338 Manufacturing jobs

Renaissance LLC All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or other legally protected status. Overview The Process Mechanic- Electromechanical will perform activities including, but are not limited to mechanical, electrical, pneumatic, and troubleshooting and repair of packaging and production machines while following FDA regulations, cGMPs, OSHA requirements, company practices and company policies. This position may also include light facilities maintenance. This is a 3rd shift position. Responsibilities • Perform Line change over, set-up, start-up, including vision system training and data collection • Identify parts needed for repairs using parts manual for specific equipment and will assemble requisition for supervisor to order parts. • Responsible for on-going preventative maintenance of machinery or equipment • Required skills include, but are not limited to, mechanical, electrical, pneumatic, and troubleshooting and repair of packaging and production machines. • Maintain, repair and troubleshoot electronics on all production equipment on the sterile filling and packaging lines to minimize production downtime. • Use computer and logic controllers to perform system analysis of equipment. • Troubleshoot and repairs logic controls/PLC, steam regulators, steam traps, steam strainers, steam valves, temperature control loops associated with autoclaves, tunnels, ovens. • Troubleshoot vision systems and automated weight checkers • Fabricate and install simple control systems to enhance line performance. • Perform changeover of packaging line equipment from one size and product to another accurately documenting the activities in accordance with procedures. • Ability to be a team player; works cooperatively with others to solve problems and proactively helps others when assistance is needed. • Experience in FDA regulated environment • Shift flexibility per business needs, and willingness to work overtime • Demonstrated ability to be flexible and open to change, self-directed, motivated, and task oriented • Make effective decisions and take action based on deductive reasoning and potential product impact. • Identify improvement opportunities in given processes / procedures • Possess strong team skills with the ability to promote clear and thorough communication both written and oral as well as through electronic means. • Must be able to be gowned qualified and maintain gowning status Qualifications High school degree, with a Minimum of 5 years of relevant mechanical experience; or equivalent combination of advanced education and experience. Experience in an aseptic/pharmaceutical packaging environment preferred. PI119423693

Renaissance LLC All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or other legally protected status. Overview This is an entry level position to the Compounding Department with emphasis on ensuring that equipment used to process aseptic and non-aseptic products has been cleaned, sanitized or sterilized, as required by specific documentation or procedures. This entails performing automated and manual equipment cleaning prior to sterilization, placing cleaned equipment into autoclaves, starting and monitoring autoclaves, unloading equipment from autoclaves, and delivering equipment to areas of use. Perform Clean-In-place (CIP) and Steam-In-Place (SIP) functions as required by specific documentation or procedures. Maintain work area and equipment on a daily basis to ensure compliance. Work area is maintained at level to sustain organization of supplies and equipment. Area is kept clean and sanitized as required by current and applicable procedures. Equipment is kept in an organized and compliant manor. Introduction to compounding functions as deemed necessary by operations management and functions where qualified to perform. Responsibilities Follow manufacturing procedures specific to the task being performed. Support to compounding functions as deemed necessary by operations management and functions where qualified to perform. Support may include active batching functions. Operation of processing equipment, and the execution of manual and automated cleaning, sanitizing, and sterilization of tanks and equipment. Perform integrity testing of filters using automated filter integrity test equipment. Able to follow detailed diagrams and written instructions to assemble or disassemble equipment, configure equipment to be washed, configure equipment to be autoclaved. Show progression in competency in all aspects of the position. Demonstrate aptitude and capability to perform multiple tasks at the same time. Able to successfully pass sterile gowning qualification within a 1 month time limit. Perform environmental monitoring at grade level C and D room classifications Utilize knowledge to actively demonstrate process trouble-shooting capabilities whenever possible. Ability to maneuver drums and equipment in excess of 50 lbs and the capability to lift weights up to 50 lbs. Maintain accurate and complete documentation in fulfillment of all duties. Understand and comply with current SOP and GMP requirements relevant to the position. Maintain professional, courteous, and effective communication with all co-workers, customers, and contractors in the execution of all job functions. Perform job responsibilities in a safe and efficient manner, maintaining a clean work environment. Assist supervisors and process manager in all other duties as assigned. Proper use of personal protective equipment at all times is required. Perform routine maintenance on process equipment. Perform area cleaning to maintain compliance using phenolic cleaners and sporicidal agent. A full face respirator or PAPR will be required to be worn for this position. Review MBRs throughout process to assure compliance to good documentation practices. Be available for unscheduled and scheduled overtime throughout the work week and weekend when requested. Qualifications A minimum of 1-3 years of relevant experience in the pharmaceutical industry; laboratory experience at the secondary education level. Aseptic manufacturing experience preferred. PI119423689

Renaissance LLC All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or other legally protected status. Overview The Compounder's primary responsibility is for the execution of bulk product batch processing, inclusive of all process related and administrative activities, as well as Equipment Preparation activities as declared in Compounder 1. Responsibilities Follow manufacturing procedures to process bulk product. Batches to be made right the first time. Follow manufacturing procedures specific to the task being performed. Perform compounding functions as deemed necessary by operations management and functions where qualified to perform. Operation of processing equipment, and the execution of manual and automated cleaning, sanitizing, and sterilization of tanks and equipment. Perform integrity testing of filters using automated filter integrity test equipment. Able to follow detailed diagrams and written instructions to assemble or disassemble equipment, configure equipment to be washed, configure equipment to be autoclaved. Show progression in competency in all aspects of the position. Demonstrate aptitude and capability to perform multiple tasks at the same time. Able to successfully pass sterile gowning qualification within a 1 month time limit. Aptitude to perform EM monitoring and testing of grade C and D clean rooms Utilize knowledge to actively demonstrate process trouble-shooting capabilities whenever possible. Ability to maneuver drums and equipment in excess of 50 lbs and the capability to lift weights up to 50 lbs. Maintain accurate and complete documentation in fulfillment of all duties. Understand and comply with current SOP and GMP requirements relevant to the position. Maintain professional, courteous, and effective communication with all co-workers, customers, and contractors in the execution of all job functions. Perform job responsibilities in a safe and efficient manner, maintaining a clean work environment. Assist supervisors and process manager in all other duties as assigned. Proper use of personal protective equipment at all times is required. Perform routine maintenance on process equipment. Perform area cleaning to maintain compliance using phenolic cleaners and sporicidal agent. A full face respirator or PAPR will be required to be worn for this position. Review MBRs throughout process to assure compliance to good documentation practices. Qualifications EDUCATION: High school diploma or general education degree (GED) required. EXPERIENCE: A minimum of 1-3 years of relevant experience in the pharmaceutical industry; laboratory experience at the secondary education level. Aseptic manufacturing experience preferred. PI119423691

Renaissance LLC All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or other legally protected status. Overview Entry level position to Compounding Department with emphasis on ensuring that equipment used to process aseptic and non-aseptic products has been cleaned, sanitized or sterilized, as required by specific documentation or procedures. This entails performing automated and manual equipment cleaning prior to sterilization, placing cleaned equipment into autoclaves, starting and monitoring autoclaves, unloading equipment from autoclaves, and delivering equipment to areas of use. This is a 2nd shift position. Responsibilities Follow manufacturing procedures specific to the task being performed. Support to compounding functions as deemed necessary by operations management and functions where qualified to perform. Support may include active batching functions. Operation of processing equipment, and the execution of manual and automated cleaning, sanitizing, and sterilization of tanks and equipment. Perform integrity testing of filters using automated filter integrity test equipment. Able to follow detailed diagrams and written instructions to assemble or disassemble equipment, configure equipment to be washed, configure equipment to be autoclaved. Show progression in competency in all aspects of the position. Demonstrate aptitude and capability to perform multiple tasks at the same time. Able to successfully pass sterile gowning qualification within a 1 month time limit. Perform environmental monitoring at grade level C and D room classifications Utilize knowledge to actively demonstrate process trouble-shooting capabilities whenever possible. Ability to maneuver drums and equipment in excess of 50 lbs and the capability to lift weights up to 50 lbs. Maintain accurate and complete documentation in fulfillment of all duties. Understand and comply with current SOP and GMP requirements relevant to the position. Maintain professional, courteous, and effective communication with all co-workers, customers, and contractors in the execution of all job functions. Perform job responsibilities in a safe and efficient manner, maintaining a clean work environment. Assist supervisors and process manager in all other duties as assigned. Proper use of personal protective equipment at all times is required. Perform routine maintenance on process equipment. Perform area cleaning to maintain compliance using phenolic cleaners and sporicidal agent. A full face respirator or PAPR will be required to be worn for this position. Review MBRs throughout process to assure compliance to good documentation practices. Be available for unscheduled and scheduled overtime throughout the work week and weekend when requested. Qualifications EDUCATION: High school diploma or general education degree (GED) required. EXPERIENCE: A minimum of 1-3 years of relevant experience in the pharmaceutical industry; laboratory experience at the secondary education level. Aseptic manufacturing experience preferred. PI119423687

Renaissance LLC All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or other legally protected status. Overview The Director of MS&T is responsible for development, scale up, and transfer of production processes into commercial manufacturing. This is a salaried position and exempt from overtime pay. Responsibilities • Responsible for developing new production processes including the establishment of batch size, equipment selection, determining critical process parameters, and execution of engineering batches. • Responsible for tech transfer of existing processes into Manufacturing. • Responsible for troubleshooting and process improvement for existing commercial products. • Partners with Product Development, Manufacturing and Validation to ensure a robust New Product Development Lifecycle. • Ensures that all safety requirements are understood and followed. • Ensures that all operations are compliant with current Good Manufacturing Practices. • Ensures that all operations are compliant with DEA and other regulatory requirements. • Develops future leaders, Supervisors and Managers with a focus on accountability and servant leadership. • Ensures appropriate training is available to all team members. • Partners with the Director of Operational Excellence to drive a culture of continuous improvement. • Partners with the Director of Engineering to develop or acquire new automation and production technology. • Responsible for ensuring appropriate resources and outstanding execution to achieve business objectives and customer requirements. Qualifications • A minimum of 10 years of leadership in Pharmaceutical Development or Tech Transfer. • Demonstrated expertise in aseptic and injectable manufacturing. • Excellent coaching and mentoring skills. • Excellent tech writing and problem solving skills. • Masters Degree in Engineering, Chemistry, or Pharmaceutical Science; PhD or MBA Preferred. PI119423679

Fabcon Inc. Location: Mahanoy City, PA Working at Fabcon Do you want to work at the top tier pre-fabricated concrete wall manufacturing and construction company in the East Coast and Midwest? Do you see yourself at a company on the cusp of rapid growth due to creative products, lean manufacturing expertise, and market dominance? Do you dream of being on a team that values leadership development and career growth opportunities? If so, a career at Fabcon may be for you. We are the precast wall panel industry leader in the United States. Purpose/Scope: Perform production labor work necessary to assist with the manufacture of high quality concrete products including, but not limited to, wall panels, highway traffic barriers, columns, and sound walls. Essential Duties and Responsibilities: Operate jackhammer, forklift, bobcat Follow appropriate work instructions to clean and upkeep all equipment Cut and install wood block outs Set up equipment used for casting bands and finishes Proper placement of concrete on the bed to match the piece drawings Monitor bed heat at computer Lay out the bed with the proper dimensions on each piece drawing and for the overall length of the bed Set up the bed according to the specs on piece drawings including all form side reveals and bottom steel/plates Responsible for washing exposed aggregate (panels/full beds) Responsible for correct dunnage placement of finished product in yard Grind ends of panels Grind clean pallet of bed Scrape clean side forms and chamfer and oil Correctly set clamp/hook-ups to panel Dedication to safety, customer satisfaction, first time quality and efficiency Responsible for calling attention to any problems with finish Compliance to the "Fabcon Way" - "Every single day a little better than the day before" Basic Qualifications: Other Required Qualifications: Ability to read tape measure, cast book and blue prints Good communication and teamwork skills Ability to operate machinery safely Ability to work extensive overtime when required Trouble shooting skills Knowledge of concrete mixes Mathematical aptitude Preferred Qualifications: High school diploma or GED Physical Requirements: Plant/Yard: Move minimum of 50lbs., spatial awareness/depth perception, walk, climb, bend at the waist, reach, forceful use of hand tools, vocal projection Work Environment: Plant/Yard: All types of weather conditions (year-round, Mid-west and Northeast), dirt/dust, noise from heavy machinery/vehicles, vibrations from machinery and vehicles, loud noises, little to no climate control, varying amounts of light, stairs, narrow walkways Must be legally authorized to work in country of employment without sponsorship for employment visa status (e.g., H1B status). Affirmative Action/Equal Opportunity Employer Fabcon is an Affirmative Action/Equal Opportunity Employer. We welcome job applications from qualified individuals without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, ancestry, family care status, veteran status, marital status, or any other lawfully protected status. Minorities, women, disabled persons, and veterans are encouraged to apply. If you need a reasonable accommodation to complete the application process, please contact our Human Resources Department. Qualified applicants are subject to pre-employment drug testing and background check upon receipt of conditional job offers. Our Drug Free Workplace Policy is available for inspection in the Human Resources office in Minnesota or our plant locations in Ohio, Kansas and Pennsylvania during normal business hours. We participate in E-Verify and if you are hired, we will provide the Social Security Administration (SSA) and, if necessary, the Department of Homeland Security (DHS), with information from your Form I-9 to confirm work authorization. If the government cannot confirm that you are authorized to work, we are required to provide you with written instructions and an opportunity to contact DHS and/or the SSA before taking adverse action against you. Please refer to the posters on our website or DHS for more information on E-verify PI119422580

Advanced Drainage Systems EEO Statement: Advanced Drainage Systems is proud to be an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. Line Operator US-OH-Napoleon Job ID: 2020-7075 Type: Regular Full-Time # of Openings: 1 Category: Manufacturing Advanced Drainage Systems Overview Headquartered in Hilliard Ohio, Advanced Drainage Systems, Inc (ADS) is the leading manufacturer of high performance thermoplastic corrugated pipe, providing a comprehensive suite of water management products and drainage solutions. Our innovative products and superior drainage solutions are used across a broad range of end markets and applications, including residential, non-residential, agriculture and infrastructure applications. We have established a leading position in many of these end markets by leveraging our national sales and distribution platform, overall product breadth and scale, and our manufacturing excellence. Founded in 1966, we operate a global network of 3,700 employees, 63 manufacturing plants and 31 distribution centers. In July, 2014 we became a public company traded on the NYSE®. To enable our continued growth, we are looking to add top talent to our dynamic organization. Responsibilities A Line Operator is responsible for performing and maintaining the daily activities associated with a production line. This includes housekeeping, safety, quality, maintaining production efficiencies, repair and maintenance and minimizing downtime. This position requires the flexibility to work 40+ hours per week and weekends as required. Ability to work varying shifts is also required due to equipment changeovers. A Line Operator reports directly to the shift Production Supervisor. The responsibilities of this position include, but are not limited to: Maintaining a safe work environment through practicing proper PPE and housekeeping compliance. Immediately communicate unsafe conditions, acts or injuries to the Production Supervisor Practice proper forklift operation and preventive maintenance. Completion of shift production and reporting paperwork. Meet ADS and AASHTO quality specifications for all products produced. Adhere to ADS product sampling schedule. Assist with Preventative Maintenance program as required Meet or exceed standard production efficiencies on all production lines. Maintain ability to operate various production lines and process effectively, earn certifications Maintain and build job skills through company training programs. Troubleshoot process and mechanical problems and perform repairs and adjustments to meet production needs as required. Perform tooling changeovers in an efficient manner Meet wired plant compliance metrics Job Skills: This position should possess the following skills/knowledge: Mechanical troubleshooting and repair abilities. Basic computer skills. Analytical thinking and problem solving skills Ability to operate heavy machinery, i.e. forklifts, in a safe manner Reading and Writing skills Self-motivated Educational Requirements: High School Diploma or equivalent. Preferred Experience: Previous manufacturing machine operation or extrusion experience 1-2 years experience as ADS Down Stream Technician Physical Requirements: Ability to perform physical labor for extended periods of time in temperature extremes. Position requires full range of body motion including twisting, bending, reaching, squatting and ability to mount/dismount industrial equipment and vehicles. Ability to stand and be mobile for a minimum of 8 continuous hours. Ability to use hands, arms and legs to physically handle and transport finished goods. PI119414313

EIS Legacy, LLC All qualified applicants will receive consideration for employment without regard to race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or other legally protected status. About Us EIS is a leading North American distributor of process materials, production supplies, specialty wire and cable and value-added fabricated parts for the electrical OEM, motor repair and assembly markets. Our culture is highly innovative, collaborative and focused on building and maintaining relationships that allow us to surpass our customers’ expectations. We embrace the qualities that make each of our team members unique and develop each other’s skillsets so that together we can be stronger than the sum of our parts. Fabrico's services include product engineering, material sourcing, prototyping, converting, laminating, digital printing, die-cutting, water jet and laser cutting, assembly and performance packaging. And Fabrico's advanced assembly capabilities apply design-for-manufacturing principles to complex, high-value projects in electronics, medical, military and defense and more. Job Description The Production Supervisor schedules, effectively delegates, and manages hourly employees to efficiently meet production requierements for multiple operations in a fast-paced work environment. Essential Functio ns: Manage staff to ensure they are productive and working towards client satisfaction Making quick decisions and changing plans/schedules to meet customer requirements Understanding and involved in 5S, Lean, and Kaizen events Demonstrate strong leadership and employee motivational skills Responsible for resolving HR issues, employee reviews and employee record keeping Have verbal and written communications with all levels of the organization Need ability to recognize opportunities and improve processes to increase efficiency Use and understand SAP for systems and reporting Use of MS Office components as a tool and for presentations Understanding of work standards Qualification Associates or Technical Degree preferred 1-3 yrs. Production experience – Supervisor or Lead position preferred Excellent communication and relationship building skills Excellent analytical skills Strong verbal and written skills Able to work in a team environment and fulfilling objectives with minimum direct supervision This job description is not intended to be an exhaustive list of all requirements and responsibilities and as such, is subject to change without notice based on the needs of the business and/or department. PI119413803

Computer Aid, Inc It is the policy of Computer Aid, Inc.(CAI) not to discriminate against any employee or applicant for employment because of race, color, religion, sex, sexual orientation, gender identity, national origin, age, marital status, genetic information, disability or because he or she is a protected veteran. It is also the policy of CAI to take affirmative action to employ and to advance in employment, all persons regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, age, marital status, genetic information, disability or protected veteran status, and to base all employment decisions only on valid job requirements. This policy shall apply to all employment actions, including but not limited to recruitment, hiring, upgrading, promotion, transfer, demotion, layoff, recall, termination, rates of pay or other forms of compensation and selection for training, including apprenticeship, at all levels of employment. Employees and applicants of CAI will not be subject to harassment on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, age, marital status, genetic information, disability or because he or she is a protected veteran. Additionally, retaliation, including intimidation, threats, or coercion, because an employee or applicant has objected to discrimination, engaged or may engage in filing a complaint, assisted in a review, investigation, or hearing or have otherwise sought to obtain their legal rights under any Federal, State, or local EEO law is prohibited. Ref No: 20-00452 Location: Baltimore,Maryland Job Profile Summary: The main function of a Production Analyst is to perform the analysis, design, implementation, modification, and daily functional support of all applications. Duties & Responsibilities: Works with key stakeholders within all business functions to align technology solutions with business strategies Gathers requirements from business units and translate those to programmers and developers Prepares cost-benefit and return-on-investment analyses to aid in decisions on system implementation Demonstrates an informed knowledge of business functions to resolve problems and capitalize on improvement opportunities Supports one or more highly complex business processes Works on multiple projects as a project team member Serves as a liaison between the business community and the IT organization in order to provide technical solutions to meet user needs Qualifications: Bachelor's degree in a technical field such as computer science, computer engineering or related field required. MBA or other related advanced degree preferred 2-4 years experience required Basic knowledge of programming languages in order to comprehend reading code and basic functions Ability to create business solutions that increase competitive advantage Ability to exercise good judgment in selecting methods and techniques for obtaining solutions Project management skills in order to handle diverse projects, often times simultaneously, and meet aggressive deadlines Ability to solve technical problems/ processes and understand complex details Ability to increase operating efficiency with produce high quality technical solutions A high level of interpersonal and verbal communication skills necessary to relate to other people at their systems knowledge level Ability to analyze complex situations and problems and do the necessary research using multiple sources of information to arrive at innovative solutions Physical Demands: Ability to safely and successfully perform the essential job functions consistent with the ADA and other federal, state and local standards Sedentary work that involves sitting or remaining stationary most of the time with occasional need to move around the office to attend meetings, etc. Ability to conduct repetitive tasks on a computer, utilizing a mouse, keyboard and monitor If you are interested in this position, please apply using the "Apply" option. If you have questions, or would like to speak with a Recruiter directly, send an email to the contact person below and note the job identification number in the subject line. Kassandra Mantz Technical Recruiter 610.530.5153 kassandra.mantz@cai.io www.cai.io PI119412908

Amgen Job ID: R-96822 Location: West Greenwich, RI, US 02817 Amgen Rhode Island is one of the premier biologics drug substance manufacturing sites in the world with a long history of operational excellence and highly successful commercial and clinical operations. Solutions Prep is looking for an Associate Manufacturing. The successful incumbent will join a day shift team working a 12-hour shift. The shift pattern will be 7AM-7PM with a two-week rotation covering 7 days per week. The rotating shift offers several benefits, with an average of 14 days on shift per month with every other weekend off. In addition, any Sundays worked receive Premium pay. Under general supervision the Associate Manufacturing will perform batching and transfer of Buffers and Medias in appropriate areas according to Standard Operating Procedures (SOPs). Associate will be responsible for good GMP practices, as well as follow and document in batch records. Associate will perform and monitor critical processes, execute routine validation protocols, and regularly draft and revise documents such as Manufacturing Procedures, SOPs, and technical reports. Associate will work within teams and adhere to the floor operating principles. Associate will also perform basic troubleshooting and assist in the review of documentation for assigned functions. In addition, Associate may identify, recommend, and implement improvements related to routine functions. Basic Qualifications : Bachelor's degree OR Associate's degree and 4 years of Manufacturing or Operations experience OR High School diploma/GED and 6 years of Manufacturing or Operations experience. Preferred Qualifications : Bachelor's degree in Science or Engineering Knowledge of large-scale biotechnology operations such as purification, cell culture, aseptic processing, etc. Knowledge of Single-use-Systems CFR and Regulatory knowledge Mechanical ability/expertise Basic statistical mathematical skills Ability to interpret and apply GMP knowledge Understanding of analytical methods for manufacturing area Demonstrated technical writing capability Able to demonstrate project management skills and presentation skills Ability to understand, apply and evaluate basic chemistry, biology and physical principles Basic troubleshooting skills on production equipment Experience with Delta V Experience with lab equipment/testing Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential Join Us If you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen. Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. PI119411805

Amgen Job ID: R-96343 Location: Juncos, PR, US 00777 Are you looking for a meaningful new opportunity to test and growth your technical skills? We have an immediate need for a various Engineer to join AML's Inspection & Packaging a Non Standard Shift Organization. This is an outstanding opportunity to seek a variety of challenges and responsibilities in support to our manufacturing facility at Amgen Manufacturing Limited in Juncos, Puerto Rico. The Role The Line Owner/System Owner will work under general supervision, owns all the technical aspects in a manufacturing line. The processes were the SO/LO Engineer shall be familiar with are: characterization of process optimization strategies and/or troubleshooting of operational issues in the packaging operations, manufacturing, pilot technologies or capital projects. Applies basic engineering principles to the design and implementation of system modifications, experiments and/or capital projects. Organizes, analyzes and presents interpretation of results for operational issues or engineering projects of minor scope and complexity. As a technical resource of an area, Engineers shall interact and provide direction to technical resources such as Mechanics, Automation Techs and IS teams. At the same time, the System Owner/Line Owner Engineer shall be able to define designs requirement to the service providers to fulfill area technical and equipment needs. Various positions available SPECIFIC RESPONSIBILITIES INCLUDE BUT ARE NOT LIMITED TO: Available for Non Standard Shift Provide solutions to a variety of technical problems of moderate scope and complexity. Under general supervision will evaluate, select and apply standard engineering techniques and procedures. Assistance given for unusual problems. Perform assignments that have clear and specific objectives and require investigation of limited number of variables. Initiate and complete routine technical tasks. Operations Engineering: Function as a technical specialist to equipment or systems regarding troubleshooting operations. Frequently become actively involved in daily operations when required to meet schedules or to resolve complex problems. Routinely audit the operational performance and regulatory compliance of a moderate number of equipment items or systems of large complexity. Work with research, manufacturing, maintenance, process development, utilities, facilities, quality assurance and/or validation departments in developing requirements and recommendations for system modifications. Design Engineering: Work under the direct supervision of project managers to complete design, engineering, and construction projects within schedule and budget constraints. Work with consultants, architects and engineering firms on development of standard design documents. Obtain and critique quotes for equipment modifications or installations. Generate rudimentary project cost estimates and schedules. Basic education & experience Master's degree in Engineering or Bachelor's degree in Engineering & 2 years of Packaging manufacturing or Automation controls experience in pharmaceutical, medical device or biotechnology industry Beyond that, the preferred qualifications are: Availability for Non Standard Shifts Written and verbal communication skills in English and Spanish Working knowledge of pharmaceutical/biotech processes Familiarity with validation processes for Packaging areas Familiarity with serialization process and networking Familiarity with documentation in a highly regulated environment Ability to operate specialized equipment, tools and computers as appropriate. Ability to interpret and apply GMPs. Ability to apply engineering science to production. Able to develop solutions to routine technical problems of limited scope Comprehensive understanding protocol execution requirements. Proven skills in the following areas: Problem solving and applied engineering. Basic technical report writing on English and Spanish Verbal communication on English and Spanish Basic technical presentations Personal Organization Protocol and script testing Writing Dealing with and managing change Packaging Equipment Technical knowledge Analytical Problem Solving Computer Literacy The benefits Our broad approach is one of the reasons why we are regularly recognized as a 'Best Place To Work'. We offer a superior benefits package that includes an award-winning retirement and stock plan. And between the paid time off, and wellness program - and on-site child care and fitness facilities - you will find us Our culture is what makes Amgen a special place to work. We have a powerful shared purpose around our mission - to serve patients. We respect one another, recognize contributions, and have embedded collaboration, trust, empowerment and inclusion in all that we do. We equip all our staff members to live well-rounded, healthy lives. Most recently, Amgen added benefits for transgender employees and continues to pride itself on industry-leading, family-friendly offerings for families of all compositions. Amgen focuses on areas of high unmet medical need and uses its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. Join Us If you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen. Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. PI119411900

Motion Industries We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. Category: Warehouse Job Id: 275533 Brand: Motion Industries Location: Cincinnati, OH Major Market: OH - Cincinnati Date Posted: March 28, 2020 Apache, a division of Motion Industries Apache is widely recognized across the US for the variety and quality of our hose, belting, custom fabrications, on-site belting services, and consumer products. Specializing in the value-added fabrication of belt, hose, and cut & molded products, Apache products are used across a wide array of industries and applications. We strive to provide a workplace built on teamwork, comprised of team players who take pride in a job well done while consistently achieving results that exceed our customer's expectations. Essential Duties and Responsibilities Maintain a safe, organized, respectful, productive work environment that promotes teamwork. Ensure production and customer satisfaction objectives are achieved by your team (e. g., shipping product on time, surpassing customer-defined quality levels). Utilize the ERP, warehouse management and scheduling systems proficiently. Create, adjust and communicate production schedules. Be actively engaged in managing performance and developing reports by regularly communicating standards and expectations and holding the team accountable. Discuss business unit needs (e.g., equipment, supplies, and labor) and Improvement Projects with Operations Management and/or Technical Services. Create and/or improve department processes by utilizing lean manufacturing tools and methods. Stay current on area metrics and trends driving them. Respond to emergencies as a trained First Responder Attend work regularly and predictably and uphold Company values in all work aspects. Requirements High school diploma plus at least one of the following 3 years of experience in a supervisory position or at least 3 years of experience in conveyor belting or rubber product fabrication or hose assembly or Equivalent combination of education and work experience. Post High school education is highly preferred. Strong leadership, decision making and problem solving skills Strong Interpersonal skills including speaking and listening skills for understanding Ability to read and interpret documents Ability to work under pressure and meet tight deadlines Ability to motivate and develop others as well as handle conflict while maintaining self-control Ability to bend, reach, push and pull, and lift and/or move 10- 50 pounds This job description is intended to convey information essential to understanding the scope of the job and the general nature and level of work performed by job holders within this job. But, this job description is not intended to be an exhaustive list of qualifications, skills, efforts, duties, responsibilities or working conditions associated with the position. Apache Inc. reserves the right to change, amend, add, delete and otherwise assign any and all duties, responsibilities and position titles as it deems necessary to meet the needs of the business. GPC believes the fair and equitable treatment of employees, customers, suppliers and other persons is critical to fulfilling its vision and goals. GPC conducts its business without regard to sex, race, creed, color, religion, marital status, national origin, age, pregnancy, sexual orientation, gender identity, genetic information, disability, military status, status as a veteran, or any other protected characteristic. GPC's policy is to recruit, hire, train, promote, assign, transfer and terminate employees based on their own ability, achievement, experience and conduct and other legitimate business reasons. PI119411364

Motion Industries We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability status, protected veteran status, or any other characteristic protected by law. Category: Inventory Job Id: 275407 Brand: Motion Industries Location: Danvers, MA Major Market: MA - All Locations Date Posted: March 26, 2020 Axis New England part of the Automation Solutions Group of Motion Industries located in Danvers, MA. We have expertise providing robotic and motion control solutions for factory automation. We service the biomedical, semiconductor, electronic assembly, defense, and general-purpose automation markets. We are currently seeking to fill a Production Scheduler. This individual will be responsible for coordinating material requirements for all Production and systems builds. This includes reviewing reports and other system information to determine and mitigate late deliveries from vendors to ensure material availability for the production group. The position would also include limited buying responsibilities associated with systems builds, RMAs and general consumables used in production. List of Responsibilities: Continuously review of material supply and demand reports to ensure material availability for open work orders Work with warehouse personnel & production manager to determine ready to build work orders Report capacity and material issues to Production Manager Production completion of finished goods into inventory to fulfill open orders Review expected delivery reports and review with Vendors and Internal buyers order status Drive JIT initiatives to maximize warehouse space while meeting material requirements Work with commodity vendors to drive down cost of parts Required Skills: Comfortable in Microsoft office suite Strong written and verbal communication skills Experience working with internal and external stakeholders Minimum of 3-5 years related experience required Experience working in Microsoft Dynamics SL and Sharepoint a plus GPC believes the fair and equitable treatment of employees, customers, suppliers and other persons is critical to fulfilling its vision and goals. GPC conducts its business without regard to sex, race, creed, color, religion, marital status, national origin, age, pregnancy, sexual orientation, gender identity, genetic information, disability, military status, status as a veteran, or any other protected characteristic. GPC's policy is to recruit, hire, train, promote, assign, transfer and terminate employees based on their own ability, achievement, experience and conduct and other legitimate business reasons. PI119411507

Amgen Job ID: R-97015 Location: West Greenwich, RI, US 02817 The Amgen Rhode Island Pilot Plant is seeking a Front Line Manager (FLM) to lead a team of staff responsible for daily cell culture and purification bioprocessing operations. This position will execute a variety of production-related operations, including but not limited to: equipment set up, operational execution, detailed scheduling, leading new product introductions and managing staff. Additionally, the FLM is accountable for ensuring a premier safety culture, continuously seeking to implement LEAN concepts for the improvement of efficiency and productivity as well as ensuring data integrity. The ARI Pilot Plant is responsible for all aspects of production planning and execution to support pipeline development runs for material and data generation, life cycle management to support commercial process optimization and tech transfer of new programs being introduced into AR-5 and AR-30. The Pilot Plant's capabilities include a mix of Single Use and Stainless Steel bioreactors up to 500L scale and full purification to generate drug substance for non-GMP use. The equipment is highly automated via Delta V distributed control system and GE Unicorn execution software. The operations are driven by Standard Operating Procedures (SOPs) and data recorded in electronic batch records. The environment is challenging, fast-paced and ever-changing with varying degrees of process definition, but very rewarding for those that like hands-on science and want to make process improvements in a development space. Basic Qualifications: Doctorate OR Master's degree and 3 years of Manufacturing/ Operations experience Or Bachelor's degree and 5 years of Manufacturing / Operations experience Or Associate's degree and 10 years of Manufacturing/Operations experience Or High school diploma / GED and 12 years of Manufacturing/Operations experience And Previous managerial experience directly managing people and/or experience leading teams, projects, programs or directing the allocation of resources Preferred Qualifications Solid knowledge of upstream and/or downstream, as well as a general knowledge of the associated analytical, and solution preparation techniques (media and buffer) Upbeat and technically-minded, with strong interpersonal and organizational skills Demonstrate the ability to learn new systems and applications, and various purification techniques Work effectively in team and/or project environments; possess strong math and computer skills, as well as the ability to apply science-based thinking to practical applications Experience in cGMP production environment Bachelor's degree in Biology, Chemistry, or Chemical/Biological Engineering (or other relevant field) and 1 or more years of managerial experience in Life Sciences field Our culture is what makes Amgen a special place to work. We have a powerful shared purpose around our mission - to serve patients. We respect one another, recognize contributions, and have embedded collaboration, trust, empowerment and inclusion in all that we do. We equip all our staff members to live well-rounded, healthy lives. Most recently, Amgen added benefits for transgender employees and continues to pride itself on industry-leading, family-friendly offerings for families of all compositions. Amgen focuses on areas of high unmet medical need and uses its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. Amgen is an Equal Opportunity employer and will consider you without regard to your race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. Join Us If you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen. Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. PI119411653

Amgen Job ID: R-96969 Location: Thousand Oaks, CA, US 91360 The Sr Associatewill assume the responsibility for investigating deviations supporting the Amgen Thousand Oaks (ATO) Manufacturing and Clinical Supply Organization, inclusive, but not limited to, Drug Substance manufacturing, Drug Product manufacturing, Device Assembly, Packaging, Labeling, Supply Chain, and Warehouse Operations. The individual is responsible for owing and leading the investigation into deviations which includes determining the scope, product impact, root cause, andidentifyingcorrective/preventative actions (CAPAs) to eliminate the root cause. This individual will play an integral role collaborating within a cross-functional team that includes Manufacturing, Quality, Process Engineering, Process Development, Analytical Sciences, Quality Control, Supply Chain, and Regulatory Affairs. The individual will be responsible for: Own deviation records and investigation Own investigation report to support the investigation Ensuring records are comprehensive and compliant per procedures Timely closure of records in relation to procedural guidance and/or disposition timelines Right the first time investigation reports and records Clear communication of investigations to impacted areas and leadership Presenting investigations to auditors and inspectors Basic Qualifications Master's degree OR Bachelor's degree and 2 years of Biotech/Pharma experience OR Associate's degree and 6 years of Biotech/Pharma experience OR High school diploma / GED and 8 years of Biotech/Pharma experience Preferred Qualifications: Bachelor's or Master's degree in Chemical Engineering, Mechanical Engineering, the Physical Sciences, or a related field 4years of bio-pharmaceutical experience within bio-pharmaceuticals manufacturing facility Analytically assess information and apply deductive reasoning Clear and concise technical writing Leadership skills to drive teams during the investigation Ability to clearly communicate status of the investigation to leadership and to auditors and inspectors Project management skills and being well organized Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. Join Us If you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen. Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. PI119411672

Amgen Job ID: R-97090 Location: West Greenwich, RI, US 02817 Amgen Rhode Island is one of the premier biologics drug substance manufacturing sites in the world with a long history of operational excellence and highly successful commercial and clinical operations. Solutions Prep is looking for a Manufacturing Associate. The successful incumbent will join a night shift team working a 12-hour shift (D shift). The shift pattern will be 7PM-7AM with a two-week rotation covering 7 days per week. Under general supervision the Manufacturing Associate will perform batching and transfer of Buffers and Medias in appropriate areas according to Standard Operating Procedures (SOPs). Associate will comprehend and apply good GMP practices, as well asfollow and document in batch records. Associate will perform and monitor critical processes, execute routine validation protocols, and regularly draft and revise documents such as Manufacturing Procedures, SOPs, and technical reports. Associate will work within teams and adhere to the floor operating principles. Associate will also perform basic troubleshooting and assist in the review of documentation for assigned functions. In addition, Associate may identify, recommend, and implement improvements related to routine functions. Basic Qualifications : Bachelor's degree OR Associate's degree and 4 years of Manufacturing or Operations experience OR High School diploma/GED and 6 years of Manufacturing or Operations experience. Preferred Qualifications : Bachelor's degree in Science or Engineering Knowledge of large-scale biotechnology operations such as purification, cell culture, aseptic processing, etc. Knowledge of Single-use-Systems CFR and Regulatory knowledge Mechanical ability/expertise Basic statistical mathematical skills Ability to interpret and apply GMP knowledge Understanding of analytical methods for manufacturing area Demonstrated technical writing capability Able to demonstrate project management skills and presentation skills Ability to understand, apply and evaluate basic chemistry, biology and physical principles Basic troubleshooting skills on production equipment Experience with Delta V Experience with lab equipment/testing Amgen is committed to unlocking the potential of biology for patients suffering from serious illnesses by discovering, developing, manufacturing and delivering innovative human therapeutics. This approach begins by using tools like advanced human genetics to unravel the complexities of disease and understand the fundamentals of human biology. Amgen focuses on areas of high unmet medical need and leverages its expertise to strive for solutions that improve health outcomes and dramatically improve people's lives. A biotechnology pioneer since 1980, Amgen has grown to be one of the world's leading independent biotechnology companies, has reached millions of patients around the world and is developing a pipeline of medicines with breakaway potential. Join Us If you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen. Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. PI119411710

Amgen Job ID: R-97113 Location: Thousand Oaks, CA, US 91360 This Specialist Manufacturing position will support the drug substance manufacturing operations in Thousand Oaks, CA. This role requires an experienced and well qualified individual to focus primarily on Quality Systems record ownership (Change Control, deviation, CAPA), in addition to managing projects. This individual will play a key role in managing multiple Change Records with varying complexity. Also the staff member will be leading the investigation of nonconforming events related to the manufacturing operations. The candidate will lead root cause analysis, definition of event scope and lot-tying strategy, assessment of product impact and development and coordination of corrective actions to prevent recurrence. The role may also require management of document revisions, as necessary. Under general direction, assume primary responsibility for execution of the Change Control/deviation/CAPA process in manufacturing. The job will also require trending of nonconforming events to identify systemic issues that need improvement, and tracking and reporting key quality systems metrics to management. Apply process, operational, scientific expertise, compliance knowledge, analytical and troubleshooting skills to support manufacturing operations. Candidates should have good project management skills. Job Scope and responsibilities: Assume ownership of critical Change Record, and nonconforming event investigations within Amgen's Quality Management System (Change Control/ Deviation /CAPA) using the Trackwise database. Represent the manufacturing support team internally within the plant and externally at the site level. Serve as department subject matter expert for the Change Control/ deviation/CAPA process, including metrics reporting and trending. Prepare, coordinate, and present complex information at cross-functional team meetings, teleconferences, various governance meetings, and management review. Ensure good progress, participation, communication and timely outcomes through cross functional team members who support MFG Apply scientific reasoning and troubleshooting techniques to solve complex process, compliance, and analytical problems in order to ensure MFG production success. This may include support of any of the following; process improvements, operational excellence initiatives, project management, and new product introductions Will work with other functions (Quality, Engineering, Automation, Facilities, Environmental Health & Safety, Process Development, etc.) in troubleshooting nonconforming events, conducting problem solving and RCAs, owning major deviations, complex change records, and developing CAPAs to prevent recurrence. Collaborate with Regulatory and Quality partners to manage records and respond to regulatory questions and/or audit findings. Basic Qualifications: Doctorate degree OR Master's degree & 3 years of manufacturing and operations experience OR Bachelor's degree & 5 years of manufacturing and operations experience OR Associate's degree & 10 years of manufacturing and operations experience OR High school diploma / GED & 12 years of manufacturing and operations experience Preferred Qualifications: Advanced Degree in Engineering or Life Sciences Experience in GMP Technical Support roles, GMP operations, Engineering, or Process Development. Technical knowledge of drug substance processing and broad understanding of related disciplinary areas Demonstrated project management abilities Experience in contamination investigations, recovery, and prevention including aseptic technique and clean room behavior. Ability to organize, analyze, and interprets technical data through trend analysis. Ability to effectively communicate complex technical information with internal and external colleagues of varying organizational levels in both presentation and technical writing forms Significant experience with Quality Systems Record ownership Ability to drive results through leadership of cross-functional teams. Join Us If you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen. Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. PI119411767

Amgen Job ID: R-97099 Location: Thousand Oaks, CA, US 91360 The successful candidate will direct a team of manufacturing associates responsible for manufacture of GMP DSI/DS in both stainless and single-use equipment. The manager will foster a safe and compliant production environment through structured on-the-floor presence. The incumbent will also be an active participant and role model in Lean culture and continuous improvement programs with responsibility to translate onto the manufacturing floor. The successful candidate must demonstrate strong leadership skills and technical understanding of production operations. Responsibilities include: Staff selection, training, oversight, performance evaluations, and development Daily schedule alignment Partner with QA and other groups to ensure deviations are initiated and closed within target timelines Utilize appropriate systems to perform job duties (SAP/MES, QMTS, LIMS etc.). Interact with business partners and internal/external audit teams and regulatory authorities. Identify and implement process and safety improvements. Work with business partners to support scheduling of maintenance tasks, engineering support, and quality investigations. Effectively elevate critical and impactful events to senior management. Make real-time processing decisions to support compliant and safe production. Ensure batch record review is completed accurately to support disposition timeline. Flexible work schedule, including night/graveyard shift and weekend/holiday work as decided by business needs. Basic Qualifications Doctorate degree Or Master's degree and 3 years of manufacturing or operations experience Or Bachelor's degree and 5 years of manufacturing or operations experience Or Associate's degree and 10 years of manufacturing or operations experience Or High school diploma / GED and 12 years manufacturing or operations experience Preferred Qualifications 5+ years of related manufacturing experience. 3+ years of experience as a production area Lead, Specialist or Manager Strong technical understanding of Cell Culture and Purification processes and equipment Demonstrated presentation and leadership skills Proven experience with continuous improvement methodologies Previous managerial experience directly managing people and/or experience leading teams, projects, programs or directing the allocation of resources Strong quality system and GMP knowledge Strong troubleshooting skills with laboratory and process equipment Energetic and technically-minded, with strong interpersonal and organizational skills Demonstrated ability to learn new systems and applications, and various new technologies Degree in Life Science, Chemistry or Engineering Join Us If you're seeking a career where you can truly make a difference in the lives of others, a career where you can work at the absolute forefront of biotechnology with the top minds in the field, you'll find it at Amgen. Amgen, a biotechnology pioneer, discovers, develops and delivers innovative human therapeutics. Our medicines have helped millions of patients in the fight against cancer, kidney disease, rheumatoid arthritis and other serious illnesses. As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other but compete intensely to win. Together, we live the Amgen values as we continue advancing science to serve patients. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. PI119411786

Metalcraft of Mayville Senior Safety Coordinator US-WI-Mayville Job ID: 2020-1772 Type: Regular Full-Time # of Openings: 1 Category: Manufacturing Metalcraft of Mayville, Inc. Overview The Safety Coordinator will report to the Safety Manager, providing safety, workman's compensation and environmental leadership to Metalcraft of Mayville manufacturing operations in our Mayville location, while assisting our other locations in West Bend and Beaver Dam. Responsibilities Lead plant on individual safety topics as well as train Shop Leaders in development of programs and engagement of all employees. Maintain OSHA compliance and an overall safe work environment. Manage record keeping for safety and environmental matters Handle issues related to Workers Comp to include managing to ensure employee’s receive proper medical care while at the same time managing cost of care, minimizing lost time or time away from work. Support and provide leadership for case management of injuries OSHA record keeping associated with recordable injuries. Participates in incident investigations and reviews and supports the preparation of relevant documentation using root cause methodologies. Compile and maintain safety statistics, analyze incident data for trends and prepare advisory or alert communications. Implementation and documentation of EH&S required training. Offers innovative solutions to solve difficult issues and leads employees and contractors to work in a safe team environment. Participates and/or Lead 6S Teams in developing, improving, and executing programs that align with the companies Key Performance Indicators. All other duties assigned Qualifications Proficient in Excel, Word, and PowerPoint Knowledgeable with applicable safety regulations Excellent internal and external Customer Service Skills Problem solving skills Excellent written and verbal communication skills Education and/or Experience Bachelor's degree in Safety or related field Preferred 3-5 years of Safety or Manufacturing related experience Metalcraft of Mayville is an Equal Opportunity Employer: Minorities/females/veterans/individuals with disabilities/sexual orientation/gender identity PM17 PI119399845

Metalcraft of Mayville Estimating Manager US-WI-Mayville Job ID: 2020-1790 Type: Regular Full-Time # of Openings: 1 Category: Estimating Metalcraft of Mayville, Inc. Overview Metalcraft Overview Metalcraft’s success and thriving growth is a result of our ingenuity, expertise, and exceptional people coupled with our unparalleled focus on customer service. Our foundation and culture are based upon our values of trust, safety, teamwork, responsibility, service and stewardship. It all starts with our extraordinary people and collaborative teams. Being a part of our team means you have the passion for being part of a creative team, possess a positive and professional attitude with forward thinking, all while being able to utilizing our efficient and up to date technology. Position Overview Reporting to the V.P. Of OEM Engineering, the Estimating Manager is primarily responsible for overseeing a team of Estimators and planning, coordinating and supervising the estimating process. The Estimating Manger works closely with the Sales, Manufacturing, Engineering and Finance teams to ensure quotes meet the Customers’ expectations and that they are in line with internal processes and actual production costs . Responsibilities Demonstrate leadership and team building capabilities. Coordinate the estimating program by providing technical and administrative direction to meet corporate objectives. Maintain estimating calendar and schedule to meet quoting deadlines. Work closely with Sales Managers, Purchasing and Engineering to ensure the estimating team provides timely, accurate estimates which identify accurate manufacturing labor, material and lead times. Maintain expert knowledge of plant capabilities/limitations, resources and operational procedures. Analyze process capabilities as they pertain to quote assignments. Analyze customer drawings, CAD data and technical specifications to determine scope of work. Assist with complex estimates as needed. Review the final estimate packages to ensure accuracy and completeness and to ensure quotes meet the Customers’ expectations Lead collaborative, cross functional design/cost teams. Analyze completed projects to compare estimated costs to actual costs and determine the reason for any discrepancies. Ensure this information is used in generating new price quotes. Ensure cost estimate accuracy by researching current processes and procedures on the shop floor. Conduct and organize shop floor time studies Provide improvement recommendations to cost estimating procedures to reduce future discrepancies between estimated and actual costs. Prepare special reports by collecting, analyzing, and summarizing information and trends. Quantify historical data and organize the information into patterns and trends Organize and manage a centralized cost estimating database and a formal process to support cost estimating to ensure historical data is utilized. Work with Estimators to achieve personal development and performance goals; help train new Estimators & provide input for performance evaluations. Other duties as assigned. Qualifications To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Strong leadership, motivation, and conflict resolution skills. Ability to manage and supervise employees and hold accountable to production standards and goals. Demonstrated detail orientation, self-motivation skills and ability to multi-task. Demonstrated ability to communicate effectively in both verbal and written formats. Effectively read blueprint prints. Good computer skills are also required, as well as knowledge of manufacturing reporting software. Education and/or Experience 5 years’ experience in a manufacturing environment Previous supervisory and/or estimating experience in a manufacturing environment preferred. Associate Degree in Engineering or Manufacturing related field preferred Must be proficient in reading customer blueprints Ability to review projects using Pro E and AutoView Must be proficient in all Microsoft Office products Able to interpret GD&T information and compare to process capabilities Must be a self-starter and be highly motivated Have excellent communication skills Be exceptionally organized and flexible in a fast paced environment Great attention to detail Must have an understanding of all areas in a manufacturing environment (i.e. laser, form, manual welding, robotic welding and paint) Experience with Costimator is a plus Metalcraft of Mayville is an Equal Opportunity Employer: Minorities/females/veterans/individuals with disabilities/sexual orientation/gender identity PM17 PI119399851