14 jobs found in greenwich

Amgen Job ID: R-89008 Location: West Greenwich, RI, US 02817 Do you want to help shape the future of biopharmaceutical manufacturing? We have an opening for a Senior Associate to join the Commercial Attribute Sciences group at our Rhode Island site. This is an analytical scientific position supporting late stage/ commercial manufacturing of biopharmaceutical products. The Sr. Associate is aligned with multiple functional areas and is tasked with testing, troubleshooting, and investigating. Key Responsibilities Include: Execute routine and characterization testing using multiple analytical methods and technologies to support commercial and NPI programs. Interact and collaborate with multiple functional areas in matrix environment, both at site and network levels. Interpret results, author and review technical reports and assessments. Support technology and method lifecycle management, including method transfers, qualifications, improvements, trending and remediations Support process improvements, including analytical comparability, small-scale model support Support site Forensics team in commercial manufacturing and PD investigations. Basic Qualifications: Master's degree OR Bachelor's degree and 2 years of Scientific or Operations experience Preferred Qualifications: 3+ years of scientific experience providing and driving analytical deliverables for biopharmaceutical processes and product development Expert knowledge of analytical methods/technologies used in biologics for both routine and characterization testing using one or more of the following: HPLC, CE, ELISA, and/or other techniques Understanding of product quality attributes for biologics, their control strategies, quality attribute assessments, and Quality Target Product Profile throughout the lifecycle of a product Experience working in a matrix environment Experience in data analysis, statistical analysis, method qualifications/transfers Experience in applying troubleshooting and investigation methodologies for problem solving Familiarity with biopharmaceutical manufacturing processes Familiarity with forensics analysis Familiarity with regulatory expectations related to analytical control strategies, familiar with applicable US and worldwide regulatory requirements Strong technical writing and verbal communication skills Amgen strives to serve patients by transforming the promise of science and biotechnology into therapies that have the power to restore health or save lives. In everything we do, we aim to fulfill our mission to serve patients. And every step of the way, we are guided by the values that define us. Amgen 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. PI116106424

Carrington Transaction Management Analyst - Legal, CCM US-CT-Old Greenwich Job ID: 2019-8961 Type: Regular # of Openings: 1 Category: Other Carrington Capital Management, LLC Overview FOUNDED IN 2003, Carrington has evolved from a mortgage credit asset manager into a vertically-integrated financial services company that covers virtually every aspect of the single family residential real estate transaction, including investment in U.S. real estate and mortgage markets, loan origination and servicing, asset management and property preservation, real estate sales and rental, and title and escrow services. Carrington has built the infrastructure necessary to maximize value during any market cycle. Responsibilities The Transaction Management Analyst will support the in-house legal department with general operations of residential mortgage based investment adviser’s transaction team, servicer oversight functions, and capital markets transactions. Review, revise and manage documentation related to transactions including mortgage loan acquisitions, mortgage loan servicing acquisitions and financing transactions. Maintain corporate governance related to investments; draft and maintain corporate documents. Work closely with internal and external counsel and transaction team on a variety of matters. Perform all duties in accordance with the company’s policies and procedures, all US state and federal laws and regulations, wherein the company operates. ESSENTIAL DUTIES AND RESPONSIBILITIES: Manage transaction documents for asset acquisitions and sales. Review deal documents, assess documents for accuracy and completeness, ensure all deal terms are contained in the documents, and determine when documents are ready for execution. Review and edit confidentiality agreements, bailee letters, mortgage loan purchase agreements and other various documents. Determine suitability for execution and correct any deficiencies. Review contracts for purchase/acquisition of analytics programs, or other software and services. Recommend vendor selection. Prepare and maintain execution copies of transaction documents related to deal closings. Maintain library of legal documents, ensuring compliance to corporate and regulatory standards. Complete bidder questionnaires to receive materials for potential asset sales. Act as liaison between transaction and legal teams, resolve outstanding issues. Form and maintain new corporate entities. Draft and maintain corporate documents. Other duties as assigned. Qualifications Excellent written and verbal communication skills Proficiency in Word and Excel required Strong organizational skills and time management skills to perform multiple tasks within limited time frames Ability to interact with all levels of staff, including executive management Excellent problem-solving skills Excellent document management skills Ability to independently evaluate alternatives and recommend solutions Ability to adapt quickly to change without negative impact to performance and/or productivity Ability to work independently with minimal supervision Results oriented in a deadline driven work environment Recognize core business issues and their impact on meeting strategic objectives Strong working relationships with internal and external customers EDUCATION, EXPERIENCE AND/OR LICENSES: 4 year college degree or equivalent work experience required Bachelor’s Degree preferred Document management experience required Contract analysis experience strongly preferred Experience in the mortgage industry preferred Previous experience with a Wall Street or counterparty firm preferred We are an Equal Opportunity Employer PI116072883

Carrington Accountant,Staff,I,CCM US-CT-Old Greenwich Job ID: 2019-8990 Type: Regular # of Openings: 1 Category: Accounting/Finance Carrington Capital Management, LLC Overview Carrington is a holding company whose primary businesses include asset management, mortgages, real estate transactions and real estate logistics. Collectively, the businesses are vertically- and horizontally-integrated, and provide a broad range of real estate services encompassing nearly all aspects of single family residential real estate transactions in the United States. Carrington’s international presence includes operations in the United Kingdom and Italy. Guided by a leadership team with a wealth of industry experience and guided by a consistent philosophy, Carrington maintains the necessary infrastructure to ensure stability and maximize value during any market cycle. Join us. Responsibilities Responsible for the day to day accounting and bookkeeping functions related to the asset management business and various affiliates. Performs all duties in accordance with all company guidelines and applicable federal, state and local regulations . ESSENTIAL DUTIES AND RESPONSIBILITIES: Responsible for month-end closing process including preparation of journal entries. Build and maintain supplemental schedules including depreciation and fixed assets. Manage accounts payable and accounts receivable to ensure timely payment and proper accounting treatment. Review employee expense reports and approve reimbursement requests. Create documentation surrounding accounting procedures while identifying process improvements and opportunities for increased efficiencies. Interface with various affiliates as necessary to reconcile intercompany accounts. Ability to analyze and present financial data as required via ad hoc reporting requests. Ability to expand duties to include financial forecasting and planning Perform other duties and special projects as assigned. ESSENTIAL KNOWLEDGE, SKILLS, ABILITIES, AND COMPETENCIES: Basic working knowledge of Excel Excellent communication skills both verbal and written Strong attention to detail Qualifications Bachelor’s degree in Accounting/Finance or related field One (1) to three (3) years’ experience in accounting or bookkeeping Basic proficiency in Microsoft Excel PI116072815

Amgen Job ID: R-89211 Location: West Greenwich, RI, US 02817 The Quality Assurance Specialist will be responsible for Quality Validation, PQA On the Floor and Off the Floor activities, and may include Raw Materials and Drug Substance Disposition for Quality Assurance 1st Shift/administrative shift. This position provides the opportunity to work directly with Manufacturing staff during bulk drug substance operations to facilitate real-time decision-making regarding quality requirements and deviations. This is a unique opportunity to foster a strong partnership and learning environment between Manufacturing and Quality staff. The focus of this role will be to support Quality Validation activities but may include PQA On the Floor and Off the Floor, Raw Materials and Drug Substance Disposition activities as required by the needs of the department. Amgen's Quality Assurance Shift 1/Administrative shift provides coaching, guidance and direction to Manufacturing, Quality Control, Process Development, Supply Chain and Facilities & Engineering staff regarding compliance and quality systems. Responsibilities include the following: Provide Quality oversight to ensure that operations products are manufactured, tested, stored, and distributed according to current Good Manufacturing Practices (cGMP), Good Distribution Practices (GDP) and other applicable regulations. Ensure that facilities, equipment, materials, organization, processes, procedures and products comply with cGMP practices and other applicable regulations. Quality review and approve Validation Documents including: DT, CRSIQ/OQ, RTM, FT/FTF, protocols, and reports. Perform ownership, QA review, and QA approval of cGMP processes, procedures, documents and records, including but not limited to Nonconformance, Corrective Action/Preventative Actions (CAPA), Change Control records, validations, and Raw Materials and Drug Substance documentation. Author/review/approve quality documents, such as:SOPs, user requirements, risk assessments, training materials, engineering documents, automation documents, environmental qualification protocols/reports, validation protocols/reports. Establish and enable LEAN practices. Oversee and provide guidance during on-the-floor analytical testing. Ensure that changes that could potentially impact product quality are assessed according to procedures. Ensure that deviations from established procedures are investigated and documented per procedures. Ensure that production records and testing results are complete, accurate, and documented according to written procedures and cGMP requirements. Alert senior management of quality, compliance, supply and safety risks. Complete required assigned training to permit execution of required tasks. Drive operational improvement initiatives, programs and projects. Basic Qualifications Doctorate degree OR Master's degree and 3 years of Quality, Manufacturing, Process Development or Process Engineering experience OR Bachelor's degree and 5 years of Quality, Manufacturing, Process Development or Process Engineering experience OR Associate's degree and 10 years of Quality, Manufacturing, Process Development or Process Engineering experience OR High school diploma / GED and 12 years of Quality, Manufacturing, Process Development or Process Engineering experience Preferred Qualifications Scientific degree in Life Sciences, Physical Sciences, Applied Engineering or Manufacturing Technologies Previous Quality Assurance oversight of manufacturing, analytical and engineering activities Experience in investigations, change controls, and CAPAs processes system knowledge Direct validation experience with pharmaceutical or biopharmaceutical processes Ability to evaluate compliance issues and interact with regulatory inspectors Experience and training in EDMQ, Trackwise, Maximo, LIMS Experience in managing multiple, competing priorities in a fast-paced environment Experience leading and/or managing teams Direct bulk drug substance and drug product experience Demonstrated proficiency of written and verbal communication skills (including technical writing and presentations) with ability to communicate and collaborate effectively with technical and senior management staff Ability to solve complex problems and make scientific risk-based decisions Experience representing Amgen while interacting with representatives of regulatory agencies Experience of trending analysis Demonstrated proficiency using Excel, Word and Power Point 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. PI116045088

Amgen Job ID: R-88947 Location: West Greenwich, RI, US 02817 The Engineer reports to the Senior Manager of the ARI Facilities & Engineering Equipment Engineering group. The position is responsible for maintenance and reliability engineering assignments at ARI. Responsibilities: Apply basic engineering principles and practices in support of daily operation and maintenance of plant process systems. Recommend and implement improvements to equipment maintenance content in the Maximo computerized maintenance management system including equipment data, job plans, spare parts, safety data, planning information, and PM schedules. Work closely with multiple disciplines, including Manufacturing, Quality Assurance, Engineering, Maintenance, Process Development and Validation to ensure safe, compliant, effective and reliable operations. Organize, analyze, and effectively present results for operational issues, engineering projects or maintenance tasks of small to medium scope and complexity. Provide engineering support for design, construction, startup, commissioning and qualification of new or modified systems. Communicate proactively with supervisor and support staff, highlighting issues. Provide troubleshooting support. Provide field support to identify and resolve equipment performance issues (design, application, operations, maintenance, etc.). Support maintenance planning, scheduling and execution. Provide ad-hoc support outside normal shift including nights, weekends and holidays. Advance the use of condition based and predictive maintenance practices by incorporating advanced data analytics where applicable. Own investigations of abnormal conditions through Deviation and INCA business processes. Basic Qualifications: Master's Degree OR Bachelor's degree and 2 years of Engineering/Maintenance/Manufacturing experience OR Associate's degree and 6 years of Engineering/Maintenance/Manufacturing experience OR High school diploma / GED and 8 years of Engineering/Maintenance/Manufacturing experience Preferred Qualifications : Mechanical or Electrical Engineering Discipline preferred. Basic engineering principles and ability to apply them to resolve issues. Strong math and computer skills and possess the ability to apply science-based thinking to practical applications. Effective verbal and written communication skills. Strong interpersonal skills with ability to work collaboratively in a team-based environment. Ability to manage multiple tasks and effectively set priorities. Energetic and technically-minded individual. Ability to learn equipment and systems design, operation and maintenance requirements. Strong mechanical acumen. 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. PI116016779

Amgen Job ID: R-89180 Location: West Greenwich, RI, US 02817 Amgen's manufacturing facility in West Greenwich, RI is looking for a student with an outstanding academic record and demonstrated leadership capabilities. An internship at Amgen is a hands-on learning experience under the guidance of an Operations Manager. Interns are matched to meaningful and challenging projects. Facilities & Engineering - Infrastructure Operations / Utilities This position will provide the opportunity to work within the Facilities & Engineering Department at the Amgen RI Operations Facility. Coaching, mentorship, and guidance will be provided to the intern as they engage in the following projects: Basic Qualifications: Amgen requires that all individuals applying for an undergraduate internship or an undergraduate co-op assignment at Amgen must meet the following criteria: 18 years or older Currently enrolled in a Bachelor's Degree program from an accredited college or university with a 3.0 minimum GPA or equivalent Completion of at least one year of study from an accredited college or university prior to the internship commencing Enrolled in a full time Bachelor's program following the potential internship or co-op assignment with an accredited college or university Must not be employed at the time the internship starts Preferred Qualifications: Pursing a degree in Engineering (Mechanical, Energy, Chemical, or Electrical) GPA 3.5 or higher Strong computer skills including knowledge of MS Office Applications (Excel, Word, PowerPoint, SharePoint) Strong communication, interpersonal, organizational, project management, problem solving, analytical and quantitative skills Demonstrated personal initiative, self-motivation, flexibility and adaptability Proven leadership experience on campus (e.g., projects, clubs, organizations, sports) Only candidates who apply via www.careers.amgen.com will be considered. Please search the Keyword section for 89180. 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. PI116016944

Amgen Job ID: R-88789 Location: West Greenwich, RI, US 02817 Reporting to the Manager of Maintenance,this position is responsible for performing maintenance and repair activities throughout the Amgen Rhode Island (ARI) site. Shift: Rotating Days (7PM - 7 AM) Specific duties include: Perform advanced maintenance and repair activities on equipment and systems used in Manufacturing, the Process Develop Laboratory, the Quality Analytical Laboratory or other areas of the ARI site. Ensure activities are accomplished in a safe manner. Ensure work is completed in accordance with procedures. Ensure work activities are completed correctly. Maximize the right first time execution. Work in a highly productive and efficient manner to maximize the quantity of activities completed. Ensure work is appropriately communicated to system operators and key stakeholders. Ensure work order documentation is completed accurately and completely. Identify waste, work flow interrupters, and other opportunities for improvement, recommend solutions, and assisting with implementation. Identify opportunities to learn new skills and actively participate in development that will improve overall team performance. Provide support when required - this may be outside of normal working hours including nights, weekends and holidays. Other tasks as assigned. Basic Qualifications: Associate's degree and 4 years of Maintenance or Instrumentation experience OR High school diploma / GED and 6 years of Maintenance or Instrumentation experience Preferred Qualifications: 7+ years of combined education, training, and experience in mechanical maintenance with an emphasis on sanitary processing equipment and systems 3+ years knowledge of pneumatic, mechanical and hydraulic systems and ability to effectively perform associated maintenance activities. Knowledge and experience working in a highly regulated function - cGMP Experience executing and documenting maintenance work orders in the Maximo computerized maintenance management system Ability to interpret P&ID's. Ability to work with minimum direction Ability to effectively communicate issues and status of tasks in a timely manner Knowledge of Maximo CMMS System Ability to interact constructively with peers/teams 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. 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. 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. PI116017014

Amgen Job ID: R-88720 Location: West Greenwich, RI, US 02817 Do you want to help shape the future of biopharmaceutical manufacturing? Would you like to work with a highly motivated team of process science professionals to positively impact patients' lives? We have a position available for a Process Development Senior Associate to join our Rhode Island Site; this is a laboratory-based role. The Process Development organization at Amgen develops, characterizes and leads the commercialization of the drug substance manufacturing processes for all late-stage and commercial programs across the Amgen portfolio. This role provides opportunities to develop leadership, teamwork and communication skills through partnership with colleagues in the wider Process Development, Manufacturing, and Quality organizations. Further, the Process Development Sr. Associate will be immersed in all aspects of a world-class commercial bulk drug facility. Responsibilities Include: Apply fundamental scientific principles of cell culture and purification to execute small-scale experiments supporting the development, characterization, scale-up and optimization of commercial programs. Utilize problem-solving skills to rapidly find solutions to process challenges. Provide first principles approach and technology driven ideas to experimental designs through engagement and collaboration with a team of scientists. Demonstrate the desire to develop technical skills and scientific knowledge in both cell culture and purification, thereby further contributing to the coordinated group. Basic Qualifications: Master's degree OR Bachelor's degree and 2 years of scientific experience Preferred Qualifications (Senior Associate) Bachelor's degree in Chemical Engineering, Biochemical Engineering, Life Sciences, or other relevant sciences Upstream and downstream problem-solving experience in both a process development and commercial manufacturing support environment Understanding and hands-on experience in mammalian cell culture and protein chromatography Excellent sterile technique in the BSC as well as in closed operation transfers. Experience using and troubleshooting small-scale bioreactors, shake flask passaging, sampling and analysis, and downstream operations using AKTA and tecan. Excellent verbal communication and scientific writing skills Proven success working with a diverse team in a dynamic, multi-functional environment Familiarity with design of experiments and statistical analysis of data About Amgen Amgen discovers, develops and delivers innovative human therapeutics. A biotechnology pioneer since 1980, Amgen was one of the first companies to realize the new science's promise by bringing safe, effective medicines from lab, to manufacturing plant, to patient. Amgen therapeutics has changed the practice of medicine, helping millions of people around the world in the fight against cancer, kidney disease, rheumatoid arthritis, and other serious illnesses. With a deep and broad pipeline of potential new medicines, Amgen remains committed to advancing science to dramatically improve people's lives. 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. PI115883421

Amgen Job ID: R-88760 Location: West Greenwich, RI, US 02817 The Quality Control Manager will be responsible for supervision of all technical and operational activities within the QC Raw Material Laboratory at Amgen, Rhode Island. Responsibilities : Oversees the execution of testing including routine analysis and testing in support of technology transfer for raw materials Provides technical expertise/guidance to lab staff and within cross-functional Amgen teams Manages the Raw Materials Lab daily operations in relation to planning and management of materials, reagents, equipment and laboratory staff Own and review controlled documents, including Standard Operating Procedures, Analytical Methods, Protocols and Reports related to Raw Materials Lab activities Ensures that the Lab operations comply with applicable regulations and Amgen requirements relating to Good Manufacturing Practices, Good Documentation Practices, Safety and Laboratory Controls Represents the Raw Materials Lab during Amgen internal/external audits and inspections. Direct interaction with regulatory agencies during on-site inspections Provides oversight of Raw Materials Lab Quality Systems records including Deviations, Corrective Actions/Preventative Actions (CAPAs) and Change Controls Selects, develops and evaluates laboratory staff to ensure functional objectives are met Basic Qualifications Doctorate degree OR Master's degree and 3 years of Quality or Bioassay experience OR Bachelor's degree and 5 years of Quality or Bioassay experience OR Associate's degree and 10 years of Quality or Bioassay experience OR High school diploma / GED and 12 years of Quality or Bioassay experience AND Previous managerial experience directly managing people and/or experience leading teams, projects, programs or directing the allocation of resources Preferred Qualifications Strong knowledge in Bioassay Laboratory techniques Familiarity with method technology transfer process. Experience with validating analytical methods and ensuring that project deliverables meet established timelines Strong level of analysis skills to evaluate and interpret data to arrive at logical and quality-minded conclusions. Experience applying problem-solving tools for root cause analysis Proven leadership capabilities and experience applying GMP requirements in a Quality Control setting Demonstrated ability to develop, coach and mentor employees Excellent interpersonal, verbal and written communication skills with all levels within the organization Experience with successfully managing a team and delivering results in fast-paced and dynamic work environment 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. PI115883478

Amgen Job ID: R-88972 Location: West Greenwich, RI, US 02817 The Manufacturing Manager position is within the Purification organization at Amgen Rhode Island (ARI), a large-scale mammalian cell biotech manufacturing plant that produces multiple commercial and clinical products. This position offers the opportunity to collaborate with multiple functions on a routine basis in a dynamic environment (Quality Assurance, Quality Control, Engineering, Facilities, Maintenance, Process Development, Process Engineering, Regulatory Compliance, etc.) while developing a deep understanding of the manufacturing operations and planning activities within the facility and site. With minimal direction, the manager is responsible for leading on the floor operations and staff in manufacturing. The Manager will be responsible for supervising, coaching, hiring, and development of floor staff. The Front-Line Manager will assist in defining area objectives, identifying improvement opportunities, and leading change efforts. The Manager will need to effectively direct his/her team and deliver on short and long term Amgen Operational goals and will work closely with a second area FLM to manage the operations for the day. Scope of Responsibility Demonstrate technical mastery of purification processes Ensure safe working environment. Ensure cGMP and CFR compliance of operating areas. Resolve problems during operation. Elevate critical and impactful events to Sr. management and make real time processing decisions. Participate as a role model in Lean culture and continuous improvement programs with responsibility to translate onto the manufacturing floor. Develop, implement and assess solutions for complex problems. Ensure scheduling of production and maintenance activities. Collaborate with cross-functional teams (i.e. QA/QC, F&E, PD, Regulatory, etc.) in completing production activities and ensuring schedule adherence. Interact with business partners and internal/external audit teams including regulatory agencies as directed Ensure effective decision-making and clear and timely communication Leading Strategy Development and Execution Assists in developing and implementing departmental strategy and plans that are aligned with the broader organizational strategy Anticipates risk and builds contingencies to help mitigate impact Deliver strong business results Building a Strong Organizational Alignment Responsible for selection training, evaluation, staff relations and development of staff. Interacts with management in optimizing organizational structure and responsibilities. Ensures the right people and resources are in place and optimally allocated to achieve results Creates an environment that fosters accountability, innovation, continuous improvement, learning and knowledge-sharing Builds and develops a diverse, high performing team Works across functions to build organization and individual capabilities Develops strong relationships with staff members, provides open and clear feedback to improve individual and team performance Day Shift: (7:00am - 7:00pm rotating days) Basic Qualifications Doctorate degree OR Master's degree and 3 years of Manufacturing and Operations experience OR Bachelor's degree and 5 years of Manufacturing and Operations experience OR Associate's degree and 10 years of Manufacturing and Operations experience OR High school diploma / GED and 12 years of Manufacturing and Operations experience AND Previous managerial experience directly managing people and/or experience leading teams, projects, programs or directing the allocation of resources Preferred Qualifications Bachelor's degree in Life Sciences or Engineering Knowledge and experience within a cGMP or other highly regulated environment including a basic understanding of technical elements across engineering, biological or chemical processing Strong leadership and teambuilding skills (coaching, mentoring, counseling) Experience with staff capability and team performance improvements Experience with performance management including performance reviews Conflict Resolution skills Analytical problem solving skills Project Management skills Thorough understanding of regulatory requirements Ability to be flexible and manage change Excellent verbal and written communication (technical) skills Excellent computer skills with Microsoft, EBR/MES, Delta V, Electronic quality systems. 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. PI115859402

Amgen Job ID: R-88966 Location: West Greenwich, RI, US 02817 Amgen's 10 - 12 week internship program offers meaningful project experiences that impact patient's lives. This internship provides the opportunity for executive and social networking events and to participate in community volunteer projects while providing a competitive compensation. Limited relocation housing and/or miscellaneous allowance may be available for eligible candidates. Amgen's manufacturing facility in West Greenwich, RI is looking for studentswith outstanding academic records and demonstrated leadership capabilities. An internship at Amgen is a hands-on learning experience under the guidance of an Operations Manager. Interns are matched to meaningful and challenging projects. Participation as an intern has the potential to lead to an offer to join the Rotational Leadership Development Program or other entry-level full-time position upon college graduation in 2020, depending on available positions and an evaluation of your performance. Information Systems This position provides the opportunity to work directly with Information Systems staff supporting bulk drug substance operations. Coaching, mentorship, and guidance will be provided to the intern as they engage in the following project: Create a dashboard or data visualization that will provide business value to a business unit involved in the production of human therapeutics. This project will entail: Gathering business requirements from a business unit to solve a problem or realize an opportunity. This will give the intern exposure to the business processes used by manufacturing, supply chain, or quality. Document the report requirements and design, which will provide insight into IS procedures and the development lifecycle. Create the dashboard or data visualization using an industry standard visualization tool, such as Spotfire or Tableau. Rollout the report\visualization to the business unit and confirm that the planned business value was obtained. Information Systems - Automation This position provides the opportunity to work directly with IS - Automation staff supporting bulk drug substance operations. Coaching, mentorship, and guidance will be provided to the intern as they engage in the following project: Work with the Facilities and Engineering business unit to identify an area of improvement within the various site utility processes (Clean Utility Generation, HVAC, etc). Gather business requirements from the Facilities and Engineering business unit to solve a problem or realize an opportunity. This will give the intern exposure to the business processes used by facilities and engineering, manufacturing, process development, or quality. Document the requirements and design, which will provide insight into Automation procedures and the development lifecycle. Develop an automated solution using automation platforms such as Allen-Bradley FactoryTalk/RSLogix, Siemens Desigo, or Schneider Continuum. Rollout the solution and confirm that the planned business value was obtained. Basic Qualifications: Amgen requires that all individuals applying for an undergraduate internship or an undergraduate co-op assignment at Amgen must meet the following criteria: 18 years or older Currently enrolled in a Bachelor's Degree program from an accredited college or university with a 3.0 minimum GPA or equivalent Completion of at least one year of study from an accredited college or university prior to the internship commencing Enrolled in a full time Bachelor's program following the potential internship or co-op assignment with an accredited college or university Must not be employed at the time the internship starts Preferred Qualifications: Pursuing a degree in Data Science, Bioinformatics, Management Information Systems, or Computer Science GPA 3.5 or higher Junior standing Proven leadership experience on campus (e.g., projects, clubs, organizations, sports) Knowledge of MS Office Applications (Visio, Word, Excel, PowerPoint Familiarity with Spotfire and Tableau Strong communication, interpersonal, organizational, project management, problem solving, analytical and quantitative skills Demonstrated personal initiative, self-motivation, flexibility and adaptability Biotechnology, pharmaceutical or health care industry experience Only candidates who apply via www.careers.amgen.com will be considered. Please search the Keyword section for 87591. #LI-DNP 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. PI115859440

Amgen Job ID: R-83462 Location: Rhode Island, RI, US Job description (Senior Associate Manufacturing AR30) 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. Amgen's new plant, AR30, is responsible for drug substance manufacturing and release of Amgen's commercial product using innovative single use manufacturing platforms and technologies. We are looking for a talented Senior Associate Manufacturing to joining the manufacturing technical support function, initially to help with startup operations for our Next Generation Bio-manufacturing plant. This individual contributor position reports into the Senior Manager of the AR30 Manufacturing Support Team and interacts broadly across the site/plant to implement key business deliverables, quality initiatives, and continuous improvement projects The initial focus of this role will be part of the AR30 startup team to prepare the facility for Operational Readiness. This includes and not limited to supporting manufacturing operations team, developing training, SOPs, electronic batch records, job hazards analysis, and standard work and, participating in commissioning and qualification of process equipment. Under minimal supervision, the Senior Associate Manufacturing will support operations in the Manufacturing area. The Senior Associate Manufacturing will own, monitor and troubleshoot critical processes and regularly draft and revise documents such as Manufacturing Procedures, SOPs, and technical reports such as deviations. Senior Associate Manufacturing may participate in cross-functional teams and represent the Cell Culture and/or Purification groups. Senior Associate Manufacturing will also have the responsibility of owning at a minimum: Unit operations, SOPs, CAPA's, Change controls and Deviations. In addition, Senior Associate Manufacturing will identify, recommend, and implement improvements related to routine floor operations in solution preparation, cell culture and purification. Basic Qualifications: Masters Degree OR Bachelor's degree with 2 years of manufacturing experience OR Associate degree and 6 years of Manufacturing or Operations experience OR High School diploma/GED and 8 years of Manufacturing or Operations experience. Preferred Qualifications: Single use technology experience Cell Culture Experience Purification experience Regulatory knowledge and experience with regulatory audits Ability to interpret and apply GMP knowledge Hands on experience facilitating problem solving and root cause investigations in a biotechnology environment Mechanical expertise Knowledge of WIP lab equipment and computers, with LIMS access Basic statistical and mathematical skills Understanding of analytical methods for manufacturing area Ability to demonstrate 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 Manufacturing equipment including single use equipment Experience with Delta V/MES 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. PI115859516

Amgen Job ID: R-88301 Location: Rhode Island, RI, US Administrative Shift - with on the floor coverage as needed 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. We are looking for a talented Manufacturing Sr. Associate to help deliver opportunities for reliability, efficiency, agility and differentiation for the AR5 Manufacturing plant. This individual contributor position reports into the Senior Manager of Purification and interacts broadly across the site to implement key business deliverable, quality initiatives, and continuous improvement projects within the purification area. This role will focus on supporting operations on the floor, flexibility to support all four shifts covering 24/7 operations. Responsibilities: Supporting front line managers through on the floor presence (~60% of time on the floor) Providing subject matter expertise for area of responsibility Trouble shooting and problem-solving support to manufacturing Owning minor deviations within manufacturing Providing training to staff on the floor Identifying and autonomously implementing continuous improvement opportunities Owning and implementing corrective/preventative actions Ensuring right first-time implementation of changes through on the floor user testing and collection of staff feedback. Supporting Manufacturing specialists during complex investigations and change controls Owning and authoring SOPs Providing data to support management evaluation of performance trends Basic Qualifications : Master's degree OR Bachelor's degree and 2 years of Manufacturing or Operations experience OR Associate's degree and 6 years of Manufacturing or Operations experience OR High school diploma / GED and 8 years of Manufacturing or Operations experience Preferred Qualifications : Hands on experience facilitating problem solving in a biotechnology environment Experience owning and editing standard operating procedures Familiarity with the deviation management systems and corrective/preventative actions Project management skills with ability to multi-task and function in a dynamic environment Excellent communication skills and sense of urgency Demonstrated ability to forge and maintain strong relationships 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. PI115836641

Location: US-Shrub Oak ID: 2019-1052 # of openings: 1 Category: Receiving Overview The Dispatch/Receiving Agent supports Company yard operations by inspecting shipments for quantity accuracy; returning defective products or excess inventory; overseeing shipment of sold products and supervising yard personnel Responsibilities Essential Functions- Receiving/Dispatching • Ensures all supplies are maintained at acceptable levels while maintaining costAssist with inventory preparation and maintains inventory control • Responsible for the presentation of yard/warehouse products including, layouts, restocking, segregation and labelling of all special orders. • Plans and schedules work load of yard men in relation to receiving orders or restocking inventory, building of orders to be delivered, and general yard condition. • Supervises customer service in yard. • Responsible for security and safety procedures of yard operation. • Training and certifying new hires on forklift operation. • Arrange for upkeep/repair on forklifts/company trucks. • Handles the customer load building process with central dispatch. • Closes the store when manager is unavailable. • Periodically updates manager on any open issues. Other Duties • Assist with sales at counter as needed. • Assist with answering phones as needed. • Assist with customers in the yard as needed. • Other duties as assigned. Qualifications Competencies Reliable transportation, valid driver's license and evidence or insurability; excellent written and oral communication skills; excellent negotiation skills; pro-active planning and time management skills required. Working knowledge of construction industry and home building requirements. Required Education and Experience High school diploma, GED or equivalent. Minimum of 2 years of receiving and dispatcher related experience or demonstrated knowledge, skills and abilities to perform the above-mentioned tasks. Preferred Experience Prior product familiarization/product knowledge and experience working with building materials and in lumber yards. Prior experience in forklift operations and training employees on forklift and yard safety. Working Conditions and Physical Demands While performing the duties of this job, the employee is occasionally exposed to fumes or airborne particles, moving forklifts, noise, vibration and extreme weather conditions. Physical demands include occasional forklift driving; prolonged lifting, carrying, standing, kneeling, walking, loading, unloading; ability to lift up to 50 pounds at a time and unassisted. Position Type/Expected Hours of Work This is a full-time position. Work schedule varies and requires employee works every other Saturday and responsible for closing the store on occasion. Typical hours are Monday through Friday from 7:00am to 4:00pm, Saturdays from 8:00am to 12:00 pm. Travel: Travel to other locations as necessary for meetings and training Supervisory Responsibility Supervising yard personnel PM19 PI115560296