26 jobs found in king of prussia

WuXi AppTec US-PA-King of Prussia Job ID 2020-6587 Overview Responsible for first and second level day to day onsite support of users and systems (regulated and non-regulated). In addition, the Support Specialist II will be counted on to correctly prioritize and escalate problems and requests to other members of the IT Department. Responsibilities End user desktop, laptop, phone and software support including remote users Imaging and deployment of computer equipment. Manages and creates user accounts for on-boarding and off-boarding user and IT orientation for new hires Video and teleconference support Works with network administrators and application support staff to ensure user management, customer service and proper troubleshooting. Keeps desktop OS and desktop software up to date. Coordinates printer setup and repairs. Contacts vendors and contractors as needed. Manage repair process of those vendors. Assists with end user device security functions that may include anti-virus and malware protection. Assists in infrastructure projects that may include, but are not limited to: VoIP deployments, network upgrades, server upgrades, email system upgrades and application deployments. Trains users on IT Systems and Policies Respond to, escalate/reassign, and close helpdesk tickets Works on routine assignments per written procedures, where ability to recognize deviation from accepted practice is required. Normally receives minimal instructions on routine work and detailed instructions on new assignments. Works under close supervision from supervisor or senior personnel. Ability to work in a team environment and independently as required Ability to liaise with global operation team with strong communication skill Maybe required to work Holidays and weekends Contributes to the overall operations and to the achievement of departmental goals Perform job specific tasks in compliance with applicable Regulations, International Standards, and WuXi Biologics Policies and Standard Operating Procedures. Thorough understanding of Good Laboratory Practices and Good Manufacturing Practices Other duties as assigned May be required to assist in other departments Qualifications Experience / Education Associate's or Bachelor's degree or equivalent experience 5-8 years technical IT support experience Preferred Certification: A+, MCSA or equivalent IT certificates Knowledge / Skills / Abilities: Advanced knowledge of Windows 7/10 operating systems and MS Office 20xx/365 Advanced knowledge of PC hardware troubleshooting and repair Advanced knowledge of printers, troubleshooting and repair Advanced knowledge of Ethernet and Wi-Fi networks Proficient in Microsoft Office applications (Excel, Word, Outlook), VPN Advanced knowledge of WAN, LAN, VPN, WLAN and Remote Desktop program Advanced knowledge in setting up Backups to External Hard Drives and Network Shares Advanced understanding of networking principles and Microsoft Active Directory Previous experience in setting up and troubleshooting mobile phones (iOS/Android) Strong organizational and time-management skills Strategic thinking ability with strong analytical troubleshooting skills Proficient in Oral & Written communication skills A positive attitude and excellent customer service skills Ability and desire to provide excellent customer service Life Science company or Lab working experience is preferred Physical Requirements: Must be able to work in an office environment with minimal noise conditions. Must be able to work in Lab setting with exposure to Animals/biohazards / Chemicals (List specific Chemicals) Must be able to wear appropriate PPE Must be able to work in environment with variable noise levels Ability to stand /Sit/walk for long periods of time Ability to lift 25 lbs routinely Ability to lift 100 lbs with help of at least one other person occasionally Ability to crouch, bend, twist, and reach Ability to push/pull 100 lbs occasionally Clarity of Vision Ability to identify and distinguish colors Must be able to perform activities with repetitive motions Ability to climb Ladders / Stairs / Scaffolding An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability PI119567240

Radius Health Radius Health is an equal opportunity employer. EEO/Disabled Individuals/Veterans. If you need assistance and/or a reasonable accommodation due to a disability during the application or the recruiting process, please send a request to HRconnect@radiuspharm.com. Click here to navigate to the EEO is the Law poster. Click here to navigate Radius Healths Pay Transparency Policy. Market Access Contract Analyst US-PA-King of Prussia Job ID: 2019-2024 Type: Regular Full-Time # of Openings: 1 Category: Market Access Strategy Overview The Market Access Contract Analyst will be responsible for prompt and accurate drafting, analyzing and executing commercial Market Access agreements including but not limited to Radius’ Commercial Agreements with Specialty Pharmacies, Group Purchasing Organizations, Wholesalers, Managed Care Organizations (Commercial and Medicare Part D) as well as other segments/channels as required ensuring key procedures and tasks are followed and completed, ensuring Agreements meet necessary business, legal, operational and other requirements. Additionally, the role requires a high degree of knowledge and experience with Market Access Agreements with an in depth understanding of the dynamic biotech and pharmaceutical market access landscape. Responsibilities Timely and thorough review of all Market Access contract related documents ensuring the agreements have the necessary language to clarify the intent and to protect Radius. Draft multiple documents including redlines, NBIs, RFPs, Bids, amendments, correspondence, etc. relating to various Market Access agreements such as offers, amendments, correspondence that covers the intent of the parties. Responsible for tracking all existing contract and in negotiations terms for various internal reporting needs. Responsible for preparing and submitting all online related Bids according to the process. Establish cross-functional collaboration with internal and external stakeholders to ensure the agreements are operational, functional, and interpreted accurately for timely implementation and other contractual obligations. Collaborate with others including various stakeholders to solve issues/problems and potential future concerns. Provide requested information to Market Access Management and other stakeholders as needed. Work in conjunction and collaboratively with Finance, Account Directors, Market Access, Legal, Market Access Contracting Operations Analyst, as well as other stakeholders to confirm or request information necessary to support accurate and timely rebate and invoice processing (i.e. plan eligibility, formulary validation, etc.) Assist with the development and ongoing contract reporting needs related to Market Access Agreements for related channels on a regular and/or ad-hoc basis as requested by Market Access Management Provide support to Management related tracking tasks including Payer Membership/Clients, Formularies, Contract Expirations, Contract Terms, Renewals and other related provisions. Work Environment: The work is performed in a typical office environment with heavy computer duties. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. The noise level in the work environment is usually quiet. The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this position, the employee is regularly required to use hands to type, handle paperwork and sort, file or manipulate documents. The employee is occasionally required to stand and walk. The employee must frequently lift and/or move up to 10 pounds and occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this position include close vision, distance vision, color vision peripheral vision, depth perception and ability to adjust focus. Qualifications A four-year college degree or business experience equivalent is required. 5 years of demonstrated experience with Market Access Contracting activities in the pharmaceutical industry, specifically including specialty pharmacy, wholesalers, Group Purchasing Organizations, Managed Care Payers related to Commercial, Managed Medicaid, Medicare Part D and other channels is required. Organized, driven with high attention to detail Highly accountable Proficient skills in Microsoft Office, particularly Outlook, Word, PowerPoint and Excel. Ability to manage and prioritize multiple tasks and projects simultaneously, work independently as well as with a team, possess strong oral and written communication skills with a focus on customer service. Effectively interact with various key internal and external stakeholders as needed (i.e. Commercial Operations, Finance, Market Access, Legal, etc.) and build strong working relationships. Ability to demonstrate a thorough understanding of all aspects of applicable internal and external processes within a short time period. Flexibility and willingness to adjust schedule, as needed, during peak contracting periods. Willingness to learn new skills, systems and processes. Ability to stay focused and willingness to adjust to frequently changing priorities Excellent communication, interpersonal skills. Ability to apply learned concepts to other situations, be flexible and possess problem-solving skills. PM18 PI118867418

WuXi AppTec US-PA-King of Prussia Job ID 2020-6314 Overview WuXi Biologics (stock code: 2269.HK), a Hong Kong-listed company, is a leading global open-access biologics technology platform offering end-to-end solutions to empower organizations to discover, develop and manufacture biologics from concept to commercial manufacturing. Our company history and achievements demonstrate our commitment to providing a truly ONE-stop service offering and strong value proposition to our global clients. As of December 31, 2018, there were a total of 205 integrated projects, including 97 projects in pre-clinical development stage, 94 projects in early-phase (phase I and II) clinical development, 13 projects in late-phase (phase III) development and 1 project in commercial manufacturing. With total estimated capacity of biopharmaceutical production planned in China, Ireland, Singapore and US reaching 280,000 liters by 2022, we will provide our biomanufacturing partners with a robust and premier-quality global supply chain network. The successful candidate will be responsible for conducting experiments to support client-based processes with a focus on vaccine downstream cell culture processes. Responsibilities • Work independently on defined biopharmaceutical projects for development and/or characterization of vaccine downstream manufacturing processes. • Design and execute lab-scale experiment in supporting downstream process development, verification, characterization. • Perform purification experiments in BSL-2 labs and document experiments in lab notebooks. • Support maintenance tasks and new technology evaluations for laboratory instrumentation; interact with outside clients/vendors/suppliers Qualifications Qualifications: • The candidate should have background in one of the following fields: chemical engineering, biochemical or biological engineering, cell/molecular biology, biochemistry, or microbiology. • Hands-on experience in downstream purification process unit operations and lab scale experimental execution, preferably UFDF operations. • BS/MS degree with 0-5 years industry experience. • Strong written and verbal communication skills are required, as well as ability to take on multiple tasks simultaneously. • Excellent communication and good interpersonal skills, work well with diverse team members Physical Requirements • Must be able to work in Lab setting with Biohazards /various Chemicals • Must be able to wear appropriate PPEs • Ability to Lift 20 lbs PI119510653

WuXi AppTec US-PA-King of Prussia Job ID 2020-6470 Overview WuXi Biologics (stock code: 2269.HK), a Hong Kong-listed company, is a leading global open-access biologics technology platform offering end-to-end solutions to empower organizations to discover, develop and manufacture biologics from concept to commercial manufacturing. Our company history and achievements demonstrate our commitment to providing a truly ONE-stop service offering and strong value proposition to our global clients. As of December 31, 2018, there were a total of 205 integrated projects, including 97 projects in pre-clinical development stage, 94 projects in early-phase (phase I and II) clinical development, 13 projects in late-phase (phase III) development and 1 project in commercial manufacturing. With total estimated capacity of biopharmaceutical production planned in China, Ireland, Singapore and US reaching 280,000 liters by 2022, we will provide our biomanufacturing partners with a robust and premier-quality global supply chain network. The successful candidate will lead 2-3 junior scientists or technicians to develop and/or characterize vaccine upstream cell culture processes. Responsibilities ? Work independently on defined biopharmaceutical projects for development and/or characterization of vaccine downstream manufacturing processes. ? Manage project workflow to ensure on time delivery: from initial planning, experiment execution, to data evaluation. ? Design and execute lab-scale experiment in supporting downstream process development, verification, characterization, and tech transfer. Perform independent data analysis and interpretation and develop strategies for optimization and troubleshooting. ? Represent Vaccine Downstream Process Development Group in internal cross-functional teams and external communication with client. ? Manage technical transfer of processes into the non-GMP pilot plant or GMP production facility. ? Document development work in concise reports and provide project updates in written and oral presentations. ? Support maintenance tasks and new technology evaluations for laboratory instrumentation; interact with outside clients/vendors/suppliers Qualifications ? The candidate should have background in one of the following fields: chemical engineering, biochemical or biological engineering, cell/molecular biology, biochemistry, or microbiology. ? Hands-on experience in downstream process unit operations and lab scale experimental execution. ? PhD degree and 0-2 years industry experience, or with MS degree and at least 3 years industry experience. ? Strong written and verbal communication skills are required, as well as ability to take on multiple tasks simultaneously. ? Excellent communication and good interpersonal skills, work well with diverse team members PI119455871

WuXi AppTec US-PA-King of Prussia Job ID 2020-6426 Overview WuXi Biologics (stock code: 2269.HK), a Hong Kong-listed company, is a leading global open-access biologics technology platform offering end-to-end solutions to empower organizations to discover, develop and manufacture biologics from concept to commercial manufacturing. Our company history and achievements demonstrate our commitment to providing a truly ONE-stop service offering and strong value proposition to our global clients. As of December 31, 2018, there were a total of 205 integrated projects, including 97 projects in pre-clinical development stage, 94 projects in early-phase (phase I and II) clinical development, 13 projects in late-phase (phase III) development and 1 project in commercial manufacturing. With total estimated capacity of biopharmaceutical production planned in China, Ireland, Singapore and US reaching 280,000 liters by 2022, we will provide our biomanufacturing partners with a robust and premier-quality global supply chain network. Responsibilities Provide analytical support for later stage vaccine development in the King of Prussia lab. Perform cell culture and sample analysis using cell-based potency assay, separation assay and other bioanalytical assays as needed to the requirements of process development labs and ICH guidelines. Perform method development and qualification for potency assay and other bioanalytical assays. Manage method transfer into the non-GMP analytical science group located at the other sites or GMP QC labs. Document completed lab work and results promptly, clearly, and accurately. Prepare presentations and written reports of experimental results and analyses and effectively communicate with internal stakeholders and client. Write and revise analytical methods, testing protocols and reports, and other technical documents. Assist in the lab set-up and equipment maintenance of the potency lab and analytical lab in King of Prussia, PA. Ability to work in a team environment and independently as required. Qualifications Bachelor or Master Degree in Biochemistry, Analytical Chemistry, Molecular Biology or related discipline, and with 1-2 year industry experience. Experience with aseptic techniques, cell culture, bioassays including cell-based potency assays and ELISAs, and molecular biology techniques (qPCR, western blot) is preferred. Experience with analysis of biological molecules using techniques of HPLC/UPLC, electrophoresis, etc. Experience with vaccines/viral testing and biosafety containment levels, preferably BSL-2 is preferred. Must be able to follow and execute SOPs and report data in an accurate and timely manner. Strong aptitude and ability to work collaboratively and effectively with internal and external partners Excellent communications skills (verbal, written, and presentation skills). Good computer skills, including Microsoft Word, Excel, PowerPoint, etc. Good technical writing skills Proficiency in English is required. Must be able to work in lab settings with exposure to cells and vaccines/viruses Critical thinking, scientific reasoning, and problem solving skills Adapt to changing priorities Organized and detail-oriented Limited international travel might be needed. PI119353134

WuXi AppTec US-PA-King of Prussia Job ID 2019-6192 Overview WuXi Biologics (stock code: 2269.HK), a Hong Kong-listed company, is a leading global open-access biologics technology platform offering end-to-end solutions to empower organizations to discover, develop and manufacture biologics from concept to commercial manufacturing. Our company history and achievements demonstrate our commitment to providing a truly ONE-stop service offering and strong value proposition to our global clients. As of December 31, 2018, there were a total of 205 integrated projects, including 97 projects in pre-clinical development stage, 94 projects in early-phase (phase I and II) clinical development, 13 projects in late-phase (phase III) development and 1 project in commercial manufacturing. With total estimated capacity of biopharmaceutical production planned in China, Ireland, Singapore and US reaching 280,000 liters by 2022, we will provide our biomanufacturing partners with a robust and premier-quality global supply chain network. Responsibilities Lead a team of analytical scientists to support analytical activity of later stage vaccine development including technical transfer and process characterization in the lab. Be responsible for the highest quality analytical support while ensuring compliance with FDA/ICH guidelines/regulations, company SOPs, and safety regulations. Involved in the design, planning, and set-up of the labs of analytical development to support vaccine development. Serve as a technical expert for analytical method development, qualification and transfer. Develop/build a world-class analytical team including planning, recruiting/hiring, coaching/mentoring, and training for scientists and managers. Play a leading role in project management interaction with internal and external clients such as Process Development and Quality Control. Develop and maintain high level of scientific achievements for the company; expected to be a point of contact for project coordination, including email and client meetings. Create a safety culture, enforce safety measures and ensure analytical lab staffs working in a safe environment. Qualifications PhD degree with more than 2 years industry experience, or MS degree with at least 7 years industry experience. Candidate must possess strong and effective people management, problem solving and interpersonal skills and have a proven track record working cross-functionally across a wide variety of technical, business and operational areas. Experience with aseptic techniques, cell culture, bioassays including cell-based potency assays and ELISAs, and molecular biology techniques (qPCR, western blot), separation assays of HPLC/UPLC, etc. Experience with vaccines/viral testing and biosafety containment levels, preferably BSL-2 and above. Strong aptitude and ability to work collaboratively and effectively with internal and external partners. Ability to plan and ensure the effective deliverables of projects and tasks within established timelines. Proficiency in English is required. Excellent communications skills (verbal, written, and presentation skills). Excellent data processing skills and computer skills using windows based software. Excellent technical writing skills. Must be able to work in lab settings with exposure to cells and vaccines/viruses Critical thinking, scientific reasoning, and problem solving skills. Adapt to changing priorities. Organized and detail-oriented. PI119353182

WuXi AppTec US-PA-King of Prussia Job ID 2019-5877 Overview WuXi Biologics (stock code: 2269.HK), a Hong Kong-listed company, is a leading global open-access biologics technology platform offering end-to-end solutions to empower organizations to discover, develop and manufacture biologics from concept to commercial manufacturing. Our company history and achievements demonstrate our commitment to providing a truly ONE-stop service offering and strong value proposition to our global clients. Searching for subject matter expert in potency assay, perform cell culture/banking, qPCR based potency assay, and testing samples train junior scientists in the King of Prussia potency lab and participate in local and regional technical transfer. Responsibilities • Perform cell culture, cell banking, sample testing, and equipment maintenance according to requirements of process development labs and ICH guidelines. • Perform assay fit for purpose of potency assay. • Document completed lab work and results promptly, clearly, and accurately. • Prepare presentations and written reports of experimental results and analyses and effectively communicate with internal stakeholders and client. • Write and revise analytical methods, testing protocols and reports, and other technical documents. • Assist in the lab set-up of the potency lab in King of Prussia, PA. • Ability to work in a team environment and independently as required. Qualifications • Must be familiar with qPCR and aseptic technique. • Knowledge and expertise in the following fields: Biochemistry and immunology principles and techniques, such as cell thawing, cell culture, cell-based assays, etc. • Experience with vaccines/viral testing and biosafety containment levels, preferably BSL-2 • Demonstrates good understanding of potency assay in the biopharmaceutical/vaccine industry. • Experience in a Contract Research Organization (CRO) or Contract Manufacturing Organization (CMO) is preferred, but not required. • Limited international travel required • Proficiency in English is required. • Excellent communications skills (verbal, written, and presentation skills). • Good computer skills, including Microsoft Word, Excel, Powerpoint, etc. • Good technical writing skills • Must be able to work in lab settings with exposure to cells and vaccines/viruses • Must be able to wear appropriate PPE • Critical thinking, scientific reasoning, and problem solving skills • Adapt to changing priorities • Organized and detail-oriented PI119353294

WuXi AppTec US-PA-King of Prussia Job ID 2020-6367 Overview WuXi Biologics (stock code: 2269.HK), a Hong Kong-listed company, is a leading global open-access biologics technology platform offering end-to-end solutions to empower organizations to discover, develop and manufacture biologics from concept to commercial manufacturing. Our company history and achievements demonstrate our commitment to providing a truly ONE-stop service offering and strong value proposition to our global clients. As of December 31, 2018, there were a total of 205 integrated projects, including 97 projects in pre-clinical development stage, 94 projects in early-phase (phase I and II) clinical development, 13 projects in late-phase (phase III) development and 1 project in commercial manufacturing. With total estimated capacity of biopharmaceutical production planned in China, Ireland, Singapore and US reaching 280,000 liters by 2022, we will provide our biomanufacturing partners with a robust and premier-quality global supply chain network. Responsibilities Perform analytical testing as needed to the requirements of process development labs and ICH guidelines Document data and analyze results promptly, clearly, and accurately. Perform cell culture and sample analysis to support process development for later stage vaccine program. Use various analytical techniques including HPLC/UPLC, qPCR, ELISA, etc. Must be able to follow and execute SOPs and report data in an accurate and timely manner. Write and revise analytical methods, testing protocols and reports, and other technical documents. Ability to work in a team environment. Qualifications Bachelor or Master Degree in Biochemistry, Molecular Biology, Analytical Chemistry, Chemistry, Immunology, Virology, or related discipline. Must be able to operate and maintain analytical instrument. Knowledge and expertise in the following fields is preferred: Biochemistry and immunology principles and techniques, such as cell thawing, cell culture, cell-based assays, etc. Experience with biological molecules and/or vaccines/viral testing and biosafety containment levels, preferably BSL-2 Proficiency in English is required. Good communications skills (verbal, written, and presentation skills). Good computer skills, including Microsoft Word, Excel, PowerPoint, etc. Good technical writing skills. Must be able to work in lab settings with exposure to cells and vaccines/viruses. Organized and detail-oriented. PI119353450

WuXi AppTec US-PA-King of Prussia Job ID 2019-5865 Overview WuXi Biologics (stock code: 2269.HK), a Hong Kong-listed company, is a leading global open-access biologics technology platform offering end-to-end solutions to empower organizations to discover, develop and manufacture biologics from concept to commercial manufacturing. Our company history and achievements demonstrate our commitment to providing a truly ONE-stop service offering and strong value proposition to our global clients. Searching for a Quality Assurance Specialist that will be responsible for daily inspections and ensure manufacturing operations maintain company and global industry standards. Responsibilities Responsible for daily inspection to ensure the effective execution of operation procedures and batch records Communication between QA and other departments, report problems in time Participate in manufacturing related deviation, change, CAPA and OOS Cooperate with self - inspection, customer and regulatory audit Participate tech transfer process and review protocols and reports Review and double check all original materials before submit to official Qualifications Minimum Bachelor degree in biology, biotechnology, or relevant discipline Minimum 5 years quality experience, preferable in vaccine Lab or commercial product experience Understanding of cGMP/GLPs and ICH in the pharmaceutical industry well Good interpersonal skills and the ability to communicate well PI119352746

WuXi AppTec US-PA-King of Prussia Job ID 2020-6440 Overview WuXi Biologics (stock code: 2269.HK), a Hong Kong-listed company, is a leading global open-access biologics technology platform offering end-to-end solutions to empower organizations to discover, develop and manufacture biologics from concept to commercial manufacturing. Our company history and achievements demonstrate our commitment to providing a truly ONE-stop service offering and strong value proposition to our global clients. As of December 31, 2018, there were a total of 205 integrated projects, including 97 projects in pre-clinical development stage, 94 projects in early-phase (phase I and II) clinical development, 13 projects in late-phase (phase III) development and 1 project in commercial manufacturing. With total estimated capacity of biopharmaceutical production planned in China, Ireland, Singapore and US reaching 280,000 liters by 2022, we will provide our biomanufacturing partners with a robust and premier-quality global supply chain network. Responsibilities Provide analytical support for vaccine development in the King of Prussia lab. Involve onsite technical transfer at a local client's site. Perform sample testing using separation assay and qPCR based potency assay and other bioanalytical assays as needed, and equipment maintenance according to requirements of process development labs and ICH guidelines. Document completed lab work and results promptly, clearly, and accurately. Prepare presentations and written reports of experimental results and analyses and effectively communicate with internal stakeholders and client. Write and revise analytical methods, testing protocols and reports, and other technical documents. Assist in the lab set-up of the analytical lab in King of Prussia, PA. Ability to work in a team environment. Qualifications Must be able to follow and execute SOPs and report data in an accurate and timely manner. Must be able to operate and maintain analytical instrument with minimal supervision. Experience with analytical techniques including HPLC/UPLC, qPCR, ELISA, etc. Experience with analysis of biological molecules. Knowledge and expertise in the following fields is preferred: Biochemistry and immunology principles and techniques, such as cell thawing, cell culture, cell-based assays, etc. Experience with vaccines/viral testing and biosafety containment levels, preferably BSL-2 Demonstrates good understanding of potency assay in the biopharmaceutical/vaccine industry. Experience in a Contract Research Organization (CRO) or Contract Manufacturing Organization (CMO) is a plus. Limited international travel might be needed. Bachelor or Master Degree in Biochemistry, Molecular Biology, Analytical Chemistry, Chemistry, Immunology, Virology, or related discipline. OTHER SKILLS, ABILITIES & EXPERIENCE: Proficiency in English is required. Excellent communications skills (verbal, written, and presentation skills). Good computer skills, including Microsoft Word, Excel, PowerPoint, etc. Good technical writing skills ADDITIONAL POSITION SPECIFIC DUTIES/INFO (Not Covered in Generic Description of Job): Must be able to work in lab settings with exposure to cells and vaccines/viruses Must be able to wear appropriate PPE Critical thinking, scientific reasoning, and problem solving skills Adapt to changing priorities Organized and detail-oriented PI119352845

WuXi AppTec US-PA-King of Prussia Job ID 2020-6439 Overview WuXi Biologics (stock code: 2269.HK), a Hong Kong-listed company, is a leading global open-access biologics technology platform offering end-to-end solutions to empower organizations to discover, develop and manufacture biologics from concept to commercial manufacturing. Our company history and achievements demonstrate our commitment to providing a truly ONE-stop service offering and strong value proposition to our global clients. As of December 31, 2018, there were a total of 205 integrated projects, including 97 projects in pre-clinical development stage, 94 projects in early-phase (phase I and II) clinical development, 13 projects in late-phase (phase III) development and 1 project in commercial manufacturing. With total estimated capacity of biopharmaceutical production planned in China, Ireland, Singapore and US reaching 280,000 liters by 2022, we will provide our biomanufacturing partners with a robust and premier-quality global supply chain network. Responsibilities Provide analytical support for vaccine development in the King of Prussia lab. Involve onsite technical transfer at a local client's site. Perform sample testing using separation assay and qPCR based potency assay and other bioanalytical assays as needed, and equipment maintenance according to requirements of process development labs and ICH guidelines. Document completed lab work and results promptly, clearly, and accurately. Prepare presentations and written reports of experimental results and analyses and effectively communicate with internal stakeholders and client. Write and revise analytical methods, testing protocols and reports, and other technical documents. Assist in the lab set-up of the analytical lab in King of Prussia, PA. Ability to work in a team environment. Qualifications Must be able to follow and execute SOPs and report data in an accurate and timely manner. Must be able to operate and maintain analytical instrument with minimal supervision. Experience with analytical techniques including HPLC/UPLC, qPCR, ELISA, etc. Experience with analysis of biological molecules. Knowledge and expertise in the following fields is preferred: Biochemistry and immunology principles and techniques, such as cell thawing, cell culture, cell-based assays, etc. Experience with vaccines/viral testing and biosafety containment levels, preferably BSL-2 Demonstrates good understanding of potency assay in the biopharmaceutical/vaccine industry. Experience in a Contract Research Organization (CRO) or Contract Manufacturing Organization (CMO) is a plus. Limited international travel might be needed. Bachelor or Master Degree in Biochemistry, Molecular Biology, Analytical Chemistry, Chemistry, Immunology, Virology, or related discipline. OTHER SKILLS, ABILITIES & EXPERIENCE: Proficiency in English is required. Excellent communications skills (verbal, written, and presentation skills). Good computer skills, including Microsoft Word, Excel, PowerPoint, etc. Good technical writing skills ADDITIONAL POSITION SPECIFIC DUTIES/INFO (Not Covered in Generic Description of Job): Must be able to work in lab settings with exposure to cells and vaccines/viruses Must be able to wear appropriate PPE Critical thinking, scientific reasoning, and problem solving skills Adapt to changing priorities Organized and detail-oriented PI119352861

WuXi AppTec US-PA-King of Prussia Job ID 2019-6210 Overview The Laboratory Technician's primary duty is to support the upstream cell culture activities by performing lab/equipment maintenance and other basic experimental related work. Responsibilities • Perform general operations such as bioreactor assembly/sterilization, cleanup and turnover of bioreactor to maintain a set run schedule. • Perform general operations such as cell culture medium, supplement and tubing sets preparations. • Perform basic calibrations of instruments on process and utility equipment. Ensure that calibration paperwork, instrument files and work order documentation are completed with accurate information. • Support and perform basic troubleshooting of process equipment, such as Nova Bioprofile analyzer, cell counter, autoclaves, and other process equipment or systems. • Orderand keep track of supplies including cell culture media, cell culture stacks and other lab consumables. • Order and keep track of critical reagents inventory and non-GMP chemical storage. • All work must be completed in accordance with lab safety, regulations, and SOPs. • Perform regular certification of equipment to verify conformance to industry standards and procedures. • Other job functions that may be assigned. Qualifications • Must have the ability to work independently and as part of a team, self-motivation, adaptability and a positive attitude. • Proven ability to work in hands-on laboratory setting. • Excellent interpersonal, verbal and written communication skills preferred. • Experience working with viral systems within a Biosafety Level-2 (BSL-2) environment is strongly preferred. Education / Experience • Associate degree with 2 years of instrumentation/calibration experience, 2 years in a technical school setting with hands-on instrumentation/calibration experience, or high school diploma/GED with 4 years of instrumentation/calibration experience. Knowledge / Skills / Abilities: • Ability to effectively communicate ideas through verbal and written form. • Intermediate computer skills. • Knowledge of process or utility equipment/system maintenance. Physical Requirements: • Must be able to work in BSL-2 Lab setting with biohazards /various chemicals. • Must be able to wear appropriate PPEs. • Ability to lift 40 lbs. An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. Employees holding this position will be required to perform any other job-related duties as requested by Management. PI119352895

WuXi AppTec US-PA-King of Prussia Job ID 2019-6136 Overview WuXi Biologics (stock code: 2269.HK), a Hong Kong-listed company, is a leading global open-access biologics technology platform offering end-to-end solutions to empower organizations to discover, develop and manufacture biologics from concept to commercial manufacturing. Our company history and achievements demonstrate our commitment to providing a truly ONE-stop service offering and strong value proposition to our global clients. As of December 31, 2018, there were a total of 205 integrated projects, including 97 projects in pre-clinical development stage, 94 projects in early-phase (phase I and II) clinical development, 13 projects in late-phase (phase III) development and 1 project in commercial manufacturing. With total estimated capacity of biopharmaceutical production planned in China, Ireland, Singapore and US reaching 280,000 liters by 2022, we will provide our biomanufacturing partners with a robust and premier-quality global supply chain network. The successful candidate will be responsible for conducting experiments to support client based processes with a focus on vaccine Downstream cell culture processes. Responsibilities Work independently on defined biopharmaceutical projects for development and/or characterization of vaccine downstream manufacturing processes. Design and execute lab-scale experiment in supporting downstream process development, verification, characterization. Perform purification experiments in BSL-2 labs and document experiments in lab notebooks. Support maintenance tasks and new technology evaluations for laboratory instrumentation; interact with outside clients/vendors/suppliers Qualifications Qualifications: The candidate should have background in one of the following fields: chemical engineering, biochemical or biological engineering, cell/molecular biology, biochemistry, or microbiology. Hands-on experience in downstream purification process unit operations and lab scale experimental execution, preferably UFDF operations. BS/MS degree with 0-5 years industry experience. Strong written and verbal communication skills are required, as well as ability to take on multiple tasks simultaneously. Excellent communication and good interpersonal skills, work well with diverse team members Physical Requirements Must be able to work in Lab setting with Biohazards /various Chemicals Must be able to wear appropriate PPEs Ability to Lift 20 lbs PI119352916

WuXi AppTec US-PA-King of Prussia Job ID 2019-6127 Overview WuXi Biologics (stock code: 2269.HK), a Hong Kong-listed company, is a leading global open-access biologics technology platform offering end-to-end solutions to empower organizations to discover, develop and manufacture biologics from concept to commercial manufacturing. Our company history and achievements demonstrate our commitment to providing a truly ONE-stop service offering and strong value proposition to our global clients. As of December 31, 2018, there were a total of 205 integrated projects, including 97 projects in pre-clinical development stage, 94 projects in early-phase (phase I and II) clinical development, 13 projects in late-phase (phase III) development and 1 project in commercial manufacturing. With total estimated capacity of biopharmaceutical production planned in China, Ireland, Singapore and US reaching 280,000 liters by 2022, we will provide our biomanufacturing partners with a robust and premier-quality global supply chain network. Responsibilities • Work independently on defined biopharmaceutical projects for development and/or characterization of vaccine downstream manufacturing processes. • Design and execute lab-scale experiment in supporting downstream process development, verification, characterization. • Perform purification experiments in BSL-2 labs and document experiments in lab notebooks. • Assist the director to coordinate the work between the downstream development group and other functional groups to meet the project objectives and timelines. • Oversee the process scale-up and technology transfer between the process development team and manufacturing team. • Coach the group leads and staff on the process development and design of experiments • Support maintenance tasks and new technology evaluations for laboratory instrumentation; interact with outside clients/vendors/suppliers • The candidate should have background in one of the following fields: chemical engineering, biochemical or biological engineering, cell/molecular biology, biochemistry, or microbiology. • Hands-on experience in downstream purification process unit operations and lab scale experimental execution, preferably UFDF operations, virus purification. • Familiar with biological/chemical/physical product characterization assays • Strong written and verbal communication skills are required, as well as ability to take on multiple tasks simultaneously. • Excellent communication and good interpersonal skills, work well with diverse team members Qualifications • MS with 12+ years, or PhD with 8+ years downstream process development experience. Physical Requirements • Must be able to work in Lab setting with Biohazards /various Chemicals • Must be able to wear appropriate PPEs • Ability to Lift 20 lbs PI119352937

WuXi AppTec US-PA-King of Prussia Job ID 2020-6485 Overview The successful candidate will be responsible for conducting experiments to support client based processes with a focus on vaccine upstream cell culture processes. Responsibilities • Work on defined biopharmaceutical projects for development and/or characterization of vaccine upstream manufacturing cell culture processes. • Perform bench scale and pilot scale bioreactor operations in supporting upstream process development, verification, characterization, and tech transfer. • Support technical transfer of processes into the non-GMP pilot plant or GMP production facility. • Keep accurate record of cell culture parameters and results into datasheets and/or laboratory notebooks. • Support maintenance tasks and new technology evaluations for laboratory instrumentation. Monitor and communicate inventory needs to the lab management group. Interact with outside clients/vendors/suppliers. Qualifications Job Requirements: • The individual must have proven ability to work in hands-on laboratory setting. • Hands-on experience in mammalian cell culture or vaccine process development/manufacturing using various scales of controlled-bioreactors is strongly preferred. • Experience working with viral systems within a Biosafety Level-2 (BSL-2) environment is strongly preferred. • Experience in statistical design of experiments (e.g., JMP, Design Expert) and/or statistical data analysis is highly desirable. • The individual must have the ability to work independently and as part of a team, self-motivation, adaptability and a positive attitude. • This position will require occasional off hour and weekend work. • Authorization to work in the United States indefinitely without restriction or sponsorship is required. Education / Experience • The candidate should have background in one of the following fields: chemical/biochemical engineering, biomedical engineering, cell/molecular biology, biochemistry, microbiology, or equivalent. • B.S./M.S. with 0-2 years of relevant experience. Job title will be experience/qualifications dependent. Knowledge / Skills / Abilities: • The individual must have strong communication (verbal and written in English) and interpersonal skills, the ability to work flexibly in a cross-functional team environment and take on multiple tasks simultaneously, and the ability to build / maintain relationships with partners and collaborators. Physical Requirements: • Must be able to work in BSL-2 Lab setting with Biohazards /various Chemicals • Must be able to wear appropriate PPEs • Ability to lift up to 30 lbs An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. Employees holding this position will be required to perform any other job-related duties as requested by Management. Management Approval: Date: Employee Signature: Date: PI119353044

WuXi AppTec US-PA-King of Prussia Job ID 2020-6484 Overview The successful candidate will be responsible for conducting experiments to support client based processes with a focus on vaccine upstream cell culture processes. Responsibilities • Work on defined biopharmaceutical projects for development and/or characterization of vaccine upstream manufacturing cell culture processes. • Perform bench scale and pilot scale bioreactor operations in supporting upstream process development, verification, characterization, and tech transfer. • Support technical transfer of processes into the non-GMP pilot plant or GMP production facility. • Keep accurate record of cell culture parameters and results into datasheets and/or laboratory notebooks. • Support maintenance tasks and new technology evaluations for laboratory instrumentation. Monitor and communicate inventory needs to the lab management group. Interact with outside clients/vendors/suppliers. Qualifications • The individual must have proven ability to work in hands-on laboratory setting. • Hands-on experience in mammalian cell culture or vaccine process development/manufacturing using various scales of controlled-bioreactors is strongly preferred. • Experience working with viral systems within a Biosafety Level-2 (BSL-2) environment is strongly preferred. • Experience in statistical design of experiments (e.g., JMP, Design Expert) and/or statistical data analysis is highly desirable. • The individual must have the ability to work independently and as part of a team, self-motivation, adaptability and a positive attitude. • This position will require occasional off hour and weekend work. • Authorization to work in the United States indefinitely without restriction or sponsorship is required. Education / Experience • The candidate should have background in one of the following fields: chemical/biochemical engineering, biomedical engineering, cell/molecular biology, biochemistry, microbiology, or equivalent. • B.S./M.S. with 0-2 years of relevant experience. Job title will be experience/qualifications dependent. Knowledge / Skills / Abilities: • The individual must have strong communication (verbal and written in English) and interpersonal skills, the ability to work flexibly in a cross-functional team environment and take on multiple tasks simultaneously, and the ability to build / maintain relationships with partners and collaborators. Physical Requirements: • Must be able to work in BSL-2 Lab setting with Biohazards /various Chemicals • Must be able to wear appropriate PPEs • Ability to lift up to 30 lbs An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. Employees holding this position will be required to perform any other job-related duties as requested by Management. PI119353061

WuXi AppTec US-PA-King of Prussia Job ID 2020-6438 Overview WuXi Biologics (stock code: 2269.HK), a Hong Kong-listed company, is a leading global open-access biologics technology platform offering end-to-end solutions to empower organizations to discover, develop and manufacture biologics from concept to commercial manufacturing. Our company history and achievements demonstrate our commitment to providing a truly ONE-stop service offering and strong value proposition to our global clients. As of December 31, 2018, there were a total of 205 integrated projects, including 97 projects in pre-clinical development stage, 94 projects in early-phase (phase I and II) clinical development, 13 projects in late-phase (phase III) development and 1 project in commercial manufacturing. With total estimated capacity of biopharmaceutical production planned in China, Ireland, Singapore and US reaching 280,000 liters by 2022, we will provide our biomanufacturing partners with a robust and premier-quality global supply chain network. The successful candidate will be responsible for conducting experiments to support client based processes with a focus on vaccine upstream cell culture processes. Responsibilities • Work on defined biopharmaceutical projects for development and/or characterization of vaccine upstream manufacturing cell culture processes. • Perform bench scale and pilot scale bioreactor operations in supporting upstream process development, verification, characterization, and tech transfer. Perform data analysis and interpretation, and develop strategies for optimization and troubleshooting. • Support technical transfer of processes into the non-GMP pilot plant or GMP production facility. • Keep accurate record of cell culture parameters and results into datasheets and/or laboratory notebooks. • Support maintenance tasks and new technology evaluations for laboratory instrumentation. Monitor and communicate inventory needs to the lab management group. Interact with outside clients/vendors/suppliers. Qualifications Job Requirements: • The individual must have proven ability to work in hands-on laboratory setting. • Hands-on experience in mammalian cell culture or vaccine process development/manufacturing using various scales of controlled-bioreactors is strongly preferred. • Experience working with viral systems within a Biosafety Level-2 (BSL-2) environment is strongly preferred. • Experience in statistical design of experiments (e.g., JMP, Design Expert) and/or statistical data analysis is highly desirable. • The individual must have the ability to work independently and as part of a team, self-motivation, adaptability and a positive attitude. • This position will require occasional off hour and weekend work. • Authorization to work in the United States indefinitely without restriction or sponsorship is required. Education / Experience • The candidate should have background in one of the following fields: chemical/biochemical engineering, biomedical engineering, cell/molecular biology, biochemistry, microbiology, or equivalent. • BS./M.S. with 1-2 years of relevant experience. Job title will be experience/qualifications dependent. Knowledge / Skills / Abilities: • The individual must have strong communication (verbal and written in English) and interpersonal skills, the ability to work flexibly in a cross-functional team environment and take on multiple tasks simultaneously, and the ability to build / maintain relationships with partners, collaborators, and customers Physical Requirements: • Must be able to work in BSL-2 Lab setting with Biohazards /various Chemicals • Must be able to wear appropriate PPEs • Ability to lift up to 30 lbs An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability PI119352513

WuXi AppTec US-PA-King of Prussia Job ID 2020-6312 Responsibilities Set up and optimize EHS management system, implement EHS procedure and action. Develop and enforce organization environment, safety and health programs in compliance with all relevant local, state and Federal regulations and guidelines and industry best practices. Be responsible to respond to hazardous material emergencies, providing technical guidance and active support. Conduct EHS incident investigation and follow up CAPA. SME on technical issues in the areas of biosafety, industrial hygiene, and occupational safety, and assist in hazard identification, hazard evaluation, and the development of controls appropriate to the work being performed. Identify potential lab operation risks and facilitate the operation process to eliminate or minimize the impact on the lab operation and employees. Responsible for client and external EHS agencies' inspection and make sure the corrective actions are fully implemented. Perform other responsibilities assigned by the management, e.g. EHS training etc. Qualifications Bachelor degree and above in biology, molecular biology, microbiology, cellular biology, biochemistry, genetics or related field. 5 year pharmaceutical company EHS working experience and 2-year EHS management experience at least, Professional certification such as Registered Biosafety Professional or certified Biological Safety Professional is desirable. Advanced degree preferred. Familiar with EHS management system such as ISO14001, ISO45001 etc. Good communication and coordination skill. Strong verbal and written communication skills. Ability to establish working relationships with diverse groups. Must work both independently & as a team member. PI119352544

WuXi AppTec US-PA-King of Prussia Job ID 2020-6477 Overview Responsible for first and second level day to day onsite support of users and systems (regulated and non-regulated). In addition, the Support Specialist II will be counted on to correctly prioritize and escalate problems and requests to other members of the IT Department. Responsibilities • End user desktop, laptop, phone and software support including remote users • Imaging and deployment of computer equipment. • Manages and creates user accounts for on-boarding and off-boarding user and IT orientation for new hires • Video and teleconference support • Works with network administrators and application support staff to ensure user management, customer service and proper troubleshooting. • Keeps desktop OS and desktop software up to date. • Coordinates printer setup and repairs. • Contacts vendors and contractors as needed. Manage repair process of those vendors. • Assists with end user device security functions that may include anti-virus and malware protection. • Assists in infrastructure projects that may include, but are not limited to: VoIP deployments, network upgrades, server upgrades, email system upgrades and application deployments. • Trains users on IT Systems and Policies • Respond to, escalate/reassign, and close helpdesk tickets • Works on routine assignments per written procedures, where ability to recognize deviation from accepted practice is required. • Normally receives minimal instructions on routine work and detailed instructions on new assignments. • Works under close supervision from supervisor or senior personnel. • Ability to work in a team environment and independently as required • Ability to liaise with global operation team with strong communication skill • Maybe required to work Holidays and weekends • Contributes to the overall operations and to the achievement of departmental goals • Perform job specific tasks in compliance with applicable Regulations, International Standards, and WuXi Biologics Policies and Standard Operating Procedures. • Thorough understanding of Good Laboratory Practices and Good Manufacturing Practices • Other duties as assigned • May be required to assist in other departments Qualifications Job Requirements: Experience / Education • Associate's or Bachelor's degree or equivalent experience • 2-3 years technical IT support experience • Preferred Certification: A+, MCSA or equivalent IT certificates Knowledge / Skills / Abilities: • Advanced knowledge of Windows 7/10 operating systems and MS Office 20xx/365 • Advanced knowledge of PC hardware troubleshooting and repair • Advanced knowledge of printers, troubleshooting and repair • Advanced knowledge of Ethernet and Wi-Fi networks • Proficient in Microsoft Office applications (Excel, Word, Outlook), VPN • Advanced knowledge of WAN, LAN, VPN, WLAN and Remote Desktop program • Advanced knowledge in setting up Backups to External Hard Drives and Network Shares • Advanced understanding of networking principles and Microsoft Active Directory • Previous experience in setting up and troubleshooting mobile phones (iOS/Android) • Strong organizational and time-management skills • Strategic thinking ability with strong analytical troubleshooting skills • Proficient in Oral & Written communication skills • A positive attitude and excellent customer service skills • Ability and desire to provide excellent customer service • Life Science company or Lab working experience is preferred Physical Requirements: • Must be able to work in an office environment with minimal noise conditions. • Must be able to work in Lab setting with exposure to Animals/biohazards / Chemicals (List specific Chemicals) • Must be able to wear appropriate PPE • Must be able to work in environment with variable noise levels • Ability to stand /Sit/walk for long periods of time • Ability to lift 25 lbs routinely • Ability to lift 100 lbs with help of at least one other person occasionally • Ability to crouch, bend, twist, and reach • Ability to push/pull 100 lbs occasionally • Clarity of Vision • Ability to identify and distinguish colors • Must be able to perform activities with repetitive motions • Ability to climb Ladders / Stairs / Scaffolding An Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, or protected veteran status and will not be discriminated against on the basis of disability This job description does not state or imply that the above are the only duties and responsibilities assigned to this position. Employees holding this position will be required to perform any other job-related duties as requested by Management. PI119352370

AmeriGas AmeriGas is a Drug Free Workplace. Candidates must be able to pass a pre-employment drug screen and a criminal background check. AmeriGas is an Equal Opportunity Employer. Location: King Of Prussia, PA, US Company: AmeriGas Propane, Inc. When you work for AmeriGas, you become a part of something BIG! Founded in 1959, AmeriGas is the nation's premiere propane company, serving over 2 million residential, commercial, industrial and motor fuel propane customers. Together, our 8,500 dedicated professionals will deliver 1.5 billion gallons of propane from 1,400 distribution points across the United States. Posting Job Summary (Purpose): The Category Associate will act on behalf of AmeriGas to minimize the cost of acquiring goods and services across specific categories and be relied on to provide category/commodity subject matter information to both internal customer and vendors. This role will be accountable for executing against specific sourcing and procurement strategies across a number of categories such as tanks, cylinders and MRO. They will also be challenged with managing associated supplier relationships tied with their category responsibility. Key Characteristics: • Demonstrated commitment to customer service; proactively communicates and responds promptly to customer needs • Must have strong relationship building abilities. • Must be comfortable with negotiating with suppliers with a key focus on achieving cost savings. • Solid understanding of procurement tactics and operational/business contracting practices Duties and Responsibilities: • Act as the point of contact for vendors within assigned scope of responsibility • Manage day to day vendor relationships, including but not limited to delivery, quality and billing issues • Resolve or assist with purchase order invoice discrepancies as required or needed • Monitor vendor service levels and performance and address issues as required • Demonstrate a solid understanding of assigned commodities and/or categories and be comfortable serving as the main Procurement point of contact for those commodities • Conduct and support RFx solicitations for the acquisition of goods and services, adhering to standard sourcing principles and processes • Monitor and evaluate contract compliance with all agreements within assigned commodities • Support, train and provide guidance to junior team members as directed • Maintain focus on delighting the customer; ensure that customer requests are met both timely and with high quality • Responsible for developing metrics and key performance indicators for vendors within assigned commodities • Complete and/or assist with supplier score carding and quality audits comparing vendor performance against what has been contractually agreed upon • Work with vendors to establish and maintain punch out or static catalogues within company Ariba P2P solution • Analyze spending patterns and perform data mining to uncover sourcing opportunities and spend optimization • Assist tactical procurement team members with operational tasks as required • Adhere to established processes and policies and identify continuous improvement opportunities • Assist with Ariba P2P training, usage and adoption • Act as a source of information to AmerGas field locations for assigned commodities Knowledge, Skills and Abilities: • Excellent interpersonal and communication skills • Familiarity with Ariba P2P preferred • Strong project management skills desired • Comfortable with "managing up" to Procurement leaders regarding project and operational statuses. • Proficiency with Microsoft Office tools • Expertise in negotiations and supplier management Education and Experience Required: • BA/BS in relevant field, including Business Admin, Supply Chain, Finance. • 3-5 years' procurement related experience required • Background that includes negotiations, contract management, and vendor management is strongly desired. Nearest Major Market: Philadelphia Job Segment: Category Manager, Supply, Procurement, Project Manager, Data Mining, Retail, Operations, Technology PI119122283