- Catalent Pharma Solutions (Chelsea, MA)
- ** Quality Assurance Specialist II - Night** **Position Summary:** Catalent is a global, high-growth, public company and a leading partner for the ... in North America. Catalent Pharma Solutions is hiring a Quality Assurance Specialist II -...production activities, including area clearance, issuance and review of batch records, and making decisions on initiation of Discrepancies;… more
- Catalent Pharma Solutions (Harmans, MD)
- ** Specialist II , MTO** **Summary:** _Our FDA-licensed, state-of-the-art CGMP manufacturing facility for Gene Therapies is located on the Harmans/BWI campus. The ... AAV and other viral vector-based therapies and vaccines._ The ** Specialist II , MTO** will provide support to...MTO** will provide support to Manufacturing Associates to meet batch record review/disposition schedule to adhere to lot release… more
- Mallinckrodt Pharmaceuticals (Hobart, NY)
- Job Title Operations Compliance Specialist II - Third Shift Requisition JR000014264 Operations Compliance Specialist II - Third Shift (Open) Location ... - $36,467 - $58,348 Plus $3.00 Per Hour Shift Differential Ensures quality procedures are followed and evaluates the organization's products, materials, and… more
- Bristol Myers Squibb (Summit, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . **Title: Senior Specialist , Engineer II , External MS&T** **Location: Warren, NJ or ... Summit, NJ** The **Senior Specialist , Engineer II , External MS&T** is responsible...CMOs including creation, changes, and enhancements to process documentation ( batch records, work instructions, SOPs, etc.) occurring at CMOs.… more
- Randstad US (Swiftwater, PA)
- usa-regulatory affairs specialist ii (clinical)- first shift. + swiftwater , pennsylvania + posted 6 days ago **job details** summary + $55 - $57.20 per hour + ... occupations + reference49310 job details job summary: The Regulatory CMC Specialist in Regulatory Site Office supports regulatory compliance for marketed products… more
- Gilead Sciences, Inc. (Foster City, CA)
- …Description** **Role and Responsibilities:** + Interact with contract manufacturers to resolve quality issues with minimal supervision + Performs a wide variety of ... requirements. + Participates in developing Standard Operating Procedures (SOPs) to ensure quality objectives are met. + Maintains routine programs and processes to… more
- Adecco US, Inc. (Swiftwater, PA)
- …Healthcare & Life Sciences is hiring a contract hybrid Regulatory Affairs Specialist for our Pharmaceutical Manufacturing partner in Swiftwater, PA. The anticipated ... upon meeting eligibility criteria Overview of the Position The Regulatory CMC Specialist will work closely with the Regulatory Site Office, Manufacturing and Supply… more
- Danaher Corporation (Madison, WI)
- …solutions that safeguard and improve human health. This position is part of the Quality Department located in Madison. Wisconsin and will be on-site. At Aldevron, we ... lay the groundwork for vital new discoveries worldwide. You will be a part of the Quality Assurance team and report to the Director of Quality . In this role you… more
- Randstad US (Lake Forest, CA)
- regulatory affairs specialist ii . + lake forest , california + posted october 10, 2024 **job details** summary + $50 - $58.79 per hour + contract + bachelor ... + reference49136 job details job summary: Immediate opportunity for a Regulatory Affairs Specialist II with a leading, global eye care company located in… more
- Danaher Corporation (Fargo, ND)
- …that safeguard and improve human health. This position is part of the Operational Quality Assurance department located in Fargo, ND and will be onsite working a ... discoveries worldwide. You will be a part of the Quality Assurance team and report to the Operational ...traceability of final material + Review GMP and GMP-S Batch Record Documentation + Complete review of Packaging generated… more
- Novo Nordisk (West Lebanon, NH)
- …products. This position has QA signature authority on the review of individual batch records, supporting test records and other ancillary support records. Will be a ... of NNUSBPI Manufacturing facilities + Releases product based on Quality Assurance record review and approval by Manager, ...Quality Assurance record review and approval by Manager, Quality Assurance + Review and assess Corrective and Preventive… more
- Fujifilm (College Station, TX)
- …in the hub of innovation, representing a source of pride for the area. The Quality Assurance (QA) Specialist II , QA Validation, under general direction, will ... of basic and technical documentation; Drafting and reviewing of internal Quality policies and procedures; Assisting in and performing product related activities;… more
- Grifols Shared Services North America, Inc (Clayton, NC)
- …countries and regions. Hours: Monday to Friday - 8:00 am - 4:30 pm The Quality Supervisor II /III in the QA Fractionation business unit will be responsible for ... including activities to support department cycle time goals. The Quality Supervisor II /III is a fully qualitied.../III will also perform tasks for Pooling through Fractionation Batch Release and other related Quality functions.… more
- University of Pennsylvania (Philadelphia, PA)
- …and wellness programs and resources, and much more. Posted Job Title Quality Assurance Specialist (Regulatory) CVPF(Center for Cellular Immunotherapy) Job ... Profile Title Research Coordinator Senior Job Description Summary The Quality Assurance Specialist will work within the Clinical Cell and Vaccine Production… more
- Actalent (Allendale, NJ)
- Job Title: Quality Assurance SpecialistJob Description As a Quality Assurance Specialist , you will be responsible for ensuring compliance with all cGMP and ... You will perform raw material inspections, issue and review batch records, and maintain all quality documentation....and review batch records, and maintain all quality documentation. Your role is critical in maintaining compliance… more
- ThermoFisher Scientific (Detroit, MI)
- …fine chemicals used in bioproduction and culture media. **How will you make an impact?** The Quality Specialist II will report to the Quality Assurance ... + Support Quality record reviews including, but not limited to, batch history records, equipment and calibration documentation, QC records, and shipping records.… more
- City of New York (New York, NY)
- …Senior Director of Systems Development & IT Support, (Computer Systems Manager, NM- II ), with wide latitude for the exercise of independent initiative and judgment, ... the Computer Specialist (Software) IV, functions as Systems Development Manager oversees...security of simple to extremely complex web-based applications, scheduled batch processes, database management systems and/or ad-hoc reports related… more
- Deloitte (Charlotte, NC)
- …testing, integration testing, and support user acceptance testing to ensure high- quality deliverables. + Initiate, lead, and deliver Salesforce projects, including ... requirements. + Perform code reviews, mentor junior developers to maintain high- quality coding standards, and ensure best practices are followed. Qualifications… more
- Deloitte (Gilbert, AZ)
- …testing, and support user acceptance testing to ensure the delivery of high- quality products. + Ability to effectively debug and resolve issues and/or defects ... Salesforce configuration and customizations using Apex, Visualforce, Triggers, Scheduled and Batch classes etc. + Knowledge of the Product Development Lifecycle,… more
- CGI Technologies and Solutions, Inc. (San Diego, CA)
- …sorting and affixing postage to sealed envelopes. Must be able to perform quality checks for standard fee information on individual applications. Due to the nature ... * Operate various equipment for high speed scanning, image review, book print, quality control, mail out and metering mail. * When operating a four-printer pod,… more