- Regeneron Pharmaceuticals (Rensselaer, NY)
- We are currently looking to fill a Quality Assurance Specialist position. This position performs activities supporting dispositioning product and/or raw ... materials while ensuring compliance with Quality Assurance policies and procedures, cGMPs, SOPs,...amount of relevant experience for each level: + Associate QA Specialist - 2+ years + … more
- Actalent (Foster City, CA)
- Opportunity to gain experience in the pharmaceutical / biotech industry! + Executes batch record review + Performs a wide variety of activities to ensure ... requirements. + Participates in developing Standard Operating Procedures to ensure quality objectives are met. + Maintains programs and processes to ensure… more
- Actalent (Foster City, CA)
- …routine work, general instructions on new assignments. Skills: batch record review , Quality assurance , standard operating procedure, glp, gmp environment ... Description: Executes batch record review Performs a wide...requirements. Participates in developing Standard Operating Procedures to ensure quality objectives are met. Maintains programs and processes to… more
- Actalent (Foster City, CA)
- …all aspects of producing quality products. Skills: batch record review , Quality assurance , standard operating procedure, glp, gmp environment ... requirements. Participates in developing Standard Operating Procedures to ensure quality objectives are met. Maintains programs and processes to...* 2+ years of experience relevant to job description. QA / batch record review … more
- Regeneron Pharmaceuticals (Troy, NY)
- We are currently looking to fill a Quality Assurance Specialist ( Batch Disposition) position. This position performs activities supporting dispositioning ... product and/or raw materials while ensuring compliance with Quality Assurance policies and procedures, cGMPs, SOPs,...amount of relevant experience for each level: + Associate QA Specialist - 2+ years + … more
- Integra LifeSciences (Cordova, TN)
- …headway to help improve outcomes. **JOB DESCRIPTION** The Specialist , Quality Assurance ( QA ) is responsible for batch record release, donor record/ ... data entry, auditing, and investigations. The Specialist , QA is responsible for quality assurance...+ Perform quality reviews of donor and batch records + Review and analyze test… more
- Bristol Myers Squibb (Bothell, WA)
- …patients, there's no better place than here at BMS with our Cell Therapy team. The Quality Assurance Specialist position plays a key role in supporting the ... a regulated cGMP environment. The primary focus of the QA Specialist role will be to support...- Wednesday, 9 pm - 7:30 am **Responsibilities:** + Review executed batch records to ensure compliance… more
- Abeona (Cleveland, OH)
- Position Overview The Specialist I, Quality Assurance - Operations performs routine activities associated with manufacturing of cell and gene therapy ... management ensuring procedural and regulatory compliance throughout the manufacturing process. The Specialist , Quality Assurance - Operations will report to… more
- Actalent (Bedford, MA)
- …as needed. Skills: Quality assurance , Compliance, GMP, Document control, Batch Record, Batch Record Review , product release, investigations, Root ... the Bedford, MA area! **Must have quality assurance experience as well as CAPAs, Batch ... assurance experience as well as CAPAs, Batch Record Review , investigations, deviations experience** If… more
- Editas Medicine (Cambridge, MA)
- …life science and 8+/6+ years respectively of relevant industry experience in Quality Assurance in a Pharmaceutical/Biotech GMP environment. + Experience ... and facility start-up, floor operations, MBR and SOP generation/revision, record review , controlled document generation, batch release, training, materials… more
- Actalent (Wilson, NC)
- Description: The Batch Record Quality Specialist II... review /release in QA . Skills: documentation review , GMP, SOP, Quality Assurance Top ... will be responsible for conducting thorough reviews of manufacturing batch records for completeness and that the required information...record. These individuals will be doing a less technical review as they will be focused on ensuring records… more
- Cambridge Isotope Laboratories, Inc. (Tewksbury, MA)
- Cambridge Isotope Laboratories (CIL) has an outstanding opportunity for a Quality Assurance Specialist I to join the team responsible for the quality of ... Annual Product Review Reports, as needed + Contributor to various QA Quality Program functions when needed (eg Deviation, CAPA, Supplier Management,… more
- System One (Bothell, WA)
- Job Title: Quality Assurance Specialist Location: Bothell, WA Hours/Schedule: 9:00pm - 7:30am, Sun - Wed Compensation: $37.00 - $42.41/hr Type: Contract, ... Potential for extension or conversion to permanent Responsibilities + Review executed batch records to ensure compliance with approved procedures and communicate… more
- Novo Nordisk (Durham, NC)
- …potential? Join Team Novo Nordisk and help us make what matters. The Position Performs quality review & approval of Batch Production Records (BPRs), Change ... presence & process confirmation on shop floor. Relationships Manager, Quality Assurance . Essential Functions + Ensures site...& how to apply required + Understanding of the Batch Review Processes required + Understanding of… more
- Novo Nordisk (Clayton, NC)
- …Manager, Quality Assurance . Essential Functions + Perform activities related to Batch review + Review API/Intermediate Batch documentation in ... release of API materials, minor deviations, minor change controls, review & approval of SOPs, QA presence...apply required + Understanding of the Batch review Processes preferred + Understanding of quality … more
- Takeda Pharmaceuticals (Social Circle, GA)
- …As a Quality Insurance Specialist II, you will provide Quality Assurance support for Manufacturing process, Critical utilities, provide Quality ... leadership. **How you will contribute:** + Responsible ongoing, daily departmental Quality Assurance support for Manufacturing process or Critical utilities.… more
- Novo Nordisk (Clayton, NC)
- …(Authorized Qualified Person), if role is in batch release. Serve as Quality oversight, review & approval of validation activities associated with projects, ... & process confirmation across FP, utilizing LEAN principles. Relationships Senior Manager, Quality Assurance . Essential Functions + Make decisions on quality… more
- Element Materials Technology (Santa Rosa, CA)
- **Overview** Element has an exciting opportunity for a ** Quality Assurance ( QA ) Specialist ** to join our team, located in Santa Rosa, California. The **( ... QA ) Specialist ** ensures the cGMP system is...Standard Operating Procedures and all other cGMP documentation + Review of executed batch records, validation, qualification,… more
- Novo Nordisk (Clayton, NC)
- …& other documentation. Perform Self Audits (in conjunction with line of business (LoB)), Quality Assurance ( QA ) presence & process confirmation on shop floor ... with stakeholder. Relationships Senior Manager, Quality Assurance . Essential Functions + Ensure site...SOPs + Review & approve documentation for Quality approval - components/raw material, batch records,… more
- Catalent Pharma Solutions (Chelsea, MA)
- **We're hiring for a rotating night shift Quality Assurance Specialist I to provide QA support for cGMP manufacturing activities, at our facility in the ... healthier lives. The ** Quality Assurance Specialist I** is responsible for supporting the QA... of production activities, including area clearance, issuance, and review of batch records. + Support of… more