- Legend Biotech USA, Inc. (Raritan, NJ)
- …in the treatment of multiple myeloma. Legend Biotech is seeking a QC Data Reviewer as part of the Quality team based in Raritan, NJ. Role Overview The ... QC Data Reviewer is an...is an exempt level position responsible for reviewing all data produced by the Quality Control...interacting with inspectors. Due to the nature of the Data Review process, this role is 100%… more
- BioAgilytix (Durham, NC)
- …right at home here at BioAgilytix.Essential ResponsibilitiesPerform Quality Control ( QC ) technical, scientific, and compliance review of data and ... will be a critical part of our beginning-to-end client data quality processes. Through your technical reviews...GMP).Identify deviations, OOS and OOT associated with Bioanalytical Operations data as applicableIssue QC review … more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …multiple myeloma. Legend Biotech is seeking a Lead QC Microbiology Data Reviewer as part of the Quality team based in Raritan, New Jersey. Role Overview ... The Lead QC Microbiology Data Reviewer is...commercial operations in a controlled cGMP cleanroom environment. Create, review and approve relevant QC documents, logbooks,… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …under the direction of the QC Manager. Relationships Reports to: Quality Control Manager Number of subordinates with direct/indirect referral: no direct ... and QC for the coordination of process/equipment improvements, sample testing and data trending/analysis Review of completed QC documentation Ability to… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs). Ensures quality control activities are aligned with industry, regulatory and ... to a better tomorrow for our patients. Ethics and quality are held in the highest regard, and a...microbiological assays, techniques and industry practices Participates in the review of microbiological trending data and writing… more
- Tris Pharma (Monmouth Junction, NJ)
- …results using instrument specific data processing software. Complete timely compendial review to maintain QC lab compliance, + work w/ rel departments ... QC Lab Operations Specialists for Tris Pharma, Inc....+ Dissolution Apparatus (Distek). Initiate + draft investigations. Create, review + revise SOPs. Assess equip. perf. Execute equip.… more
- Merck & Co. (Millsboro, DE)
- …reliable supply to customers and patients on time, every time, across the globe.The Quality Control ( QC ) Associate Specialist, with Guidance from the ... QC Manager, ensures product/process quality through the review of GMP documentation...requirementsSAP transactions, inventory control , GMP documentation and data integrityResponsible for the review and release… more
- Aequor (West Greenwich, RI)
- …GMP operations and Environmental/Water monitoring. 2. Perform testing and possible data review for compendia, non-compendia methods, and routine laboratory ... responsible for activities including microbiology & analytical testing, sample and data management and equipment and instrumentation operation and maintenance in a… more
- BioAgilytix (Boston, MA)
- …to GxP guidelines)Essential Responsibilities: Data Review & DocumentationPerform Quality Control ( QC ) technical and scientific and compliance ... GLP, GMP) and non-regulatedIdentify deviations, OOS and OOT associated with Bioanalytical Operations data as applicableIssue QC review observations and work… more
- Lundbeck (Bothell, WA)
- …use in GMP testing) Oversee routine analytical testing and coordinate study support across Quality Control ( QC ) and Process Development (PD) groups Oversee ... optimizing new potency assays and then supporting transfer to QC , including supporting QC (as needed) with...will interact with Lundbeck Seattle Upstream, Downstream, Formulation, and Quality Control groups so strong interpersonal skills… more
