- Novo Nordisk Inc. (Boulder, CO)
- …and scale-up processes from laboratory to pilot plant scale Author and/or review batch documentation and generate automated equipment methods Execute ... are driving change. Are you ready to make a difference? The Position The Specialist , API Manufacturing works in Novo Nordisk's Boulder, Colorado Pilot Plant and is… more
- Merck & Co. (Durham, NC)
- …formulation vessel, lyophilizers, etc.).Provide QA shop floor support in the execution and review of GMP documentation such as IQ, OQ and other technical ... product inspection, and quality control laboratories. The Quality Assurance Specialist will support this expansion. Project activities requiring support include… more
- Novo Nordisk Inc. (Durham, NC)
- …Records (BPRs) & relevant quality processes are compliant with regulations. Performs quality review & approval of Change Requests (CR's) & other documentation ... compliance with Regulations, ISO standards, corporate & local SOPs Reviews & approves documentation for Quality approval - batch records & other documentation … more
- Novo Nordisk Inc. (Durham, NC)
- …Novo Nordisk and help us make what matters. The Position Performs quality review & approval of Batch Production Records (BPRs), Change Requests (CR's), Deviations & ... other documentation (in conjunction with LoB) & QA presence &...Handles release of raw materials & provides quality oversight, review & approval of validation activities associated with minor… more
- Merck & Co. (Rahway, NJ)
- …job that provides both technical and project management responsibility. The Specialist - Manufacturing Automation position will report to the Director, Engineering, ... production, utility systems and associated infrastructure.- Responsibilities of the Specialist - Manufacturing Automation include the following:The automation engineer… more
- Lovelace Biomedical Research Institute (Albuquerque, NM)
- OverviewUnder specific direction, the Accounts Payable Specialist will be responsible for timely and accurate processing of accounts payable disbursements and ... ensuring compliance with internal controls.Will review reconcile vendor statements and invoices, process all accounts payable transactions for payments, process… more
- Aequor (Seattle, WA)
- …procedure. Review training form submissions for adherence to good documentation principals, accuracy and completion. Oversee the creation, edit and/or retirement ... Utilize a consultative approach and powerful questions in customer interactions and review training requests in order to address actual vs. stated training need.… more
- Merck & Co. (Durham, NC)
- Job DescriptionPosition Description: Senior Specialist , Manufacturing Automation The Senior Specialist Manufacturing Automation person is primarily responsible ... the automation systems in compliance with cGMPs. The Manufacturing Automation Sr. Specialist must actively support, participate and embrace an empowered team culture… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionPosition Description: Executive Transportation Specialist Working in a dynamic, fast paced environment, the Executive Transportation Driver reports ... Director, Executive & Personnel Protection, Global Security.The Executive Transportation Specialist is an experienced professional responsible for the safe and… more
- Novo Nordisk Inc. (Durham, NC)
- …The Position Plan, manage & perform laboratory validation activities. Routine review of laboratory validation procedures & completed validation protocols for ... Support systematic problem solving related to equipment qualification Reviews documentation for accuracy & completeness Contribute to process confirmations Maintain… more
- Catalent (Manassas, VA)
- …to help create engaging new products consumers will love.The Document Control Specialist - 2nd Shift is responsible for creating and maintaining the Quality ... System documentation . Communicate any deviations to management. Assist the Quality...Quality Systems and Regulatory Manager in complete, appropriate detail; Review and verify the operators' paperwork to ensure they… more
- BioAgilytix (Durham, NC)
- …at BioAgilytix.Essential ResponsibilitiesPerform Quality Control (QC) technical, scientific, and compliance review of data and documentation generated by the ... OOS and OOT associated with Bioanalytical Operations data as applicableIssue QC review observations and work closely with the scientific staff to ensure data… more
- Catalent (Manassas, VA)
- …to help create engaging new products consumers will love.The Quality Assurance Specialist I - Quarantine is responsible for auditing the products and processes ... incoming labels and packaging materials and well as reviews receiving documentation . Responsible for maintaining Raw Materials and Finished Goods' Quarantine log;… more
- Merck & Co. (Rahway, NJ)
- …in supporting the process automation systems within clinical manufacturing.-The Automation Specialist - Engineering Auto Eng position will report to the Director, ... and develop appropriate system validation, change control, and testing documentation .Maintain familiarity with system life cycle documentation methodology… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of an immunotherapy in the treatment of multiple myeloma. Legend Biotech is seeking QC Specialist , Lab Services - I, II, III as part of the Quality team based in ... Raritan, NJ. Role Overview The QC Specialist , Lab Services, is responsible for sample management. The QC Specialist is encouraged to work independently on… more
- Aequor (New Brunswick, NJ)
- …experience in GMP environment. Job Description: 100% onsite Responsibilities: Review and approve vendor-executed calibration, maintenance, repair, and performance ... verification work. Prepare documentation for Quality Assurance approval prior to work execution. Monitor schedules to ensure timely completion of calibration,… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …accurate and performed in a timely manner in accordance with the procedures. Review and inspect documentation in support of Final Product Shipments. Generates ... Biotech is seeking a QA Warehouse Incoming Raw Material Specialist as part of the Quality team based in...and record results to complete receipt process. Reviews inspection documentation (C of A or other Material Certifications) for… more
- Aequor (Swiftwater, MN)
- …cycle and lead the investigation or trouble shooting. o Ability to review and analyze data. Cleaning Validation experience o Acceptance criteria determination o ... in a GMP setting MS Project experience Skills Proficiency in utilizing documentation system to author protocols and reports Experience participating in teams and… more
- Exela Pharma Sciences, LLC (Lenoir, NC)
- …and other regulatory requirements are adhered to as it relates to review and approval of engineering/validation specific documentation . He/she must ensure ... The QA Specialist II - Engineering/Validation is responsible for cGMP...the Engineering and Validation departments. Job Responsibilities Perform Quality review /approval of URS, FAT, SAT, IQ,OQ,PQ protocols and summary… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …is responsible for performing reviews of manufacturing and support documentation and records to certify compliance with in-house specifications/standards and ... for all NNUSBPI products. This position has QA signature authority on the review of individual batch records, supporting test records and other ancillary support… more
