- Parexel (Sacramento, CA)
- …activities CALIBRATIONS: + Execute "Before-Use" calibrations prior to performing testing + Review calibration data within the ELN + Prepare and submit ... Skills and Experience** + Experience in working in a GMP Pharmaceutical environment with specific experience environmental monitoring +...reports + Able to clearly interpret adverse vs desirable data + Mold investigations and studies + PSIM work… more
- BeOne Medicines (Pennington, NJ)
- …cGMP/EU GMP . + Strong knowledge of regulatory requirements for data management and compliance. + Impressive, demonstrable track record and skills/experience ... Quality Control (QC) laboratory instrumentation and metrology activities to support GMP manufacturing, testing, and release of materials, intermediates, and finished… more
- BeOne Medicines (Pennington, NJ)
- **General Description:** Review QC data and test records in accordance with BeOne procedures to support GMP testing and release of materials, intermediates, ... regulations and other applicable international standards. **Essential Functions of the job:** + Review and validate QC data and test records. + Support… more
- BeOne Medicines (Pennington, NJ)
- …results in support of manufacturing operations. + Review , interpret, and report analytical data in accordance with GMP regulations and internal ... other junior level analysts and new hires on instrumentation, GMP practices, and data analysis. + Serving...of test results in support of manufacturing operations. + Review of laboratory test results, ensuring adherence to Good… more
- BeOne Medicines (Pennington, NJ)
- …results in support of manufacturing operations. + Review , interpret, and report analytical data in accordance with GMP regulations and internal ... procedures. + Lead troubleshooting efforts for analytical methods and instrumentation related to CE. + Conduct...junior level analysts and new hires on CE instrumentation, GMP practices, and data analysis. + Serving… more
- BeOne Medicines (Pennington, NJ)
- …results in support of manufacturing operations. + Review , interpret, and report analytical data in accordance with GMP regulations and internal ... procedures. + Lead troubleshooting efforts for analytical methods and instrumentation related to CE. + Conduct...junior level analysts and new hires on CE instrumentation, GMP practices, and data analysis. + Serving… more
- CSL Behring (Kankakee, IL)
- …Improvement** + Lead equipment-related changes through formal change control processes, ensuring GMP compliance, data integrity, and controlled risk. + Drive ... comply with GMP , EHS, and ISO 55000/55001 requirements. + Author, review , and approve SOPs/, change controls, deviations, and CAPAs. + Lead and support… more
- Quad (Franklin, WI)
- …departments. + Manage documentation, reporting, and closure of compliance issues. + Review GMP documents for compliance with SOPs, quality systems, and ... internal audit teams. + Hold monthly leadership meetings to review YTD costs of quality, trends, and system performance....industry standards for packaging and food safety. + Strong analytical skills with the ability to interpret data… more
- Caris Life Sciences (Phoenix, AZ)
- …jack, and/or forklift to safely transport materials. + Use ERP system to review purchase order (PO) and process receipt accordingly. + Use eQMS (electronic Quality ... Management System) to review and print material specification forms. + Verify that...maintain cleaning log. + Adhere to good manufacturing practices ( GMP ). + Maintain organized workstations and warehouse by applying… more
- Parexel (Phoenix, AZ)
- …determines, and discusses with LSAD the correct timing and type of visits. + Performs Source Data Review (SDR), Case Report Form (CRF) review and Source ... maintenance. Tasks may include Site Qualification Visits, collection, preparation, review and tracking of documents for the application process; submission… more
- Parexel (Des Moines, IA)
- …determines and discusses with LSAD the correct timing and type of visits. + Performs Source Data Review (SDR), Case Report Form (CRF) review and Source ... maintenance. Tasks may include Site Qualification Visits, collection, preparation, review and tracking of documents for the application process; submission… more
- ALBEMARLE (Charlotte, NC)
- …acumen, Customer focus, understanding of the industry and customer expectations. + Data -based decision making, Analytical thinking. + Strong technical foundation ... accordance with corporate and regulatory standards (eg, ISO 9001, GMP , IATF 16949) + Partner with site teams to...Builds trust and alignment across functions and cultures. + ** Analytical Thinking:** Uses data to identify root… more
- Kerry (Fort Worth, TX)
- …o Accurately complete detailed documentation and maintain precise records of production data , test results, and traceability information. o Review and reconcile ... checks. o Conduct micro swabs, allergen swabs, thermometer calibrations, and other analytical tests as required. o Perform additional analytical testing as… more
- Kerry (Norwich, NY)
- …and maintain laboratory equipment within the Quality Control Laboratories + Review Production Batch Records to ensure compliance with manufacturing procedures, both ... required to handle hazardous waste + Entry of testing data as well as releasing of product in SAP...combination years of experience and education. + Microbiology / Analytical experience?a plus. + 1-2 years of laboratory experience… more
- Coty (Hunt Valley, MD)
- …Manufacturing Process Engineer, you will lead continuous improvement activities through detailed data analysis and root cause problem solving tools to achieve a ... methodology and process capability studies + Analyze critical line data to make recommendations for improvement from trends +...KPI's for the manufacturing facility + Follow all site GMP policies and procedures + Other duties as assigned… more
- Post Holdings Inc. (Wakefield, NE)
- …RESPONSIBILITIES:** + Utilize CMMS to support the maintenance function including review , execution and documentation of scheduled/unscheduled work on a daily basis. ... in all jobs and tasks. + Adhere to Quality work practices, follow all GMP 's, maintain sanitary conditions and ensure that product quality is maintained. Report to… more
- Bristol Myers Squibb (Summit, NJ)
- …an environment and culture to keep our employees safe. + Utilize state-of-the-art data acquisition and analytical technology to drive asset performance while ... BMS with our Cell Therapy team. The Senior Manager, GMP Facilities provides leadership and direction to the 24/7...class maintenance and reliability KPI's and ensure the appropriate review process is in place so actions are being… more
- ThermoFisher Scientific (Middleton, WI)
- …biopharmaceutical compounds in a variety of formulations. You will be responsible for review and compilation of results and data comparison against SOP ... Shift (Days) **Environmental Conditions** Adherence to all Good Manufacturing Practices ( GMP ) Safety Standards, Office, Some degree of PPE (Personal Protective… more
- Eurofins US Network (Rensselaer, NY)
- …looking for a rewarding career, apply with us today! ** **Job Description** ** Data Review Responsibilities** + Review of GMP data generated by ... international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to...the chain of custody integrity for samples tested + Review of audit trails to confirm adherence to actions… more
- Eurofins US Network (Lancaster, PA)
- …data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations. + Review simple and complex routine and non-routine ... international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to... data for accuracy, clarity, and adherence to GMP and/or GLP regulations + Review simple… more
