B.S. with 12+ years, M.S. with 10+ years or PhD, with 6+ years industrial experience in biopharmaceutical industry, such as Biology, Biochemistry, Analytical Chemistry or related field, particularly in the area of assessing product activities of biological products,
5+ years of supervisory and managerial experiences
• Good statistical analysis, analytical and trouble shooting skills and effective multi-tasking skills.
• Must have excellent technical writing skills and high attention to detail
• Knowledge in cGMP, CFR and other regulations in order to assure laboratory compliance.
• Able to seek additional tasks or non-routine functions and accomplish them with minimal supervision
• Overcome conflicts with priorities; consult supervisor regarding major conflicts
• Have knowledge of compendia methods performed in a cGMP environment.
• Have knowledge of assay transfer, validation and implementation.
• Enthusiasm to identify and evaluate new assays and new technology in improving proficiency in laboratory operations.
• Strong organizational skills in record keeping, data analysis, and strong computer skills.
• Good verbal and written communication ability and team oriented with strong interpersonal skills.
• Have ability to plan budget for the group
Why GSK? Because GSK's Biopharm business vision is to leverage its experience and technical capabilities to launch, supply, and manage Biopharmaceutical products around the world. It will fulfill GSK's Mission to Do More, Feel Better, and Live Longer by living its values: Integrity: Always doing the right thing; Commitment to the Patient: Making the Patient the #1 Priority; Customer Service: Commit to delivering on promises to internal & external customers; Compliance - Being accountable for quality and safety.
GSK Biopharm in Rockville MD has an opening for a QC Supervisor. In this role, you will plan and prioritize resource allocation in Rockville quality control bioassay laboratory to meet testing requirements for raw material programs. Oversee the operation of QC Raw Materials group. Responsible for training quality control analysts, transferring assays from development group, qualifying and validating new assays and implementing assays to be used for quality control purposes to support manufacturing and marketing of the product. Other functions: conduct laboratory investigations related to raw material testing, compile reports in support of product filings with the regulatory agencies. Review and release of test results, and ensure full cGMP compliance in the laboratory operations. Prepare documents (IND, BLA and MAA) to support regulatory filing.
• Responsible for training quality control analysts, transfer assays from development group, qualify and validate new assays and implement assays to be used for quality control purposes to support manufacturing and commercial products.
• Conduct laboratory investigations related to product testing.
• Compile reports in support of product filings with the regulatory agency.
• Review and release of test results.
• Ensure group compliance with laws, regulations, guidelines, procedures and practices governing bioassay QC testing, including departmental and corporate standard operating procedures and safety procedures
• Ensure technical and professional growth of QC analysts, encouraging excellence and continuous improvement in their performance
• Collaborate and work effectively within the Quality Control groups as well as other departments.
• Represent the quality control department and departmental functions on company projects/committees. Review, update regulatory documents (IND, EOP2, IMPD), as required.
You may apply for this position online by selecting the Apply now button.
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