QA Specialist (Biotech) needs 3 years of experience in the biotech/pharmaceutical industry within research and development or commercial organizations.
QA Specialist (Biotech) requires:
- Pharma Biotech industry
- Veeva
- cGMP manufacturing environment
- FDA
- Kneat
- Slinshot
- SAP
- Blue mountain RAM
- Knowledge of manufacturing batch record review and/or analytical analyses for the biotech/pharmaceutical
- Degree in Chemistry biological or other
QA Specialist (Biotech) duties:
- Responsible for performing inspection and disposition of raw materials and components by:
- Supporting incoming material release activities within the ERP system ensuring compliance with applicable regulations and internal procedures.
- Get Certificates of Analysis (CoA) Certificates of Compliance (CoC) and other required documentation from vendors in alignment with the Master Specification
- Conduct thorough reviews of logbooks and Work Orders across Manufacturing Engineering Quality and Warehouse departments to ensure entries are complete accurate and compliant with company policies and procedures.
- Responsible for providing QA review/approval of the completed Manufacturing batch records in a timely manner and ensuring that the entries adhere to the company policies and procedures.
QA Specialist (Biotech) needs 3 years of experience in the biotech/pharmaceutical industry within research and development or commercial organizations. QA Specialist (Biotech) requires: Pharma Biotech industryVeevacGMP manufacturing environmentFDAKneatSlinshotSAPBlue mountain RAMKnowledge of manufa...
QA Specialist (Biotech) needs 3 years of experience in the biotech/pharmaceutical industry within research and development or commercial organizations.
QA Specialist (Biotech) requires:
- Pharma Biotech industry
- Veeva
- cGMP manufacturing environment
- FDA
- Kneat
- Slinshot
- SAP
- Blue mountain RAM
- Knowledge of manufacturing batch record review and/or analytical analyses for the biotech/pharmaceutical
- Degree in Chemistry biological or other
QA Specialist (Biotech) duties:
- Responsible for performing inspection and disposition of raw materials and components by:
- Supporting incoming material release activities within the ERP system ensuring compliance with applicable regulations and internal procedures.
- Get Certificates of Analysis (CoA) Certificates of Compliance (CoC) and other required documentation from vendors in alignment with the Master Specification
- Conduct thorough reviews of logbooks and Work Orders across Manufacturing Engineering Quality and Warehouse departments to ensure entries are complete accurate and compliant with company policies and procedures.
- Responsible for providing QA review/approval of the completed Manufacturing batch records in a timely manner and ensuring that the entries adhere to the company policies and procedures.
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