Role Summary:
Work both as individual contributor and in collaboration with team to facilitate & support regulatory requirements quality systems and best practices in drug product development
Main Accountabilities:
Review of quality control activities at analytical development lab and subcontracted
facilities.
Compliance in Analytical lab and maintain as per Global requirement.
Tracking and maintaining the documents in Analytical as per Regulatory requirement.
Participation in the local Manufacturing Review Board (MRB) provide quality input on IMP and manufacturing processes during development.
Role Summary: Work both as individual contributor and in collaboration with team to facilitate & support regulatory requirements quality systems and best practices in drug product development Main Accountabilities: Review of quality control activities at analytical development lab an...
Role Summary:
Work both as individual contributor and in collaboration with team to facilitate & support regulatory requirements quality systems and best practices in drug product development
Main Accountabilities:
Review of quality control activities at analytical development lab and subcontracted
facilities.
Compliance in Analytical lab and maintain as per Global requirement.
Tracking and maintaining the documents in Analytical as per Regulatory requirement.
Participation in the local Manufacturing Review Board (MRB) provide quality input on IMP and manufacturing processes during development.
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