summary

hyderabad, telangana
temporary

job category
engineering

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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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quality assurance service consultant.

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experience

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