Job Description

• Visiting to Quality Control Labs to ensure that activities are being carried out by following GMP requirements and as per approved procedures.
• To ensure that labs are maintained to be GMP ready always. Follow-up to close the findings as per established procedures.
• Handling of QC Lab incidents, Deviations, change controls, OOS, OOT, OOL, QRM, CAPA management and related investigations throughout the year.
• Verification of analytical test results and approval through SAP. (In-process, Intermediate, DS, FB, DP and additional study reports if any).
• Batch Release activity for intermediates and In-process (i.e.: Media, buffers and so on).
• Review of SOPs/ STPs/ Specifications and any other documents as per GMP requirements for QC/QA department.
• Ensure that stability studies/ testing of samples are being carried out by following approved procedure/protocols.

Work Experience
1-5 years
Education
Post Graduation in Life Science or Biotechnology
Competencies
1. Strategic Agility
2. Innovation & Creativity
5. Result Orientation
Quality
Technical Skills