Dear Applicants, Greeting from Biophore India pharmaceutical Pvt Ltd, We have opening for Formulation DQA Department-Development Quality Assurance

Job description
-3
- 6 Yrs
- Handling of QMS documents and Ensure the SOP compliance
- Review of Formulation Analytical Development Documents & Formulation Product Development Documents.
- Method Validation and Transfer Protocols and Reports
- Product development with QbD approach
- Responsible for ensuring GMP/GLP/GDP compliance in the Formulation and Analytical areas as per the respective SOPs.
- Review of FRD activities (LNBs, BDRs, PDR’s, MFR’s and MPR’)
- SOP’s and Guidelines Preparation and Review and Approval of SOP’s.
- Responsible for conducting Internal Audits/External Audits for Cross functional
- Departments in Formulation Division and External Division.
- Conducting and Coordinating Employee Trainings.
- Responsible for Review and Approval of Vendor Qualification
- Should have experience in IPQA and Analytical QA (OSD/Injectable)
- Ref to Friends or colleagues.
- Please Share update resume: [email protected]
- Total Exp:
- Current CTC:
- Exp CTC :
- Notice Period:
- Designation:

📌 Executive/Sr Executive For Formulation (Hyderabad)
🏢 Biophore
📍 Hyderabad