Intas Pharmaceuticals Ltd. extends an invitation for walk-in interviews for positions in Quality Assurance. The available roles include Officer to Senior Officer in the Documentation Cell, focusing on PQR/APQR, requiring 1 to 4 years of experience and an educational background in M.Sc or B.Pharm, with a strong emphasis on QA documentation skills. Additionally, there are openings in the CQA department for Senior Officer to Manager roles, necessitating 3 to 15 years of experience and qualifications in B.Pharm, M.Pharm, or M.Sc. The Manager position entails vendor audits for various materials, regulatory audit preparation, and oversight of audit reports, while the Senior Officer/Executive role involves vendor management documentation, SAP management, and risk assessments related to raw materials. Furthermore, the Senior Officer position in Artwork requires expertise in reviewing printed packaging materials and vendor management.
Walk-in interview details
Date & Time: 18th February , 9.00 AM – 2.00 PM
Venue: Plot No. 5 to 14, Pharmez, Nr. Village Matoda, Sarkhej – Bavla National Highway, No. 8- A, Taluka: Sanand, Dist: Ahmedabad – 382213 Gujarat (India)
Department – Documentation Cell – QA
Section – Documentation Cell (PQR / APQR )
Role- Officer to Sr. Officer
Experience – 1 to 4 Yrs of relevant experience
Qualification – M.Sc. / B. Pahrma
Skill Set – Have good exposure in QA Documentation Area PQR / APQR)
Department – CQA
Section – Vendore / Artwork / Documentation
Role- Sr. Officer to Manager
Experience – 3 to 15 Yrs
Qualification – B.Pharma / M.Pharma / M.Sc
Skill Set:
Manager Position – Vendor Section Vendor
- Audit for API/ Excipient /KSM/ Intermediates/ PM/ contract labs etc.
- Review of audit reports and SAP management, Review of CAPA, change, investigation
- Preparation for regulatory audits
Sr. Officer / Executive – Vendor Section
- Review of Vendor management documents
- SAP management, QMS software,
- Raw material complaint management,
- Elemental impurity risk assessment
- Nitrosamine risk assessment of raw material
- Technical agreement preparation
- Review of Vendor management documents
- Preparation and review of Software qualification documents
- Review of change control, impact assessment,
- Deviation, investigation related to vendor assessment.
- Raw material complaint management,
- Elemental impurity risk assessment
- Nitrosamine risk assessment of raw material
- Technical agreement preparation
- To perform the audit as co-auditor along with audit risk assessment.
- Regulatory audit preparation and audit compliance
Sr. Officer – Artwork
- Artwork review for printed packaging material
- Vendor management