Virtual Walk In Drive for B.Pharm, M.Pharm as Manufacturing Executive at Intas Pharma

Intas is one of the leading multinational pharmaceutical formulation development, manufacturing and marketing companies in the world. Today, Intas is present in more than 85 countries worldwide and is growing at 20% CAGR. Around 70% of its revenues come from the international markets, particularly the highly regulated markets of EU and US. At Intas, everyday and everyone works to create a world of good health, happiness and hope.

Virtual Walk In Drive

Post : Executive

Experience : 2-5 Years

Department : Manufacturing - Filling

Qualification : B.Pharm / M. Pharm

Job Location : Ahmedabad, Intas Plasma Fractionation Centre

Roles and Responsibilites
1. Responsible for In-process production related activities in DP manufacturing, filling, and packing sections
2. Preparation of batch manufacturing records, process validation protocol/report of DP area and its associated records
3. Responsible for calibration and qualification program of equipment of DP area
4. Execution and review of IQ, OQ, PQ of equipments
5. Perform the Qualification/Verification of equipments and compilation of PV documents of the DP Area
6. Handling of Equipments and process related to DP manufacturing, filling, and packing sections
7. To manage the product related activity, in absence of primary responsible person
8. To check and ensure to carry out all the process activities in the plant with compliance of cGMP standards.
9. To ensure safe working conditions, safe operating practices and usage of PPE by all workers and staff.
10. Ensure to identify and resolving engineering issues to keep availability of equipment and utilities as per production planning and thereby ensure zero production loss due to breakdown.

11. Check that all equipments used in area are calibrated, qualified, clean and in good condition for intended use.
12. Ensure to check area, equipment cleanliness & environmental condition before commencement of Manufacturing & packaging of products.
13. Ensure that Manufacturing & Packaging of batches is carried out strictly as per the procedure laid down in respective BPCR/BPR
14. To ensure availability of consumables, and material issue required for the DP area.
15. To ensure proper utilization of resources with high productivity with zero wastage
16. Ensure to maintain all documents required for regulatory compliance are maintained properly. To check online filling of records and submission to QA department.

Date : 5 July 2025 (Saturday)
Time : 09:00 am to 01:00 pm
Mode : Virtual - MS Teams

• Please apply for your candidature as per the given link in the description latest by 4th July 2025
• Shortlisted candidates will be confirmed with MS Teams link
• Require experience in biotech industry