Panacea Biotec career in Production and Quality Assurance QMS

Panacea Biotec is a leading research based Health Management Company, with an annual turnover of approx. Rs. 830 Crores. We are engaged in research, development, manufacture & marketing of Vaccines, Bio-Pharmaceuticals and Pharmaceuticals (Rx & OTC) of international quality and Health Services. All Panacea Biotec plants are accredited by international agencies and they follow current Good Manufacturing Practices, as per WHO guidelines.

Post : Executive - Production, QMS

Executive - Production
Experience : 5 - 10 Years

Description
1. Cleaning and operation of autoclave,
2. Cleaning and operation vial washing machine and dehydrogenation tunnel
3. Cleaning and preparation of different autoclave loads (machine parts, manufacturing accessories etc.)
4. Disinfectant preparation, distribution, disinfectant filtration, decartoning of vial.
5. Operation and cleaning of leak test apparatus, neutralization cabinet, filter integrity machine and other d area equipment’s
6. Garments washing, drying, inspection and preparation of Garment load sterilization.
7. Completion of autoclave area documents & system implementation as per cGMP.
8. Daily work completion as per production plan
9. Operation & Cleaning of other equipment’s of production department, like Dynamic pass box, Autoclave, Leak test apparatus, laminar air flow, cRAB, CIP/SIP docking station, NVPC, GLR skid,etc.

Executive - Quality Assurance (QMS)
Experience : 4 - 8 Years

Description
1. Preparation, Review and compliance of Standard Operating Procedures.
2. Initiation, logging, Review, Implementation, effectiveness and closure of Change Control Process.
3. Initiation, logging, Review, Investigation, trending, approval and closure of Deviations.
4. Initiation, logging, Review, Investigation, approval and closure of Nonconformance reports.
5. Review, logging and closure of OOS/OOT (Raw material, FG & Stability) and Multi stage failure.
6. Review, logging, approval and closure of concurrent, Skip and reduce testing reports.
7. Initiation, review, approval and closure of CAPA.
8. Review, approval and distribution of Artworks.
9. Preparation, review and execution of MQR/QQR.
10. Responsible for review of investigation, performed in context to deviation and Non conformances reports.
11. Responsible for logging & handling of market complaints.
12. To perform any other work as and when assigned by Head of department.

Last Date : 20th January 2026