Integrated Biopharma AND Pharma Solution is hiring.
Position: Principal, Quality associate.
Qualification: Master’s degree in Biotechnology / Pharma / Biochemistry / Chemical Engineering.
- Working in the biopharma industry producing for US / EU markets (drug substance or drug product experience is mandatory) with experience of 9-10 years.
- Firsthand experience of facing FDA / EU inspections in the past 5-6 years will be an added advantage.
- The candidate must have work experience in a regulated GMP environment, specifically producing for the US/ EU market and said regulation.
- Clear understanding of biopharmaceutical processes, equipment and facilities and system qualification / validation.
- Hands on experience of writing documents like SOPs, protocols, technical reports, etc. Strong communication skills and willingness to travel domestic/overseas is must.
Contact Mahesh Rao at email@example.com