QMS - Production
Job Description:
Job title : Supervisor - GMP Documentation
Desired Qualifications : BSc./MSc./Diploma (Chemical)
Experience Required : 3 Years+
Industry : Pharmaceutical/ Fine/Speciality Chemicals
Job Function Dept- : Production (GMP)
Location : Dahej
Technical:
? Having Batch processing experience on shop floor and familiar with equipment like reactor,
centrifuge, dryer etc.
? Having basic awareness about unit operation and unit process.
? Having good command on basic computer operation specially MS Office (MS Word).
Job Description:
? Review the executed Batch Manufacturing Record (BMR) and other GMP documents on
daily basis.
? Resolve the review comments related to BMR by discussed with shopfloor team and
IPQA team.
? Taking plant round on daily basis to ensure online filling of BMR, daily cleaning record,
daily verification record and other GMP related documents.
? Support shopfloor team for online documentation and area readiness as per audit/visit.
? If required prepare draft BMR and other GMP documents for review purpose.
Key Skills :
Company Profile
--- --- finds its roots in 4 years of engineering during which we saw a dream to carve out a niche for ourselves in Pharmaceutical Industry. As a part of the final year project, We worked on cost reduction of "Aceclofenac" which fetched us four national awards including one from Consultancy Development Center, Government of India.
At ---, We aim to develop and provide quality,cost effective and sustainable solutions to our Customers by empowering people to think beyond the traditional norms of Chemistry and Engineering to come up with different and innovative solutions to the problems.
Apply Now
- Interested candidates are requested to apply for this job.
- Recruiters will evaluate your candidature and will get in touch with you.