Posted:4 hours ago| Platform:
Work from Office
Full Time
Roles & Responsibilities: Daily R.M. /P.M. planning and issuing as per production schedule. Manpower allotment in shifts and to give and take proper shift charge from reliever. To review BMR, BCR, documents and to submit to QA. To check the processing is being done as per instructions written in BMR. To report any kind of deviation/abnormal incident to HOD immediately. To ensure safety, GMP, discipline & housekeeping in plant. To ensure that all production related documents are filled on line & accurately. To give training to subordinates, prepare and maintain training related all activity and documents. To prepare, issue and submit all documents like BMR, BCR, SOP etc. as draft for production processes and to get approval from QA. To ensure that all persons working in plant are fit as per predetermined fitness criteria. To report any kind of maintenance job immediately & ensure completion of it. To ensure that equipment cleaning is done as per schedule and ensures approval of QA to cleaning after completion of campaign before starting the next campaign. To ensure process related deviation, CAPA, change control to QA and get it documented To ensure that sampling of finished product is done and the same is transferred to ware house after approval. To ensure the quality & yield of batches within acceptable limits. To ensure tracking of department objectives & take actions accordingly. To ensure PSD and complete analysis results and pack final material as per customer requirements. To ensure the process and cleaning validation is done as per schedule. Ensure that all work relevant to his area is carried out under his supervision in Accordance with company procedures as regards Safety, Health and Environmental protection. To perform the internal audit and prepared the audit report. Desired Candidate Profile: Experience: 8-10 years of experience in pharmaceutical industry with expertise in Batch Manufacturing Records, Continuous Improvement, Documentation & Reporting, Gmp Compliance, Regulatory Compliance. Qualification: Bachelor's degree in Chemistry (B.Sc)& Master's degree in Science (MS/M.Sc) Job Location: Boisar (Tarapur).
Upload Resume
Drag or click to upload
Your data is secure with us, protected by advanced encryption.
16.0 - 18.0 Lacs P.A.
6.0 - 8.4 Lacs P.A.
8.0 - 10.0 Lacs P.A.
Experience: Not specified
Salary: Not disclosed
5.0 - 6.0 Lacs P.A.
Experience: Not specified
8.0 - 11.0 Lacs P.A.
0.2 - 0.4 Lacs P.A.
0.1 - 0.25 Lacs P.A.
Salary: Not disclosed
Experience: Not specified
Salary: Not disclosed