54 Job openings found

1 Opening(s)
15.0 Year(s) To 17.0 Year(s)
15.00 LPA TO 17.00 LPA
Sr. Manager- Quality Assurance (QA QC)   Job Responsibilities?:-  Planning and execution of daily QA, QC operation activities for production in Injectable section to smooth Functioning work culture.  To prepare and review the   SOPs of QA QC departments. Ensure qualification/ validation status of equipment’s   QA, QC of Internal and external Manufacturing as per SOP.  Experience of handling ...
1 Opening(s)
1.0 Year(s) To 5.0 Year(s)
2.00 LPA TO 4.00 LPA
Position Junior Executive - IPQA CTC Range Up to 4 LPA Educational Qualification B.Sc., B.Pharm, D.Pharm, M.Sc. Total Experience 1 to 2 Years Preferred Industry Pharmaceutical (Parenteral Manufacturing unit) Job Description Batch Manufacturing record review Batch manufacturing record issuance. Line clearance Calibration activity Operation of Viable / Non-Viable monitoring Preparation of annual product quality review.
1 Opening(s)
5.0 Year(s) To 8.0 Year(s)
3.00 LPA TO 7.00 LPA
Following GMP during operation of the equipment and handling of products. Responsible for Operation of moisture analyzer and ERH apparatus. Responsible for the following SOPS and BMR’S in the area without any deviations. Responsible for integrity of punches & dies and sieves, screens, finger bags. Responsible for the Maintenance of change parts and punch ...
10 Opening(s)
5.0 Year(s) To 8.0 Year(s)
3.00 LPA TO 7.00 LPA
Following GMP during operation of the equipment and handling of products. Responsible for Operation of moisture analyzer and ERH apparatus. Responsible for the following SOPS and BMR’S in the area without any deviations. Responsible for integrity of punches & dies and sieves, screens, finger bags. Responsible for the Maintenance of change parts and punch ...
1 Opening(s)
2.0 Year(s) To 3.0 Year(s)
2.40 LPA TO 2.50 LPA
Job Description• To perform IPQA activities at shop floor in each and every stage of sterile manufacturing and packing.• QA overview for clean room behavior and aseptic activity.• Review of batch processing records.• Review of all documents relating to the manufacturing, Packaging & analysis report prior to batch release.• Review ...
4 Opening(s)
2.0 Year(s) To 5.0 Year(s)
3.00 LPA TO 4.00 LPA
Hiring for Quality Executive/Officer Designation: Quality Executive/Officer Qualification: B. Pharmacy Experience: Minimum 3 Years  Salary:- up to 4LPA. Candidate should have experience in Process Validation   Job Profile: Responsible for Batch file preparation & review of batch manufacturing record. Trend analysis. Responsible for change control filing of all revised documents. Line clearance. Issuance of all documents. Review all analysis reports and COA. Responsible to check daily updating of ...
4 Opening(s)
2.0 Year(s) To 8.0 Year(s)
2.40 LPA TO 5.00 LPA
Hiring for API / Pilot Plant Designation: Production Executive/ Sr. Executive Qualification: B.Sc. / M.Sc chemistry Designation: Executive/ Sr. Executive. Experience: Minimum 2 to 8 years in must have experience in API Production / Pilot Plant Equipment handled -: Reactors, Centrifuge, Dryers, Sifter, and Blender etc. Job Profile: Responsible For All Activity in Plant during Shift as an Officer. Ensuring that ...
1 Opening(s)
5.0 Year(s) To 10.0 Year(s)
6.00 LPA TO 10.00 LPA
Leading and Management of IPQA team.Performing IPQA activity (Line clearance, in-process checks, sampling, etc.) at shop floor for Dispensing, Manufacturing, and Packing area.Review of executed Batch Processing Records and related cGMP documents for the on-time release of the batch.Preparation of SOP for execution on shop floor IPQA related activities. Review of ...
3 Opening(s)
3.5 Year(s) To 5.4 Year(s)
7.00 LPA TO 11.00 LPA
Role : Business and Integration Architect  Role Description : Work directly with the client gathering requirements to align technology with business strategy and goals and. Experts internally and externally for their deep functional or industry expertise, domain knowledge, or offering expertise.                    ...
8 Opening(s)
0 To 3.0 Year(s)
2.00 LPA TO 3.00 LPA
Department - QA Job Locaion - ambernath Willingness should be there to work in all shifts Job Description Experience in issuing of line clearance at every step of Batch Manufacturing Hands on performing In-process quality assurance checks for Tablets, Capsules and Intermediates. Stability Sample Handling as well as Stability Chamber. Monitoring and Executing Process Validation and Sampling of the same. Carry out In-house Calibration and External Calibration of Balance, Instrument, Equipments, LAF and HVAC validation. Periodic checking of Retention Sample and Handling of the same. Documentation of Records. BMR and BPR Preparation and reviewing. Carry out Destruction Activities for Rejected and Expired Raw and Packing Materials. Preparation of PQR & APQR.

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