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Jamp Pharma CQA, DQA Jobs for msc, B pharm and M pharmacy Candidates 2021

JAMP PHARMA&GROUP QA WALK-IN INTERVIEW on 13th & 14th November, 2021

We are looking for competent QA personnel to be an integral part of our team based at our Ahmedabad Office. Date 13th November, 2021-Saturday & Day: 14th November, 2021-Sunday

Time: 11:00 AM to 04:00 PM


JAMP India Pharmaceuticals Pvt. Ltd., 6th Floor, 606, Shapath-V, Opp. karnavati Club, S.G. Highway, Ahmedabad – 380015

Candidates with Regulated Market (OSD/Semi Solid / Injectable / Ophthalmic Dosage Forms) Experience only need to apply

Department: Quality Assurance (“DQA”, “CQA”)

Qualification: B Pharmacy / M Pharm / MSc

Designation: Manager I Deputy Manager (5 positions)

Experience: 12-15 yrs

Desired Exposure in:

Reviews and comments all manufacturing documents related to submission dossiers of the various development projects in accordance with Good Manufacturing Practices (GMP) and Canadian regulations (Health Canada)

Participates in the development of validation protocols and/or reviews validation protocols as requested for development projects. Reviews and approves process validation and packaging reports for products in development

Ensures third party operation (CMO/CDMO) with respect to GMP and Canadian regulations.

Reviews and evaluates the change controls and QMS documents

Reviews all Clarifax from Health Canada which are related to module 3 of the submission file

Knowledge on the risk assessment approach as per ICH Q9/ Health Canada quality risk Management including Elemental impurity and Nitrosamine

Department: Quality Assurance (“DQA”, “CQA”)
Designation: Assistant Manager (5 positions)
Experience: 8-11 yrs

Desired Exposure in:
Review and approve the document during the product development phase (Formulation & Analytical)

Review & approve all the commercial Master and Executed documents (Spec. STP, BMR. BPR, MFC &Others)

Review of documents related to Clarifax from Health Canada

Fill out the follow-up table of all the received documents and

Review of Process validation Analytical validation protocol and reports

Department: Quality Assurance (“DQA”, “CQA”)
Designation: Sr. Executive I Executive / Sr. Officer (15 positions)
Experience: 4-7 yrs

Desired Exposure in:
Validation process (manufacturing and packaging) and analytical method validation and transfer. The request in both execution on the floor and documentation review in terms of evaluation and strategy.

GMP requirements and compliance to Heath Canada guidance, USP/EP/BP monograph as well as ICHI WHO requirement.

Stability program requirement, determination of shelf-life and appropriate packaging components. Review and evaluation of Master documents (finish product specification, MBR, validation protocol. stability protocol, BHT protocol)

Precautions to be taken due to COVID: Mandatorily wear face mask and also maintain social distancing

Candidates who are unable to attend the interview may send their updated resume on
Candidates who have appeared for an interview at JAMP Pharmaceuticals in last one month are requested not to apply

Please note that JAMP India Pharmaceuticals Pvt. Ltd. does not hire through consultants/ agents who promise interviews/jobs for monetary consideration/registration fees. Beware of such fraudulent calls
Contact Person: Mr. Dakshesh Thaker