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Openings in Pharma Quality Assurance at JAMP Pharmaceuticals - CQA, DQA

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Openings in Pharma Quality Assurance at JAMP Pharmaceuticals - CQA, DQA

The JAMP group is a proud Canadian owned company with its international headquarters located in Boucherville, 20 minutes from downtown Montreal, Quebec, Canada. The JAMP Pharma Group is active in all sectors of the pharmaceutical industry with our JAMP Pharma Generics, Orimed branded products, our Wampole and Laboratoire Suisse natural health supplements and our Cosmetic Import beauty and personal care products. The JAMP Pharma Group has also made a major investment in biosimilars which is one of the fastest growing markets in the pharmaceutical industry.
looking for competent QA personnel to be an integral part of our team based at our Ahmedabad office

Post: Manager / Deputy Manager / Asst. Manager / Sr. Executive - Quality Assurance - Department: Quality Assurance (DQA, CQA)

Manager / Deputy manager - 5 positions
Experience: 12-15 years
Desired Exposure in:
Reviews and comments all Manufacturing documents related to submission dossiers or the various development projects in accordance with Good Manufacturing Practices (GMP) and  Canadian regulations (Health Canada)
Participate in the development of validation protocols and/or reviews validation protocols as requested tor development projects. Reviews an 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 evaluate the changes controls and QMS documents
Reviews all Clarifax from Health Canada with related to module 3 of submission file
Knowledge on the risk assesment approach as per ICH Q9 / Health Canada quality risk Management including elemental purity and Nitrosamine

Assistant manager - 5 positions
Experience: 8-11 years
Desired Exposure in:
Review and approve the document during the product development phase (Formulation an Analytical)
Review & approve all the commercial Master and Executed documents (Spec.STP, BMR. BPR, MFC & Others)
Review of documents related to Clarifax from Heath Canada
Fill out the follow up table of all the received documents and trending
Review of process validation / Analytical Validation protocols and reports


Sr Executives / Executives / Sr officers - 15 positions
Experience: 4-7 years
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 monographs as well as ICH/WHO requirement.
stability program requirement, determination of shelf life an appropriate components.
Review an evaluation of master documents (finish product specification, MBR, validation protocol, stability protocol, BHT protocol

Candidates with regulated market OSD, Semi-Solid, Injectable, Ophthalmic dosage forms can apply. Only experienced candidates require to apply


Date of Walk-In Interview: 13th & 14th Nov 2021 i.e. Saturday & Sunday
Time: 11:00 AM to 4:00 PM
Venue:
JAMP INDIA Pharmaceutical Pvt. Ltd.
Office No. 606, 6th Floor, Shapath V,
Near to Hotel Crown Plaza, Sarkhej – Gandhinagar Hwy,
Prahlad Nagar, Ahmedabad, Gujarat 380015

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 d.thaker@jamppharma.com
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. Be aware of such fraudulent calls.

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