Looking For Quality Assurance Officer

Job Description

Job Opening: Quality Assurance (QA) Officer with IPQA Responsibilities

Location: On-site Nalagarh, Himachal Pradesh

Experience: 3+ years mandatory experience

Qualification: B. Pharm / M. Pharm

Language & Software Skills: Proficiency in English and Microsoft Office (Word, Excel, PowerPoint) Mandatory

About the Role:

We are hiring a knowledgeable and proactive Quality Assurance (QA) Officer to join our pharmaceutical manufacturing unit in Nalagarh. This role combines core QA responsibilities with In-Process Quality Assurance (IPQA) oversight on the production floor. The ideal candidate will ensure regulatory compliance, documentation accuracy, and continuous quality improvement throughout the production lifecycle.

Key Responsibilities: Core QA Functions:

Review and approve Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR).

Manage deviations, validations (mandatory), change controls, CAPAs, and maintain documentation as per regulatory norms.

Conduct internal quality audits and assist in external audits by clients or regulatory agencies.

Maintain and update SOPs, manuals, and master documents in accordance with current regulations.

Oversee document control systems and archival processes.

Train employees on cGMP practices and quality systems.

In-Process QA (IPQA) Responsibilities:

Monitor critical stages of manufacturing and packing operations to ensure GMP compliance.

Line clearance before batch start-up and between changeovers.

Sampling of in-process materials and verification of critical process parameters.

Real-time review and recording of BMR/BPR entries during production.

Ensure proper gowning, hygiene, and sanitation compliance on the shop floor.

Immediate reporting and documentation of any deviation or non-conformance observed.

Desired Profile:

B. Pharm / M. Pharm with a strong academic and technical background.

Minimum 3 years of QA experience in a regulated pharmaceutical manufacturing unit.

Hands-on experience with IPQA activities and on-floor quality monitoring.

Excellent written and spoken English communication skills Mandatory

Proficiency in Microsoft Office (Word, Excel, PowerPoint) Mandatory

Good understanding of WHO-GMP, Schedule M, and other applicable quality regulations.

Strong coordination skills, attention to detail, and documentation accuracy.

Join a team committed to delivering excellence through quality-first manufacturing.

If you're passionate about compliance, process integrity, and hands-on QA work we invite you to apply!

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  • Experience

    3 Years

  • No. of Openings

    5

  • Education

    B.Pharma, B.Sc, M.Pharma, M.Sc

  • Role

    Quality Assurance Officer

  • Industry Type

    Manufacturing / Production / Quality

  • Gender

    [ Male / Female ]

  • Job Country

    India

  • Type of Job

    Full Time

  • Work Location Type

    Work from Office

  • Face interview location

    Village Mehsa Tibba, P.O. Manjholi, Tehsil Nalagarh, Distt, Solan, HP,INDIA , 174101

About Magbro Healthcare Private Limited

MAGBRO Founded in 2003, is a professionally managed fast growing pharmaceutical formulations manufacturing company, having its state of the art manufacturing facility located near Nalagarh(HP) for manufacturing Tablets, Capsules, Liquid Orals and External Ointments, Lotions, Continuing towards our aim of achieving excellence in quality, MAGBRO got the WHO GMP certification for its manufacturing facility in December 2010.
After that we have not looked back and presently our plant is approved by the drugs control authorities of Afghanistan, Benin, Cambodia, Georgia, Ghana, Guinea, Ivory Coast, Kenya, Mynamar, Nigeria, Phillipines, Sri Lanka, Togo & Uzbekiston. We are regularly exporting our products to these countries and as of now we have about 200 product registrations in these countries with many more in progress.
We at MAGBRO are committed to achieve our long term vision of making available medicines of highest quality at affordable costs to all sections of society.
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