PHARMA BHARAT
PHARMACEUTICAL JOB PORTAL
No new notifications

Ad

Avantika Medex QA Jobs 2026 | IPQA Officer & Assistant Manager QA

Published on

Ad

If you are looking for a rewarding career in the pharmaceutical industry, Avantika Medex Pvt. Ltd. has announced exciting opportunities for experienced professionals in its Quality Assurance Department. The company is inviting applications for Officer/Sr. Officer โ€“ IPQA and Assistant Manager โ€“ QA (Validation) positions at its manufacturing facility in Ahmedabad, Gujarat.

Candidates with qualifications such as B.Pharm, M.Pharm, and M.Sc. and relevant pharmaceutical experience are encouraged to apply through email.


Job Overview

Company Name: Avantika Medex Pvt. Ltd.

Department: Quality Assurance

Job Location: Gallops Industrial Park, Ahmedabad, Gujarat

Mode of Application: Email

Email ID: hr@avantikamedex.com

Available Positions

  • Officer / Sr. Officer โ€“ IPQA
  • Assistant Manager โ€“ QA (Validation)

Eligibility Criteria

1. Officer / Sr. Officer โ€“ IPQA

Qualification

  • B.Pharm
  • M.Pharm
  • M.Sc.

Experience

  • 2โ€“4 Years

2. Assistant Manager โ€“ QA (Validation)

Qualification

  • B.Pharm
  • M.Pharm

Experience

  • 8+ Years

Roles & Responsibilities

Officer / Sr. Officer โ€“ IPQA

  • Perform in-process quality checks during manufacturing and packing activities.
  • Ensure compliance with cGMP, GDP, SOPs, and regulatory requirements.
  • Monitor line clearance and in-process controls (IPC).
  • Verify equipment and area cleanliness before production activities.
  • Review Batch Manufacturing Records (BMR) and Batch Packing Records (BPR).
  • Report deviations and support CAPA implementation.
  • Coordinate with Production and other departments to ensure product quality.

Assistant Manager โ€“ QA (Validation)

  • Plan, execute, and monitor process validation activities.
  • Execute cleaning validation for equipment and manufacturing areas.
  • Perform equipment qualification (IQ, OQ, PQ).
  • Prepare and review validation protocols and reports.
  • Ensure compliance with cGMP guidelines, regulatory requirements, and data integrity.
  • Support regulatory audits and inspections.
  • Collaborate with cross-functional teams for successful validation activities.

Required Qualifications

Candidates should possess any of the following qualifications depending on the position:

  • B.Pharm
  • M.Pharm
  • M.Sc.

Applicants must also have the relevant pharmaceutical industry experience mentioned for the respective role.


Salary & Benefits

The salary package will depend on the candidate’s qualifications, experience, and interview performance.

Expected Salary Range

  • โ‚น4.5 LPA โ€“ โ‚น14 LPA (Approx., based on role and experience)

Additional employee benefits may include:

  • Competitive compensation
  • Professional growth opportunities
  • Exposure to Quality Assurance and Validation systems
  • Learning-oriented pharmaceutical work environment

How to Apply

Interested and eligible candidates can send their updated CV to:

Email: hr@avantikamedex.com

Candidates are advised to mention the position applied for in the email subject line to facilitate the recruitment process.

Ad

Share This Job

โœ… Copied!