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Officer - Qa

Intas Pharmaceuticals
Intas pharmaceuticals
2-3 years
Not Disclosed
Ahmedabad, India
10 Feb. 18, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Officer – Quality Assurance (QA)

Job Category: Quality Assurance / Validation / Pharmaceutical Manufacturing

Job Type: Full-Time

Company: Intas Pharmaceuticals

Location: SEZ, Ahmedabad, Gujarat, India, 382213

Travel: 0%


About Intas Pharmaceuticals
Intas Pharmaceuticals is a leading global pharmaceutical company specializing in the research, development, manufacturing, and marketing of high-quality pharmaceutical formulations. The company is committed to addressing unmet medical and societal needs through a fully integrated pharmaceutical value chain operating in over 85 countries.

With key markets across North America, Europe, Latin America, and the Asia-Pacific under the Accord Healthcare brand, Intas has achieved rapid growth through strategic acquisitions and organic expansion. The company adheres to stringent quality standards, with products approved by USFDA, MHRA, and EMA.

Intas invests in substantial in-house R&D capabilities and focuses on advanced areas such as Biosimilars and New Chemical Entities (NCEs), reflecting its commitment to innovation in global healthcare. At Intas, the workforce is the cornerstone of success, with an empowering culture that fosters innovation, accountability, and professional growth.

Recruitment Fraud Disclaimer
Intas Pharmaceuticals does not request or accept any fees during recruitment. Any request for payment in our name is fraudulent. Suspected scams should be reported to local authorities or cybercrime units.


Job Purpose
The Officer – QA will support parenteral qualification activities and regulatory documentation submissions, ensuring compliance with global regulatory standards and maintaining high-quality operational standards.


Key Responsibilities

  • Prepare and review media fill and qualification summaries.

  • Track and maintain all qualification and validation activities.

  • Develop, execute, and review protocols and reports for equipment and facility validation (IQ/OQ/PQ, DQ, FAT).

  • Coordinate with production and other user departments for qualification and validation activities.

  • Ensure accuracy and completeness of technical documentation received from suppliers.

  • Compile and review qualification validation reports in a timely manner.

  • Review equipment calibration reports and ensure document correctness.

  • Conduct Factory Acceptance Testing (FAT) as required.

  • Coordinate with external agencies for execution of qualification activities.

  • Identify deviations through review and observations.

  • Prepare annual re-qualification/validation schedules and update VMP and QA SOPs as needed.


Qualifications & Experience

  • B.Pharm / M.Pharm / M.Sc. in a relevant field.

  • 2–3 years of experience in QA/validation at USFDA, MHRA, or TGA-approved pharmaceutical plants.

  • Knowledge of parenteral manufacturing processes, media fill procedures, and validation protocols.

  • Strong analytical, documentation, and communication skills.


Life at Intas Pharmaceuticals
For over three decades, Intas has thrived through the talent and dedication of its people. The company fosters a collaborative environment that encourages professional growth, innovation, and collective success. Employees are empowered to contribute meaningfully to healthcare innovation and global pharmaceutical excellence.

Posting Date: 11 February 2026

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