QA Executive(Documentation) Jobs in Centaur Pharmaceuticals Pvt. Ltd - Pune, Maharashtra

QA Executive(Documentation) Jobs in Centaur Pharmaceuticals Pvt. Ltd - Pune, Maharashtra

work outline icon0 - 5 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Centaur Pharmaceuticals Pvt. Ltd

time outline iconPune, Maharashtra, India

Posted on 19-02-2026

1 Vacancy

Description

  1. Job Title: QA Executive (Documentation)
  2. Location: Centaur Pharmaceuticals Pvt. Ltd - Pune, Maharashtra
  3. Qualification: Mpharm / Bpharm
  4. Work Experience: 0 to 5

Job Requirement

  1. Ensure implementation and compliance with cGMP, GDP, and regulatory guidelines across operations.
  2. Review, approve, and control SOPs, BMRs, BPRs, protocols, and quality documents.
  3. Monitor in-process activities and support IPQA to ensure product quality and compliance.
  4. Handle deviations, change controls, OOS/OOT, and CAPA activities effectively.
  5. Support qualification, validation, and revalidation of equipment, systems, and processes.
  6. Conduct internal audits and support regulatory inspections and customer audits.
  7. Prepare and review APQR/PQR reports and trend quality data.

Take this opportunity to join Centaur Pharmaceuticals Pvt. Ltd - Pune, Maharashtra as a QA Executive (Documentation) in Pune, Maharashtra and build a successful career in the healthcare industry. Apply today for this job opportunity and grow with a leading healthcare organization.

Category

Pharmaceuticals

Functional Area

Pharma Quality Assurance (QA)

Preferred Education

MPharm (Master Of Pharmacy)BPharm (Bachelor Of Pharmacy)

Key Skills

Team working SkillsDecision-Making SkillsGood CommunicationAttention to Detail

About Organization

The organization Centaur Pharmaceuticals Pvt. Ltd is a major integrated pharmaceutical company with manufacturing and quality systems in Pune, focusing on finished dosage formulations and export-oriented production with a strong commitment to regulatory compliance and quality. It emphasizes adherence to GMP standards, documentation accuracy, and continuous quality improvement across production and QA functions. The company maintains structured quality assurance and documentation processes to support regulated pharmaceutical manufacturing. Teams work collaboratively across departments to ensure compliance with internal SOPs and external regulatory requirements. The work environment prioritizes quality systems, documentation integrity, and professional standards in pharmaceutical operations.

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