QA Officer (Documentation)Jobs in Centaur Pharmaceuticals Pvt. Ltd - Pune, Maharashtra
Centaur Pharmaceuticals Pvt. Ltd
Pune, Maharashtra, India
Posted on 19-02-2026
1 Vacancy
Description
- Job Title: QA Officer (Documentation)
- Qualification: BPharm
- Location: Centaur Pharmaceuticals Pvt. Ltd - Pune, Maharashtra
- Work Experience: 4 to 8 Years
Job Description
- Develop, review, and control all quality documents (SOPs, policies, manuals, forms).
- Ensure proper document numbering, version control, and approval tracking.
- Maintain Master Document Register and ensure obsolete documents are withdrawn.
- Ensure compliance with quality standards (NABH/ISO or internal QMS).
- Coordinate with departments for timely document revision and updates.
- Support internal and external audits with required documentation.
- Monitor corrective and preventive action (CAPA) documentation.
- Ensure safe storage, retrieval, and confidentiality of records.
Take this opportunity to join Centaur Pharmaceuticals Pvt. Ltd - Pune, Maharashtra as a QA Officer (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
Key Skills
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.
Aggregated job.
Learn more