Company Description VHA Biopharma Private Limited is committed to providing quality healthcare solutions that make a meaningful difference in patients’ lives. The company focuses on delivering effective cures across key therapeutic areas, including antibiotics, pain management, gastrointestinal care, gynecological products, and nutritional and health supplements. VHA strives to meet the needs of both external customers and internal stakeholders through its pursuit of excellence.

The organization continues to expand into additional therapeutic categories, offering growth opportunities for team members who want to contribute to a broader healthcare impact.

Role Description This full time on-site role, based in Delhi, India, is for QA Sr/Jr Executives specializing in Injectable and Oral Solid Dosage (OSD) formulations. The position involves executing and monitoring quality assurance activities across manufacturing and packaging operations, ensuring compliance with WHO-GMP, cGMP, and internal QMS procedures. Day-to-day responsibilities include reviewing batch manufacturing records, validation protocols and reports, SOPs, and change control documents; supporting internal and external audits; and coordinating with cross-functional teams to address deviations, CAPA, and regulatory requirements.

The role also requires maintaining up-to-date documentation,



participating in training programs, and supporting continuous improvement initiatives in quality systems and regulatory compliance.

Qualifications

- Strong foundation in Quality Assurance and Quality Control to oversee product quality across Injectable and OSD manufacturing.
- Experience in Quality Management and Quality Auditing to implement, monitor, and improve QMS processes.
- Hands-on knowledge of Good Manufacturing Practice (GMP), including WHO-GMP and cGMP compliance in a regulated pharma environment.
- 3+ years of pharmaceutical QA experience, preferably in sterile/Injectable and OSD facilities.
- B.Pharm, M.Pharm, M.Sc, or an equivalent life sciences degree from a recognized institution.
- Familiarity with validation activities (process, cleaning, equipment, utilities) and regulatory compliance requirements.
- Ability to interpret regulatory guidelines, prepare documentation, and support regulatory inspections.
- Strong analytical, documentation, and problem-solving skills with attention to detail.
- Effective communication skills and ability to collaborate with production, QC, regulatory, and other cross-functional teams.
- Willingness to work in an on-site, fast-paced manufacturing environment and adapt to evolving quality standards.

📌 QA Sr/Jr Executives – Injectable/OSD | 3+ Years Pharma QA Experience | B.Pharm/M.Pharm/M.Sc | WHO-GMP, cGMP, QMS, Validation & Regulatory Compliance | Delhi
🏢 VHA Biopharma Private
📍 Delhi