Company Description VHA Biopharma Private Limited is committed to providing quality healthcare solutions that make a meaningful difference in patients’ lives. The organization focuses on delivering effective therapies across multiple treatment areas, including antibiotics, pain management, gastrointestinal care, gynecological products, and nutritional and health supplements.

VHA aims to meet the needs of both external customers and internal stakeholders by maintaining high standards of product quality and service. The company continues to expand into additional therapeutic categories, offering opportunities for growth and innovation for its team members.

Role Description This is a full-time, on-site role based in Baddi, Himachal Pradesh, focused on GLP Compliance within Quality Control for injectable pharmaceutical products. The role involves ensuring adherence to Positive Laboratory Practice (GLP) standards, maintaining data integrity in line with ALCOA+ principles, and overseeing documentation and record-keeping in QC laboratories.

The professional in this position will review analytical data, monitor compliance with internal SOPs and regulatory guidelines, and participate in internal and external audits.



Daily responsibilities include coordinating with cross-functional teams to resolve compliance issues, implementing corrective and preventive actions (CAPA), supporting training on GLP and data integrity, and preparing reports for management and regulatory authorities.

Qualifications

- Strong skills in Compliance Management and Regulatory Compliance relevant to pharmaceutical injectables.
- Proficiency in Legal Compliance and understanding of applicable national and international quality guidelines.
- Solid Analytical Skills for data review, trend analysis, and investigation of deviations.
- Effective Communication skills for clear reporting, audit support, and cross-functional coordination.
- 4–5 years of experience in Quality Control for injectable formulations in a GLP-compliant environment.
- Hands-on knowledge of GLP, data integrity, ALCOA+ principles, and audit preparation and participation.
- Bachelor’s or Master’s degree in Pharmacy, Chemistry, or a related life science discipline.
- Familiarity with GMP, quality systems, CAPA processes, and laboratory instrumentation used in injectable QC.
- Ability to work accurately under regulatory timelines, with attention to detail and strong documentation practices.

📌 GLP Compliance – Quality Control | 4–5 Years Pharma Injectable Experience | GLP, Data Integrity, ALCOA+, Audits & Compliance | Baddi, Himachal Pradesh
🏢 VHA Biopharma Private
📍 Baddi