Company Description VHA Biopharma Private Limited is dedicated to delivering quality healthcare solutions that create a meaningful difference in patients’ lives. The organization focuses on excellence and aims to consistently satisfy both external customers and internal stakeholders. VHA offers effective therapies across key segments including antibiotics, pain management, gastrointestinal conditions, gynecological care, and nutritional and health supplements.

The company continues to expand into other therapeutic categories, providing a growing portfolio of pharmaceutical products. Professionals joining VHA can expect to work in a purpose-driven workplace centered on patient well-being and product quality.

Role Description The QA Manager – Pharma will oversee quality assurance activities related to tablets and capsules, with a strong focus on documentation and compliance with regulatory and company standards. This full-time, on-site role is based in the Amritsar/Ludhiana area and involves managing and reviewing batch manufacturing records, SOPs, validation documents, and quality-related reports. The role includes coordinating with production, QC, and regulatory teams to ensure that products meet defined quality specifications and are manufactured in line with GMP requirements.

The QA Manager will lead investigations of deviations and non-conformities, implement corrective and preventive actions, and support internal and external audits. IPQA experience is not required, but the role demands consistent monitoring of documentation practices,



training of team members on QA procedures, and contributing to continuous improvement initiatives. The position offers a monthly salary range of ₹30,000–₹60,000, depending on experience and qualifications.

Qualifications

- Formal education in pharmacy: B.Pharm or M.Pharm, with 3–4 years of experience in pharmaceutical quality assurance, preferably in solid oral dosage (tablets and capsules).
- Strong knowledge of QA documentation practices, including preparation, review, and control of batch records, SOPs, validation and qualification documents, and change control forms.
- Understanding of GMP, GLP, and relevant national and international regulatory requirements applicable to pharmaceutical manufacturing.
- Experience collaborating with cross-functional teams such as Production, QC, Regulatory Affairs, and Warehouse to maintain product quality and compliance.
- Ability to conduct investigations of deviations, OOS/OOT results, and non-conformities, and to implement effective CAPA and risk mitigation measures.
- Proficiency in data analysis, documentation accuracy, and maintaining audit-ready records; familiarity with quality management systems is an advantage.
- Strong organizational, planning, and time-management skills, with the ability to manage multiple batches and documentation workflows simultaneously.
- Clear written and verbal communication skills in English; ability to prepare concise reports, summaries, and training materials.
- Leadership qualities to guide and mentor QA staff, support training on QA procedures

📌 Hiring: QA Manager – Pharma (Tablets & Capsules, Documentation; IPQA Experience Not Required) | B.Pharm/M.Pharm | 3–4 Years’ Experience | Salary: ₹30,000–₹60,000 per Month (India)
🏢 VHA Biopharma Private
📍 India