Company Description Ipca Laboratories Limited is a consumer-led global pharmaceutical company that has been contributing to healthcare since 1949. The organization operates with a strong sense of responsibility, integrity, and commitment to high quality standards, focusing on the safety of both employees and patients.

Ipca is a fully integrated pharmaceutical manufacturer, producing over 350 formulations and 80 APIs across multiple therapeutic segments, and serving millions of people in more than 120 countries on six continents. The company is among the world’s largest manufacturers and suppliers of a dozen-plus APIs, with fully automated, globally approved facilities recognized by authorities such as UK-MHRA, EDQM-Europe, and WHO-Geneva. Ipca holds leadership positions in DMARDs for rheumatoid arthritis, as well as in pain, rheumatology, antimalarials, and hair care therapies, with several formulations ranking among the top brands in the Indian pharmaceutical market.

Role Description This full-time, on-site Quality Assurance Specialist role is based at Ipca Laboratories Limited’s facility in Indore.

The Quality Assurance

Specialist will oversee adherence to quality standards across manufacturing processes, ensuring compliance with company policies, regulatory requirements, and Good Manufacturing Practices (GMP). Daily responsibilities include reviewing and approving batch records and validation documents, monitoring in-process controls, investigating deviations and non-conformances, and supporting corrective and preventive actions (CAPA).



The role involves conducting internal quality audits, collaborating with Quality Control and production teams, and contributing to continuous improvement initiatives. The Specialist will also assist in maintaining documentation and training records, supporting inspections by regulatory bodies, and promoting a culture of safety, integrity, and quality throughout the site.

Qualifications

- Demonstrated expertise in Quality Assurance and Quality Management, with the ability to implement and maintain robust quality systems.
- Strong foundation in Quality Control practices, including review and interpretation of test results and batch documentation.
- Hands-on experience with Good Manufacturing Practice (GMP) in a pharmaceutical or similarly regulated manufacturing environment.
- Proficiency in Quality Auditing, including planning, conducting, and reporting internal audits and supporting external inspections.
- Bachelor’s or master’s degree in Pharmacy, Chemistry, Life Sciences, or a related discipline.
- Knowledge of regulatory requirements and guidelines applicable to pharmaceutical manufacturing and APIs.
- Analytical mindset, attention to detail, and strong problem-solving skills for root cause analysis and CAPA implementation.
- Effective written and verbal communication skills, with the ability to work collaboratively with cross-functional teams in office.
- Prior experience in a pharmaceutical QA function and familiarity with documentation management systems is highly beneficial.

📌 Quality Assurance Specialist (Indore)
🏢 Ipca Laboratories
📍 Indore