Ipca Laboratories Limited, a globally recognized pharmaceutical company headquartered in Mumbai, India, is a leading manufacturer and supplier of Active Pharmaceutical Ingredients (APIs), pharmaceutical formulations, and medicinal products worldwide. With a strong international presence, Ipca sells its APIs and intermediates globally, solidifying its position as one of the world’s largest producers in this crucial sector. We are committed to delivering high-quality medications and are constantly seeking talented individuals to join our growing team.
Join Our Team: Analytical Method Validation Officer/Senior Officer
We are currently seeking highly motivated and dynamic candidates for the position of Analytical Method Validation Officer/Senior Officer at our state-of-the-art formulation (OSD Plant) facility in Athal (Silvassa). This is a fantastic opportunity to contribute to the advancement of pharmaceutical science within a large, established, and reputable organization.
Key Responsibilities:
- Method Validation: Play a crucial role in validating analytical methods used in quality control, ensuring the accuracy, reliability, and consistency of our products.
- Routine and Non-Routine Analysis: Conduct a range of analytical tests, meticulously documenting results and adhering to stringent quality standards. This involves working with various analytical instruments and techniques.
- Data Compilation and Analysis: Accurately record, analyze, and interpret laboratory data, ensuring compliance with regulatory requirements and internal procedures.
- Visual Inspection: Conduct thorough visual inspections of materials and products, identifying and documenting any discrepancies.
- Stability Sample Analysis: Perform stability testing of pharmaceutical products, following established protocols and standard operating procedures (SOPs). Contribute to the determination of product shelf life and stability profiles.
- Compliance and Documentation: Maintain meticulous records, ensuring complete compliance with Good Laboratory Practices (GLP), Good Manufacturing Practices (GMP), and relevant regulatory guidelines.
Ideal Candidate Profile:
- Education: B.Pharm, M.Pharm, B.Sc (Chemistry), or M.Sc (Chemistry)
- Experience: 1 to 3 years of relevant experience in analytical method validation within the pharmaceutical industry.
- Skills: Strong analytical skills, meticulous attention to detail, proficiency in laboratory techniques, excellent data management and documentation skills. Experience with various analytical instruments (e.g., HPLC, GC, UV-Vis) is highly desirable.
- Attributes: A proactive and results-oriented individual with strong communication and teamwork skills. A commitment to maintaining high quality and adhering to strict regulatory standards is essential.
Why Choose Ipca Laboratories?
Ipca Laboratories Limited offers a stimulating and rewarding work environment, fostering professional growth and development. We provide opportunities for continuous learning and advancement within a global pharmaceutical organization. We are committed to our employees’ well-being and offer a competitive compensation and benefits package.
Walk-in Interview Details:
Don’t miss this exciting opportunity to join our team! We invite you to attend our walk-in interview.
- Venue: Hotel Sovereign, Sea Face Road, Nani – Daman, Daman – UT of Daman & Diu 396210.
- Date: Sunday, May 11, 2025
- Time: 10:00 AM to 4:00 PM
Important Note: Ipca Laboratories Ltd. does not solicit or charge any fees for job applications. Beware of fraudulent recruitment activities. If you encounter any suspicious requests for money, please report them immediately.
