Indoco Remedies, a leading pharmaceutical company with a 77-year legacy of excellence and strong global presence, including approvals from the US FDA and UK MHRA, is conducting a walk-in interview for an Analytical Method Development Officer at its R&D Centre in Rabale, Navi Mumbai. This is an exceptional opportunity to join a well-established organization committed to innovation and quality in the pharmaceutical industry.

About Indoco Remedies:

For 77 years, Indoco Remedies has been a trusted name in the pharmaceutical world, consistently delivering high-quality medications to patients globally. Our commitment to research and development, coupled with our rigorous adherence to international regulatory standards (US FDA and UK MHRA approved), positions us as a leader in the industry. We offer a dynamic and rewarding work environment where innovation and professional growth are encouraged.

Position: Analytical Method Development Officer (Formulations)

This crucial role within our Analytical Method Development team focuses on the development and validation of analytical methods for pharmaceutical formulations. The successful candidate will contribute significantly to ensuring the quality, safety, and efficacy of our products. This is a fantastic opportunity for a highly motivated and skilled analytical chemist to contribute to a company with a proven track record of success.

Key Responsibilities:

• Method Development and Validation: Develop, validate, and optimize analytical methods (HPLC, GC, UV-Vis Spectroscopy, Dissolution testing) for assay, related substances, and dissolution testing of pharmaceutical formulations. This includes writing and executing method validation protocols in accordance with cGMP guidelines.
• Analytical Testing: Perform analysis of prototype and stability samples according to established procedures, ensuring accurate and reliable results.
• Dissolution Profile Evaluation: Evaluate and interpret multimedia dissolution profiles to ensure consistent drug release and bioavailability.
• Compatibility Studies: Conduct various compatibility studies, including:
  • Drug-excipient compatibility studies
  • Filter compatibility studies
  • Forced degradation studies
  • Material contact and tubing compatibility studies
  • Diluent compatibility studies
  • Photostability studies
  • Excursion studies
  • Freeze-thaw stability studies
• Solubility Studies: Conduct solubility studies to determine the solubility profiles of drug substances.
• Instrumentation: Calibrate and maintain analytical instruments, ensuring accurate and reliable performance.
• Data Analysis and Reporting: Accurately record, analyze, and report experimental data, adhering to all regulatory guidelines and company SOPs.

Qualifications and Skills:

• Education: M.Sc. or M.Pharm. in Chemistry or a related field.
• Experience: 2-5 years of hands-on experience in analytical method development and validation within the pharmaceutical industry.
• Technical Skills:
  • Proven expertise in HPLC, GC, UV-Visible Spectroscopy, and Dissolution testing.
  • Proficiency in Empower-3 software (or similar chromatography data systems).
  • Strong understanding of analytical chemistry principles and techniques.
  • Experience with regulatory guidelines (e.g., ICH guidelines) and industry best practices.
• Soft Skills:
  • Excellent analytical and problem-solving skills.
  • Strong attention to detail and accuracy.
  • Ability to work independently and as part of a team.
  • Excellent communication and documentation skills.

Walk-in Interview Details:

• Date: Saturday, April 19, 2025
• Time: 10:00 a.m. to 4:00 p.m.
• Venue: INDOCO REMEDIES LIMITED, R&D Centre, R-92/93, TTC Industrial Area, MIDC, Thane – Belapur Road, Near Fire Brigade, Rabale, Navi Mumbai – 400 701.

Contact:

For any queries, please contact:

• Gauri.deo@indoco.com
• Sakshi.pande@indoco.com

Website: www.indoco.com

Only experienced candidates should attend the interview. Please bring your updated resume and relevant documents. We look forward to meeting you!

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