Career Opportunity: Research Associate / Sr. Research Associate at Macleods Pharmaceuticals
Job Summary:
Macleods Pharmaceuticals is seeking experienced and dynamic professionals for the position of Research Associate / Senior Research Associate within its Product Development (PDR/R&D) department. This is a full-time opportunity based in Mumbai, focused on driving innovation in generic medicines and formulation development for highly regulated global markets, including the US and EU.
About the Company
Macleods Pharmaceuticals is a leading global pharmaceutical company with a formidable reputation for excellence in the manufacturing of generic medicines, advanced formulations, and active pharmaceutical ingredients (API). With a strong emphasis on research and development, quality-driven manufacturing processes, and the delivery of affordable, world-class healthcare solutions, we continue to expand our footprint across international regulated markets. We invite passionate researchers to join our team and contribute to our mission of advancing global health.
Position Overview
- Role: Research Associate / Sr. Research Associate
- Department: PDR (Product Development / R&D)
- Employment Type: Full-Time
- Location: Andheri East, Mumbai
- Experience Required: 3 – 7 Years
- Salary: As per industry standards (Not Disclosed)
Educational Qualifications
- Degree: M.Pharm (Master of Pharmacy)
- Experience: Candidates must possess 3–7 years of proven experience specifically in formulation and development within the pharmaceutical industry.
Roles and Responsibilities
The successful candidate will be responsible for the end-to-end development of pharmaceutical products, ensuring compliance with international regulatory standards. Key duties include:
- Formulation Development: Spearheading the development of solid oral and liquid oral dosage forms.
- R&D Execution: Conducting rigorous product development activities specifically tailored for US and EU regulated markets.
- Process Optimization: Enhancing existing formulation and manufacturing processes to improve efficiency and quality.
- Documentation: Managing comprehensive R&D and regulatory documentation, ensuring accuracy and audit readiness.
- Compliance: Strictly adhering to USFDA and EU regulatory guidelines throughout the product lifecycle.
Key Skills Required
- Expertise in Formulation Development.
- Strong technical knowledge of Solid Oral Dosages (Tablets/Capsules).
- Experience with Liquid Oral Formulations.
- In-depth understanding of USFDA/EU regulatory requirements.
- Proficiency in maintaining high-quality R&D documentation.
- Strong analytical and problem-solving capabilities regarding complex formulation challenges.
Walk-In Interview Details
We are conducting walk-in interviews for eligible candidates. Please find the details below:
- Date: 4 April 2026
- Time: 9:00 AM onwards
- Venue: Plot 60, Street No. 14, MIDC Phase II, Andheri East, Mumbai – 400093
- Contact Information: 7208877803 / 8291054728
Documentation Required
Please carry the following documents for the interview process:
- Updated CV (Resume).
- Salary Structure (CTC breakup).
- Aadhaar Card for identification.
Important Notes
- Eligibility: This position is strictly for experienced professionals. Freshers are not eligible to apply.
- Mandatory Requirements: Candidates must have hands-on experience in formulation development and a comprehensive understanding of the standards required for regulated markets (US/EU).
We look forward to meeting candidates who are committed to excellence in pharmaceutical research and are ready to contribute to our global growth.
