Macleods Walk-In Regulatory Affairs & R&D

Macleods Pharma Walk-In 2026 – Regulatory Affairs & R&D Jobs in Mumbai for MPharm BPharm MSc Candidates

Macleods Pharmaceuticals has announced a major walk-in drive for its R&D center in Mumbai, offering multiple openings across Regulatory Affairs and Product Development (PDR) departments. The company is hiring for roles including Officer, Executive, Assistant Manager, Manager, Research Associate, and Senior Research Associate. This hiring is open for candidates with 2 to 15 years of experience in regulatory affairs and 3 to 7 years of experience in formulation R&D.

The walk-in interview is scheduled for 4th April 2026 at Andheri East, Mumbai. Candidates with M.Pharm, B.Pharm, and M.Sc qualifications are eligible based on role requirements. This opportunity is especially valuable for professionals working in global regulatory submissions, dossier preparation, and formulation development for regulated markets such as US, EU, Canada, Australia, and South Africa.

Company Overview

Macleods Pharmaceuticals is one of India’s leading pharmaceutical companies with a strong presence in regulated and emerging markets. The company is known for its expertise in formulation development, regulatory compliance, and global product registrations.

With advanced R&D facilities and a strong pipeline of products, Macleods plays a key role in delivering affordable and high-quality medicines worldwide. The Mumbai R&D center is a critical hub for regulatory affairs, formulation development, and global submissions.

Working at Macleods provides exposure to:

• Global regulatory frameworks including USFDA, EMA, and ICH guidelines
• Dossier preparation for multiple international markets
• Formulation development for solid oral and liquid dosage forms
• Cross-functional collaboration across R&D, QA, and regulatory teams

This environment is ideal for professionals aiming to grow in regulatory affairs, formulation R&D, and global pharma compliance.

Job Role & Responsibilities

Regulatory Affairs (Officer to Manager Level)

• Prepare and review regulatory dossiers for global markets (EU, Canada, AU, NZ, South Africa)
• Ensure compliance with FDA, EMA, and ICH guidelines
• Handle submissions, variations, renewals, and regulatory queries
• Coordinate with internal departments for documentation and approvals
• Support lifecycle management and regulatory strategy

Product Development (PDR – Research Associate / Sr. Research Associate)

• Work on formulation development for solid oral dosage and liquid orals
• Conduct trials, scale-up activities, and process optimization
• Prepare development reports and documentation
• Support regulatory submissions with formulation data
• Ensure compliance with regulatory standards for US and EU markets

These roles are essential in ensuring successful product development and global regulatory approvals.

Eligibility / Qualifications

Required Education

Candidates must have relevant pharmaceutical or science qualifications.

Accepted courses include:

M.Pharm, B.Pharm, M.Sc, Pharmaceutical Sciences, Pharmaceutics, Chemistry

Experience Requirements

• Regulatory Affairs: 2 to 15 years
• PDR (R&D): 3 to 7 years

Additional Requirements

• Strong knowledge of global regulatory guidelines
• Experience in dossier preparation and submissions
• Exposure to regulated markets preferred

Location & Salary

Location:

• R&D Center, Plot No. 60, MIDC Phase II, Andheri East, Mumbai

Salary:

• Salary is not disclosed
• Roles in regulatory affairs and R&D typically offer high growth and competitive compensation in pharma industry

Walk-In Interview Details

• Date: 4th April 2026
• Time: 09:00 AM onwards
• Venue: Plot 60, Street No. 14, MIDC Phase II, Andheri East, Mumbai – 400093

Documents to Carry:

• Updated CV
• Salary structure (CTC breakup)
• Aadhaar card

Application Process

Candidates can directly attend the walk-in interview.

For queries:

Contact: 7208877803 / 8291054728

Candidates are advised to:

• Highlight experience in regulatory affairs or formulation R&D
• Mention exposure to global markets and submissions
• Ensure all documents are ready for verification

Why This Opportunity Stands Out

• Multiple openings across regulatory and R&D departments
• Opportunity to work on global submissions and regulated markets
• Strong career growth in high-demand pharma domains
• Exposure to formulation development and compliance systems

This hiring drive is ideal for professionals aiming to build or advance careers in regulatory affairs, formulation development, and global pharmaceutical operations.

FAQs

Is this a walk-in interview?

Yes, candidates can directly attend the walk-in on the specified date.

What roles are available?

Regulatory Affairs (Officer to Manager) and R&D (Research Associate roles).

What experience is required?

2–15 years for regulatory roles and 3–7 years for R&D roles.

What qualifications are required?

M.Pharm, B.Pharm, and M.Sc candidates are eligible.

How to apply?

Candidates can attend the walk-in interview directly.

Summary Table

Company	Macleods Pharmaceuticals
Vacancies	Regulatory Affairs (Officer to Manager), Research Associate (PDR)
Required Education	M.Pharm, B.Pharm, M.Sc, Pharmaceutics, Chemistry
Experience	2–15 years (Regulatory), 3–7 years (R&D)