Regulatory Affairs & R&D Jobs

Tyropharma; Navi Mumbai; On-site; INR 600,000 - 1,500,000; Full time

Job summary

Tyropharma is conducting a walk-in drive for Regulatory Affairs and R&D roles in Navi Mumbai on 18 January 2026. Applicants must have M.Sc or M.Pharm qualifications and relevant experience. Positions include handling regulatory submissions and formulation development activities.

Candidates should carry an updated CV and other documents. The walk-in will start at 09:30 AM at The Fern Residency. This is a great opportunity to join a leading pharmaceutical company.

Qualifications

• M.Sc or M.Pharm qualifications as specified.
• 2–15 years experience for Regulatory Affairs.
• 2–7 years experience for AMD (Formulation).

Responsibilities

• Handling regulatory submissions for global markets.
• Formulation and analytical development activities.
• Supporting product development lifecycle.

Skills

Regulatory submissions knowledge (FDA, EMA, ICH)

Analytical method development (OSD)

Documentation and compliance understanding

Education

M.Sc or M.Pharm

Job description

Macleods Pharma Walk-In Drive – Regulatory and R&D Jobs, Navi Mumbai

TyroPharma 1/14/2026 2 minute read

Macleods Pharmaceuticals is conducting a walk-in drive for Regulatory Affairs and R&D (Formulation & Analytical) departments. Eligible candidates with M.Sc or M.Pharm qualifications can attend the walk-in interview on 18 January 2026 at Navi Mumbai.

Company Overview

Macleods Pharmaceuticals Ltd is an Indian pharmaceutical company engaged in formulation development, analytical research, and regulatory submissions for global markets.

Eligibility Criteria

• M.Sc or M.Pharm qualification as specified
• Relevant pharmaceutical industry experience as mentioned
• Applicable only for experienced candidates

Positions and Responsibilities

• Regulatory Affairs – Handling regulatory submissions for global markets, ensuring compliance with regulatory guidelines.
• AMD (Formulation) – Formulation and analytical development activities, analytical method development (OSD), documentation and compliance understanding.
• PDR – Solid oral dosage & liquid oral formulation development activities, supporting product development lifecycle.

Qualifications & Experience

• Regulatory Affairs: M.Sc / M.Pharm; 2–15 years in pharmaceutical regulatory affairs.
• AMD (Formulation): M.Sc / M.Pharm; 2–7 years in Analytical Method Development (OSD).
• PDR: M.Pharm; 3–7 years in solid oral dosage & liquid oral formulation development.

Skills Required

• Regulatory submissions knowledge (FDA, EMA, ICH)
• Analytical method development (OSD)
• Documentation and compliance understanding

Salary & Benefits

Salary and benefits will be as per company norms.

Walk-In Interview Details

• Date: 18 January 2026
• Time: 09:30 AM onwards
• Venue: The Fern Residency, Plot No. 1, Sector 20, Turbhe, Navi Mumbai – 400705
• Documents Required: Updated CV, Salary structure (CTC breakup), Aadhaar card
• Contact Numbers: 8291054728 / 7208877803 / 8291331272

How to Apply

Eligible candidates can attend the direct walk-in interview. Prior registration is required through the official link.