Macleods Pharma Hiring For PDR-DQA Department

Macleods Pharma is inviting applications from qualified M.Pharm Pharmaceutics candidates for an opportunity in the PDR-DQA Department in Andheri, Mumbai. Candidates with 1–3 years of relevant PDR-DQA experience can apply for this pharmaceutical quality assurance opportunity.

The position involves documentation review, SOP management, Product Development Report (PDR) review, laboratory compliance activities, Master Manufacturing Formula review, qualification documentation support and coordination with cross-functional teams.

For M.Pharm professionals looking for PDR-DQA jobs in Mumbai, this opening provides an opportunity to work across pharmaceutical development documentation and quality assurance processes.

Job Overview

Key Responsibilities

Selected candidates for the Macleods Pharma PDR-DQA job are expected to handle responsibilities including:

1. Prepare and review Standard Operating Procedures (SOPs), guidelines and associated quality documentation.
2. Provide training on applicable SOPs and guidelines and maintain/archive relevant training records.
3. Review and approve Product Development Reports (PDRs) and Laboratory Note Books (LNBs).
4. Conduct laboratory rounds and verify that equipment is within its applicable calibration period and carries appropriate equipment identification.
5. Verify laboratory cleanliness and physical environmental standards as part of routine quality oversight.
6. Review Master Manufacturing Formula (MMF) documentation.
7. Provide documentation support for Installation Qualification (IQ), Operational Qualification (OQ) and Performance Qualification (PQ) activities.
8. Maintain and archive PDR data backup files and associated records.
9. Communicate and coordinate with cross-functional departments for quality and product-development activities.

Qualification and Experience

Candidates interested in this PDR-DQA vacancy at Macleods Pharma should meet the following criteria:

• Qualification: M.Pharm in Pharmaceutics
• Experience: 1–3 years of relevant experience in PDR-DQA
• Understanding of pharmaceutical quality documentation and SOP systems
• Knowledge of PDR, LNB and Master Manufacturing Formula review
• Familiarity with IQ/OQ/PQ documentation
• Understanding of laboratory equipment calibration and compliance requirements
• Good documentation, communication and cross-functional coordination skills

Skills Relevant for PDR-DQA Jobs

Candidates may benefit from practical knowledge of GMP documentation, SOP preparation and review, document control, data archival, laboratory compliance, equipment qualification, calibration controls, Product Development Reports, Master Manufacturing Formula documentation and pharmaceutical quality systems.

Attention to detail and the ability to review technical documentation are particularly important because PDR-DQA functions provide quality oversight during pharmaceutical product development activities.

Why Consider This Opportunity?

This role can provide relevant exposure to pharmaceutical development quality assurance, particularly for M.Pharm Pharmaceutics professionals building careers in Development Quality Assurance (DQA).

The position offers exposure to SOP management, product-development documentation, qualification activities, laboratory compliance, documentation review and collaboration with multiple pharmaceutical functions.

Salary Estimate

The employer has not disclosed an official salary in the provided recruitment information.

For structured-data purposes, an estimated market range of approximately ₹4,00,000–₹7,00,000 per year may be considered for a 1–3 year PDR-DQA professional in Mumbai. This is an indicative estimate only and should not be interpreted as salary offered or confirmed by Macleods Pharma.

How to Apply for Macleods Pharma PDR-DQA Jobs

Eligible candidates can send their updated CV to:

Email: vishalb@macleodspharma.com