Manufacturing Science & Technology (MSAT) Team Member

Company Description

Dr. Reddy's Laboratories Ltd. is an integrated global pharmaceutical company committed to providing affordable and innovative medicines for healthier lives. We have a commercial presence in more than 40 countries and 23,000 employees worldwide are part of our success. Our purpose is to accelerate access to affordable medicines because we believe Good Health Can’t Wait .

Situated in the heart of West Yorkshire, our Active Pharmaceutical Ingredient (API) manufacturing site in Mirfield, is part of Dr. Reddy’s global network of API and formulation manufacturing sites. Our Mirfield team specializes in producing complex APIs in accordance with the quality standards of the MHRA and international regulatory authorities. We also make intermediates and activated mPEGs which make us independent from global supplies. Today, we have produced pharmaceutical ingredients for more than three decades (since 1986).

We are looking for MSAT team member who will serve as the technical bridge between process development and commercial production. Operating within a cGMP environment, this role provides end-to-end technical oversight, process engineering expertise, and scientific support to ensure the robust, scalable, and safe manufacture of Active Pharmaceutical Ingredients (APIs). The successful candidate will drive technology transfers, lead complex root-cause investigations, and champion continuous process improvement (CPI) to optimize product yield and quality.

Responsibilities

Support the technical transfer of new API / Intermediate chemical synthesis processes from MSAT lab or external customers into commercial-scale manufacturing.; Conduct laboratory experiments for feasibility studies and / or continuous improvement purpose.; Perform facility-fit assessments, chemical engineering calculations (e.g., mass/energy balances, heat transfer, mixing dynamics), and scale-up modeling.; Draft, review, and execute Technology Transfer Protocols, Campaign Summary Reports, and regular technical risk assessments (FMEA).; Support to the EHS department in analysis the process safety data and interpretation.; Support to the Validation program Process / clean protocols and Continued Process Verification (CPV) plans in alignment with ICH guidelines and Quality compliance requirements.; Provide real-time shop floor technical support during active manufacturing campaigns and validation batches.; Act as the Technical Subject Matter Expert (SME) for manufacturing deviations, batch failures, and out-of-specification (OOS) results.; Utilize structured root-cause analysis (RCA) tools (e.g., Fishbone, 5 Whys) to determine technical root causes and implement robust Corrective and Preventive Actions (CAPAs).; Identify and implement process optimization initiatives to enhance yield, minimize impurity profiles, reduce solvent consumption, and cut cycle times.; Manage technical aspects of lifecycle changes, authoring technical justifications for change controls.; Support the technical queries for regulatory filing queries.; Participate as a technical SME during regulatory inspections and client audits.

Requirements

Bachelor’s, Master’s, or Ph.D. in Chemical Engineering, Chemistry, Pharmaceutical Sciences, or a closely related technical discipline; Minimum 5 Years of experience in pharmaceutical industry.

Benefits

Defined contribution pension scheme; Life assurance; Private health insurance for self and family; Sickness Absence; Income Protection Scheme; Travel Insurance- Business and Personal; Sports and Health club membership fee reimbursement; Cycle to work scheme; Enhanced Maternity / Paternity leave