Manufacturing Science & Technology (MSAT) Team Member

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).

About Dr Reddy's Laboratories Limited

• Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait.
• This is our credo as well as the guiding principle behind all our actions.
• We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit.
• And to do this, we foster a culture of empathy and dynamism.
• People are at the core of our journey over the last few decades.
• They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success.
• We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic.
• 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).

Responsibilities

• The successful candidate will drive technology transfers, lead complex root-cause investigations, and champion continuous process improvement (CPI) to optimize product yield and quality.
• 1.
• Transfer & Scale-Up 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.
• 2.
• Validation & Monitoring 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.
• 3.
• Deviation, Investigation & CAPA Management 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).
• 4.
• & Lifecycle Management 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.
• 5.
• Regulatory & Compliance Support Support the technical queries for regulatory filing queries.
• Participate as a technical SME during regulatory inspections and client audits.

Requirements

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

Benefits

• We offer competitive salary and comprehensive benefits like

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

Our Work Culture Ask any employee at Dr.