MSAT Engineer: Tech Transfer & Continuous Improvement for APIs

Dr Reddy'S Laboratories Limited; West Yorkshire; On-site; GBP 55,000 - 85,000; Full time

Benefits offered by this job

Defined contribution pension scheme

Life assurance

Private health insurance for self and/

Sickness Absence

Income Protection Scheme

Travel Insurance - Business and Travel

Sports and Health club membership

Cycle to work scheme

Enhanced Maternity / Paternity leave

Job summary

Dr. Reddy’s Laboratories Limited is seeking an MSAT team member to bridge process development and commercial production in a cGMP environment. You will oversee technology transfer, scale-up, validations, and continuous process improvement to optimize yield and quality.

The role requires strong technical skills in process engineering, RCA, and CAPA, with the ability to operate across lab and manufacturing facilities. Join a team focused on robust APIs and lifecycle management.

Qualifications

• 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.
• Experience in cGMP environment and technology transfers welcome.

Responsibilities

• Technology transfer & scale-up support from MSAT lab to commercial manufacturing.
• Conduct lab feasibility studies and continuous improvement experiments.
• Perform facility-fit assessments and scale-up modeling, with mass/energy balance calculations.
• Draft and review Technology Transfer Protocols, Campaign Summary Reports, and risk assessments (FMEA).
• Support process validation, CPV plans, and regulatory queries as SME during inspections.

Skills

Process engineering

Root-cause analysis

Continuous process improvement

Scale-up modeling

Education

Bachelor’s/Master’s/PhD in Chemical Engineering, Chemistry, Pharmaceutical Sciences

Tools

FMEA

Job description

Dr. Reddy’s Laboratories Limited is seeking an MSAT team member to bridge process development and commercial production in a cGMP environment. You will oversee technology transfer, scale-up, validations, and continuous process improvement to optimize yield and quality.

The role requires strong technical skills in process engineering, RCA, and CAPA, with the ability to operate across lab and manufacturing facilities. Join a team focused on robust APIs and lifecycle management.