Technical Specialist Validation Services

Introduction

Join our Validation Services team as a Technical Specialist Validation Services and play a key role in delivering high-quality validation testing services. By executing laboratory protocols in line with internal standards and regulatory requirements, you will contribute to customer satisfaction and operational excellence, supporting better health for more people. The position is based in Bangalore.

Grow with us – Your Responsibilities

Coordinate and execute microbiological and physicochemical studies for filter validation activities (Confidence Projects) based on validation protocols and SOPs, following Good Laboratory Practices (GLP) and considering GMP principles as applicable

Complete laboratory data forms, interpret results, submit records for final approval, and document test results in the specified format according to Good Documentation Practices

Inform the Manager of deviations related to validation protocols and test execution, and initiate and complete investigations related to protocol deviations or out-of-specification results

Prepare SOPs, EOPs, qualification protocols, qualification reports, technical reports, and other related documentation

Support routine maintenance of departmental instruments, oversee maintenance and repairs performed by third parties, and support inventory management

Ensure the validation laboratory complies with Company Laboratory Quality Assurance and Safety Manuals, and prepare for and participate in customer and ISO audits

Ensure proper storage and disposal of hazardous waste, maintain safety records and Material Safety Data Sheets, coordinate the preparation and maintenance of microbial culture strains, culture media, test solutions and reagents according to SOPs or specific test requirements, and conduct other laboratory-related tasks as specified by the Manager

What will convince us

Master’s degree in Microbiology or Biotechnology, or a postgraduate qualification in a related field

2–5 years of professional experience within the pharmaceutical industry, biopharma, or a contract manufacturer

Knowledge of analytical testing procedures, including microbiological tests such as growth promotion testing and media preparation; awareness of calibration and qualification activities; and knowledge of sterilizing-grade filter applications within pharma or biopharma

Good understanding of GMP and GDP requirements

Knowledge or hands-on experience with LIMS, ELN, and Microsoft tools

About Sartorius

Sartorius is part of the solution in the fight against cancer, dementia, and many other diseases. Our technologies help translate scientific discoveries into real-world medicine faster, so that new therapeutics can reach patients worldwide.

We look for ambitious team players and creative minds, who want to contribute to this goal and advance their careers in a dynamic global environment.

Join our global team and become part of the solution. We are looking forward to receiving your application.

www.sartorius.com/careers