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

Work arrangement
No