Job Summary

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.

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

Qualifications

- 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

- Positive understanding of GMP and GDP requirements

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

Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.

Role: Technical Lead,

Industry Type: Pharmaceutical & Life Sciences,

Department: Engineering - Software & QA,

Employment Type: Full Time, Permanent

Role Category: Software Development

Education

UG: Any Graduate

PG: Any Postgraduate

Key Skills analytical testingauditsbiotechnologycancercustomer satisfactioninventory managementmaintenancemedia preparationmicrobiologymicrosoft toolspharmapharmaceuticalpharmaceutical industryquality assurancequality validation

📌 Technical Specialist Validation Services (Bengaluru)
🏢 Sartorius
📍 Bengaluru