Sartorius is hiring for the position of Technical Specialist – Validation Services in Bangalore, Karnataka. The role focuses on microbiological and physicochemical testing for filter validation, laboratory documentation, quality compliance, and validation activities in the pharmaceutical and biopharmaceutical industries.
Candidates with a postgraduate qualification in Microbiology, Biotechnology, or a related field and 2–5 years of relevant industry experience can apply through the official Sartorius careers portal.
Job Details
| Particulars | Details |
|---|---|
| Company | Sartorius |
| Job Title | Technical Specialist – Validation Services |
| Location | Bangalore, Karnataka |
| Job Type | Full-time |
| Experience | 2–5 years |
| Qualification | Master’s degree in Microbiology, Biotechnology, or a related postgraduate qualification |
| Job Requisition ID | R42554 |
| Application Mode | Online |
About Sartorius
Sartorius develops technologies that help translate scientific discoveries into real-world medicines. Its work supports the development of therapeutics for diseases including cancer and dementia, helping medicines reach patients worldwide.
Positions Available
- Technical Specialist – Validation Services
Job Responsibilities
The selected candidate will be responsible for:
- Coordinating and executing microbiological and physicochemical studies for filter validation according to validation protocols and SOPs.
- Performing laboratory activities in accordance with Good Laboratory Practices (GLP) and applicable Good Manufacturing Practices (GMP).
- Recording laboratory data, interpreting results, and submitting records for final approval according to Good Documentation Practices (GDP).
- Reporting protocol deviations and initiating and completing investigations related to deviations or out-of-specification results.
- Preparing SOPs, EOPs, qualification protocols, qualification reports, technical reports, and related documentation.
- Supporting routine laboratory instrument maintenance, third-party repairs, and inventory management.
- Ensuring compliance with laboratory quality assurance and safety requirements.
- Preparing for and participating in customer and ISO audits.
- Managing hazardous waste, safety records, and Material Safety Data Sheets.
- Coordinating the preparation and maintenance of microbial culture strains, culture media, test solutions, and reagents.
Eligibility and Qualifications
Candidates must meet the following requirements:
- A Master’s degree in Microbiology or Biotechnology, or a postgraduate qualification in a related field.
- 2–5 years of professional experience in the pharmaceutical industry, biopharma, or a contract manufacturing organization.
Required Skills and Knowledge
- Knowledge of analytical testing procedures.
- Understanding of microbiological testing, including growth promotion testing and media preparation.
- Awareness of calibration and qualification activities.
- Knowledge of sterilizing-grade filter applications in pharmaceutical or biopharmaceutical settings.
- Good understanding of GMP and GDP requirements.
- Knowledge of or hands-on experience with Laboratory Information Management Systems (LIMS) and Electronic Lab Notebooks (ELN).
- Proficiency with Microsoft tools.
- Knowledge of laboratory documentation, quality assurance, and safety procedures.
