Assistant Research

TÜV SÜD; Bengaluru; On-site; INR 700,000 - 900,000; Full time

Job summary

TÜV SÜD South Asia Pvt. Ltd. in Bangalore, India, is seeking a life sciences professional to execute and support in vitro toxicity and mutagenicity/genotoxicity assays for medical devices in line with ISO standards.

The role includes cell culture, sample preparation, and routine lab activities in a regulated setting. The candidate should hold an M.Sc. in Life Sciences or related fields with 1–2 years of relevant experience.

Qualifications

• Post-graduation (M.Sc.) in Life Sciences, Biotechnology, Microbiology, Toxicology, or a related discipline.
• 1 to 2 years of relevant experience in in vitro toxicity, genotoxicity, or mutagenicity studies.

Responsibilities

• Execute and support in vitro toxicity and mutagenicity/genotoxicity assays for medical devices according to ISO Standards.
• Perform cell culture, sample/test item preparation, and routine laboratory activities.
• Prepare study documentation, worksheets, raw data records, and reports in accordance with GLP requirements.
• Perform statistical analysis of biological data and support data interpretation.
• Assist in maintaining laboratory records, inventory, and study-related documentation.
• Support study execution while ensuring compliance with applicable quality and regulatory requirements

Education

M.Sc. in Life Sciences / Biotechnology / Microbiology / Toxicology

Job description

At TÜV SÜD Group we are passionate about technology. Innovations impact our daily lives in countless ways, and we are dedicated to being a part of that progress. We test, we audit, we inspect, we advise. We never stop challenging ourselves for the safety of society and its people. We breathe technology, we strive for professional excellence, and we leave a mark. We take the future into our hands. We are TÜV SÜD Group.

Your Tasks

• Execute and support in vitro toxicity and mutagenicity/genotoxicity assays for medical devices according to ISO Standards.
• Perform cell culture, sample/test item preparation, and routine laboratory activities.
• Prepare study documentation, worksheets, raw data records, and reports in accordance with GLP requirements.
• Perform statistical analysis of biological data and support data interpretation.
• Assist in maintaining laboratory records, inventory, and study-related documentation.
• Support study execution while ensuring compliance with applicable quality and regulatory requirements

Your Qualifications

• Post-graduation (M.Sc.) in Life Sciences, Biotechnology, Microbiology, Toxicology, or a related discipline.
• 1 to 2 years of relevant experience in in vitro toxicity, genotoxicity, or mutagenicity studies.

At TÜV SÜD Group, we have employees from more than 100 different countries collaborating together. People of different backgrounds, skills, and pursuing different life goals. Our strength comes from these countless and varied perspectives.

We are committed to be an inclusive and diverse workplace by welcoming people of all backgrounds. We want Diversity & Inclusion (D&I) to be a foundation of our company and create an environment where all our employees can trust they will be treated with respect, regardless of gender, nationality, ethnic background, faith, beliefs, disabilities, age, sexual orientation, or identity. As such, our employees are expected to behave at all times in a manner consistent with TÜV SÜD Group Code of Ethics and Company values. We firmly believe embedding D&I in the heart of what we do will inherently contribute to the success of TÜV SÜD Group.

Work Area: Medical Devices & Healthcare

Country/Region: India

Job Location: Bangalore

Working Model : Onsite

Employment Type: Full time / regular

Company: TUV SUD South Asia Pvt. Ltd.

Org Unit Code

Requisition ID: 7568