Thermo Fisher Hiring Quality Specialist
Thermo Fisher jobs in Bangalore offer a rare chance for professionals in the life sciences sector, as Thermo Fisher Scientific invites applications for the position of Quality Specialist II. This opportunity is ideal for candidates with 1–3 years of experience in medical devices, IVD, regulatory affairs, or quality assurance.
About Thermo Fisher Scientific
Thermo Fisher Scientific is a global leader in serving science, providing essential products and services for life sciences research, diagnostics, and clinical development. The company has a significant presence in India, supporting various scientific functions and contributing to advancements in healthcare and research.
Company: Thermo Fisher Scientific
Job Title: Quality Specialist II
Location: Bangalore, India
Work Mode: Fully Onsite
Employment Type: Full Time
Work Schedule: Monday–Friday
Experience: 1–3 years
Qualification: Bachelor’s degree in Life Sciences, Biomedical Sciences, Pharmacy, or related fields
Primary Area: Post-Market Surveillance / Quality
Industry: Medical Devices / IVD / Life Sciences
Thermo Fisher Jobs in Bangalore: Job Description
The Quality Specialist II post-market surveillance role will support global Business Unit Post-Market Surveillance teams through a centralized Center of Excellence model. The position primarily involves updating previously approved PMS documentation using analyzed data supplied by Business Unit teams. The specialist will work with standardized templates and processes to maintain consistency, traceability, accuracy, and audit readiness.
Key Responsibilities
- Updating approved PMS reports using data provided by Business Unit PMS teams.
- Maintaining and updating PMSR, PSUR, PMPF, and literature review documentation.
- Ensuring annual or periodic PMS documentation updates are completed on time.
- Maintaining document version control and traceability.
- Compiling and integrating Business Unit data into standardized templates.
- Reviewing documents for clarity, accuracy, consistency, and audit readiness.
- Identifying inconsistencies or potential safety signals and escalating them to appropriate Business Unit teams.
- Collaborating with global PMS teams to collect required inputs.
Eligibility Criteria
- Bachelor’s degree in Life Sciences, Biomedical Sciences, Pharmacy, or a related field.
- 1–3 years of experience in medical devices, IVD, regulatory affairs, or quality environments.
- Experience specifically involving PMS, medical device regulatory documentation, MDR, IVDR, PSUR, PMSR, PMPF, or literature surveillance is advantageous.
Required Skills
- Strong technical writing skills.
- Data interpretation ability.
- Analytical skills.
- High attention to detail.
- Strong documentation skills.
- Knowledge of Microsoft Office.
- Ability to work with standardized templates.
- Understanding of regulated quality environments.
How to Apply
Interested candidates can apply through the following link: CLICK HERE FOR THE ORIGINAL NOTIFICATION / APPLY ONLINE
Conclusion
This post-market surveillance position at Thermo Fisher Scientific offers an excellent opportunity for professionals looking to advance their careers in the life sciences sector, particularly in post-market surveillance and quality assurance. Candidates are encouraged to apply at the earliest to seize this opportunity.
