Mumbai, Maharashtra, India
16 hours ago
Manager - Quality Assurance

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Office

Job Description

About the company

Thermo Fisher Scientific Inc. (NYSE: TMO) is the world leader in serving science, with annual revenue of approximately $45 billion. Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Whether our customers are accelerating life sciences research, solving analytical challenges, growing efficiency in their laboratories, improving patient health through diagnostics, or developing and manufacturing life-changing therapies, we are here to support them. Our distributed team delivers an outstanding combination of innovative technologies, purchasing convenience, and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD. Our Innovative Laboratory technologies & Services makes it easier for customers.

Education Qualification : B.Sc. / M.Sc. in Chemistry

Experience : Min 10 years of experience in Quality Control and Quality Assurance in Chemicals

Skill :

- Sound Technical Knowledge in Chemicals

- Hands on experience on the equipment like GC, GC-MS/HS, HPLC, ICP, AAS, IR etc.

- Good Communication Skill - Experience in Quality Management Systems of ISO 9001, ISO 17025 and ISO 17034

Roles and Responsibilities :

1. Management of Quality complaints and customer interactions to facilitate effective problem-solving.

2. Addressing technical inquiries from customers.

3. Fulfilling specific customer requirements, including vendor questionnaires and product declarations.

4. Overseeing customer audits and providing responses to audit findings.

5. Implementing Quality Management Systems across all toll sites as per ISO 9001 which includes all Toll sites Documentation as well as Internal Quality Audits (IQA).

6. Managing documentation, such as Standard Operating Procedures (SOPs) and formats, in alignment with ISO 9001 Quality Management System (QMS) requirements.

7. Conducting vendor / supplier evaluations, as well as audits, to promote quality improvement.

8. Implementing the Quality Management System for ISO 17025 accreditation.

9. Implementing the Quality Management System for ISO 17034 accreditation.

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