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Regulatory Affairs Assistant
Thermo Fisher Scientific
Bengaluru
1+ Years
Regulatory Affairs
Clinical Research
🏢 About Thermo Fisher Scientific
Thermo Fisher Scientific is a global leader in life sciences, analytical instruments, biotechnology, and clinical research services. The company supports scientific innovation and regulatory compliance across pharmaceutical, biotechnology, and healthcare industries worldwide.
📌 Job Overview
- Role: Principal Regulatory Affairs Assistant
- Company: Thermo Fisher Scientific
- Location: Bengaluru, Karnataka, India
- Experience: 1+ Years
- Work Mode: Fully Onsite
- Employment Type: Full-Time
🔬 Key Responsibilities
- Support preparation and submission of regulatory documentation under EUCTR guidance
- Coordinate regulatory deliverables and client submissions
- Track project plans and provide status updates to stakeholders
- Maintain compliance with internal and client SOPs
- Evaluate client requirements against timelines and quality expectations
- Collaborate with cross-functional teams to resolve regulatory issues
- Prepare documentation, reports, and regulatory deliverables
- Assist with preparation of bids, proposals, and contract revisions
🎓 Eligibility Criteria
- Bachelor’s or Master’s degree in Pharmacy, Life Sciences, or related discipline
- Minimum 1+ year experience in Regulatory Affairs or Clinical Research
- Familiarity with EUCTR regulatory submissions
- Strong documentation and coordination skills
- Ability to manage multiple regulatory projects
- Excellent communication and stakeholder management abilities
⭐ Benefits & Career Growth
- Exposure to global regulatory affairs and clinical research operations
- Opportunity to work with international regulatory frameworks
- Career growth in regulatory affairs and clinical compliance
- Structured learning environment within a global organization
- Competitive industry salary and benefits
📌 Note Before You Apply:
Kindly read the entire job description carefully before applying. Candidates with experience in regulatory submissions, EUCTR documentation, and clinical research compliance may have an advantage.
Kindly read the entire job description carefully before applying. Candidates with experience in regulatory submissions, EUCTR documentation, and clinical research compliance may have an advantage.
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