Apply online for Remote Job Regulatory Affairs Openings at Thermo Fisher Scientific Join global compliance and documentation teams.
Overview
Thermo Fisher Scientific, one of the world’s leading science and technology companies, is hiring Regulatory Affairs Specialist I (Admin) professionals to support Regulatory Compliance Review (RCR) operations. This fully remote opportunity allows skilled candidates to work from home while contributing to the integrity, safety, and compliance of global pharmaceutical documentation. Remote Job Regulatory Affairs Openings at Thermo Fisher Scientific
If you are detail-oriented, passionate about regulatory processes, and looking for a meaningful career with flexibility, this is an excellent chance to grow with a globally recognized organization. The role is based remotely, with the company’s primary regulatory hub in Bangalore, India. Remote Job Regulatory Affairs Openings at Thermo Fisher Scientific
About Thermo Fisher Scientific
Thermo Fisher Scientific is a multinational biotechnology and pharmaceutical leader, known for advancing science through innovative solutions, instruments, and analytical support. The company’s mission, “to enable our customers to make the world healthier, cleaner, and safer,” drives every aspect of its work. Remote Job Regulatory Affairs Openings at Thermo Fisher Scientific
Through the PPD clinical research business, Thermo Fisher delivers integrated drug development, laboratory, and regulatory services to pharmaceutical, biotechnology, and healthcare organizations worldwide.
Joining Thermo Fisher’s Regulatory Affairs team means becoming part of a global network of scientists, compliance specialists, and regulatory professionals working together to bring life-saving medicines to patients safely and efficiently. Remote Job Regulatory Affairs Openings at Thermo Fisher Scientific
About the Role
The position of Regulatory Affairs Specialist I (Admin) focuses on supporting Regulatory Compliance Review (RCR) and documentation processes. The role is vital to ensuring all essential study documents meet international quality standards and regulatory requirements. Remote Job Regulatory Affairs Openings at Thermo Fisher Scientific
This is a remote-based position, offering the flexibility to work from home while managing global compliance operations. You will coordinate across project teams, maintain accurate regulatory documentation, and uphold the company’s commitment to quality and transparency. Remote Job Regulatory Affairs Openings at Thermo Fisher Scientific
Key Responsibilities
As a Regulatory Affairs Specialist I, you will be responsible for maintaining regulatory consistency and supporting project teams through documentation review and management. Your daily activities will include:
- Performing global regulatory compliance reviews of essential study documents supporting the customization of Essential Document Checklists (EDCs).
- Responding to project team queries regarding document requirements and regulatory standards.
- Facilitating discussions on deviations from the RCR process, ensuring proper documentation and justification.
- Coordinating and managing the Essential Document Checklist process to ensure regulatory completeness and efficiency.
- Maintaining knowledge of PPD Standard Operating Procedures (SOPs), client directives, and current global regulatory guidelines.
- Reviewing, finalizing, and posting EDCs accurately and within the required timelines.
- Supporting version control and consistency across document submissions to ensure full regulatory traceability.
- Assisting with process improvements, documentation audits, and corrective actions when required.
This role requires exceptional accuracy, documentation expertise, and a proactive approach to compliance and quality control. Remote Job Regulatory Affairs Openings at Thermo Fisher Scientific
Educational Qualification
- Bachelor’s degree in Science, Pharmacy, Life Sciences, Biotechnology, or Information Technology.
- Candidates with a Master’s degree such as M.Pharm, Pharm.D, or M.Sc will be preferred.
This role is ideal for professionals with a strong academic background in the pharmaceutical, biomedical, or scientific domains who wish to transition into global regulatory operations. Remote Job Regulatory Affairs Openings at Thermo Fisher Scientific
Experience Required
- 1 to 3 years of professional experience in Regulatory Affairs, Clinical Documentation, or Quality Compliance.
- Experience working with Essential Document Checklists (EDCs), Clinical Trial Master Files (TMFs), or Regulatory Information Management (RIM) systems is advantageous.
- Prior exposure to Good Clinical Practice (GCP) and international regulatory standards will be an asset.
Essential Skills and Competencies
The Regulatory Affairs Specialist I position requires a balanced mix of technical expertise and communication ability. The key skills include:
- Excellent English communication skills, both written and verbal.
- Strong attention to detail and commitment to documentation accuracy.
- Proficiency in Microsoft Word, Excel, and PowerPoint.
- Capability to adapt to new software and document management technologies.
- Strong organizational and time management skills to handle multiple tasks efficiently.
- Ability to work independently and collaboratively with global teams.
- Familiarity with global and regional regulatory submission processes.
- Analytical, investigative, and problem-solving mindset to maintain compliance standards.
- Editorial and proofreading skills for document quality checks.
Key Benefits of Working with Thermo Fisher Scientific
Thermo Fisher Scientific is committed to providing employees with a supportive and inclusive workplace that fosters professional growth. As a Regulatory Affairs Specialist, you’ll enjoy the following benefits: Remote Job Regulatory Affairs Openings at Thermo Fisher Scientific
- Work-from-Home Flexibility
- 100% remote opportunity, allowing you to contribute from anywhere in India.
- Global Exposure
- Gain hands-on experience working on international regulatory projects and documentation systems.
- Career Advancement
- Structured career development paths with opportunities to move into senior specialist or manager roles.
- Work-Life Balance
- Standard weekday schedule (Monday to Friday) ensures consistent, predictable hours.
- Learning & Upskilling Programs
- Access to professional training and global certification programs to enhance your regulatory knowledge.
- Collaborative Work Environment
- Work with a diverse, supportive team of scientists, regulatory experts, and data specialists.
Work Schedule and Location
- Work Type: Full-time
- Work Mode: 100% Remote (Work from Home)
- Base Location: Bangalore, India
- Work Days: Monday to Friday (Standard Office Hours)
Career Path and Growth Opportunities
A role at Thermo Fisher Scientific is just the beginning. Starting as a Regulatory Affairs Specialist I, you can progress to:
- Regulatory Affairs Specialist II
- Senior Specialist or Lead – Regulatory Compliance
- Regulatory Affairs Manager or Global Operations Lead
With every level, you’ll gain more responsibility, exposure to strategic compliance projects, and the opportunity to lead teams handling critical regulatory submissions.
Who Should Apply
This role is suitable for professionals who:
- Have a background in Life Sciences, Pharmacy, or Biotechnology.
- Possess strong documentation and analytical abilities.
- Are seeking remote job opportunities in Regulatory Affairs.
- Aspire to work for a globally recognized pharmaceutical and research organization.
Fresh graduates with strong academic records and internship experience in regulatory or clinical documentation are also encouraged to apply. Remote Job Regulatory Affairs Openings at Thermo Fisher Scientific
How to Apply
Interested and qualified candidates can apply online through the official Thermo Fisher Scientific careers page. Remote Job Regulatory Affairs Openings at Thermo Fisher Scientific
Step-by-Step Application Process:
- Visit the official Thermo Fisher Scientific Careers Portal.
- Search for the position titled “Regulatory Affairs Specialist I (Admin)” or Job ID: R-01330620.
- Click on “Apply” to begin the application process.
- Create an account or log in with existing credentials.
- Fill out the online application form and upload your updated resume and cover letter.
- Review all information carefully and submit your application.
💡 Tip: Tailor your resume to highlight experience in regulatory documentation, data review, and quality compliance. Mention tools or systems you’ve used for document management to strengthen your profile. Remote Job Regulatory Affairs Openings at Thermo Fisher Scientific
Important Details
- Company: Thermo Fisher Scientific (PPD Division)
- Position: Regulatory Affairs Specialist I (Admin)
- Location: Bangalore, India (Remote)
- Experience Required: 1–3 years
- Qualification: B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, or Life Sciences Degree
- Work Type: Full-Time (Work from Home)
- Application Mode: Online
- Posted On: November 6, 2025
- Last Date to Apply: Apply as soon as possible
Conclusion
The Regulatory Affairs Specialist I (Admin) position at Thermo Fisher Scientific is an exceptional opportunity for professionals who wish to combine remote flexibility with global regulatory exposure. Working within the company’s PPD clinical research business, you will play a vital role in maintaining documentation quality and ensuring compliance with international standards. Remote Job Regulatory Affairs Openings at Thermo Fisher Scientific
If you’re driven by precision, passionate about regulatory systems, and ready to grow in a multinational organization that values innovation and collaboration, this role is ideal for you.
Start your journey with Thermo Fisher Scientific today — apply online and be part of the team that’s redefining excellence in global regulatory affairs.
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