Remote Hiring for eCTD / Regulatory Submissions at Thermo Fisher Scientific
Introduction
Thermo Fisher Scientific, a global leader in scientific solutions, is currently hiring for the position of Regulatory Publishing Specialist. This remote job opportunity is based in India and is ideal for professionals with a background in pharmacy, life sciences, or regulatory affairs. With over $40 billion in annual revenue and operations in more than 100 countries, Thermo Fisher offers a rewarding career path for individuals looking to contribute to global health and innovation. Remote Hiring for eCTD / Regulatory Submissions
In this article, we’ll cover all the important details about the position, including roles, responsibilities, qualifications, benefits, and how to apply online.
About Thermo Fisher Scientific
Thermo Fisher Scientific Inc. is a Fortune 500 company renowned for its mission to make the world healthier, cleaner, and safer. Through its PPD® clinical research portfolio, the company provides leading-edge contract research organization (CRO) services. These services support pharmaceutical and biotechnology companies worldwide in their drug development and clinical trial processes.
This recruitment drive is part of Thermo Fisher’s strategic effort to strengthen its regulatory submissions team and maintain its leadership in the global life sciences sector.
Job Role: Regulatory Publishing Specialist
Job Type:
- Full-time, Permanent
- Work from Home (India-based)
Department:
- Regulatory Affairs / Clinical Research
Experience Required:
- Minimum 2 years
Key Responsibilities
As a Regulatory Publishing Specialist at Thermo Fisher Scientific, you will be responsible for preparing, formatting, and submitting high-quality regulatory submissions in accordance with international standards. Your key duties will include:
- Preparing and managing eCTD (electronic Common Technical Document) and other electronic submission formats as per ICH, FDA, EMA, and other global regulatory authorities’ guidelines.
- Performing document formatting, hyperlinking, bookmarking, and quality control checks using industry-standard publishing tools.
- Collaborating with cross-functional teams including regulatory affairs, medical writing, and quality assurance to ensure timely and compliant submissions.
- Managing document version control, ensuring completeness, accuracy, and regulatory compliance.
- Supporting sponsor-specific submission requirements and maintaining communication for ongoing projects.
- Keeping regulatory documentation systems and records up to date and compliant with internal and external requirements. Remote Hiring for eCTD / Regulatory Submissions
Required Qualifications
To qualify for this position, applicants must have the following educational and professional background: Remote Hiring for eCTD / Regulatory Submissions
Educational Criteria:
- B.Pharm, M.Pharm, M.Sc, B.Sc, or a degree in Regulatory Affairs or any Life Sciences discipline.
Professional Skills and Experience:
- Minimum 2 years of hands-on experience in regulatory publishing, document management, or eCTD submissions.
- In-depth knowledge of global regulatory submission standards (including ICH, FDA, and EMA guidelines).
- Familiarity with tools like Microsoft Word, Excel, Adobe Acrobat, and regulatory publishing software.
- Strong attention to detail and organizational skills.
- Excellent communication skills and the ability to handle multiple projects under tight deadlines.
Benefits of Working with Thermo Fisher
This remote opportunity is not only flexible but also offers several benefits that make it an attractive role for professionals in the regulatory and pharmaceutical sector. Remote Hiring for eCTD / Regulatory Submissions
Key Benefits:
- Remote work opportunity with global exposure.
- Competitive salary package.
- Annual performance-based bonuses.
- Health insurance and other medical benefits.
- Career development and internal promotion opportunities.
- Exposure to global regulatory practices and documentation standards.
- Inclusive and innovation-driven work culture.
Career Growth and Learning Opportunities
Working at Thermo Fisher Scientific provides access to world-class training programs, mentorship opportunities, and the chance to work on international projects. Regulatory professionals joining the company often move into more advanced roles within regulatory strategy, global submissions, or leadership positions within a few years. Remote Hiring for eCTD / Regulatory Submissions
Who Should Apply?
This job is ideal for:
- Regulatory Affairs professionals looking to work remotely with a globally recognized organization.
- Individuals with experience in preparing and managing eCTD or other regulatory submission formats.
- Professionals aiming for career advancement in pharmaceutical documentation and compliance.
- Candidates seeking a work-from-home job with international exposure and long-term stability.
How to Apply
Interested candidates can apply online through the official Thermo Fisher careers portal or verified pharmaceutical job platforms such as Pharmabharat. Before applying, make sure your resume highlights your experience in regulatory publishing and any tools or systems you have worked with.
Important: Ensure that all documents are properly formatted and up to date. Include a well-written cover letter that demonstrates your understanding of regulatory compliance, document standards, and your ability to manage submissions. Remote Hiring for eCTD / Regulatory Submissions
Final Words
Thermo Fisher Scientific is known for its innovation, ethical practices, and commitment to employee growth. If you have experience in regulatory publishing and are looking for a remote job that offers a great balance between flexibility and career growth, this is an excellent opportunity. Remote Hiring for eCTD / Regulatory Submissions
Apply now to become part of a dynamic team working to support global health and regulatory standards.
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