Life Science Job at Meril
Looking for a rewarding Life Science Job in the medical device industry? A job at Meril brings an exciting opportunity for talented Biotechnology, Pharmacy, Biomedical Engineering, and Life Science professionals to join as a Documentation Executive in the R&D – Women’s Genesis division. If you have experience in regulatory documentation, quality systems, and technical documentation, this role offers an excellent chance to work on innovative healthcare products while building your career with one of India’s leading medical technology companies.
About Meril
Meril is a prominent medical device company specialising in innovative solutions for healthcare. Operating in the biomedical engineering sector, Meril focuses on developing advanced medical devices that enhance patient care. The organisation is headquartered in Vapi, Gujarat, and is committed to maintaining high standards in quality and regulatory compliance throughout its operations. This life science job at Meril is crucial for supporting the company’s mission to deliver safe and effective medical products.
Job Details:
- Job Title: Documentation Executive
- Department: Research & Development (R&D) – Women Genesis
- Location: Vapi, Gujarat
- Reports To: Manager / Senior Manager
Job Purpose:
The Documentation Executive will prepare, review, control, and maintain design, technical, quality, and regulatory documentation throughout the product development lifecycle for Women’s Healthcare medical devices. This life science job ensures compliance with applicable regulatory standards, Quality Management System (QMS) requirements, and company procedures while supporting R&D, product development, validation, technology transfer, and regulatory submissions.
Job Description
This life science job at Meril involves a variety of responsibilities that are essential for the successful development and commercialisation of medical devices. The role requires strong attention to detail and a thorough understanding of regulatory requirements, ensuring that all documentation meets the necessary standards for quality and compliance.
Key Responsibilities
- Prepare, review, and maintain Design History Files (DHF), Design Inputs, Design Outputs, Design Verification & Validation documents, and technical specifications.
- Develop and maintain Technical Files supporting product development and commercialisation.
- Prepare documentation for regulatory submissions including Test License, CDSCO, CE MDR, and ROW.
- Coordinate timely submission of project documents to the Regulatory Affairs department.
- Maintain document revision history, version control, approvals, and archival in accordance with document control procedures.
- Collaborate with cross-functional teams to ensure timely completion and approval of project documents.
- Support internal audits, external audits, and regulatory inspections by providing accurate documentation.
- Assist in CAPA implementation and continuous quality improvement initiatives.
Eligibility Criteria
- Bachelor’s degree in Biomedical Engineering, Biotechnology, Life Sciences, or a related discipline.
- 2–3 years of experience in documentation, Quality Assurance, Regulatory Affairs, or technical documentation within the medical device, pharmaceutical, or healthcare industry.
- Experience in regulated medical device documentation and product development is preferred.
Required Skills
- Strong knowledge of ISO 13485, CE MDR, CDSCO, and medical device Quality Management Systems.
- Excellent technical writing, documentation, and organizational skills.
- Proficiency in Microsoft Office applications and Electronic Document Management Systems (eDMS).
- Strong analytical abilities with exceptional attention to detail.
- Effective communication and cross-functional coordination skills.
- Self-motivated with a proactive approach to continuous improvement and regulatory compliance.
Why Join Meril?
Joining Meril offers an opportunity to work in a dynamic environment focused on innovation in the biomedical engineering field. This life science job is integral to the company’s commitment to quality and regulatory compliance in the development of medical devices. Employees benefit from a collaborative culture that values professional growth and continuous improvement, making it an ideal place for those passionate about healthcare and technology.
Summary
Documentation executive jobs at Meril present an excellent opportunity for qualified candidates to contribute to the healthcare sector. With a focus on regulatory compliance and documentation quality, this life science job is vital for the development of innovative medical devices. Interested individuals are encouraged to apply before the deadline to seize this opportunity in Vapi, Gujarat.
