MSc Biotechnology Jobs at Meril Apply Now for a Quality Assurance Role!
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MSc Biotechnology Jobs at Meril 

Meril, Vapi, Gujarat is hiring a Regulatory Documentation Specialist, a Quality Assurance Role to manage IVF buffer media and sterile life science product documentation. MSc Biotechnology Jobs at Meril offers candidates a vast experience & expertise in regulatory compliance, DCGI submissions, ISO 13485 QMS documentation, and audit support to ensure product approvals and renewals.

Job Details:

  • Job Role: Regulatory Documentation Specialist – IVF & Sterile Life Science Products
  • Company: Meril Life Sciences
  • Location: Vapi, Gujarat, India
  • Employment Type: Full-time

About Meril:

Meril Life Sciences is a globally recognized medical device and life science company committed to advancing healthcare solutions through innovation and quality. With a strong presence in India and international markets, Meril focuses on manufacturing high-standard, compliant medical technologies that enhance patient outcomes and align with international regulatory standards.

About the Job:

Regulatory Documentation Specialist Jobs at Meril focused on IVF buffer media and sterile life science products. The ideal candidate for the MSc Biotechnology Jobs will have a strong background in regulatory compliance and documentation.

Qualifications:

  • Master’s in Biology / Biotechnology / Life Sciences
  • 3–5 years’ experience in regulatory documentation for sterile or IVF-related products

Key Responsibilities of the Jobs at Meril:

  • Prepare and maintain regulatory dossiers, technical files, and SOPs
  • Collaborate with QA, RA, and R&D teams for regulatory submissions
  • Support audits, product registrations, and renewals
  • Ensure compliance with DCGI, CE marking, and MDR/IVDR requirements
  • Maintain documentation under ISO 13485:2016 and WHO-GMP standards

Skills Required:

  • Expertise in DCGI submissions and Product/Site Master Files
  • Strong understanding of ISO 13485:2016 QMS documentation
  • Knowledge of CE marking, MDR/IVDR compliance, and WHO-GMP standards
  • Familiarity with Drugs & Cosmetics Act and Medical Device Rules (2017)
  • Excellent documentation, communication, and coordination skills

To apply, kindly email your updated resume to [email protected]

Career Growth & Opportunities of Jobs at Meril:

At Meril, employees are encouraged to grow within the regulatory and life sciences domain through structured career development paths, continuous learning opportunities, and exposure to international compliance frameworks. Successful professionals can advance to senior regulatory, quality assurance, or product compliance roles.

Benefits of Jobs at Meril:

  • Competitive salary package with performance-based incentives
  • Health and medical insurance coverage
  • On-site facilities and wellness programs
  • Continuous professional development and training programs
  • Work-life balance and employee engagement activities

CLICK HERE TO APPLY THROUGH LINKEDIN

Shekhar
Shekhar Suman is the Co-founder of BioTecNika Info Labs Pvt. Ltd. He is an Entrepreneur, Writer, Public Speaker, and a Motivational Coach. In his career, he has mentored more than 100,000+ students toward success in the Biopharma Industry. He heads the BioTecNika Group, which comprises BioTecNika.com, BioTecNika.org, and Rasayanika.com. An avid reader and listener who is passionate about BioSciences. Today Biotecnika is India's largest Biotech Career portal, with over 5 Million subscribers from academia & Industry. It's ranked among the top 50 websites worldwide in the Biology category.

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