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Urgent! IVF Documentation - Local Job Opening in Vapi

IVF Documentation



Job description

Join our team as a
Regulatory Documentation Specialist
focused on
IVF buffer media and sterile life science products
.

The ideal candidate will have strong expertise in
regulatory compliance & documentation.

Qualifications:

Master's in Biology / Biotechnology / Life Sciences

3–5 years' experience in regulatory documentation for sterile or IVF-related products

Key Skills:

DCGI submissions & Product/ Site Master Files

ISO 13485:2016 QMS documentation

CE marking, MDR/IVDR compliance

Knowledge of Drugs & Cosmetics Act, Medical Device Rules (2017)

Knowledge of
WHO-GMP
standards.

Responsibilities:

Prepare and maintain regulatory dossiers, technical files & SOPs

Collaborate with QA, RA & R&D for submissions

Support audits, product registrations & renewals

Kindly mail your update resume on


Required Skill Profession

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