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Quality Control, Pharma Industry, R and D, CSIR, Food Industry, Pathology, Medical Writing, coding

Multiple Vacancies in Production, Microbiology, Quality Control, Quality Assurance, Analytical R and D , Warehouse, Packing

THEON LIFESCIENCES LTD IS ORGANISING  WALK IN INTERVIEW FOR VARIOUS DEPARTMENTS  Details are provided below  Date: 11th APRIL 1. Department: Production  2. Positions :  Operators  Eye Drops  Ampoules  Executives / Officers  Eye Drops  Ampoules  1. Department: Microbiology  2. Positions:  Officer Executive Trainee 1. Department: Quality Control ( QC)  2. Positions :  Executive Officer 1. Department: Quality Assurance ( QA)  2. Positions :  Validations AM/DM Product Development QMS Trainees 1. Department: Analytical R&D ARD (ARD Department) 1. Department: Warehouse  Officer 1. Department: Packing  Supervisor Technician Required for:Blister Packings Cartonator/PFS hrl@theonlifesciences.com Click Here for Details
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Required Documentation Specialist - IVF Media-B.Pharm / M.Pharm / M.Sc. / B.Sc. (Biotech / Life Sciences /Pharmacy)

Meril Life Sciences Pvt Ltd is Hiring Documentation Specialist - IVF Media
Meril Life Sciences is looking for experienced professionals to join their Quality team in IVF Media documentation & compliance.
Details are provided below 
1. Role Overview:
-Drive quality documentation, ensure regulatory compliance, and support quality systems for sterile IVF media products in line with global standards.
2. Key Responsibilities:
-Implement and maintain ISO 13485 Quality Management Systems
-Prepare & review SOPs, BMRS, BPRs, validation protocols, and technical documents
-Manage change control, deviations, CAPA, and risk management
-Ensure compliance in aseptic
manufacturing, sterility, and contamination control
-Support audits (internal, external, regulatory) and documentation readiness
-Collaborate with cross-functional teams for QA and regulatory requirements
3. Qualification :
B.Pharm / M.Pharm / M.Sc. / B.Sc. (Biotech / Life Sciences /Pharmacy) 
4. Experience: 3-4 years in QA for sterile products, injectables, biologics, or IVF/cell culture media
5. Key Skills:
-ISO 13485 | WHO & CE compliance | GMP | Aseptic processes | CAPA |
-Audit readiness
6. Added Advantage: Exposure to CDSCO, EU MDR, or ISO 14971
7. How to Apply: 
If you have a strong eye for quality and compliance, kindly connect:
ankita.rajput@merillife.com/vaishnavi.kadam@merillife.com

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