BioMatrix Healthcare - Walk-In Interviews for B.Pharm / ITI / M.Sc Candidates on 26th May' 2026 - Pharmawisdom.co.in

BioMatrix Healthcare Pvt. Ltd. is conducting walk-in interviews for multiple openings in Production, Packaging, QC, and QC-Microbiology departments at its Ahmedabad manufacturing facility. The company manufactures and exports oral solids, liquids, and dry syrups and is backed by EU-GMP, Health Canada, and WHO-GMP certifications along with strong R&D capabilities.

Walk-In Interview Details

Details Information
Interview Date 26 May 2026 (Tuesday)
Registration Time 09:30 AM – 01:00 PM
Interview Venue Survey No.-624, Sarkhej-Bavla Highway, Village Rajoda, Ahmedabad, Gujarat
Job Location Ahmedabad, Gujarat

Production Department Openings

Designation Qualification Experience Key Skills
Executive M.Sc / B.Pharm 8 – 10 Years Shift handling, tablet capsule plant operations, QMS activities, SOP implementation
Operator ITI 2 – 5 Years Granulation, Compression, Tablet & Capsule manufacturing

Packaging Department Openings

Designation Qualification Experience Key Skills
Officer to Executive B.Sc / M.Sc 2 – 10 Years Primary & secondary packaging, GMP compliance, QMS activities
Operator ITI 2 – 5 Years Auto Cartonator, Blister Packing, Strip Packing

Quality Control (QC) Openings

Designation Qualification Experience Key Skills
Officer to Sr. Officer B.Sc / M.Sc / B.Pharm 2 – 6 Years HPLC, GC, analytical testing, AMV, GMP/GLP compliance

QC – Microbiology Openings

Designation Qualification Experience Key Skills
Officer to Sr. Officer B.Sc / M.Sc in Microbiology 2 – 6 Years Microbiological analysis, environmental monitoring, GMP/GLP documentation

Contact Details

Email IDs

Contact Numbers

  • 63574 10551
  • 63589 70525
  • 97259 01031
  • 92288 93058

Important Instructions

  • Candidates should carry updated resumes and relevant educational and experience documents.
  • Experience in pharmaceutical manufacturing, QC, packaging, and microbiology operations will be preferred.
  • Knowledge of GMP, GLP, QMS, and regulatory documentation is desirable for most roles

 

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