Pharma Jobs in Ahmedabad – BioMatrix Healthcare Walk-In Drive for QA, QC & Production Positions

BioMatrix Healthcare Announces Walk-In Interviews for Multiple Pharmaceutical Positions in Ahmedabad

BioMatrix Healthcare, a globally recognized pharmaceutical manufacturer, has announced a walk-in recruitment drive for various roles in Quality Assurance, Quality Control, and Production. The interviews are scheduled for November 16, 2025 (Sunday), from 9:00 AM to 12:00 PM, at the company’s corporate office in Ahmedabad.

This recruitment initiative aims to fill several key positions across departments, offering roles ranging from Officer to Executive levels, as well as technical Operator positions. With certifications from EU-GMP and Health Canada, BioMatrix stands as a trusted name in pharmaceutical manufacturing, committed to global health under its mission of “Supporting Life Worldwide.”

Interview Details:

Date: 16th November 2025 (Sunday)

Time: 9:00 AM – 12:00 PM

Venue:

    Corporate Office, 502-B, Times Square Grand, Sindhu Bhavan Road, Thaltej,
Ahmedabad – 380059

Open Positions & Eligibility

1. Quality Assurance (QA) – Officer to Executive

· Qualifications: B.Pharm / M.Pharm / M.Sc

· Experience: 2–8 years

· Role Includes: IPQA & Documentation (OSD), in-process quality checks, documentation review, equipment qualification

2. Quality Control (QC) – Officer to Executive

· Qualifications: B.Sc / M.Sc / B.Pharm

· Experience: 2–8 years

· Role Includes: HPLC operation, stability studies, analytical method validation (AMV), QC documentation, cGMP compliance

3. Production – Officer to Executive

· Qualifications: B.Pharm / M.Pharm

· Experience: 2–8 years

· Role Includes: Overseeing Oral Solid Dosage (OSD) manufacturing processes

4. Production – Operator

· Qualifications: ITI

· Experience: 2–6 years

· Role Includes: Hands-on work in Compression and Granulation processes (OSD)

Why Join BioMatrix Healthcare?

BioMatrix is known for:

· Adherence to international regulatory standards (Health Canada, EU-GMP)

· A focus on innovation and quality in pharmaceutical manufacturing

· A supportive and professional work environment

· Opportunities for career growth across departments

How to Apply?

Interested and eligible candidates can:

· Walk in directly on the specified date with their updated CV, educational certificates, and experience documents.

· Pre-submit their resume via email to:

career@biomatrixhealthcare.com

    hr@biomatrixhealthcare.com

Contact for Queries:

    63574 10551, 63589 70525

    97259 01031, 92288 93058 (WhatsApp available)

Website: www.biomatrixhealthcare.com

FAQ:

1. What type of products are manufactured under the Oral Solid Dosage (OSD) division at BioMatrix Healthcare?

BioMatrix Healthcare’s OSD division manufactures a wide range of solid oral formulations, including tablets, capsules, and granules, in compliance with EU-GMP and Health Canada guidelines. The facility follows strict quality control and documentation systems aligned with international standards.

2. What analytical instruments and techniques are used in the Quality Control (QC) department?

The QC department utilizes advanced analytical instruments such as HPLC, UV-Visible Spectrophotometers, FTIR, Dissolution Testers, and Karl Fischer Titrators. Analysts are expected to have hands-on experience with method validation, stability testing, and data integrity compliance under cGMP norms.

3. What are the key responsibilities of IPQA personnel in the Quality Assurance department?

In-process Quality Assurance (IPQA) personnel are responsible for monitoring in-process manufacturing activities, verifying batch documentation, ensuring compliance with Standard Operating Procedures (SOPs), and conducting line clearance and process validation checks during production to maintain consistent product quality.

4. What manufacturing processes are covered under Production (OSD) roles?

Production roles include operation and supervision of granulation, compression, coating, and packing processes. Candidates are expected to understand batch manufacturing records (BMR), handle GMP documentation, and ensure process compliance for oral solid dosage formulations.

5. What qualifications or experience are preferred for candidates handling HPLC in QC?

Candidates should hold a B.Sc / M.Sc / B.Pharm degree with 2–8 years of experience in a pharmaceutical QC laboratory. Hands-on experience in HPLC operation, system suitability, calibration, method validation, and stability sample analysis will be highly preferred.