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Join BioMatrix Healthcare Private Limited, a 100% export-oriented pharmaceutical company headquartered in Ahmedabad, Gujarat, established in 2007 with a mission of “Supporting Life Worldwide.”
We are hiring dedicated professionals for our Analytical Development Laboratory (ADL) and Quality Control (QC) departments to support our expansion into EU, LATAM, GCC, and SEA markets. Our WHO-GMP and EU-GMP accredited facility complies with ANVISA, UKMHRA, and USFDA regulations, exporting oral solids, liquids, and dry syrups to over 30 countries.
Event Details
- Date: Sunday, June 8, 2025
- Time: 9:00 AM to 12:00 PM
- Venue: BioMatrix Healthcare Pvt. Ltd., 502-B, Times Square Grand, Sindhu Bhavan Road, Thaltej, Ahmedabad, Gujarat 380059
- Note: Bring updated CV, one passport-size photo (mandatory for interview), educational certificates, last 3 months’ payslips, and Aadhaar/PAN copies. USFDA/EU-GMP exposure preferred.
Job Opportunities
| Department | Designation | Qualification | Experience | Key Responsibilities |
|---|---|---|---|---|
| ADL | Officer to Executive | B.Sc / M.Sc / B.Pharm | 2-6 Years | Develop and validate analytical methods (HPLC, GC, UV), prepare documentation, support regulatory filings |
| QC | Officer to Executive | B.Sc / M.Sc / B.Pharm | 2-6 Years | Perform RM/PM/FP testing using HPLC, GC, dissolution; ensure cGMP/GLP compliance, manage QMS |
Key Responsibilities
Analytical Development Laboratory (ADL):
- Develop and validate analytical methods for oral solids, liquids, and dry syrups using HPLC, GC, UV, and dissolution apparatus
- Prepare analytical development reports (ADR) and stability study protocols
- Support regulatory submissions for EU, USFDA, and ROW markets
- Maintain lab documentation per cGMP and GLP standards
- Collaborate with R&D for formulation development
Quality Control (QC):
- Conduct testing of raw materials (RM), packaging materials (PM), and finished products (FP) using HPLC, GC, and dissolution
- Perform stability studies and ensure compliance with cGMP, GLP, and SOPs
- Manage QMS activities, including deviations, CAPA, and OOS investigations
- Operate lab software (e.g., Empower, LIMS) and support USFDA/EU-GMP audits
- Review analytical data and maintain accurate documentation
Desired Profile
- 2-6 years of experience in ADL or QC within pharmaceutical formulation (OSD/liquids)
- Proficiency in HPLC, GC, UV, dissolution, and analytical method validation
- Strong knowledge of cGMP, GLP, SOPs, and regulatory requirements (USFDA, EU-GMP, WHO-GMP)
- Familiarity with lab software (Empower, LIMS) and QMS processes
- Excellent analytical, communication, and documentation skills
- Ability to work in a fast-paced, audit-ready environment
Why Join BioMatrix Healthcare?
BioMatrix Healthcare, with 700+ professionals across 30+ countries, is a fast-growing, multicultural CRO rated 3.8/5 on AmbitionBox for work culture and 4.0/5 for skill development.
Our Ahmedabad facility, located at Rajoda and Thaltej, supports over 1,000 product registrations globally. Benefits include a supportive environment, UDAAN cultural initiatives, and export-focused growth, though some reviews note restrictive leave policies (22 days/year limit, no increment if exceeded) and a 3.2/5 salary rating. Learn more at BioMatrix Healthcare.
How to Apply
- Walk-In: Attend with required documents on June 8, 2025.
- Email: Send CV to career@biomatrixhealthcare.com.
- Contact: Call +91 6357410551 or +91 9725901031 for queries.
- Note: Mention “ADL/QC Officer to Executive” in email subject. Passport-size photo mandatory for interview. No fees charged.
Additional Information
Explore QC/ADL career trends at PharmaVoice. Join BioMatrix to support life worldwide through innovative pharmaceuticals!
Disclaimer: BioMatrix Healthcare does not charge fees for recruitment or use free email services for job offers. Verify offers through official channels (e.g., hr@biomatrixhealthcare.com).
Note: Shortlisting based on qualifications, analytical expertise, and regulatory exposure.