BioMatrix Walk-in QA, QC & Production (OSD)

B.Pharm, M.Pharm Openings | QA, QC & Production | BioMatrix Ahmedabad

BioMatrix hiring Officers & Executives for QA, QC & Production (OSD). Walk-in on 16 Nov 2025 at Ahmedabad.

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BioMatrix Healthcare Pvt. Ltd., a globally recognized pharmaceutical company with EU-GMP and Health Canada approvals, invites experienced professionals for a Walk-In Interview in Quality Assurance (QA), Quality Control (QC), and Production (OSD). This is a fantastic opportunity for motivated individuals looking to grow in a world-class manufacturing environment driven by innovation and quality.

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Company Overview

BioMatrix Healthcare Pvt. Ltd. is one of India’s fastest-growing pharmaceutical companies with a mission to deliver high-quality healthcare solutions worldwide. With approvals from EU-GMP, Health Canada, and WHO, BioMatrix specializes in Oral Solid Dosage (OSD) and injectable formulations for regulated and semi-regulated markets. The company upholds stringent GMP standards, advanced technology, and continuous innovation in drug manufacturing.

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Job Role & Responsibilities

1. Department: Quality Assurance (QA)

Designation: Officer to Executive
Experience: 2–8 Years
Qualification: B.Pharm, M.Pharm, M.Sc

Responsibilities:

• Manage IPQA and Documentation (OSD) activities in manufacturing areas.
• Review and ensure accuracy of batch manufacturing records and SOPs.
• Support equipment qualification and validation processes.
• Conduct process inspections and ensure compliance with cGMP, GDP, and regulatory guidelines.
• Handle deviations, CAPA, and ensure documentation integrity.

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2. Department: Production (OSD)

Designation: Officer to Executive
Experience: 2–8 Years
Qualification: B.Pharm, M.Pharm

Responsibilities:

• Supervise and operate Oral Solid Dosage (OSD) manufacturing processes.
• Oversee granulation, compression, and coating operations.
• Maintain batch records and coordinate with QA for line clearance.
• Monitor yields, material reconciliation, and maintain high productivity.
• Ensure adherence to cGMP, EHS, and data integrity standards.

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3. Department: Quality Control (QC)

Designation: Officer to Executive
Experience: 2–8 Years
Qualification: B.Sc, M.Sc, B.Pharm

Responsibilities:

• Conduct HPLC operations, stability testing, and analytical method validation (AMV).
• Perform testing for raw materials, finished products, and stability samples.
• Prepare analytical documentation, protocols, and reports.
• Maintain calibration records and ensure compliance with cGMP and GLP.
• Participate in internal audits and laboratory data integrity programs.

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4. Department: Production (Operator)

Designation: Operator
Experience: 2–6 Years
Qualification: ITI

Responsibilities:

• Operate compression and granulation machines for OSD manufacturing.
• Conduct in-process checks and ensure production within defined parameters.
• Maintain area cleanliness and perform equipment cleaning as per SOPs.
• Support validation and documentation activities for process control.

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Eligibility / Qualifications

Education: B.Pharm, M.Pharm, M.Sc, B.Sc, or ITI (based on role).
Experience: 2–8 years in pharmaceutical QA, QC, or OSD production.

Relevant Courses (comma-separated): Industrial Pharmacy, Analytical Chemistry, cGMP & GLP, Pharmaceutical Quality Management, Validation & Calibration, Regulatory Affairs, OSD Manufacturing Practices.

Skills:

• In-depth knowledge of cGMP, GLP, and data integrity standards.
• Proficiency in handling analytical instruments (HPLC, UV, FTIR).
• Strong communication, documentation, and problem-solving skills.

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Location & Salary

Interview Venue: Corporate Office, 502-B, Times Square Grand, Sindhu Bhavan Road, Thaltej, Ahmedabad – 380059
Interview Date: 16th November 2025 (Sunday)
Time: 09:00 AM – 12:00 PM
Work Location: Ahmedabad
Salary: Best in the industry, based on experience and qualifications.

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Application Process

Interested candidates may attend the Walk-In Interview with their updated resumes, educational certificates, and ID proof. Those unable to attend can share their profiles via email.

Email IDs:
career@biomatrixhealthcare.com
hr@biomatrixhealthcare.comContact Numbers:
63574 10551 | 63589 70525 | 97259 01031 | 92288 93058

Website: www.biomatrixhealthcare.com

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Why Join BioMatrix Healthcare?

• Work in an EU-GMP & Health Canada-approved facility.
• Exposure to international regulatory audits and global markets.
• Hands-on learning with modern analytical and production systems.
• A collaborative, growth-oriented work environment.
• Competitive pay and career advancement opportunities.

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FAQs

1. When is the walk-in interview scheduled?
The interview will be held on 16th November 2025 (Sunday) from 9:00 AM to 12:00 PM.

2. What positions are open?
Positions available in QA, QC, and Production (Officer to Executive) and Operator levels.

3. What qualifications are required?
Candidates with B.Pharm, M.Pharm, M.Sc, B.Sc, or ITI can apply based on their area of expertise.

4. Is BioMatrix approved by international agencies?
Yes, BioMatrix is EU-GMP and Health Canada-approved, ensuring a global-standard work environment.

5. How can I apply?
You can attend the walk-in or email your resume to career@biomatrixhealthcare.com or hr@biomatrixhealthcare.com.

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Job Summary Table

Category	Details
Company	BioMatrix Healthcare Pvt. Ltd.
Vacancies	QA, QC & Production (OSD)
Required Education	B.Pharm / M.Pharm / M.Sc / B.Sc / ITI
Experience	2–8 Years
Location	Ahmedabad, Gujarat
Interview Date	16th November 2025
Email	career@biomatrixhealthcare.com / hr@biomatrixhealthcare.com
Contact	63574 10551 / 63589 70525 / 97259 01031 / 92288 93058