Marksans Pharma Ltd., a fast-growing global pharmaceutical company specializing in oral solid dosage (OSD) formulations, is seeking dedicated professionals for Quality Control (QC) and Quality Assurance (IPQA) roles at our USFDA-approved facility in Verna, Goa.
With a presence in over 20 countries and a focus on regulated markets like the US, UK, and Australia, Marksans is committed to quality and innovation. Join our team to contribute to high-quality pharmaceutical manufacturing in a dynamic, regulatory-compliant environment. Goan domicile candidates are preferred.
Job Details
- Location: Marksans Pharma Ltd., Plot No. L-82, L-83, Verna Industrial Estate, Verna, Goa – 403722
- Application Deadline: Open until filled (immediate joiners preferred)
- Contact: Email resumes to muskan.shaikh@marksanspharma.com or call +91 9607909656 for inquiries.
Open Positions
1. Quality Control (QC)
- Designation: Officer / Senior Officer / Executive
- Qualification: B.Sc / M.Sc (Chemistry, Analytical Chemistry)
- Experience: 3–7 years in QC for pharmaceutical manufacturing
- Vacancies: Multiple (exact number TBD)
Responsibilities:
- Perform analytical testing of raw materials, in-process samples, and finished products using HPLC, GC, UV Spectrophotometer, and KF Titrator.
- Conduct stability studies, method validation, and transfer activities.
- Ensure compliance with cGMP, GLP, and regulatory standards (USFDA, MHRA).
- Maintain accurate documentation and support regulatory audits.
Key Skills:
- Proficiency in QC instruments and analytical method validation.
- Strong knowledge of regulatory requirements and data integrity.
- Attention to detail and problem-solving skills.
2. Quality Assurance (IPQA)
- Designation: Officer / Senior Officer / Executive
- Qualification: B.Pharm / M.Pharm
- Experience: 2–7 years in IPQA for pharmaceutical manufacturing
- Vacancies: Multiple (exact number TBD)
Responsibilities:
- Conduct in-process quality checks and line clearance for OSD manufacturing and packing.
- Review Batch Manufacturing Records (BMR) and Batch Packing Records (BPR) for accuracy.
- Manage deviations, CAPA, and OOS investigations.
- Ensure adherence to cGMP, GDP, and regulatory standards during production.
- Support internal and regulatory audits (USFDA, MHRA).
Key Skills:
- Strong understanding of cGMP, GDP, and regulatory compliance.
- Excellent documentation and observational skills.
- Ability to coordinate with production and QC teams effectively.
Why Join Marksans Pharma?
- Global Reach: Contribute to a company with a strong presence in regulated markets, including 70%+ exports to the US, UK, and Australia, and a 25% CAGR.
- Regulatory Excellence: Work in a USFDA, MHRA, and TGA-approved facility, recognized for zero 483 observations in recent audits.
- Career Growth: Join a team of 1,500+ employees with opportunities for skill development, though AmbitionBox rates career growth at 3.5/5 due to moderate increments.
- Supportive Environment: Benefit from a 4.0/5 work-life balance rating (AmbitionBox) and a focus on employee-friendly policies, especially for Goan domicile candidates.
How to Apply
- Submission: Email your updated resume to muskan.shaikh@marksanspharma.com, mentioning the specific role (e.g., “QC Officer” or “IPQA Executive”) in the subject line. Include total experience, current CTC, expected CTC, and notice period.

Required Documents:
- Updated resume
- Educational certificates (B.Sc / M.Sc / B.Pharm / M.Pharm)
- Last 3 months’ payslips and increment letter (if applicable)
- Aadhar card and PAN card
- Passport-size photographs (2)
Note:
- Goan domicile candidates are preferred.
- Candidates must have experience in regulated plants (USFDA, MHRA).
- Those interviewed at Marksans in the last 6 months are ineligible.
About Marksans Pharma
Founded in 1992, Marksans Pharma Ltd. is a Mumbai-based global pharmaceutical company headquartered at Kirti Tower, Mumbai, with manufacturing facilities in Verna, Goa, and other locations. Specializing in OSD formulations, we cater to regulated markets with over 80% of revenue from exports.
Our Verna facility is a state-of-the-art, USFDA-approved plant producing tablets, capsules, and soft gels. Marksans is committed to quality, innovation, and employee well-being, making it a preferred employer in Goa. Learn more at www.marksanspharma.com.
Important Disclaimer
Marksans Pharma Ltd. does not charge any fees for recruitment or authorize agencies to collect payments. Report suspicious job offers or requests to muskan.shaikh@marksanspharma.com.
Join Marksans Pharma and contribute to quality healthcare in a globally recognized, employee-friendly organization!
I am interested on job
I am intrested in QA roles
Total experience 3 years