Marksans Pharma Ltd, Goa, a reputed pharmaceutical company known for its WHO-GMP compliant manufacturing facilities, is inviting applications for Operators and Officers in the Liquid Manufacturing Department. This is an excellent opportunity for candidates looking to build a career in pharmaceutical manufacturing and production operations.
About Marksans Pharma Ltd
Marksans Pharma Ltd is a globally recognized pharmaceutical company engaged in the manufacturing and marketing of high-quality pharmaceutical formulations. The company follows strict GMP guidelines and offers a professional work environment with excellent growth opportunities.
Job Details
Particulars Details
Company Name
Marksans Pharma Ltd
Location
Goa
Department
Liquid Manufacturing
Position
Operators / Officers
Experience
1–9 Years
Qualification
ITI, D.Pharm, B.Pharm, B.Sc, M.Sc
Industry
Pharmaceutical Manufacturing
Facility
WHO-GMP Compliant
Key Responsibilities
Operator
Operation of liquid manufacturing equipment.
Batch preparation and processing as per BMR.
Equipment cleaning and line clearance activities.
Monitoring manufacturing parameters.
Maintaining GMP documentation.
Officer
Supervision of manufacturing activities.
Batch record review and compliance monitoring.
Process validation and troubleshooting.
Coordination with QA, QC, and Engineering departments.
Ensuring regulatory compliance and production targets.
Required Skills
Knowledge of GMP, cGMP, and SOP compliance.
Understanding of liquid manufacturing processes.
Experience in syrup, suspension, and oral liquid production.
Documentation and batch record handling.
Equipment operation and troubleshooting skills.
Good communication and teamwork abilities.
Why Join Marksans Pharma?
WHO-GMP compliant manufacturing facility.
Career growth opportunities.
Professional working environment.
Learning and development support.
Exposure to advanced pharmaceutical manufacturing technologies.
How to Apply
Interested candidates can send their updated CV to:
📧 vaishnavi.naik@marksanspharma.com
📞 Contact: 7447488738
Technical FAQs
1. What is Liquid Manufacturing in the pharmaceutical industry?
Liquid manufacturing involves the production of pharmaceutical syrups, suspensions, oral solutions, and liquid formulations using controlled mixing, filtration, and filling processes while maintaining GMP compliance.
2. What GMP documents are commonly used in liquid manufacturing?
Common documents include Batch Manufacturing Records (BMR), Standard Operating Procedures (SOPs), Equipment Log Books, Cleaning Records, and Line Clearance Checklists.
3. Why is line clearance important before manufacturing?
Line clearance ensures that the production area is free from previous product materials, labels, and documents, preventing mix-ups and cross-contamination.
4. What qualifications are suitable for a Liquid Manufacturing role?
Candidates with ITI, D.Pharm, B.Pharm, B.Sc, or M.Sc qualifications and relevant pharmaceutical manufacturing experience are generally preferred.
5. What are the critical process parameters in liquid manufacturing?
Important parameters include mixing speed, temperature, pH, viscosity, filtration efficiency, batch yield, and cleaning validation to ensure product quality and consistency.
Conclusion
Marksans Pharma Ltd Goa is offering a promising opportunity for experienced pharmaceutical professionals in the Liquid Manufacturing Department. Candidates with 1–9 years of experience and qualifications such as ITI, D.Pharm, B.Pharm, B.Sc, or M.Sc are encouraged to apply and become part of a growing pharmaceutical organization committed to quality, compliance, and excellence.

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