India's DMPLOI - Jobs & Networking AppMarksans Pharma Ltd., a globally recognized pharmaceutical company, has announced an exciting recruitment opportunity for experienced professionals in the Quality Control (QC) department at its Verna, Goa manufacturing facility. Candidates with strong analytical laboratory experience in HPLC, GC, Chromatography, and Finished Product testing are encouraged to apply.
If you are looking to build your career in a regulated pharmaceutical environment with exposure to cGMP, GLP, and international quality standards, this is an excellent opportunity.
Job Overview
Particular Details
Company Name
Marksans Pharma Ltd.
Job Location
Verna, Goa
Department
Quality Control (QC)
Qualification
B.Sc., M.Sc.
Experience
3–9 Years
Industry
Pharmaceutical Manufacturing
Employment Type
Full Time
Eligibility Criteria
Candidates should possess:
B.Sc. or M.Sc. in a relevant science discipline.
3–9 years of experience in a regulated pharmaceutical company.
Strong analytical and documentation skills.
Knowledge of cGMP, GLP, and Data Integrity requirements.
Required Technical Skills
Applicants should have practical experience in:
High Performance Liquid Chromatography (HPLC)
Gas Chromatography (GC)
Chromatography techniques
Analysis of Finished Products (FP)
Stability Sample Testing
Laboratory Documentation
Analytical Data Review
Key Responsibilities
The selected candidates will be responsible for:
Analysis of raw materials, in-process samples, and finished products.
Performing HPLC and GC analysis according to approved methods.
Conducting stability sample testing and maintaining records.
Reviewing analytical data and laboratory documentation.
Ensuring compliance with cGMP, GLP, SOPs, and Data Integrity guidelines.
Investigating OOS (Out of Specification), OOT (Out of Trend), and deviations.
Maintaining laboratory instruments and following calibration procedures.
Supporting internal and external regulatory audits.
Why Join Marksans Pharma?
Opportunity to work with global quality standards.
Career growth and learning opportunities.
Professional and collaborative work environment.
Strong focus on quality and compliance.
Exposure to regulated pharmaceutical manufacturing.
How to Apply
Interested and eligible candidates can share their updated resume through the official recruitment contact.
Email: vaishnavi.naik@marksanspharma.com
Contact Number: 7447488738
Work Location: Marksans Pharma Ltd., Verna, Goa
Technical FAQs
1. What analytical instruments should candidates be familiar with?
Candidates should have hands-on experience with HPLC, Gas Chromatography (GC), and other chromatography techniques used for pharmaceutical quality control analysis.
2. What is the role of Stability Sample Testing in Quality Control?
Stability testing evaluates whether pharmaceutical products maintain their identity, strength, quality, and purity throughout their shelf life under defined storage conditions.
3. What do OOS and OOT mean in pharmaceutical Quality Control?
OOS (Out of Specification): Test results that fall outside predefined acceptance criteria.
OOT (Out of Trend): Results that deviate from the normal historical trend and require investigation.
4. Why are cGMP, GLP, and Data Integrity important?
These quality systems ensure pharmaceutical products are consistently manufactured, tested, documented, and controlled according to regulatory requirements while maintaining reliable and traceable laboratory data.
5. What documentation is expected from a QC Analyst?
QC professionals should maintain:
Analytical worksheets
Instrument logbooks
Calibration records
Stability records
Raw data
Test reports
SOP compliance documentation
Investigation reports for OOS/OOT cases
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