Marksans Pharma Ltd Goa Recruitment 2026 – Quality Control Department Jobs for B.Sc & M.Sc Graduates

 

Marksans Pharma Ltd Goa Recruitment 2026 – Quality Control Department Hiring | Apply Now

Marksans Pharma Ltd., one of the leading pharmaceutical manufacturing companies in Goa, has announced recruitment for experienced professionals in its Quality Control (QC) Department. The company is inviting applications from eligible candidates with B.Sc. or M.Sc. qualifications and relevant experience in pharmaceutical quality control.

This recruitment offers an excellent opportunity for science graduates and postgraduates who wish to build or advance their careers in the pharmaceutical industry. Candidates having experience in analytical testing, chromatography, HPLC, GC, and regulatory compliance are encouraged to apply.

Interested candidates should carefully review the eligibility criteria, required experience, and responsibilities before submitting their resumes.

Company Name

Marksans Pharma Ltd.

Job Location

Verna, Goa

Department

Quality Control (QC)

The recruitment is specifically for the Quality Control Department, which plays a vital role in ensuring that pharmaceutical products meet the highest standards of quality, safety, and regulatory compliance.

Educational Qualification

Candidates must possess one of the following qualifications:

• Bachelor of Science (B.Sc.)
• Master of Science (M.Sc.)

The company is looking for science graduates and postgraduates with a strong analytical background.

Experience Required

Applicants should have 3 to 9 years of relevant experience in the regulated pharmaceutical industry.

The advertisement specifies experience in the following areas:

• HPLC (High Performance Liquid Chromatography)
• GC (Gas Chromatography)
• Chromatography techniques
• Analysis of Finished Products (FP)
• Stability Sample Testing

Candidates with hands-on laboratory experience and exposure to pharmaceutical analytical instruments will have an advantage.

About the Quality Control Department

The Quality Control Department is responsible for ensuring that raw materials, in-process materials, and finished pharmaceutical products meet all quality standards before reaching patients.

Professionals in Quality Control perform laboratory testing, analytical evaluations, documentation, and regulatory compliance activities to ensure product quality and safety.

The department plays a crucial role in maintaining Good Manufacturing Practices (GMP) and meeting national and international pharmaceutical regulations.

Key Responsibilities

According to the recruitment advertisement, selected candidates will be responsible for:

• Analysis of Raw Materials.
• Analysis of In-process Materials.
• Analysis of Finished Products.
• Operating HPLC and GC instruments.
• Performing Chromatography analysis.
• Stability Sample Analysis.
• Documentation of analytical results.
• Reviewing analytical data.
• Reviewing laboratory documentation.
• Ensuring compliance with cGMP.
• Following GLP guidelines.
• Maintaining Data Integrity.
• Investigating OOS (Out of Specification) results.
• Investigating OOT (Out of Trend) observations.
• Handling deviations and corrective actions.

These responsibilities require strong analytical skills, technical knowledge, and attention to detail.

Skills Preferred

Candidates applying for this position should ideally possess:

• Good analytical skills.
• Knowledge of pharmaceutical testing procedures.
• Experience handling HPLC and GC systems.
• Understanding of GMP and GLP guidelines.
• Knowledge of stability studies.
• Documentation skills.
• Problem-solving abilities.
• Good communication skills.
• Teamwork and coordination.
• Time management skills.

Why Join Marksans Pharma?

Marksans Pharma has highlighted several advantages of working with the organization.

Quality Focused Environment

Employees work in an environment committed to maintaining the highest pharmaceutical quality standards.

Career Growth

The company provides opportunities for learning, skill development, and professional growth within the pharmaceutical sector.

GMP Compliance

Employees gain valuable experience working under globally accepted Good Manufacturing Practices.

Collaborative Team Culture

The organization promotes teamwork and encourages collaboration among professionals from different departments.

Exposure to Modern Pharmaceutical Manufacturing

Working in the Quality Control Department allows professionals to gain experience with advanced analytical equipment and internationally accepted laboratory practices.

Career Scope in Quality Control

Quality Control remains one of the most sought-after career paths in the pharmaceutical industry. Professionals with laboratory experience in analytical chemistry and pharmaceutical testing are in demand across manufacturing companies, contract research organizations, formulation units, and regulatory laboratories.

Candidates experienced in HPLC, GC, chromatography, and stability studies can pursue long-term careers in:

• Quality Control Analyst
• Senior QC Analyst
• QC Executive
• QC Officer
• Senior Executive – Quality Control
• Laboratory Scientist
• Analytical Scientist

With continuous learning and industry experience, professionals can also progress to supervisory and managerial roles.

Documents to Keep Ready

Before applying, candidates should keep the following documents ready:

• Updated Resume.
• Passport-size Photograph.
• Educational Certificates.
• Degree Certificates.
• Mark Sheets.
• Experience Certificates.
• Identity Proof.
• Address Proof.
• Previous Employment Details (if applicable).

Ensure that the resume clearly highlights your analytical laboratory experience and technical expertise.

How to Apply

Interested candidates should share their resumes through email.

Email ID:

vaishnavi.naik@marksanspharma.com

Candidates should ensure that their resume is updated with their latest educational qualifications, work experience, technical skills, and contact information.

Contact Number

For further details regarding the recruitment, candidates may contact:

7447488738

Applicants are advised to communicate professionally if contacting the company regarding the vacancy.

Work Location

The selected candidates will be working at:

Marksans Pharma Ltd.
Verna, Goa

Verna Industrial Estate is one of Goa's major pharmaceutical and industrial hubs, providing excellent career opportunities for professionals in manufacturing and quality assurance.

Tips for Applicants

To improve your chances during the recruitment process:

• Update your resume before applying.
• Highlight your experience in HPLC and GC.
• Mention pharmaceutical analytical techniques you have worked with.
• Include GMP and GLP knowledge.
• List your stability study experience.
• Mention any exposure to OOS or OOT investigations.
• Clearly mention total years of experience.
• Keep all educational and experience certificates ready.

Selection Process

The advertisement does not specify the exact selection process. However, shortlisted candidates may be contacted by the company's Human Resources department for further stages of recruitment, which could include interviews, technical discussions, or other assessments as determined by the employer.

Recruitment Highlights

• Company: Marksans Pharma Ltd.
• Location: Verna, Goa
• Department: Quality Control
• Qualification: B.Sc. / M.Sc.
• Experience: 3–9 Years
• Industry: Pharmaceutical
• Skills Required: HPLC, GC, Chromatography, Stability Sample Testing, Finished Product Analysis
• Email for Resume: vaishnavi.naik@marksanspharma.com
• Contact Number: 7447488738

Final Words

Marksans Pharma Ltd., Verna, Goa is offering an excellent opportunity for experienced B.Sc. and M.Sc. graduates to join its Quality Control Department. Candidates with 3 to 9 years of experience in pharmaceutical quality control, including HPLC, GC, chromatography, stability testing, and regulatory compliance, should consider applying for this recruitment. Interested applicants should send their updated resumes to vaishnavi.naik@marksanspharma.com and ensure that their qualifications and experience match the company's requirements. This is a valuable opportunity to work with a reputed pharmaceutical company known for its commitment to quality, compliance, and employee development. 

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