Marksans Pharma Ltd. Hiring 2026 announcement brings excellent opportunities for experienced professionals in Quality Control (QC) and Quality Assurance (IPQA).

Marksans Pharma Ltd. is actively recruiting Sr. Officer and Officer-level professionals for its USFDA-approved manufacturing facility in Goa, offering exposure to regulated markets and advanced analytical systems.

About Marksans Pharma Ltd.

Marksans Pharma Ltd. is a globally recognized pharmaceutical company specializing in:

• Oral Solid Dosage (OSD) formulations

• Generic medicines for regulated markets

• High-quality manufacturing and compliance

The company operates multiple facilities approved by:

• United States Food and Drug Administration

• Medicines and Healthcare products Regulatory Agency

• World Health Organization

Its facility in Verna is a state-of-the-art plant focused on delivering high-quality pharmaceutical products for global markets.

Job Details – Marksans Pharma Ltd. Hiring

Available Job Roles

Quality Control (QC) – Sr. Officer / Officer

• Experience: 5–9 Years

• Qualification: M.Sc / B.Sc

Key Skills:

• HPLC & GC operation

• Dissolution testing

• Stability studies

• Analytical method validation

• OOS/OOT investigations

Quality Assurance (IPQA) – Sr. Officer / Officer

• Experience: 1–7 Years

• Qualification: B.Pharm / M.Pharm

Key Skills:

• IPQA activities & line clearance

• Batch record review

• Validation protocols

• Deviation handling & CAPA

• Real-time process monitoring

Key Skills Required

Candidates applying for Marksans Pharma Ltd. Hiring should have:

• Hands-on experience in:

  • HPLC, GC, dissolution apparatus

  • Stability chambers and analytical software

• Strong knowledge of:

  • GMP & GLP compliance

  • ICH guidelines

  • Regulatory documentation

• Ability to:

  • Handle deviations and investigations

  • Ensure audit readiness

  • Work in cross-functional teams

Key Responsibilities

• Perform RM/IP/FP/stability testing using analytical instruments

• Conduct IPQA checks and line clearance

• Execute process and cleaning validation

• Investigate OOS/OOT and deviations

• Maintain documentation and ensure data integrity compliance

• Prepare stability protocols and reports

Why Join Marksans Pharma Ltd.?

Joining Marksans Pharma Ltd. offers:

• Work experience in a USFDA-approved facility

• Exposure to regulated international markets

• Hands-on learning in advanced QC and QA systems

• Strong career growth in quality functions

• Competitive salary and performance incentives

How to Apply

📧 Email Your CV: vaishnavi.naik@marksanspharma.com
📱 WhatsApp Resume: 7447488738

👉 Mention the position applied for in the subject line/message.

Industry Background – Growing Demand for QC & QA Professionals

India’s pharmaceutical sector is expanding rapidly, especially in:

• Generic drug manufacturing

• Regulated market exports (US, UK, EU)

• Quality-driven production systems

Locations like Goa are emerging as major centers for OSD manufacturing and quality operations, creating high demand for skilled QC and QA professionals.

Authoritative Sources

For pharmaceutical quality standards and regulatory compliance:

• United States Food and Drug Administration

• World Health Organization

• Central Drugs Standard Control Organization

• International Council for Harmonisation

FAQs – Marksans Pharma Ltd. Hiring 2026

What experience is required for QC roles?

Candidates need 5–9 years of experience with strong expertise in HPLC, GC, and stability studies.

Is regulatory experience required?

Experience in USFDA or regulated environments is highly preferred.

What is the job location?

The job is based in Verna, Goa.

How can I apply?

You can apply by emailing your resume or sending it via WhatsApp to the provided contact details.

What skills are important for QA roles?

Key skills include IPQA, validation, deviation handling, CAPA, and GMP compliance.