Pharma QC & QA Jobs – Marksans Pharma Ltd., a globally recognized pharmaceutical company, is actively hiring Quality Control (QC) and Quality Assurance (IPQA) professionals for its USFDA-approved facility in Verna, Goa.
This is an excellent opportunity for experienced candidates skilled in HPLC, GC, stability, dissolution, IPQA, validation, and investigation coordination to join a quality-focused organization with strong growth in regulated markets.
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About the Company
Marksans Pharma Ltd. is a leading global pharmaceutical company specializing in oral solid dosage formulations, with a strong presence in regulated markets including the US, UK, and Europe. The company operates multiple USFDA, MHRA, and WHO-GMP approved manufacturing facilities, including its state-of-the-art plant in Verna, Goa.
Marksans is known for its commitment to quality excellence, regulatory compliance, continuous improvement, and innovation in generic medicines. With a focus on patient-centric healthcare and sustainable growth, the company provides a professional, progressive environment for talent in quality control, assurance, and manufacturing.
Job Details
- Company Name: Marksans Pharma Ltd.
- Experience: QC: 5–9 Years | QA (IPQA): 1–7 Years
- Qualification: M.Sc / B.Sc (QC) | B.Pharm / M.Pharm (QA)
- Location: Verna, Goa
- Work Type: On-site
Job Description
Marksans Pharma Ltd. is strengthening its quality functions at the Verna facility to support high-volume OSD production under stringent regulatory standards. These roles are critical for ensuring product quality, compliance, and continuous process improvement in a fast-paced, USFDA-compliant environment.
Sr. Officer / Officer – Quality Control (QC)
- Department: Quality Control
- Market: Pharmaceuticals – OSD Formulations
- Role: Sr. Officer / Officer – QC
- Experience: 5–9 Years
- Education/Qualification: M.Sc / B.Sc
Sr. Officer / Officer – Quality Assurance (IPQA)
- Department: Quality Assurance
- Market: Pharmaceuticals – OSD Formulations
- Role: Sr. Officer / Officer – IPQA
- Experience: 1–7 Years
- Education/Qualification: B.Pharm / M.Pharm
Skills/Qualifications
- Hands-on proficiency with HPLC, GC, dissolution apparatus, stability chambers, and instrument software
- Strong experience in analytical method validation, stability studies, and OOS/OOT investigation coordination
- Expertise in in-process QA (IPQA), line clearance, validation protocols, and real-time monitoring
- Knowledge of GMP, GLP, ICH guidelines, and regulatory compliance
- Excellent documentation, problem-solving, and teamwork skills
Key Responsibilities
- Perform RM/IP/FP/stability sample analysis using HPLC, GC, dissolution
- Calibrate and maintain QC instruments; handle software and data integrity
- Conduct in-process QA checks, line clearance, and batch record review
- Execute validation protocols and support process/cleaning validation
- Investigate deviations, OOS/OOT results, and implement CAPA
- Prepare stability protocols, reports, and ensure audit readiness
Benefits/Perks
- Career growth in a USFDA/MHRA-approved global pharma company
- Exposure to advanced analytical and quality systems
- Opportunities for skill enhancement and professional development
- Competitive salary and performance-based rewards
- Positive work culture focused on quality, compliance, and teamwork
How to Apply
Send your updated CV highlighting relevant HPLC/GC/stability/IPQA/validation experience to vaishnavi.naik@marksanspharma.com. You can also WhatsApp your resume to 7447488738. Mention the position applied for in the subject line or message.
For more pharma jobs, QC/QA openings, Goa pharma careers, and updates, visit Pharma Recruiter.
Apply now and become part of Marksans Pharma’s commitment to quality and excellence!
Why You Should Join
Marksans Pharma Ltd. offers a stable, high-compliance environment in a globally respected organization with strong regulatory credentials.
Employees benefit from exposure to advanced OSD manufacturing, continuous learning in analytical techniques and validation, career progression in quality functions, and the opportunity to contribute to affordable, high-quality medicines in regulated markets.
Joining Marksans means working in a supportive, growth-driven culture focused on excellence and patient well-being.
FAQs
What experience is required for the QC Officer/Sr. Officer role?
5–9 years with strong hands-on experience in HPLC, GC, dissolution, stability, and investigation coordination.
Is USFDA or regulated market experience mandatory?
While not explicitly stated, it is highly preferred given the USFDA-approved facility and nature of the roles.
Where is the job location?
Verna, Goa – Marksans Pharma’s USFDA-approved OSD formulation facility.
How do I apply for these QA/QC positions?
Email your CV to vaishnavi.naik@marksanspharma.com or WhatsApp to 7447488738 with your updated resume and relevant experience details.
