Marksans Pharma Hiring QC Investigation Coordinator in Goa – Apply Now | ₹10 LPA Pharma Job 2026
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(Marksans Pharma Hiring QC Investigation Coordinator in Goa) |
Introduction
If you are an experienced pharmaceutical professional looking to grow in Quality Control (QC) investigations, then this opportunity at Marksans Pharma Ltd. can be a game-changer for your career. With increasing demand for regulatory compliance and quality assurance in pharma manufacturing, companies are actively hiring skilled professionals who can handle investigations, documentation, and compliance effectively.
This job role is ideal for candidates with hands-on experience in OOS, OOT, deviation handling, and CAPA documentation. If you want to work in a regulated environment and build a long-term career in pharmaceutical quality systems, this role is highly relevant.
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About The Company
Marksans Pharma Ltd. is a globally recognized pharmaceutical company known for manufacturing high-quality generic formulations. The company has a strong presence in regulated markets such as the US, UK, and Europe.
Headquarters: Mumbai, India
Founded: 1992
Employees: 2000+ (approx.)
Global Presence: USA, UK, Australia, and other regulated markets
Marksans Pharma focuses on quality, compliance, and innovation, making it one of the preferred employers in the pharmaceutical manufacturing sector. Working here provides exposure to global regulatory standards like the USFDA and MHRA.
Job Overview Summary
Marksans Pharma is hiring for the position of Investigation Coordinator in the Quality Control department at its Goa facility. This role focuses on managing investigations related to OOS, OOT, deviations, and ensuring compliance with regulatory standards.
Candidates will work closely with cross-functional teams and play a crucial role in maintaining product quality and audit readiness. This is a mid-level role suitable for professionals with 6–9 years of pharma QC experience.
Vacancy Details (Official)
- Company: Marksans Pharma Ltd.
- Department: Quality Control (QC)
- Role: Investigation Coordinator
- Location: Verna, Goa, India
- Experience: 6–9 Years
- Employment Type: Full-Time
Responsibility Explanation (Simplified)
In this role, you will be responsible for handling critical quality investigations that directly impact product safety and compliance. Your main job will be to identify issues, analyze root causes, and implement corrective actions.
You will manage OOS (Out of Specification) and OOT (Out of Trend) cases, ensuring proper documentation and timely closure. Writing detailed investigation reports and CAPA (Corrective and Preventive Action) plans will be a key part of your daily work.
Additionally, you will coordinate with production, QA, and regulatory teams to resolve deviations and maintain compliance with global standards. This role requires strong analytical thinking, documentation skills, and attention to detail.
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Eligibility (Official)
- Qualification:
B.Pharm / M.Pharm / M.Sc (Relevant Discipline) - Experience:
6–9 years in Quality Control (Pharma Industry) - Domain Knowledge:
OOS, OOT, Deviations, CAPA, Regulatory Compliance
Skills Required (Own Words)
To succeed in this role, candidates must have a strong understanding of pharmaceutical quality systems and investigation processes.
Key skills include:
- Strong analytical and problem-solving ability
- Excellent technical writing and documentation skills
- Deep understanding of GMP and regulatory compliance
- Ability to handle audits and inspections
- Good communication and coordination skills
- Knowledge of USFDA, MHRA, and global guidelines
Salary Estimate (Unique)
Based on current industry standards for QC investigation roles in India, the estimated salary for this position is:
₹6 LPA – ₹10 LPA
Candidates with strong investigation experience and regulatory exposure may negotiate higher packages. Additional benefits include job stability, growth opportunities, and exposure to international audits.
Interview Details (Official)
- Mode: Shortlisting + Interview (HR + Technical)
- Rounds:
- Resume Screening
- Technical Interview (QC + Investigation)
- HR Discussion
Shortlisted candidates will be contacted directly by the company.
Required Documents (Own Words)
Before applying, make sure you have the following documents ready:
- Updated Resume (CV)
- Educational Certificates
- Experience Letters
- Salary Slips (last 3 months)
- ID Proof (Aadhar/PAN)
- Passport-size Photograph
Make sure your resume highlights your experience in OOS/OOT investigations and CAPA documentation.
How to Apply
Interested candidates can apply using the details below:
👉 Tip: Mention “QC Investigation Coordinator Application” in the subject line.
FAQs Section
1. What is the role of an Investigation Coordinator in pharma?
An Investigation Coordinator handles OOS, OOT, and deviation investigations, ensuring proper documentation and compliance with regulatory standards.
2. Is this job suitable for freshers?
No, this role requires 6–9 years of experience in Quality Control within the pharmaceutical industry.
3. What is OOS and OOT in pharma?
OOS (Out of Specification) and OOT (Out of Trend) are investigation processes used to identify quality issues in pharmaceutical products.
4. What is the salary for QC roles in pharma?
QC professionals with 6–9 years of experience can earn between ₹6 LPA and ₹10 LPA, depending on skills and company.
5. Is Marksans Pharma a good company to work for?
Yes, Marksans Pharma is a reputed company with global presence and strong regulatory compliance standards.
Final Conclusion
This job opportunity at Marksans Pharma is ideal for experienced QC professionals who want to specialize in investigation handling and regulatory compliance. With strong exposure to global standards, documentation practices, and cross-functional collaboration, this role can significantly boost your career in the pharmaceutical industry.
If you have the required experience and skills, don’t miss this opportunity. Apply as soon as possible and take the next step in your pharma career.
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Disclaimer
Note: Pharma Duniya does not charge any money for job information. Candidates are advised to verify details from the official company website.
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