PHARMA BHARAT
PHARMACEUTICAL JOB PORTAL
No new notifications

Advertisement

Marksans Pharma is Hiring for QC Investigation Coordinator

Published on

Advertisement

Marksans Pharma Ltd., a well-established pharmaceutical company, is inviting applications from experienced professionals for its Quality Control (QC) department at Verna, Goa. This opportunity is ideal for candidates who have strong expertise in investigation handling, compliance, and documentation within regulated environments.

If you are looking to advance your career in pharmaceutical quality control with a reputed organization, this role offers excellent growth and exposure.

Job Overview

Company Name

Marksans Pharma Ltd.

Job Location

Verna, Goa, India

Department

Quality Control (QC)

Role

Investigation Coordinator

Experience Required

6 to 9 Years


Key Responsibilities

As an Investigation Coordinator in QC, the selected candidate will be responsible for:

  • Handling OOS (Out of Specification) and OOT (Out of Trend) investigations
  • Managing incident and deviation investigations effectively
  • Preparing and reviewing change control documentation
  • Writing detailed investigation reports and CAPA (Corrective and Preventive Action) reports
  • Ensuring compliance with regulatory guidelines and internal SOPs
  • Coordinating with cross-functional teams for timely closure of investigations
  • Maintaining proper documentation and audit readiness

Required Qualifications & Skills

  • B.Pharm, M.Pharm, or M.Sc. in a relevant discipline
  • 6โ€“9 years of experience in Quality Control within the pharmaceutical industry
  • Strong knowledge of OOS, OOT, deviations, and incident management
  • Excellent documentation and technical writing skills
  • Hands-on experience in investigation and CAPA report writing
  • Good understanding of regulatory requirements (USFDA, MHRA, etc.)

Salary & Benefits

  • Estimated Salary: โ‚น6,00,000 โ€“ โ‚น10,00,000 per annum (based on experience)
  • Opportunity to work in a reputed pharmaceutical company
  • Exposure to regulatory compliance and global standards
  • Career growth and skill development opportunities
  • Professional and collaborative work environment

How to Apply

Interested candidates can apply by sharing their updated CV using the details below:

Make sure your resume highlights your experience in QC investigations, OOS/OOT handling, and CAPA documentation.

Advertisement

Share This Job

โœ… Job Details Copied!
Ad Popup