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Complaint Handling Specialist Job in Saraca Solutions

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Looking to advance your career in pharmacovigilance and complaint handling? A promising opportunity is now open for a Complaint Handling Specialist in Hyderabad with 2โ€“6 years of experience in the pharma or medical devices industry. This role focuses on diabetes care product complaints, regulatory reporting, and patient safetyโ€”making it ideal for professionals aiming to strengthen their expertise in MDR/ADE reporting and compliance.

If you have a background in Pharmacy, Biomedical, Biotechnology, or Pharma sciences, this could be your next career move in a high-impact safety and quality domain.

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๐Ÿ“Œ Job Overview

  • Role: Complaint Handling Specialist
  • Location: Hyderabad, India
  • Experience: 2โ€“6 Years
  • Industry: Pharmaceutical / Medical Devices
  • Function: Complaint Handling, Pharmacovigilance, Regulatory Affairs

๐Ÿ”‘ Key Responsibilities

  • Manage and evaluate product complaints related to diabetes care devices
  • Perform MDR (Medical Device Reporting) and ADE (Adverse Drug Event) reporting
  • Ensure compliance with global regulatory guidelines (FDA, EU MDR, etc.)
  • Conduct root cause analysis (RCA) and recommend corrective actions
  • Maintain accurate documentation for audits and inspections
  • Collaborate with cross-functional teams for quality and safety improvements
  • Support patient safety initiatives and risk management processes

๐ŸŽ“ Qualifications & Skills

  • Bachelorโ€™s or Masterโ€™s degree in Pharmacy, Biomedical, Biotechnology, or related field
  • 2โ€“6 years of experience in complaint handling (pharma or medical devices)
  • Strong understanding of regulatory compliance and vigilance reporting
  • Analytical mindset with excellent problem-solving skills
  • Good communication and documentation capabilities
  • Familiarity with quality systems and pharmacovigilance processes

๐Ÿ’ผ Benefits & Career Scope

  • Opportunity to work in high-impact patient safety roles
  • Exposure to global regulatory frameworks (MDR, ADE reporting)
  • Career growth in pharmacovigilance, quality assurance, and regulatory affairs
  • Dynamic and collaborative work environment
  • Competitive salary and industry-standard benefits

๐Ÿ“ฉ How to Apply

Interested candidates can share their updated CV at:
๐Ÿ“ง rahul@saracasolutions.com

Make sure your resume highlights your complaint handling experience, regulatory exposure, and safety reporting expertise to improve your chances of selection.

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