Complaint Handling Specialist Job in Saraca Solutions
- Bose Informatics HR
- May 2
- 2 min read
Looking to advance your career in pharmacovigilance and complaint handling? A promising opportunity is now open for a Complaint Handling Specialist in Hyderabad with 2–6 years of experience in the pharma or medical devices industry. This role focuses on diabetes care product complaints, regulatory reporting, and patient safety—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.
📌 Job Overview
Role: Complaint Handling Specialist
Location: Hyderabad, India
Experience: 2–6 Years
Industry: Pharmaceutical / Medical Devices
Function: Complaint Handling, Pharmacovigilance, Regulatory Affairs
🔑 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
🎓 Qualifications & Skills
Bachelor’s or Master’s degree in Pharmacy, Biomedical, Biotechnology, or related field
2–6 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
💼 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
📩 How to Apply
Interested candidates can share their updated CV at:




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