PMS Analyst-Medical Devices/Complaint Handling

HCLTech

Madurai

In loco

INR 600.000 - 1.000.000

Tempo pieno

14 giorni+

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Descrizione del lavoro

A global technology company is seeking a PMS Analyst in Madurai, Tamil Nadu. The role involves managing medical device complaints and requires 2 to 7 years of relevant experience. Candidates should possess working knowledge of medical device regulations and the ability to work efficiently in a team-driven environment. The position offers full-time employment with immediate joiners preferred.

Competenze

  • 2 to 7 years of experience in medical devices complaints handling or PMS activities.
  • Working knowledge of global medical device regulations like CFR Parts 803, 806 and 820, ISO 13485, ISO 14971.
  • Ability to adapt to cross cultural differences.

Mansioni

  • Handle medical devices complaints management process.
  • Organize and manage daily work allocation.
  • Collaborate with cross-functional teams for project execution.

Conoscenze

Medical devices complaints handling
Knowledge of medical device regulations
Ability to work in a timeline driven environment

Descrizione del lavoro

Overview

Job Position: PMS Analyst – Medical Devices Complaints Handling

Job Description: To handle medical device customer allegations in complaints management system . Candidate with knowledge on Medical devices usage, Medical devices reporting including post-market surveillance (PMS)

Responsibilities
  • To work on medical devices Complaints handling Process.
  • Work with lead in completing daily assignation
  • Organize and manage daily work allocation
  • Complaints remediation using work instruction, compliance to process
  • To drive efficiency and continuous improvement.
  • Collaborate with of cross function team (CFT) such as Intake, MDR, Investigation to execute the project and initiative.
  • Daily status to lead associate
Qualifications
  • 2 to 7 years of experience in Medical devices complaints handling or any PMS activities
  • Working knowledge of appropriate global medical device regulations, requirements, and standards such as: CFR Parts 803, 806 and 820, ISO 13485, ISO 14971
  • Adopt to cross cultural differences
  • Ability to work in a timeline driven environment
Experience
  • Total working experience (TEX): 2 to 7 years
  • Relevant experience (REX): 2+ years
Employment details
  • Employment type: Full-time
  • Job function: Information Technology
  • Industries: IT Services and IT Consulting
Location

Madurai, Tamil Nadu, India

Additional info

Immediate joiners will be given preference

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