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Medical Device Regulatory Affairs ( Central ) #HYT

$ 5,000 - $ 5,500 / month

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8-Month Contract Opportunity: Regulatory Affairs Specialist (Maternity Cover)

Location: Novena


Tentative Start Date: May/June 2025
Salary: $5,000/month

Key Responsibilities:

  • Review and approve documentation for product development and manufacturing processes.
  • Prepare and submit comprehensive documentation packages to regulatory agencies.
  • Track project timelines and milestones related to regulatory submissions.
  • Stay on top of evolving regulations and guidance, evaluating their impact on ongoing projects.
  • Oversee labeling and product documentation to meet regulatory requirements.
  • Assist with regulatory agency inspections and audits, ensuring compliance.
  • Maintain and manage detailed tracking databases for submission progress.
  • Act as the key liaison between internal teams (sales, marketing, clinical) and regulatory agencies.

Requirements:

  • 3-5 years of experience in medical device regulatory affairs
  • Strong understanding of regulations for medical devices across different markets
  • Ability to manage documentation, submissions, and compliance processes effectively

All qualified applicants, please click “ APPLY NOW”

Or you may send in your resume to:

Whatsapp: https://wa.me/+6597430026

Email : [email protected]

Kimmy Low Yi Ting (Kim) | CEI Registration Number: R23112122

Recruit Express Pte Ltd Company Reg. No. 199601303W | EA LICENCE Number: 99C4599

8-Month Contract Opportunity: Regulatory Affairs Specialist (Maternity Cover)

Location: Novena


Tentative Start Date: May/June 2025
Salary: $5,000/month

Key Responsibilities:

  • Review and approve documentation for product development and manufacturing processes.
  • Prepare and submit comprehensive documentation packages to regulatory agencies.
  • Track project timelines and milestones related to regulatory submissions.
  • Stay on top of evolving regulations and guidance, evaluating their impact on ongoing projects.
  • Oversee labeling and product documentation to meet regulatory requirements.
  • Assist with regulatory agency inspections and audits, ensuring compliance.
  • Maintain and manage detailed tracking databases for submission progress.
  • Act as the key liaison between internal teams (sales, marketing, clinical) and regulatory agencies.

Requirements:

  • 3-5 years of experience in medical device regulatory affairs
  • Strong understanding of regulations for medical devices across different markets
  • Ability to manage documentation, submissions, and compliance processes effectively

All qualified applicants, please click “ APPLY NOW”

Or you may send in your resume to:

Whatsapp: https://wa.me/+6597430026

Email : [email protected]

Kimmy Low Yi Ting (Kim) | CEI Registration Number: R23112122

Recruit Express Pte Ltd Company Reg. No. 199601303W | EA LICENCE Number: 99C4599