Technical Specialist - Product Development

CameleonHR; Thomson (GA); On-site; USD 65,000 - 85,000; Full time

Job summary

A recruitment agency is seeking a Technical Specialist for a full-time role in the medical device industry. The ideal candidate will hold a Bachelor's degree and have 2+ years of experience in a regulated environment. Key responsibilities include executing product design and ensuring compliance with industry standards.

Qualifications

• 2+ years of experience in a regulated medical device environment (R&D, Quality, Compliance or Regulatory).
• Ability to support audits and remediation activities.

Responsibilities

• Execute product design and development activities for medical devices.
• Support design control execution.
• Ensure compliance with relevant regulations.

Skills

Regulated medical device experience

Ability to work in multi-stakeholder environment

Education

Bachelor's degree in engineering, science or related field

Job description

Technical Specialist - Product Development

4 days ago Be among the first 25 applicants

At Caméléon RH, we believe that the right match goes far beyond technical skills. Our mission is to connect talent with the right environment: where they can grow, contribute meaningfully, and have real impact.

About the Role

We are currently supporting Medicom, a global leader in the medical device industry, in the recruitment of a Technical Specialist. This role is 100% on-site. In this position, you will contribute directly to the development and improvement of medical device products, while ensuring robust execution of design control activities in a highly regulated environment.

Key Responsibilities

• Execute product design and development activities (medical device)
• Support both new product development and sustaining engineering initiatives
• Participate in design control execution: specifications, V&V, design reviews, labeling, risk management
• Support design transfer to manufacturing
• Ensure compliance with CMDR, FDA QSR, ISO 13485, CDC NIOSH and EU MDR requirements
• Support audits (FDA, notified bodies) and remediation activities if needed

What We’re Looking For

• Bachelor’s degree in engineering, science or related technical field
• 2+ years of experience in a regulated medical device environment (R&D, Quality, Compliance or Regulatory)
• Ability to work in a multi-stakeholder / contract manufacturing context

Assets

• Master’s degree or relevant technical certification
• Experience in continuous improvement or design transfer

If this role aligns with your background and you want to contribute to impactful products used in healthcare every day – we’d love to connect with you!

Seniority level

Entry level

Employment type

Full-time

Job function

Medical Equipment Manufacturing