Technical Specialist - Product Development

Technical Specialist - Product Development

Technical Specialist - Product Development Thomson, Georgia Permanent

Do you think you have what it takes to work in an organization where creativity, ambition and initiative are valued, and where integrity drives everything we do?

Medicom has been in business for over 35 years and has retained its entrepreneurial spirit. By working with us, you will have the opportunity to get involved, make a real impact and contribute to the continued growth of the company. We live our values every day by focusing on customer satisfaction while promoting teamwork, accountability and empathy.

Our team thrives in fast-paced environments. You will benefit from flexibility to balance your work, personal life and well-being.

Medicom is looking for a Technical Specialist to join our team. This role is 100% on-site and focused on supporting product design and development activities for our medical device portfolio. You will play a key role in the successful execution of design control, technical development, and process improvement initiatives to bring new and enhanced products to market while ensuring compliance with global regulatory and quality standards.

• Execute product design and development tasks supporting Medicom’s United Medical Enterprise (UME) contract manufacturing operations and NAM Product Development objectives
• Support new product development and sustaining engineering projects from concept to commercialization
• Participate in design control activities: specification definition, verification & validation, design reviews, labeling development, and risk management
• Support design transfer and continuous improvement initiatives across manufacturing sites
• Ensure compliance with medical device standards and regulations including CMDR, FDA QSR, ISO 13485, CDC NIOSH, and EU MDR
• Support regulatory audits (FDA, notified bodies) and remediation projects related to design control documentation

• Bachelor’s degree in Engineering, Science, or related technical field
• Minimum of 2 years of experience in a regulated medical device environment (R&D, Quality, Compliance, or Regulatory)
• Strong understanding of design control and product development processes
• Ability to collaborate in a multi-site and contract manufacturing setting Assets
• Master’s degree or relevant professional certification
• Experience in continuous improvement, design transfer, or regulatory audits

• A mission-driven environment focused on improving safety and performance in the medical device industry
• The opportunity to collaborate with cross-functional teams across the globe
• Competitive compensation and growth opportunities within a global organization

Medicom is an equal opportunity employer. We consider all applicants without regard to age, gender, gender identity or expression, sexual orientation, race, ethnic or national origin, religious beliefs, sex (including pregnancy and breastfeeding), disability, or marital or family status. We welcome applications from all qualified individuals and encourage Indigenous persons, persons of color, LGBTQ+ and gender-nonconforming persons, persons with disabilities, women, and members of any other marginalized group.

Ready to take on this challenge? Apply today!