MEDICAL WRITER

Are you passionate about making a difference in the medical device industry? Join our dynamic team at CONMED as a Medical Writer! In this pivotal role, you’ll leverage your expertise in global regulations to proactively collect and analyze market and customer feedback on our medical devices. Your work will ensure compliance with Medical Device Regulation (EU 2017/745) and other global standards, driving innovation and excellence in healthcare.

QUALIFICATIONS:

• Bachelor’s degree in clinical research, health sciences, or a related field. Alternatively, 5+ years of experience with medical devices in an Operating Room setting as a CST, CSFA, or RN.
• 0-2 years of experience in the medical device and/or pharmaceutical industry.

PREFERRED SKILLS:

• Experience with medical device complaint investigation, CAPAs, Recalls, or Post Market Surveillance.
• Proficiency in creating PMS plans, PMSRs, or PSURs.
• Strong knowledge of risk management, product design practices, and Good Manufacturing Practices (GMP).
• Understanding of medical device regulations and adverse event reporting.
  Disclosure as required by applicable law, the annual salary range for this position is $62,000 to $97,000. The actual compensation may vary based on geographic location, work experience, education, and skill level. The salary range is CONMED’s good faith belief at the time of this posting.
  This job posting is anticipated to close on August 15, 2025. We may, however, extend this time period, in which case the posting will remain available on careers.conmed.com. Please submit your application as soon as possible as we will be reviewing applications on a rolling basis as we receive them.

KEY RESPONSIBILITIES:

• Develop and refine strategies and processes for market and customer feedback collection.
• Assist in creating medical device market research protocols and Case Report Forms.
• Craft and update post-market surveillance plans, Periodic Safety Update Reports, and Post Market Surveillance reports.
• Collaborate with cross-functional teams and surgeons for Post Market Clinical Follow-up studies.
• Keep relevant procedures up-to-date.

WHAT YOU’LL DO:

• Utilize your knowledge of medical devices and In-Vitro Diagnostic products to gather proactive customer feedback per Medical Device Regulation (EU 2017/745) and In-Vitro Diagnostic Medical Device Regulation (EU 2017/746)
• Create market research protocols, deploy questionnaires, and compile technical reports.
• Review and provide feedback on (Periodic Safety Update Reports) and PMSRs (Post-Market Surveillance Reports)
• Author and update post-market surveillance plans for upcoming and existing medical devices.
• Interface with engineering, medical, safety, regulatory, quality, and manufacturing teams to complete surveillance activities.
• Ensure timely creation of deliverables to prevent project delays.
• Develop proactive customer feedback templates and process workflows.
• Communicate roadblocks and escalate issues promptly to stakeholders.