Senior Medical Writing Specialist - Orthopedic Implants

🏢 ABOUT THE COMPANY

Stryker is a world-leading medical technology company founded in 1941, headquartered in Kalamazoo, Michigan, USA, with a rich history of innovation and commitment to improving lives through medical technology. Our mission is to make healthcare better, with a strong focus on our core values: Quality, Integrity, Teamwork, Leadership, and Innovation. With over 32,000 employees worldwide and a global presence, Stryker is a great place to work for those who share our passion for making a difference. Our company has achieved numerous milestones and has been recognized as one of the best companies to work for in the world.

🎯 ROLE OVERVIEW

As a Senior Medical Writing Specialist, you will play a key role in developing high-quality, regulatory-compliant content for our orthopedic implants portfolio. You will work closely with cross-functional teams, including R&D, regulatory, and marketing, to create compelling medical content that meets the needs of our customers and stakeholders. Reporting to the Medical Writing Manager, you will have the opportunity to impact the development and commercialization of our innovative orthopedic implants.

📋 KEY RESPONSIBILITIES

Develop high-quality, user-friendly, and compliant medical content, including instruction manuals, product information sheets, and labeling for our orthopedic implants.

Create and maintain complex documentation, including clinical study reports, regulatory submissions, and post-marketing surveillance reports.

Collaborate with regulatory, R&D, and marketing teams to ensure alignment with company policies and regulatory requirements.

Conduct literature reviews, summarize clinical studies, and develop scientific content to support regulatory submissions and marketing materials.

Mentor and train junior medical writers to develop their skills and expertise.

Identify and implement process improvements to increase efficiency and quality in medical writing processes.

Ensure compliance with regulatory requirements, company policies, and industry standards.

Review and revise content for consistency, accuracy, and clarity.

Stay up-to-date with regulatory changes, industry developments, and scientific advancements to ensure that content remains current and relevant.

✅ REQUIRED QUALIFICATIONS

M.Sc. or Ph.D. in a life science discipline (e.g., biology, biochemistry, pharmacology, medicine).

A minimum of 5 years of experience in medical writing, preferably in the medical device industry.

Proven track record of successfully developing high-quality medical content for regulatory submissions and marketing materials.

Excellent writing and communication skills, with the ability to adapt to different audiences and styles.

Strong understanding of regulatory requirements, including FDA, EU, and ISO guidelines.

Ability to work independently and collaboratively as part of a cross-functional team.

⭐ PREFERRED QUALIFICATIONS

Experience with regulatory submissions, including 510(k) and PMA applications.

Familiarity with medical device software, such as MDS2 or Veeva.

Certification in medical writing, such as the American Medical Writers Association (AMWA).

B.A. or M.A. in a related field (e.g., English, communications, journalism).

💰 WHAT WE OFFER

We offer a competitive salary range of 60,000 - 80,000 EUR per year, depending on experience.

A comprehensive health insurance package, including medical, dental, and vision coverage.

A retirement plan with a company match.

Generous vacation days and flexible work arrangements.

A dedicated learning and development budget for professional growth and development.

The opportunity to work with a dynamic and talented team in a remote or hybrid setting.

A growth-oriented culture that values innovation, teamwork, and continuous improvement.

👥 ABOUT THE TEAM

Our medical writing team is a collaborative and supportive group of professionals who share a passion for creating high-quality content. We work closely with cross-functional teams to ensure that our content meets the needs of our customers and stakeholders. Recent wins include the successful launch of several new orthopedic implants and the development of a comprehensive product portfolio for our joint reconstruction business.

📨 HOW TO APPLY

If you are a motivated and detail-oriented medical writer with a passion for creating high-quality content, please submit your application, including your resume and a cover letter, to [insert contact information]. We look forward to hearing from you.

📋 Job Details

Job Type	🌐 Remote
Location	Remote, DE
Salary	EUR 60,000 – 80,000 / year
Industry	General
Company	Stryker
Valid Until	2026-09-13

📨 How to Apply

Submit your updated CV and a brief cover letter to Stryker. Applications are reviewed on a rolling basis. Only shortlisted candidates will be contacted within 2 weeks of applying.