Important Informartion:

Location: JnJ Groningen, Fully remote job.

Language: English is a must, Dutch a nice to have

Working hours: 32 hours or 40 hours possible

Contract: the first contract for 6 months, probably extended for another 6 months but not guaranteed yet, depends on business need and performance.

No perspective for a perm contract as project-related

Focus on: document writing for products in medical devices (e.g. intraocular lenses,…)

Key Responsibilities:

• Plan, write, and review technical documentation under Design Control.
• Conduct technical reviews to ensure document accuracy and compliance to local procedures, Johnson & Johnson guidelines, and regulatory requirements.
• Partner with cross-functional team members to define the impact of regulatory requirements and industry trends/practices.
• Manage daily activities to ensure timelines are met.

Experience and Skills:

• Related job experience with an advanced degree is required.
• Experience within the medical device industry and knowledge of MDR regulatory requirements is preferred.
• Strong verbal and written communication skills and interpersonal relationships are required.
• Demonstrated knowledge and experience in quality regulatory compliance, adverse event reporting, medical device risk management processes, and common statistical methods are preferred.
• Regulatory/Notified Body audit experience is preferred

Qualifications

Experience:

4-6 years of experience as a technical writer in the field of medical devices

Education:

BA, BS, or BSN is required in areas of Engineering, Biomedical Engineering, or other life science discipline. An advanced degree is preferred.