Technical Writer
Location:
Littleton, MA
Hours:
- Monday – Friday 8 – 5
Position Duties:
- Strong experience in the clinical medical device regulatory field – Preferred
- Create, revise, and manage technical documentation including:
- User Manuals and Instructions for Use (IFUs)
- Installation and Service Manuals
- Technical Bulletins
- Training Materials
- Regulatory submissions and labeling documents
- Ensure all documents are developed in compliance with applicable regulatory requirements (FDA, EU MDR, NMPA, etc.) and internal quality systems.
- Collaborate with engineers, regulatory specialists, and product managers to extract technical information and translate it into clear, concise content.
- Organize content using structured authoring tools and templates.
- Conduct editorial and format reviews to ensure accuracy, consistency, and quality.
- Assist with document control and change management processes in accordance with Quality System Regulations.
Pay Rate:
- $60 – 65/ Hour Depending on Experience
…Pay Statement and Pay Transparency Laws: rate of pay listed is on a per hour basis. You will be entitled to health insurance once employed for 60 days and you must work 30 hours per week, on average, per month to enroll and maintain health insurance through Complete Staffing Solutions. Once both qualifiers are met you must complete the enrollment packet and your benefits will start on the first of the subsequent month. ..It is our policy to provide equal employment opportunity to all individuals regardless of race, color, sex, sexual orientation, religion, disability, age, veteran status, ancestry, national or ethnic origin or any other legally protected class. We are committed to a diverse workforce. We value all employees’ talents and support an environment that is inclusive and respectful. We are strongly committed to this policy, and believe in the concept and spirit of the law.#ZIP