RAQA Technical Writer
Portage, MI, US
Scientific
Bachelors Degree
Full Time, Temporary
Experienced (Non-Manager)
On-site
Biotechnology/Pharmaceuticals
First Shift (Day)
Portage, MI, US
Experienced (Non-Manager)
Full Time, Temporary
Biotechnology/Pharmaceuticals
On-site
Scientific
Bachelors Degree
First Shift (Day)
Job details
RAQA Technical Writer
- Location: Portage, Michigan – 100% ONSITE ROLE
- Type: W2 contract (NO C2C OR THIRD PARTY)
- Duration: Estimated to end – 9/16/26
- Pay Rate – Negotiable depending on DIRECT-related experience
- Work Authorization: Must have CURRENT United States employment authorization documents and be physically located in United States when applying for this role WITHOUT current sponsorship transfer requirements.
Position Summary
The RAQA Technical Writer will be responsible for developing, standardizing, and maintaining clear and accurate documentation including operating procedures, work instructions, and forms. This role ensures that all documentation complies with internal standards, regulatory requirements, and best practices for clarity, consistency, and usability. The Technical Writer will collaborate closely with subject matter experts (SMEs), process owners, and cross-functional teams to capture complex processes and translate them into user-friendly documentation.
Key Responsibilities
- Develop, write, edit, and maintain operating procedures, work instructions, and forms in alignment with company policies, industry standards, and regulatory requirements.
- Partner with subject matter experts (SMEs) and process owners to gather information and ensure accuracy of technical content.
- Standardize documentation format and ensure consistency across departments.
- Review, update, and manage document revisions to reflect process improvements or regulatory changes.
- Ensure documentation complies with applicable quality management system (QMS) requirements (e.g., ISO 9001, ISO 13485, FDA, or other relevant standards).
- Create documentation that is clear, concise, and easily understood by intended users, including technical and non-technical audiences.
- Support audits and inspections by providing controlled, accurate documentation.
- Collaborate with training teams to align documentation with employee training and onboarding programs.
- Maintain document control within approved systems and ensure proper version management.
- Develop process flows that clearly illustrate the end-to-end solution.
Qualifications
- Bachelor’s degree in Engineering, Technical Communication, English, Engineering, Life Sciences, or a related field, or equivalent experience.
- 3+ years of experience in technical writing, preferably within regulated industries (e.g., medical devices, pharmaceuticals, manufacturing).
- Strong knowledge of operating procedures, work instructions, and controlled forms.
- Familiarity with Quality Management Systems (ISO 9001, ISO 13485) and regulatory requirements preferred.
- Excellent written and verbal communication skills with a strong attention to detail.
- Ability to translate complex technical concepts into clear, concise documentation.
- Proficiency in Microsoft Office Suite and document management systems (e.g., SharePoint, MasterControl, or similar).
- Strong organizational and project management skills, with the ability to manage multiple priorities.
Work Authorization: Must have CURRENT United States employment authorization documents and be physically located in United States when applying for this role without current sponsorship requirements.
Important information: To be immediately considered, please send an updated version of your resume to Deas172@kellyservices.com.
***(Kelly Services does not expense relocation or interview costs)***
In addition to working with the world’s most recognized and trusted name in staffing, Kelly employees can expect:
Competitive pay
Paid holidays
Year-end bonus program
Recognition and incentive programs
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