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Technical Documentation Specialist
St Louis, MO, US
Engineering
High School or equivalent
Full Time, Temporary
Experienced (Non-Manager)
On-site
Medical Devices and Supplies
First Shift (Day)
St Louis, MO, US
Experienced (Non-Manager)
Full Time, Temporary
Medical Devices and Supplies
On-site
Engineering
High School or equivalent
First Shift (Day)
Job details
Manufacturing (Contract)
Join a Leader in Infection Prevention and Make Your Mark on Quality!
Are you a skilled technical writing professional with a passion for clarity and compliance? We’re seeking a meticulous and experienced Technical Documentation Specialist to join our team in St. Louis! This 3+ month contract role offers the opportunity to contribute to the manufacturing of critical infection prevention cleaning chemistries in a dynamic pharmaceutical environment.
What You’ll Do:
- Develop, edit, and maintain essential technical documents, including Standard Operating Procedures (SOPs), batch records, and validation reports.
- Collaborate with subject matter experts (SMEs) across departments to gather information and ensure accuracy.
- Ensure all documentation adheres to stringent ISO, FDA, cGMP, and other relevant regulatory requirements.
- Utilize Electronic Document Management Systems (EDMS) such as PLM (Product Lifecycle Management) and QMS (Quality Management System) for effective document control.
- Conduct thorough document reviews to guarantee accuracy, clarity, and compliance.
- Contribute to process improvement initiatives related to documentation and overall compliance.
What You’ll Bring:
- Proven experience in a GMP-regulated pharmaceutical manufacturing environment.
- Expertise in navigating, updating, and developing clear, concise, and compliant technical documents.
- A deep understanding of ISO, FDA, cGMP, and industry standards.
- Proficiency in using Electronic Document Management Systems (EDMS).
- Exceptional attention to detail and commitment to accuracy.
- Strong communication and collaboration skills.
Why Join us (Even for a Contract Role!)?
- Contribute to a company at the forefront of infection prevention, making a real difference in healthcare.
- Gain valuable experience in a highly regulated pharmaceutical manufacturing setting.
- Work alongside a dedicated team of experts.
- This is an initial 3-month contract role with possibility of extension.
If you’re a documentation expert ready to tackle a challenging and rewarding project, apply now!
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