Technical Writer Pharma (Onsite, Warren, NJ)
We are looking for a Technical Writer for our client, a Global Biopharmaceutical Company. You will support the successful implementation of laboratory equipment and systems at multi-use sites through interaction with internal customers and external service providers.
This is a 40-hour per-week, 12-month contract, 100% Onsite role in Warren, NJ (The candidate must be able to work onsite 5 days a week).
This is a W2 role as a Stage 4 Solutions employee. Health benefits and 401K are offered.
Responsibilities :
- Develop written procedures for the operation, cleaning, and maintenance of equipment and systems.
- Author risk assessments for equipment, systems, facilities, and utilities.
- Perform gap assessments for revisions to the site validation program and the corresponding impact of those changes on all applicable site-level functional areas and relevant procedures.
- Create all documents in compliance with BMS standards and policies.
- Provide excellent customer service and support. Maintain a positive relationship with all team members and site customers while promoting a positive team environment.
Requirements :
- 5+ years of experience in technical writing, with 3 years of technical writing experience in the pharmaceutical industry
- Experience writing Standard Operating Procedures, Work Instructions / Practices, and Risk Assessments
- Strong understanding of cGXP requirements and good documentation practices relating to systems, equipment, and instrumentation
- Preferred experience with Blue Mountain Regulatory Asset Manager and Veeva Vault applications.
- BA / BS degree, Bachelor of Science degree required
Please submit your resume to our network at / careers / (please apply to the Technical Writer Pharma (Onsite, Warren, NJ) role).
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