Junior Scientific Technical Writer
On-site · Ledgewood, New Jersey, United States
Job Summary
Junior Technical Writer assists the Senior Scientific Technical Writer with preparing GMP documents for the manufacturing department, including Batch Records, SOPs, and protocols. Learn to use MasterControl eBR system to support changes, gather information from subject matter experts to ensure technical accuracy, determine appropriate instruction level for the audience, ensure documents comply with Imprimis and industry standards and templates, ensure correct spelling/grammar, and facilitate documents through the change control process in Veeva. Communicate with internal customers and management to meet timelines, support compliance projects, and manage multiple projects. Willing and able to follow sterile gowning procedures to enter controlled production areas as necessary.
Required Qualifications
- Bachelor's degree preferred, (Science degree preferred)
- 1-2 years' experience creating documents in a cGMP regulated environment, preferably in a pharmaceutical manufacturing facility.
- Strong organizing and writing skills.
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint)
- Excellent written and verbal communication skills.
- Ability to work independently and as part of a team, self-motivated, adaptable, and positive attitude.
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