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St. George Tanaq Corporation
Technical Writer, Scientific II – Regulatory & cGMP Remote
Job summary
A leading recruitment firm is seeking a Technical Writer/Scientific - II to join a pharmaceutical client in West Point, PA. This is a fully remote role with a 9-month contract that could be extended. The candidate will focus on authoring and reviewing Analytical Test Methods and regulatory documentation while collaborating within a multidisciplinary team. A BS/BA in life sciences/engineering and at least 2 years of experience in a cGMP environment are required. Excellent communication skills are essential. The position is also open for hybrid options.
Benefits
Qualifications
- Minimum 2 years of experience in a cGMP laboratory environment.
- Experience in biopharmaceutical manufacturing, especially in biologics or vaccines.
- Detail-oriented with excellent writing skills.
Responsibilities
- Author and review technical documents for regulatory filings.
- Ensure compliance with current cGMP practices.
- Collaborate with multidisciplinary teams.
Skills
Education
Tools
- ...
* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.