GMP Technical Writer — Precise Pharma Documentation Leader
Job in
Springfield, Union County, New Jersey, 07081, USA
Listed on 2026-01-02
Listing for:
Cedent Consulting Inc.
Full Time
position Listed on 2026-01-02
Job specializations:
-
Pharmaceutical
-
Healthcare
Job Description & How to Apply Below
A leading consulting firm is looking for a GMP Pharmaceutical Technical Writer to produce and maintain essential documentation in the pharmaceutical industry. Responsibilities include authoring Standard Operating Procedures, ensuring compliance with GMP regulations, and collaborating with cross-functional teams. The ideal candidate holds a Bachelor’s degree in Life Sciences with at least 2 years experience in a GMP-regulated environment. Strong communication skills and proficiency in document management systems are essential, along with the ability to work independently on multiple projects.
#J-18808-Ljbffr
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
Search for further Jobs Here:
×