Tris Pharma, Inc. in Monmouth, NJ seeks a Quality Assurance Documentation Lead to support QA across departments and ensure compliance with SOPs, cGMPs, and FDA standards.
You will maintain quality documentation, assist with MasterControl systems, and help manage stability data, change control, and batch records while coordinating with SMEs. Excellent English communication and attention to detail are required.
#J-18808-LjbffrQA Documentation Lead: Pharma Compliance & Records in south brunswick at Unknown Company
This position is listed as full time and onsite.