Search the 5 jobs at Arranta Bio

The EHS Manager is responsible for maintaining a robust EHS program and providing direction, oversight, and interaction of the day-to-day safety and compliance operations for Recibiopharm's biopharmaceutical manufacturing facility in Watertown, MA. They collaborate with Site Leadership to ensure workplace safety, lead the Emergency Response Team, support site-specific programs, and drive safety initiatives to prevent workplace accidents.

The Proposal Writer will be responsible for drafting proposals for customers seeking solutions for technology transfer, process development, clinical manufacturing, and fill-finish. This role requires strong technical writing skills and an outlook for career growth and development.

Quality Control Analyst III responsible for late phase and commercial quality control activities in a GMP environment. Duties include raw material testing, stability testing, environmental monitoring, method qualifications, troubleshooting, and documentation maintenance. Must have 5+ years of QC experience, proficiency in various analytical instruments, microbiology expertise, and knowledge of regulatory guidelines.

Quality Control Investigations Lead responsible for late phase and commercial quality control activities. Supports raw material testing, stability testing, and environmental monitoring. Initiates and assists in investigations adhering to cGMP and GDP practices.

The Quality Control analyst will be responsible for supporting early phase and commercial quality control activities, including raw material testing, release testing, stability testing, and environmental monitoring. The role involves data analysis, laboratory investigations, equipment calibrations, troubleshooting, and documentation maintenance in accordance with GDP.