Senior QA Specialist

Global Life Science Hub is thrilled to partner with a biologics powerhouse on the brink of exponential growth! With 2 commercial products already on the market and a third approval expected any day, they’re expanding and renovating their New Jersey facility to scale up production from 50L to 2000L.

We’re kicking things off by rapidly expanding their quality team with the hire a Senior QA Specialist. The appointed candidate will support the activities of the QA department in review of QC data and reports, and other reports such as SOPs, CAPAs, Deviations, Change Controls and OOS as needed. 

Requirements:

• Writes, revises, and reviews standard operating procedures (SOPs).
• Conduct reviews of release testing, stability testing, raw material testing, method validations, equipment qualifications and calibrations, technical protocols and reports to ensure compliance with internal procedures and policies, good documentation practices...

Navarro Research and Engineering is recruiting a Quality Assurance (QA) Specialist, Senior for Piketon, OH.

Navarro Research & Engineering is an award-winning federal contractor dedicated to partnering with clients to advance clean energy and deliver effective solutions for complex challenges in the nuclear and environmental fields. Joining Navarro means being a part of an exceptional team committed to quality and safety while also looking for innovative strategies to create value for the client’s success. Headquartered in Oak Ridge, Tennessee, Navarro has active programs in place across the nation for DOE/NNSA, NASA, and the Department of Defense.

Under general supervision, performs quality assurance support for the Quality Assurance (QA) team.  Typical job duties are routine and require use of standard techniques and procedures.

• Responsible for planning and preparation of quality assurance documents and procedures and...

At Editas Medicine, we are pioneering the possible. Our mission and commitment is to translate the power and potential of the CRISPR/Cas12a and CRISPR/Cas9 genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world.  Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for a broad class of diseases.  

Why Choose Editas?

At Editas Medicine, we’re a team of courageous problem solvers, harnessing the power and potential of CRISPR gene editing to transform the future of medicine. Driven by a shared purpose to serve people living with serious diseases, we succeed together through collaboration, mutual respect, and innovation. If you want to be part of a team where your voice is heard and respected, where you can operate at the forefront of gene editing, and push the boundaries of what’s possible in medicine, come join us and...