Under minimal supervision, this position is responsible for developing the validation program and executing validation strategies and plans for semi-solid, tablet and OTC products.
A thorough understanding of cGMPs, FDA expectations with...
AstraZeneca Pharmaceuticals LP
Do you have a desire to join a team that is improving and enriching the lives of others? Do you have a vision to be part of a world-class manufacturer of innovative medicines for patients, and a manufacturer that is admired for its performance, its...
The Manufacturing Engineer performs engineering, maintenance, and metrology activities for the company. Maintains the systems and performs the job functions by which equipment, instruments, facilities and processes are designed and implemented. ...
Ambrx, Inc. is a biopharmaceutical company with a mission to deliver breakthrough protein therapeutics. Ambrx is based on a fundamental advance in protein biosynthesis that enables the company to genetically engineer proteins with new amino acid...
ADVENT Engineering Services, Inc.
ADVENT Engineering Services is an engineering consulting firm serving the pharmaceutical and biotechnology industries. Head-quartered in San Ramon, CA with operations in the USA, including CA, MA, NC, NY/NJ, PA, as well as Toronto, Canada, and...
Driven by the passion for elevating the science and utility of genetic testing, Natera is committed to helping families identify and manage genetic diseases. Natera is a rapidly-growing diagnostics company with proprietary bioinformatics and...
City NewarkState California [CA]Title Process EngineerJob ID 723XXDate Added 7/6/2016DescriptionResponsible for supervising technology transfer and process validation activities of and will provide technical support for Depomed’s commercial...
About Pfizer A career at Pfizer offers opportunity, ownership and impact. All over the world, Pfizer colleagues work together to positively impact health for everyone, everywhere. Our colleagues have the opportunity to grow and develop a career...
Validation Engineer III (Engineering Operations) is responsible for the Equipment and Cleaning Validation at the Medimmune Boulder Manufacturing Facility. Responsibilities include: *Developing and Implementing equipment and cleaning validation...
Summary: Candidate will be responsible for qualification and validation of manufacturing process and production equipment in a cGMP environment. The qualified individual should have experience with current US and international regulations, guidance,...