experience in manufacturing, preferably in a cGMP setting, or some experience as an Associate Level I in the bio-pharma industry... to be part of a high-reaching team at Lonza, where world-class biotechnological solutions come to life. Our Manufacturing...
improve the world. And that’s the kind of work we want to be part of. The Manufacturing Services Associate I role... Hampshire, USA, this position is crucial in maintaining the flawless operation of our cGMP manufacturing production suites...
and nights worked The Manufacturing Associate I is in charge of producing therapeutic proteins (API) in accordance with current... in manufacturing; cGMP setting preferred, and/or some experience as an Associate Level I in bio-pharma industry Confirmed logic...
Job Title: Manufacturing Associate / Bio-Technologist Associate Duration: 12 Month Contract (Possible extension based... 7AM-7PM - ROTATING DAYS - ON SCHEDULE EVERY OTHER WEEKEND Job Description: The Manufacturing Associate is responsible...
as a Manufacturing Associate, you could help positively impact people’s lives all around the world. See Pharma from new angles... production facility. Provide effective training for manufacturing staff related to any new equipment or systems to be used...
to transfer in and maintain customers' processes in the production facility. Provide effective training for manufacturing staff... related to any new equipment or systems to be used in Mammalian Biology. Collaborate with the Manufacturing Leadership team...
Job Description: The Manufacturing Services Associate I is responsible for supporting all cGMP manufacturing.... Report all activities in written and electronic documents in accordance with good manufacturing practice (GMPs) and good...
Today, Lonza is one of the world’s largest healthcare manufacturing organizations operating across five continents... & Manufacturing Executions Systems (MES) Support Specialist will focus on supporting internal customers who use Syncade and DeltaV...
Job description: The Manufacturing Associate is responsible for the manufacturing of therapeutic proteins (API... production in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation...
) - gowning process is much more complicated. The Manufacturing Associate is responsible for the manufacturing of therapeutic... production in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation...
Job description: The Manufacturing Associate is responsible for the manufacturing of therapeutic proteins (API... production in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation...
you will: Job Description: The Manufacturing Associate is responsible for the manufacturing of therapeutic proteins (API) under cGMP conditions...Innova Solutions has a client that is immediately hiring for a Biotechnologist Associate Position...
Job Title: Manufacturing/Biotechnologist Associate Job location: Portsmouth, NH, 03801 Duration: 11+ months... is much more complicated. The Manufacturing Associate is responsible for the manufacturing of therapeutic proteins (API) under cGMP...
Job description: The Manufacturing Associate is responsible for the manufacturing of therapeutic proteins (API... production in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation...
and recruiting partners. Job Description Job description: The Manufacturing Associate is responsible for the manufacturing...) operations and report production in written and electronic documents in accordance with good manufacturing practice (GMPs...
Associate is responsible for the manufacturing of therapeutic proteins (API) under cGMP conditions. Associates are expected...Title: Biotechnologist Associate Duration: 12 Months (possibility of extension) Location: Portsmouth, NH 03801...
Job description: The Manufacturing Associate is responsible for the manufacturing of therapeutic proteins (API... production in written and electronic documents in accordance with good manufacturing practice (GMPs) and good documentation...
Description: Shift Timings:- 12 Hours Shift - 7:00 Am 7:00 Pm The Manufacturing Associate is responsible for the... manufacturing of therapeutic proteins (API) under cGMP conditions. Associates are expected to execute process recipes, follow...
NIGHTS - 12 HOUR SHIFTS - DAYS 7PM - 7AM - ROTATING DAYS - EVERY OTHER WEEKEND The Manufacturing Associate... is responsible for the manufacturing of therapeutic proteins (API) under cGMP conditions. Associates are expected to execute process...
Description: Shift Timings:- 12 Hours Shift - 7:00 Pm 7:00 Am The Manufacturing Associate is responsible for the... manufacturing of therapeutic proteins (API) under cGMP conditions. Associates are expected to execute process recipes, follow...