Growing firm in Western Canada requires a downstream manufacturing specialist with a background in the biopharmaceutical industry where GMP standards are required. You would have previous experience with SOPs,
Batch Records, and other related documentation. Your duties would include equipment validation, troubleshooting, training, running audits, and manufacture of products (fermentation processes) destined for trials or large scale.
Position reports to a Manager,
Please quote job #1576
Hess Associates
T: (416) 447-3355
1500 Don Mills Road, Suite 712, Toronto, ON M3B 3K4
hr.RemoveThis@hessjobs.com
http://www.hessjobs.com
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