Admin functional support 3 jobs in the Quality Assurance & Safety category and Medical Devices and Supplies industry

THERAKOS® is a global leader in advancing the science of extracorporeal photopheresis (ECP). For 25 years, THERAKOS® employees have pioneered new and industry leading technologies. As we look to drive the next phase of Therakos’ growth, we are seeking to expand our team with talented leaders and professionals in all functional areas. THERAKOS® offers a range of opportunities to work and grow in an...
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Catalent Pharma Solutions (a Blackstone Group company) is a leading Drug Development, Advanced Delivery Technology and Supply partner to the global pharmaceutical industry. A Fortune 1000 company, with over 20 locations on 5 continents, we partner with 90 out of the top 100 pharmaceutical companies and 44 of the top 50 biotech firms, as well as thousands of small innovator companies. JOB FUNCTION ...
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We have been engaged by our client to recruit their Regulatory Affairs Manager. Our client is a worldwide medical device manufacturer. This manager plays a key role for combination products representing Regulatory Affairs within the company and with global regulatory agencies. The role develops and executes strategies for global regulatory approvals to introduce new and modified medical device/dru...
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Plan, execute and manage field actions (recalls, withdrawals, field corrections and safety notices) from decision making to termination on a global scale in accordance with global regulatory requirements for products manufactured and/or distributed by Hospira and Hospira's business partners, including drugs, devices, biologics and software. Provide guidance during the decision making process for p...
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The Senior Lead Quality Auditor is responsible for aiding in the development of and subsequent implementation of quality processes associated with site internal and external audits (Suppliers), Approvals, Quality Council, Management Reviews, risk assessments, and routine company reporting. All quality processes will be in compliance to 21CFR 820, ISO requirements. Contract thru December 2013. Main...
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