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Resumes 31 - 40 of 232 |
Nashville, NC
... Production Operator Merck Pharmaceuticals - Wilson, NC October 2009 to February 2011 Packaging of tablets reading of sops bops FDA regulations and OSHA recordable weight scales calibration torqueing lot numbers expiration dates cleanup changeover ...
- 2021 Sep 06
Raleigh, NC
... FDA, EMA) Monitor onsite process monitoring and calibrate\adjust equipment such as digital\analog gauges, temperature monitoring devices and various other equipment in a process setting. Managed OEM site visits (as required) and reviewed OEM ...
- 2021 Aug 01
Wake Forest, NC
Thomas Lauria EXPERIENCE DEPTH • Computer System Validation expert with 30+ years’ experience in FDA regulated environment • Project management skills demonstrated in multiple project environments, fast track/Legacy/Greenfield projects. Managing ...
- 2021 Jul 08
Raleigh, NC
... Wrote and edited Manufacturing Process Instructions, user manuals, firmware-programming instructions, software architecture documents, and software documents for FDA 510(k) submission. Created graphics and process flows for multiple software ...
- 2021 Jun 09
Raleigh, NC
... my VP and the PMs for each region Tracked and recorded installations of nurse call communication systems Prepared and maintained FDA mandated Device History Records Created purchase orders to obtain software licenses Supervised payment of contractor ...
- 2021 May 26
Raleigh, NC, 27616
... r.postjobfree.com Phone 919-***-**** PROFILE Established leader in Validation and Technology Transfers with over twenty (20) years of experience in the Pharmaceutical and Biotech Industry with knowledge of cGMPs, FDA, EMEA, and ISO regulations. ...
- 2021 Apr 30
Raleigh, NC
... World’s only hand-held OCT solution approved by the FDA in the diagnosis of physiological and pathological conditional of the eye. • EnFocus I – Intrasurgical OCT solution for new and existing surgical microscopes. Uniquely designed objective ...
- 2021 Jan 25
Raleigh, NC
... • Worked with cross-functional teams in a contract medical device manufacturing environment to assist customers in getting their products validated and FDA cleared; worked closely with quality and regulatory to ensure products met requirements, ...
- 2021 Jan 07
Raleigh, NC
... and Word Regulation Experience: FDA, cGMP and cGLP Education Oracle Database certificate - 2020 - Wake Technical Community College Bachelor of Science Biology with Minor in Chemistry - 2006 - The University of North Carolina at Greensboro (UNCG); ...
- 2020 Dec 11
Clayton, NC
... Prepared documents for protocol, standard of procedure, audit, review, approval and support of FDA submissions. EDUCATION Master of Science in Nursing, Family Nurse Practitioner; South University, Virginia Beach, VA Bachelor of Science in Nursing; ...
- 2020 Oct 24