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Resumes 61 - 70 of 417 |
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
Cary, NC
... Proficient in JDE toolkit (OMW, RDA, FDA, UBE, TC, NER, BF), OS/400, RPG, Visual Basic/Access, JDE CNC/OMW and ODBC technologies. Extensive experience in inter-system data transfer, data integrity, validation of business practices and functional ...
- 2021 May 11
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
Chapel Hill, NC
... This consulting service provides general management consulting to the pharmaceutical and biotechnology industry, scientific reviews of product proposals and grant applications (NIH, NSF, FDA, various foundations), literature reviews for product ...
- 2021 Feb 03
Apex, NC
... Sound knowledge of ICH –GCP guidelines, US FDA and EMEA regulations. Process Lifecycle Safety data according to applicable regulations, guidelines, SOPs and project requirements. Demonstrated competence in triaging, evaluating, processing of ...
- 2021 Jan 25
Chapel Hill, NC
... India Sep 2010 – Nov 2010 Business Process Analyst – Pharmaceutical Industry tLed a Six Sigma Black Belt program for an FDA regulated client which lead to reduction in defects enabling them to adhere to regulatory requirements tKey stakeholder ...
- 2021 Jan 25
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
Durham, NC, 27704
... FDA regulated IT customers supported with a varied customer base(Clinical, Manufacturing and Laboratory). Title 21 CFR Part 11. •Various tools/products used daily to respond to customer incidents, problems and changes. Tools used to recreate, ...
- 2021 Jan 23
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
Chapel Hill, NC
... Legacy Systems EDUCATION North Carolina Central University, BBA, Business Education and Administration, 1980-1984, 2008 CERTIFICATIONS FDA Awareness Certification IBM AS/400e Performance Tuning and Capacity Aldon CMS, BMC Patrol Administration ...
- 2020 Dec 14