| Resume alert | Resumes 1 - 10 of 80 |
Quality Control Product Compliance
Greensboro, NC
... My back- ground in medical administration has equipped me with a strong understanding of regu- latory compliance, including FDA regulations and CGMP guidelines. I excel in analyzing data to identify quality improvements and am adept at collaborating ... - Apr 18
... My back- ground in medical administration has equipped me with a strong understanding of regu- latory compliance, including FDA regulations and CGMP guidelines. I excel in analyzing data to identify quality improvements and am adept at collaborating ... - Apr 18
Clinical Research Hr Manager
Chapel Hill, NC
... Submission of CIOMS (EU) and MedWatch (FDA) reports for specific clients. Rewriting OG’s, DEG’s and SOP as it pertains to the project. Review product labeling for inclusion of applicable data in MedWatch reports for Medical device studies. Identify ... - Jan 15
... Submission of CIOMS (EU) and MedWatch (FDA) reports for specific clients. Rewriting OG’s, DEG’s and SOP as it pertains to the project. Review product labeling for inclusion of applicable data in MedWatch reports for Medical device studies. Identify ... - Jan 15
Clinical Research Medical Information
Burlington, NC
... Organized and maintained FDA, IRB and GCP required regulatory documentation for individual sites and studies. Maintained ongoing study-specific clinical trial tracking documents and distributed as needed. Clinical Research Coordinator II Kelly ... - 2023 Nov 25
... Organized and maintained FDA, IRB and GCP required regulatory documentation for individual sites and studies. Maintained ongoing study-specific clinical trial tracking documents and distributed as needed. Clinical Research Coordinator II Kelly ... - 2023 Nov 25
Senior Vice President of Sales and Marketing
Greensboro, NC
... While the company dealt with Food and Drug Administration (FDA) issues, tasked to manage client expectations. Senior Vice President of North American Pharmaceutical and Nutritional Product Sales (2003–2005) Guided North American nutritional and ... - 2023 Nov 01
... While the company dealt with Food and Drug Administration (FDA) issues, tasked to manage client expectations. Senior Vice President of North American Pharmaceutical and Nutritional Product Sales (2003–2005) Guided North American nutritional and ... - 2023 Nov 01
Plant Manager
Greensboro, NC
... Ensuring compliance to all product FDA reliability conformance to specifications. Compliant with ISO Standards resulting in successful ISO audits. Managing facility equipment to avoid downtime, through a proactive preventative maintenance program. ... - 2023 Sep 02
... Ensuring compliance to all product FDA reliability conformance to specifications. Compliant with ISO Standards resulting in successful ISO audits. Managing facility equipment to avoid downtime, through a proactive preventative maintenance program. ... - 2023 Sep 02
Equipment Operator Plant Manager
Reidsville, NC
... Communication of company /customer regulatory requirements affecting each individual product or process and know regulatory aspects of FDA, EPA, OSHA and GMP. Communication of production results via SAP interface and Microsoft office spreadsheets. ... - 2023 May 16
... Communication of company /customer regulatory requirements affecting each individual product or process and know regulatory aspects of FDA, EPA, OSHA and GMP. Communication of production results via SAP interface and Microsoft office spreadsheets. ... - 2023 May 16
Process Engineer Facility
Greensboro, NC
... Wood advozt@r.postjobfree.com advozt@r.postjobfree.com SENIOR PROCESS/PROJECT/VALIDATION ENGINEER 269/929-3608 Process & Project Chemical Engineering / Multi-Site Operations / R&D / FDA Compliance Change Management /Process Design & Validation / ... - 2023 Mar 03
... Wood advozt@r.postjobfree.com advozt@r.postjobfree.com SENIOR PROCESS/PROJECT/VALIDATION ENGINEER 269/929-3608 Process & Project Chemical Engineering / Multi-Site Operations / R&D / FDA Compliance Change Management /Process Design & Validation / ... - 2023 Mar 03
Senior Quality Professional
Greensboro, NC
... In-depth knowledge of FDA regulations, ICH guidelines, domestic and global standards. Proven experience in liaising with third party suppliers and conducting test requirements of the project at all stages of process. Ability to identify quality ... - 2022 Feb 07
... In-depth knowledge of FDA regulations, ICH guidelines, domestic and global standards. Proven experience in liaising with third party suppliers and conducting test requirements of the project at all stages of process. Ability to identify quality ... - 2022 Feb 07
IT Business Analyst/Project Manager
Burlington, NC, 27215
... Experienced in developing, supporting, and deploying IT solutions in FDA regulated environments complying with Computer System Validation, SOX, and HIPAA regulations. Technical Skills and Tools Used AS400 (IBMi) Technologies - RPGLE, RPG, CL400, DB2 ... - 2021 Apr 01
... Experienced in developing, supporting, and deploying IT solutions in FDA regulated environments complying with Computer System Validation, SOX, and HIPAA regulations. Technical Skills and Tools Used AS400 (IBMi) Technologies - RPGLE, RPG, CL400, DB2 ... - 2021 Apr 01
Medical C
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
... 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