| Resume alert | Resumes 1 - 10 of 17 |
Customer Service Administrative Support
Greer, SC
... • Assured compliance with all federal and state laws working closely with the FDA and DEA. Paralegal Motley Rice – Mount Pleasant, South Carolina (May 2019 – June 2020) • Member of the Medical Devices team managing bodily injury claims for the ... - Jan 19
... • Assured compliance with all federal and state laws working closely with the FDA and DEA. Paralegal Motley Rice – Mount Pleasant, South Carolina (May 2019 – June 2020) • Member of the Medical Devices team managing bodily injury claims for the ... - Jan 19
Project Manager Program
Lyman, SC
... AMERISOURCEBERGEN / LASH GROUP, (Project Manager/Scrum Master) Contract May 2017 – October 2017 Managed and directed all aspects the FDA new drug launches to ensure that they are on time and on budget when delivered. Define project scope and ... - 2023 Oct 28
... AMERISOURCEBERGEN / LASH GROUP, (Project Manager/Scrum Master) Contract May 2017 – October 2017 Managed and directed all aspects the FDA new drug launches to ensure that they are on time and on budget when delivered. Define project scope and ... - 2023 Oct 28
Environmental Sustainability Strategic Planning
Taylors, SC
... create all annual purchase orders and maintain all updated DEA, FDA & SCBP Audit-ready Books and Documentation in preparation for site audit. Secure estimates and cost quotes in conjunction with Procurement; maintain yearly budget forecasting and ... - 2023 Oct 24
... create all annual purchase orders and maintain all updated DEA, FDA & SCBP Audit-ready Books and Documentation in preparation for site audit. Secure estimates and cost quotes in conjunction with Procurement; maintain yearly budget forecasting and ... - 2023 Oct 24
Human Resources Manager
Greer, SC
... Directed efforts to be compliant with FDA regulations regarding employee competency & training, recordkeeping & training effectiveness. Implemented Pay for Performance (PP) plan for Liquid and Nicogen manufacturing operations Recruits, interviews, ... - 2023 Sep 11
... Directed efforts to be compliant with FDA regulations regarding employee competency & training, recordkeeping & training effectiveness. Implemented Pay for Performance (PP) plan for Liquid and Nicogen manufacturing operations Recruits, interviews, ... - 2023 Sep 11
Packaging Operator Production Associate
Greer, SC
... Accountable for accurate packaging of products free from contamination in accordance with FDA cGMP requirements. Setup filler. Correctly document downtime in batch record. Operate material handling equipment. Review completed batch records for ... - 2023 Mar 01
... Accountable for accurate packaging of products free from contamination in accordance with FDA cGMP requirements. Setup filler. Correctly document downtime in batch record. Operate material handling equipment. Review completed batch records for ... - 2023 Mar 01
Library Assistant Customer Support
Boiling Springs, SC
... - Greenville, SC - September 2015 to December 29, 2016 Responsibilities – Mentored 2 technicians covering: Automation, PHP Web/Apps, Security, customer support, while maintaining QA levels for applications and system in a HIPPA, FDA, PCI compliant ... - 2023 Jan 25
... - Greenville, SC - September 2015 to December 29, 2016 Responsibilities – Mentored 2 technicians covering: Automation, PHP Web/Apps, Security, customer support, while maintaining QA levels for applications and system in a HIPPA, FDA, PCI compliant ... - 2023 Jan 25
Staff Supervisor Process Technician
Greer, SC
... Held knowledge of cGMPs, FDA and DEA guidelines, applying them effectively. Boddie Noell Supervisor 9/2000 to 1/2014 Knightdale NC Full Time Worked as the supervisor for a reputable company, providing all team members with the necessary information ... - 2021 Aug 06
... Held knowledge of cGMPs, FDA and DEA guidelines, applying them effectively. Boddie Noell Supervisor 9/2000 to 1/2014 Knightdale NC Full Time Worked as the supervisor for a reputable company, providing all team members with the necessary information ... - 2021 Aug 06
Engineer Manufacturing
Mills River, NC
... Audited device history records, dimensional part analysis, and multiple program launches, some with FDA medical devices. IQ, OQ, PQ with Quality Engineer team. oExtensive planning for audit team to include medical devices under 21 CFR 820, ISO 13485 ... - 2020 Nov 27
... Audited device history records, dimensional part analysis, and multiple program launches, some with FDA medical devices. IQ, OQ, PQ with Quality Engineer team. oExtensive planning for audit team to include medical devices under 21 CFR 820, ISO 13485 ... - 2020 Nov 27
Medical Manager
Taylors, SC
... * Real time PCR detection of HPV 16.18.31.6,11 particles from Lavage samples * Completed 12000 patients samples study from worldwide for safety, efficacy study * Ensure all clinical sample test records and documents completion for FDA inspection * ... - 2019 Nov 16
... * Real time PCR detection of HPV 16.18.31.6,11 particles from Lavage samples * Completed 12000 patients samples study from worldwide for safety, efficacy study * Ensure all clinical sample test records and documents completion for FDA inspection * ... - 2019 Nov 16
Data Science position
Columbus, NC
... • Using Quality Systems Methodology developed and implemented the process for validating a legacy application to specifications designed to meet FDA requirements. Process requirements included testing in both the development and production ... - 2018 Nov 14
... • Using Quality Systems Methodology developed and implemented the process for validating a legacy application to specifications designed to meet FDA requirements. Process requirements included testing in both the development and production ... - 2018 Nov 14