| Resume alert | Resumes 61 - 70 of 288 |
Pharmacy Medical
West Chester, PA, 19380
... Sterile and Non-Sterile Compounding • Responsible for implementing and updating USP <795>, <797>, and <800> standards, and FDA cGMP standards • Completed ongoing pharmacy policy and procedure updates • Successfully completed several state Board of ... - 2020 Sep 10
... Sterile and Non-Sterile Compounding • Responsible for implementing and updating USP <795>, <797>, and <800> standards, and FDA cGMP standards • Completed ongoing pharmacy policy and procedure updates • Successfully completed several state Board of ... - 2020 Sep 10
Salesforce QA Analyst / Application Support
Morton, PA
... Bristol-Myers Squibb, Hopewell, NJ March 2004 – May 2006 System Test Lead - Accenture ●Applied FDA 21 CFR Part 11, GCP, GMP and SOPs in the validation and implementation of in-house and COTS software applications to Oracle Clinical Trial and ... - 2020 Sep 08
... Bristol-Myers Squibb, Hopewell, NJ March 2004 – May 2006 System Test Lead - Accenture ●Applied FDA 21 CFR Part 11, GCP, GMP and SOPs in the validation and implementation of in-house and COTS software applications to Oracle Clinical Trial and ... - 2020 Sep 08
Manager Maintenance
Gilbertsville, PA, 19525
... • I was a member of 3 Green-field facility start-up teams along with associated validation efforts through FDA and EMA approval. • Led the development, planning and execution of major facility renovations and shutdowns. • Served as the site Energy ... - 2020 Aug 17
... • I was a member of 3 Green-field facility start-up teams along with associated validation efforts through FDA and EMA approval. • Led the development, planning and execution of major facility renovations and shutdowns. • Served as the site Energy ... - 2020 Aug 17
Manager Project
Malvern, PA
... Lead the validation testing for CFR21 Regulations, OQ,PQ validation protocols and FDA protocol validation testing Project Title: MMIS system upgrade 07/01/2016– 06/01/2017 Role: MMIS IV&V Lead Test Consultant Vermont, USA Client: State of Vermont ... - 2020 Jun 06
... Lead the validation testing for CFR21 Regulations, OQ,PQ validation protocols and FDA protocol validation testing Project Title: MMIS system upgrade 07/01/2016– 06/01/2017 Role: MMIS IV&V Lead Test Consultant Vermont, USA Client: State of Vermont ... - 2020 Jun 06
Pharmacy Medical
Collegeville, PA
... • Multiple clerkships spanning an extensive range of pharmacy practices from pediatric cardiology to medical affairs at The Johns Hopkins Hospital, the FDA, and Pfizer. PROFESSIONAL EXPERIENCE Pharmacy Intern. Synergy Services Long Term Care ... - 2020 May 01
... • Multiple clerkships spanning an extensive range of pharmacy practices from pediatric cardiology to medical affairs at The Johns Hopkins Hospital, the FDA, and Pfizer. PROFESSIONAL EXPERIENCE Pharmacy Intern. Synergy Services Long Term Care ... - 2020 May 01
Clinical Research Coordi, Regulatory Coordinator, Regulatory Affairs
New Castle, DE
... ●Managed and trained up to 25 staff members and clinical personnel for cross-functional duties, specific assignments, and operations according to and in compliance with SOPs, FDA regulations and ICH/GCP guidelines to meet project goals. ●Considered ... - 2020 Apr 27
... ●Managed and trained up to 25 staff members and clinical personnel for cross-functional duties, specific assignments, and operations according to and in compliance with SOPs, FDA regulations and ICH/GCP guidelines to meet project goals. ●Considered ... - 2020 Apr 27
Buyer/ Buyer Planner/Purchasing Agent
Berwyn, PA
... 1999 - 2004 Buyer-Planner/Purchasing Agent – cGMP Supply cGMP experience: FDA approval of world class manufacturing facility 3-4 months earlier than target Generated cost savings in MRO and critical inventory in excess of $270,000 over 2 yrs. ... - 2020 Mar 31
... 1999 - 2004 Buyer-Planner/Purchasing Agent – cGMP Supply cGMP experience: FDA approval of world class manufacturing facility 3-4 months earlier than target Generated cost savings in MRO and critical inventory in excess of $270,000 over 2 yrs. ... - 2020 Mar 31
Engineer Manager
Wilmington, DE
... Created IQ, OQ protocols and performed PQ testing 12 years of pharmaceutical MES out to Cloud manufacturing industry experience working with FDA and cGMP regulations and writing application codes to PLCs, SCADA, Wonderware, POMS,SAP and MES server ... - 2020 Mar 19
... Created IQ, OQ protocols and performed PQ testing 12 years of pharmaceutical MES out to Cloud manufacturing industry experience working with FDA and cGMP regulations and writing application codes to PLCs, SCADA, Wonderware, POMS,SAP and MES server ... - 2020 Mar 19
Sales Medical
West Chester, PA
... Counsel individuals on the importance of FDA regulations. Maintained daily outputs determine by the operation schedule. Responded to quality issues in the form of a corrective action EDUCATION: West Chester University: West Chester, PA. B.A. ... - 2019 Aug 02
... Counsel individuals on the importance of FDA regulations. Maintained daily outputs determine by the operation schedule. Responded to quality issues in the form of a corrective action EDUCATION: West Chester University: West Chester, PA. B.A. ... - 2019 Aug 02
Senior Scientist
Newark, DE
... Lead technical staff for conducting GLP studies based on FDA guidelines. EDUCATION Institution Years Field Degree Capital Medical University (CMU) 9/2004 - 5/2007 Neurobiology Ph.D. Capital Medical University (CMU) 9/2000 - 5/2003 Pharmacolgoy M.S. ... - 2019 Jul 16
... Lead technical staff for conducting GLP studies based on FDA guidelines. EDUCATION Institution Years Field Degree Capital Medical University (CMU) 9/2004 - 5/2007 Neurobiology Ph.D. Capital Medical University (CMU) 9/2000 - 5/2003 Pharmacolgoy M.S. ... - 2019 Jul 16