| Resume alert | Resumes 1 - 10 of 618 |
Service Representative Customer
Edison, NJ
... In depth knowledge of US FDA, GxP areas including (cGMP, GCLP, and GCP), ICH, GvP, and EU PV regulations to bring a unique perspective and contribute to growth and strengthening of the pharmaceutical sector. CORE COMPETENCIES: Global Patient Safety ... - Jun 11
... In depth knowledge of US FDA, GxP areas including (cGMP, GCLP, and GCP), ICH, GvP, and EU PV regulations to bring a unique perspective and contribute to growth and strengthening of the pharmaceutical sector. CORE COMPETENCIES: Global Patient Safety ... - Jun 11
Program Manager Project
Hillsborough, NJ
... HEITECH SERVICES, Landover, MD 4/21 – 02/22 Project Manager, Medical Device Reporting (MDR) Managed an organization responsible for handling electronic reports submitted to the Food and Drug Administration (FDA) per manufacturer and user facility ... - Jun 11
... HEITECH SERVICES, Landover, MD 4/21 – 02/22 Project Manager, Medical Device Reporting (MDR) Managed an organization responsible for handling electronic reports submitted to the Food and Drug Administration (FDA) per manufacturer and user facility ... - Jun 11
Team Member Inventory Control
Monmouth Junction, NJ
... • Follow FDA standard and keep hygiene of the facility. • Help elderly people to perform their activity. • Maintain inventory and support audit activity. Picker-Packer Jalaram Gift Shop– India Jan 2022 to Mar 2023 • Unload received items, short and ... - Jun 03
... • Follow FDA standard and keep hygiene of the facility. • Help elderly people to perform their activity. • Maintain inventory and support audit activity. Picker-Packer Jalaram Gift Shop– India Jan 2022 to Mar 2023 • Unload received items, short and ... - Jun 03
Clinical Operations Management
North Brunswick, NJ
... Study Responsible for Drug/Device protocol/ICF writings and CRF design Responsible for Drug/Device Advarra IRB and FDA IND and IDE submissions EXECUTIVE DIRECTOR OF CLINICAL SERVICES 07/2022 to 03/2023 Target Health, LLC (CRO) Carlstadt, NJ ... - Jun 02
... Study Responsible for Drug/Device protocol/ICF writings and CRF design Responsible for Drug/Device Advarra IRB and FDA IND and IDE submissions EXECUTIVE DIRECTOR OF CLINICAL SERVICES 07/2022 to 03/2023 Target Health, LLC (CRO) Carlstadt, NJ ... - Jun 02
Security Officer Law Enforcement
Green Knoll, NJ, 08807
... SECURITY OFFICER ALLIED UNIVERSAL SECURITY SERVICES - Somerset, NJ November 2018 to March 2020 FDA and STA Security Clearance. Perform walking patrols and monitor CCTV and several alarm systems. PATROL SERGEANT RUTGERS UNIVERSITY POLICE DEPARTMENT ... - Jun 02
... SECURITY OFFICER ALLIED UNIVERSAL SECURITY SERVICES - Somerset, NJ November 2018 to March 2020 FDA and STA Security Clearance. Perform walking patrols and monitor CCTV and several alarm systems. PATROL SERGEANT RUTGERS UNIVERSITY POLICE DEPARTMENT ... - Jun 02
Production Associate Qc Inspector
Flanders, NJ
... FDA environment experience GMP & SOP experience Lean Manufacturing ISO 90001. Microsoft Office (Word, Excel, Powerpoint, Outlook) ESD Training experience. Able to work under pressure and with minimal supervision. Ability to keep ahead of workflow ... - May 29
... FDA environment experience GMP & SOP experience Lean Manufacturing ISO 90001. Microsoft Office (Word, Excel, Powerpoint, Outlook) ESD Training experience. Able to work under pressure and with minimal supervision. Ability to keep ahead of workflow ... - May 29
Business Analyst Process
Somerset, NJ, 08873
... •I was very much involved and supported business in periodic review process for all GMP applications for Site and GxP System Audit Trail Review Summary Report, FDA audit,HER. •I helped business to document functional requirement, validation process ... - May 28
... •I was very much involved and supported business in periodic review process for all GMP applications for Site and GxP System Audit Trail Review Summary Report, FDA audit,HER. •I helped business to document functional requirement, validation process ... - May 28
Quality Control 1 2
Hillsborough, NJ
... ● Performed quantitative analysis for pharmaceutical drug-substances, excipients and drug products using USP/NF, EP, in-house test methods and standard protocols, maintaining full compliance with all applicable US FDA - cGMP regulations and internal ... - May 27
... ● Performed quantitative analysis for pharmaceutical drug-substances, excipients and drug products using USP/NF, EP, in-house test methods and standard protocols, maintaining full compliance with all applicable US FDA - cGMP regulations and internal ... - May 27
Social Media Digital Marketing
East Brunswick, NJ, 08816
... across the overall umbrella of products within the portfolio • Collaborated with medical and regulatory agencies in assembling FDA review packages, as well as formulating answers to FDA product queries • Maintained all project timelines, managed and ... - May 22
... across the overall umbrella of products within the portfolio • Collaborated with medical and regulatory agencies in assembling FDA review packages, as well as formulating answers to FDA product queries • Maintained all project timelines, managed and ... - May 22
Quality Assurance Software Testing
Piscataway, NJ
... Executed manual test cases using JAMA, focusing on FDA rules and IES code of conduct standards, and documented results. Logged defects and Change Control Requests in JIRA and tracked the bug resolution cycle. Conducted regression testing after ... - May 21
... Executed manual test cases using JAMA, focusing on FDA rules and IES code of conduct standards, and documented results. Logged defects and Change Control Requests in JIRA and tracked the bug resolution cycle. Conducted regression testing after ... - May 21