| Distance: | Resume alert | Resumes 411 - 420 of 25476 |
Human Resources Production Supervisor
Manteca, CA
... I ensure compliance to quality systems (FDA, GMP, QSR, ISO 13485, ISO 9001), product specifications, process instructions, safety requirements and company policies. I work and support a clean room environment (ISO 8000 certified) Technical ... - 2025 Sep 05
... I ensure compliance to quality systems (FDA, GMP, QSR, ISO 13485, ISO 9001), product specifications, process instructions, safety requirements and company policies. I work and support a clean room environment (ISO 8000 certified) Technical ... - 2025 Sep 05
Business Analyst Hr Manager
Washington, DC
... Project scope included existing custom software applications that had been in use for several years but not properly validated according to CAPA from FDA audit findings. • Experience with Legacy System -Data Migration. • Participated in an in-house ... - 2025 Sep 05
... Project scope included existing custom software applications that had been in use for several years but not properly validated according to CAPA from FDA audit findings. • Experience with Legacy System -Data Migration. • Participated in an in-house ... - 2025 Sep 05
Supply Chain Customer Service
New Jersey
... Optimize Savings KPI’s, SOP’s, Performance Dashboards OSHA, FDA, cGMP, CFR 21 & 49 Environments Manage Suppliers, Negotiate, Run Bids LEADERSHIP & CAREER CAPITAL PROVEN ORGANIZATIONAL, SUPPLY CHAIN, OPERATIONS SKILLS WITHIN CORPORATE, COMPANY & SITE ... - 2025 Sep 05
... Optimize Savings KPI’s, SOP’s, Performance Dashboards OSHA, FDA, cGMP, CFR 21 & 49 Environments Manage Suppliers, Negotiate, Run Bids LEADERSHIP & CAREER CAPITAL PROVEN ORGANIZATIONAL, SUPPLY CHAIN, OPERATIONS SKILLS WITHIN CORPORATE, COMPANY & SITE ... - 2025 Sep 05
Records Management/Documentation Specialist
Sterling, MA
... Apr 2008 – Jan 2010 ·Knowledge of the Quality System Regulation (FDA QSR 21 CFR Part 820) and ISO 9001 Quality System standard. ·Determined whether complaints were categorized appropriately for Potential Adverse Event and MDR reporting. ·Reviewed ... - 2025 Sep 05
... Apr 2008 – Jan 2010 ·Knowledge of the Quality System Regulation (FDA QSR 21 CFR Part 820) and ISO 9001 Quality System standard. ·Determined whether complaints were categorized appropriately for Potential Adverse Event and MDR reporting. ·Reviewed ... - 2025 Sep 05
Technical Project Manager
Piscataway, NJ
... Collaborated with Compliance teams to ensure adherence to regional and global regulatory requirements (GxP, FDA, GDPR). Conducted due diligence on vendor selection, focusing on operational cost-effectiveness and service quality. Partnered with ... - 2025 Sep 05
... Collaborated with Compliance teams to ensure adherence to regional and global regulatory requirements (GxP, FDA, GDPR). Conducted due diligence on vendor selection, focusing on operational cost-effectiveness and service quality. Partnered with ... - 2025 Sep 05
Pharmacy Technician Continuous Improvement
Miami, FL
... experience • Microsoft Dynamics 365 • Calipers (10+ years) • Warehouse experience (10+ years) • Compounding Medications • FDA regulations • Front desk • Manufacturing • Guest services (10+ years) • Order Entry • Facilities maintenance • Forklift ... - 2025 Sep 05
... experience • Microsoft Dynamics 365 • Calipers (10+ years) • Warehouse experience (10+ years) • Compounding Medications • FDA regulations • Front desk • Manufacturing • Guest services (10+ years) • Order Entry • Facilities maintenance • Forklift ... - 2025 Sep 05
Clinical Research Trial
Cupertino, CA
... ● Regulatory Compliance: Understanding of FDA regulations, ICH guidelines, and Good Clinical Practice (GCP) to ensure clinical trial compliance. ● Project Support: Ability to support CRAs and Regulatory teams in managing project timelines, clinical ... - 2025 Sep 05
... ● Regulatory Compliance: Understanding of FDA regulations, ICH guidelines, and Good Clinical Practice (GCP) to ensure clinical trial compliance. ● Project Support: Ability to support CRAs and Regulatory teams in managing project timelines, clinical ... - 2025 Sep 05
Production Line lead at pci for close to 5 years Forklift experience
Rockford, IL
... Experience Production Line Leader PCI Pharma Services – Rockford, IL December 2020 – May 2025 • Spearheaded the execution of packaging lines, strictly adhering to Batch Production Records, cGMP, and FDA regulatory guidelines for pharmaceutical ... - 2025 Sep 04
... Experience Production Line Leader PCI Pharma Services – Rockford, IL December 2020 – May 2025 • Spearheaded the execution of packaging lines, strictly adhering to Batch Production Records, cGMP, and FDA regulatory guidelines for pharmaceutical ... - 2025 Sep 04
Process Development Scientist
Olney, MD, 20832
... Contributed in one of the company's FDA approved drugs starting with engineering runs to conformance runs and an 80+ cGMP commercial run campaign Cross trained with large scale downstream manufacturing group Worked with process development on ... - 2025 Sep 04
... Contributed in one of the company's FDA approved drugs starting with engineering runs to conformance runs and an 80+ cGMP commercial run campaign Cross trained with large scale downstream manufacturing group Worked with process development on ... - 2025 Sep 04
Accounts Payable Receivable
Elburn, IL, 60119
... ·Handling around 470 customers oversees global supply chain and 141 customers of USA with FDA regulations. ·Using VLOOKUP, PIVOT Table, SAP, CPG Tool and analysis with Tableau Desktop. GHP Group: AR/AP Supervisor 02/2019 – 06/2022 ·I have been ... - 2025 Sep 04
... ·Handling around 470 customers oversees global supply chain and 141 customers of USA with FDA regulations. ·Using VLOOKUP, PIVOT Table, SAP, CPG Tool and analysis with Tableau Desktop. GHP Group: AR/AP Supervisor 02/2019 – 06/2022 ·I have been ... - 2025 Sep 04