Post Job Free

FDA Resumes

Sign in
Search for: Jobs   Resumes


Distance: Resume alert Resumes 11 - 20 of 25551

Data Entry

La Porte, TX
... ● Review driver paperwork of paperwork for compliance with FDA, cGMP, IMS, and local, state, or federal regulations (DOT). ● Train and assist drivers on new procedures and paperwork accuracy to meet KPIs. ● Organize office operations and procedures ... - Aug 28

All areas of Human Resources

New York City, NY
... Employment Immigration • Payroll & Benefits Administration • Regulatory Compliance (OSHA, ISO, FDA) • Performance Management • HR Policy Development • Workforce Planning & Development • Employee Relations • HRIS & Payroll Systems PROFESSIONAL ... - Aug 28

Talent Acquisition Supply Chain

Kansas City, KS
... Conducted Batch Record Reviews and FDA Audits. 04/2014 – 10/2014 Sr. Human Resource Analyst / Recruiter, Black & Veatch, Overland Contracting Subsidiary, REHIRE Overland pRk, Usa Overland Contracting is a wholly owned subsidiary of Black & Veatch, a ... - Aug 28

Project Manager Management

Elkton, MD, 21921
... Moyer, PMP PROJECT MANAGER 717-***-**** *******@*****.*** Elkton, MD 21921 Project Manager with over 20 years’ experience in cross-functional project management and business change management for regulated industries including US FDA, DoD, and ... - Aug 28

Pharmaceutical Technician

Paterson, NJ
... ●In-depth understanding of Federal Regulations Title, including FDA, DEA, and the Cosmetic Act for manufacturing. ●Knowledgeable with process Protocols, SOP’s, cGMP’s with following batch records, OSHA Safety regulations. ●FIFO with materials used, ... - Aug 28

Human Resources Employee Relations

Indianapolis, IN
... Australian Gold/New Sunshine Manufacturing: 2015 – March 2023 Plant Manager – 2021 – March 2023 Oversee the development and establishment of procedure and process to comply with FDA, GMP, and cGMP Standards. Including process flow, facility design, ... - Aug 28

Scrum Master Project Manager

Monmouth County, NJ
... Played key role in winning Pfizer’s Quality Team Award for custom SharePoint and Documentum back-end used for FDA submission tool which improved Pfizer’s global pharmaceutical portfolio’s compliance. SANOFI-AVENTIS PHARMACEUTICALS (FULL-TIME) 08 ... - Aug 27

Clinical Research Trial

West Palm Beach, FL
... • Patient-Centered Medical Strategy • Regulatory & Compliance (FDA, GCP, ICH) Key Achievements • Supported FDA approval of Biogen’s Aduhelm (Alzheimer’s) through Phase I & III clinical trials. • Contributed to the development of Lundbeck’s Vyepti ... - Aug 27

Project Management Quality Assurance

Rocky Mount, NC
LinkedIn Profile Personal page at iubix.com +1-252-***-**** ***.*@*****.*** Professional Summary As a Certified GAMP Professional with extensive experience in FDA regulations, I specialize in risk-based approaches for remediation, QMS upgrading, ... - Aug 27

Regulatory Affairs Medical Device

Parsippany, NJ
... Proven ability to navigate the complexities of FDA regulations, manage project risks, and facilitate efficient regulatory processes. Seeking to leverage my expertise in regulatory affairs, compliance, and project management as Manager, Regulatory ... - Aug 27
Previous 1 2 3 4 5 6 7 Next