| Resume alert | Resumes 11 - 20 of 24187 |
Supply Chain Customer Service
Hephzibah, GA, 30815
... Implement and follow procedures for FDA regulated Pharma manufacturing site Used critical thinking to break down problems, evaluate solutions and make decisions. Led meetings, administered budgets and coordinated subcontractor work. Feb 2005 - Jun ... - May 22
... Implement and follow procedures for FDA regulated Pharma manufacturing site Used critical thinking to break down problems, evaluate solutions and make decisions. Led meetings, administered budgets and coordinated subcontractor work. Feb 2005 - Jun ... - May 22
Quality Assurance Analyst
Fort Lauderdale, FL
... Dedicated to precision in pharmaceutical manufacturing while upholding FDA Regulations, cGMP, and safety protocols to deliver high-quality products efficiently. Passionate about ensuring a safe work environment and exceeding production standards. ... - May 22
... Dedicated to precision in pharmaceutical manufacturing while upholding FDA Regulations, cGMP, and safety protocols to deliver high-quality products efficiently. Passionate about ensuring a safe work environment and exceeding production standards. ... - May 22
Household Manager/ Nanny
San Diego, CA
... Food and Drug Administration (FDA) approved vaccine to prevent COVID-19. Read this Fact Sheet for information about the Pfizer-BioNTech COVID-19 Vaccine. Talk to the vaccination provider if you have questions. It is your choice to receive the Pfizer ... - May 22
... Food and Drug Administration (FDA) approved vaccine to prevent COVID-19. Read this Fact Sheet for information about the Pfizer-BioNTech COVID-19 Vaccine. Talk to the vaccination provider if you have questions. It is your choice to receive the Pfizer ... - May 22
Project Management Analytical Chemistry
Carver, MN, 55315
... Contract Research Organization (CRO) experiences, good knowledge of cGMP, GLP and FDA regulations for pharmaceutical industry. Authorships of SOP and Validation Protocols per industrial regulations. Ph.D in Analytical Chemistry, with expert ... - May 22
... Contract Research Organization (CRO) experiences, good knowledge of cGMP, GLP and FDA regulations for pharmaceutical industry. Authorships of SOP and Validation Protocols per industrial regulations. Ph.D in Analytical Chemistry, with expert ... - May 22
Quality Assurance Engineer
Morrisville, NC
... I have held positions of Site Quality Lead, Compliance Officer, Quality Engineer, and Senior Quality Assurance Specialist at FDA and EMA regulated companies encompassing operations including drug substance manufacturing for mAbs, parenteral drug ... - May 22
... I have held positions of Site Quality Lead, Compliance Officer, Quality Engineer, and Senior Quality Assurance Specialist at FDA and EMA regulated companies encompassing operations including drug substance manufacturing for mAbs, parenteral drug ... - May 22
Qc Inspector Department Supervisor
Bartlett, IL
... • Maintain quality system requirements in accordance with ISO 13485 and FDA 21 CFR 820. • Maintain safe work environment and follow GMP policies. • Develop technical expertise, support 5S, lean six sigma and continuous improvement projects to ... - May 22
... • Maintain quality system requirements in accordance with ISO 13485 and FDA 21 CFR 820. • Maintain safe work environment and follow GMP policies. • Develop technical expertise, support 5S, lean six sigma and continuous improvement projects to ... - May 22
Sr. Technical Recruiter
Bowie, MD
... Technical Recruiter/Business Development Extensive marketing to the Federal Government and Commercial companies to include: State Dept, HUD, FDA, DOJ, etc. Generate, coordinate, and secure new add existing business for SSD in support of the ... - May 22
... Technical Recruiter/Business Development Extensive marketing to the Federal Government and Commercial companies to include: State Dept, HUD, FDA, DOJ, etc. Generate, coordinate, and secure new add existing business for SSD in support of the ... - May 22
Mental Health Social Worker
Chicago, IL
... Enter Data into EDC and answer Queries per FDA guidelines and review them against the subject's medical record for completeness and accuracy. ●Ensure the filing and maintenance of all regulatory documents and files at the study site. ●Train back-up ... - May 22
... Enter Data into EDC and answer Queries per FDA guidelines and review them against the subject's medical record for completeness and accuracy. ●Ensure the filing and maintenance of all regulatory documents and files at the study site. ●Train back-up ... - May 22
Raw Materials Machine Operator
Kingsport, TN
... • Train new workers • Follow OSHA and FDA safety standards • Trained on industrial sewing machines (6900 JUK1. Brothers bar tack. MERROW serger. Impact sealer. etc. 2017-2018 Facility maintenance Technician-Morgan County Correctional Complex • ... - May 22
... • Train new workers • Follow OSHA and FDA safety standards • Trained on industrial sewing machines (6900 JUK1. Brothers bar tack. MERROW serger. Impact sealer. etc. 2017-2018 Facility maintenance Technician-Morgan County Correctional Complex • ... - May 22
Project Manager Specialist 1
Downingtown, PA
... Acquired proficiency in Pharma validation Projects (GxP, GMP, CFR 11 & FDA) Facilitated Release tracking and Release Management cycles internal and integration. Rama Markapuram, PMP® LinkedIn TOSCA - Specialist 2 Scrum Master - Internal ... - May 22
... Acquired proficiency in Pharma validation Projects (GxP, GMP, CFR 11 & FDA) Facilitated Release tracking and Release Management cycles internal and integration. Rama Markapuram, PMP® LinkedIn TOSCA - Specialist 2 Scrum Master - Internal ... - May 22