FDA resumes in Elkridge, MD

Silver Spring, MD
... in Bioequivalence Professional Experience Currently-Retired From FDA April 2015 Working on the Development of a Physiological Model for d and l pharmacokinetics and pharmacodynamics of extended-release methylphenidate in children and adults. ... - 2023 Apr 22

Hyattsville, MD
... Profiling Prescription Filing Information Documentation Restock Shelves Staff Leadership Prescriptions Management FDA and HIPAA Compliance Inventory and Supply Management Prescription Filling and Labeling Equipment Cleaning and Maintenance ... - 2023 Apr 17

Greenbelt, MD
... 6/2016 – 12/2017 Contracting Program Analyst (Contract) / Food and Drug Administration (FDA), Adelphi, MD Center for Drug Evaluation & Research (CDER), Strategic Programs and Initiatives (SPIS) Refined CDER Executive On-Boarding Program, workflow ... - 2023 Apr 12

Baltimore, MD
... Documentation Plan • Assisted in identifying and implementing best practices and continuous improvement plans within the department/company • Maintained working knowledge of the Company's standards/SOPs and FDA/ICH guidelines and regulations. ... - 2023 Apr 10

Essex, MD, 21221
... patient or patients that experience Adverse events from covid19 shots and input the Information into the reports then reported the cases to the FDA · Input the data from the case into the Citrix EMR system · Conduct follow up on cases if needed. ... - 2023 Mar 25

Baltimore, MD
... Maintained study regulatory binders (Ensured the following documents were signed and filed in proper position in binder: IRB roster, IRB correspondence, Investigator Brochure, Investigator and Staff CV, Protocol, Protocol Amendments, FDA 1572 Form, ... - 2023 Mar 06

Severn, MD
... Secured warehouse staff’s compliance with all regulatory requirements and ethical standards related to procurement, including USDA and FDA regulations. Followed DOT regulations and OSHA safety regulations to conduct SSOP, HACCP, etc. Conducted ... - 2023 Feb 26

Laurel, MD
... oCollaborate with the QC team to develop Standard Operating Procedures, quality, and regulatory requirements such as FDA/IND compliance. oLead the R&D level protein process development, scale up and technical support for manufacturing of proteins, ... - 2023 Feb 01

Silver Spring, MD
... and Presentation Development • Key Performance Indicator Building and Assessment • Regulatory Review, Compliance, and Inspection (FDA, USDA, EPA) • GMP, cGMP, ISO 9001, ISO 22716:2017 Classification Schemes, Product Safety Assessment, Auditing and ... - 2022 Dec 31

Lanham, MD
... ●Following FDA and research approved policies concerning nutrition, breast-feeding and safety ●Encouraging and mediating flexible communication with families through accessible and consistent means such as videos of daily activities, text messages ... - 2022 Dec 26