Fda Regulations Jobs in Milford, DE

Job Description Position: Validation Engineer Job Summary: We are seeking a motivated Entry Level Validation Engineer to join our team for a 12month contract in New Jersey. The Validation Engineer will be responsible for the execution of validation protocols for equipment facilities a More...

Job Title: Validation Engineer III Location: Santa Monica CA Duration: 06 months contract with possible extension Shift Details: 1st Shift/ MF 85 Pacific/ Onsite at least 3 days a week (Hybrid) Pay Range: $60$80/hr w2 Position Details: Responsible for developing CSV related docu More...

Job Title Validation Process Monitoring and Data Analytics Engineer Location Parsippany NJ Hybrid Onsite T/W/Th Working hours: 84:30 8:305 95:30 type of hours (most of team works 95) Job Duration: 12 months Responsibilities: Strong background in statistics process monitori More...

At Adtalem Global Education we are committed to empowering students and transforming lives through education. As a Senior Regulatory Affairs Analyst you will play a critical role in ensuring compliance with federal state and accreditor regulations helping to shape policies and process More...

(The role requires weekly to cover PST time for a couple of days) The Scientific Affairs Manager (SAM) is responsible to inform engage and influence key stakeholders (KSH) at strategic pharma and biotech companies regarding scientific and clinical data supporting Guardant Health More...

Vice President Regulatory AffairsHybrid/Remote Options AvailableAre you a strategic leader with a passion for regulatory compliance and higher education Join our team as Vice President of Regulatory Affairs where you will shape compliance strategies build key regulatory relationships More...

insightsoftware is hiring an experienced Regulatory & Export Compliance Manager to support the business develop continuously enhance scale and manage insightsoftwares regulatory and export compliance including matters pertaining to antibribery/anticorruption and ethics. A successf More...

At Adtalem Global Education we are committed to empowering students and transforming lives through education. As a Senior Regulatory Affairs Analyst you will play a critical role in ensuring compliance with federal state and accreditor regulations helping to shape policies and process More...

About This Role Leading and taking full accountability in the successful creation ownership and execution of US Medical Affairs (USMA) operational processes and activities the Sr Manager Medical Affairs Operations Lead (specialty Care) is a critical member of the US Medical Affairs te More...

The Manager Regulatory Affairs US Advertising & Promotion combines knowledge of scientific regulatory and business issues to enable products that are developed manufactured or distributed to meet required legislation. Has responsibility for 12 of the following: therapeutic area pr More...

About The Position The KIPP Foundation is seeking a Senior Director (SD) of Transformation to drive strategic change and innovation across its operations.  The SD will be responsible for leading strategic transformation efforts across KIPP Foundation teams (i.e. Finance Scho More...

The Senior BIM Consultant will have the opportunity to work alongside a highly skilled team delivering and implementing BIM from strategy level to project level for global clients.Duties:To fulfil the duties of a Senior Consultant specializing in BIM include:Able to capture client req More...

About the Role:We are seeking a highly experienced and visionary Senior Manager for our AI Foundation team. This role is pivotal in driving the strategy development and implementation of AI capabilities services and solutions to assist our organizations AI initiatives that is a mix of More...

General SummaryUnder limited supervision is responsible for the collection of the account balances from all third party payors and patients for services rendered at UMMC Kernan and Specialty Hospital. Manages the Cash Posting area and Followup. Develops and maintains the policies and More...

About This Role The Senior Manager GCP Quality Assurance & Governance in R&D Quality and Compliance provides global strategic leadership for quality and oversight of quality activities in Biogen R&Ds ongoing clinical research and development processes and programs partneri More...

The Associate Director of RCM Vendor Partnerships & Client Success will serve as the key leader responsible for managing and optimizing relationships with revenue cycle management (RCM) vendors. This role involves tracking vendor performance metrics ensuring vendor accountability More...

About This Role:Pharmacometric analyses and insight are critical in the development of drug candidates determination of product viability and maximization of commercial value at Biogen. The Associate Director Pharmacometrics has responsibility for high priority clinical development as More...

About This Role The Associate Director Statistical Programming will be reporting to the Statistical Programming & Clinical Data Sciences Lead for Biogens West Coast Hub. He/She will lead and oversee statistical programming activities of internally and externally through vendors en More...

Part of Amgens R&D Strategy & Operations organization the R&D Knowledge & Learning team serves staff across R&D and the Office of the Chief Medical Officer transforming how we learn and grow together. We are reimagining learning as an integrated longitudinal journe More...

HRIS Management:Oversee the implementation maintenance and optimization of HRIS systems with a strong focus on Workday.Create HRIS roadmap with input from HR stakeholders and collaborate with IT and internal HRIS team to ensure resources are in place to complete priorities.Ensure More...