FDA Regulations Jobs in USA

DescriptionPhlebotomist II - Draper UT Monday to Friday 7:00 AM to 4:00 PM with rotational SaturdaysPay range: $19.80 per hourSalary offers are based on a wide range of factors including relevant skills training experience education and where applicable certifications obtained. Market and organizati...

Position TitlePhlebotomistCollege Point Medical PavilionPosition Summary / Career Interest:The University of Kansas Health System Phlebotomist is a position within the clinical laboratory that is responsible for interpreting orders for lab work from providers within The University of Kansas Health S...

Sanford Health is one of the largest and fastest-growing not-for-profit health systems in the United States. Were proud to offer many development and advancement opportunities to our nearly 50000 members of the Sanford Family who are dedicated to the work of health and healing across our broad footp...

OverviewVersiti is a fusion of donors scientific curiosity and precision medicine that recognize the gifts of blood and life are precious. We are home to the world-renowned Blood Research Institute we enable life saving gifts from our donors and provide the science behind the medicine through our di...

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As the leading independent OEM-certified provider of MRI coil repair services ScanMed delivers tailored solutions designed to meet the unique needs of each customer. Our skilled technicians specialize in diagnostics refurbishment and precision repair ensuring every coil is restored to the highest st...

As a leading financial services and healthcare technology company based on revenue SS&C is headquartered in Windsor Connecticut and has 27000 employees in 35 countries. Some 20000 financial services and healthcare organizations from the worlds largest companies to small and mid-market firms rely on...

Join a dynamic and highly collaborative compliance team that plays a critical role in safeguarding the integrity of Vanguards pooled investment vehicles including those focused on alternative this influential role you will lead the development implementation and ongoing refinement of compliance pro...

The OpportunityQuidelOrtho unites the strengths of Quidel Corporation and Ortho Clinical Diagnostics creating a world-leading in vitro diagnostics company with award-winning expertise in immunoassay and molecular testing clinical chemistry and transfusion medicine. We are more than 6000 strong and d...

Current Employees:If you are a current Staff Faculty or Temporary employee at the University of Miami please click here to log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position please review this tip sheet.PGY1 Preliminary Internal Medicine...

Title: Validation Engineer with medical device Location: Irvine CA JD: Review/Creation of IQ protocols Execution of IQ protocols Review/Creation of IQ reports Review/Creation of OQ protocols Execution of OQ protocols Review/Creation of OQ reports Execution of equipment and process cha...

Job Requirements: Demonstrates commitment to principles of the patient care model and achieving the organizations nursing vision and strategy. Complies with regulatory requirements accreditation standards board of nursing requirements patient safety requirements infection control practices and other...

As a Junior Validation Engineer you take the project from the screen to the street. You are responsible for the physical execution of test protocols on Hardware-in-the-Loop (HIL) rigs and vehicle platforms providing the empirical data required for final approval.Key ResponsibilitiesProtocol Executio...

The QA Validation Analyst/Engineer is responsible for planning and overall approval of validation tasks. Responsibilities may also include executing validation activities. Under the direction of the Validation Section Manager this individual will participate in the implementation of the Validation q...

As a Development and Validation Engineer you will lead the bridge between design intent and physical performance. You are responsible for not only executing complex test protocols but also developing the procedures themselves. You will act as a primary technical lead during triage sessions identifyi...

The Manager Regulatory Affairs for Chemistry Manufacturing & Controls (CMC) Post Approval Change (PAC) is responsible for ensuring RA-CMC post approval change objectives are met by project managing marketed product variations including authoring and compilation of chemistry manufacturing and control...

The Senior Chemist is responsible for maintaining instrumentation; tuning and calibrating instrument daily; analyzing quality control and client samples; reviewing and assembling data in an efficient manner with a high degree of quality; evaluating current organizational and analytical systems; diag...

Responsible for the daily operation of the R&D Applications Lab including resourcing and scheduling of testing communicating with test submitters and developing and maintaining a State-of-the-Art test lab as part of the Materials Group North America - Mentor Innovation Center.Distribute testing for...

Hearing Instrument Specialist / Audiologist Sams Club Beaumont TX USAPart Time On CallPosition: Specialist (HIS or AuD) Job DescriptionOur Mission: Helping People Hear BetterAbout this Hearing Specialist / Audiologist opportunity in Beaumont TX: Lucid Hearing is looking for a hearing instrument spec...

Essential Job DutiesCompliance representative on product issue escalation meetings to understand the product/process issue risk clinical impact and help establish escalation decisions/conclusions.Provides guidance to stakeholders in the interpretation of FDA regulations and external regulations/stan...