Regulatory Documents Jobs in USA

DESCRIPTIONTo conceive design implement and execute specific scientific experiments which contribute to the successful completion of goals and/or projects under general guidance of and designs executes or evaluates and interprets experimental input to new processes to generate robust and reliable...

The Regulatory Affairs Specialist role is responsible for preparing and submitting the appropriate documentation for FDA 510(k) submissions and documentation for other international regulatory bodies.Responsible for managing and preparing 510(k) submissions to obtain FDA clearance to commercially di...

AskBio Inc. a wholly owned and independently operated subsidiary of Bayer AG is a fully integrated gene therapy company dedicated to developing life-saving medicines and changing lives. The company maintains a portfolio of clinical programs across a range of neuromuscular central nervous system card...

A Pharmacy Technician assists the pharmacist in his/her professional responsibilities in providing pharmacy services. Working under the direction of a licensed pharmacist participates in the preparation dispensing distribution and return of patient specific medications including intravenous admixtur...

OverviewResponsibilitiesJOB SUMMARYThis position is open to those individuals skilled in machine or appliance repair or those with an electrical or computerized hardware background. This position is responsible for assisting the Slots Operations Division with service and repair support minimizing do...

OverviewCOMPANY PROFILE:In addition to its two Seminole Hard Rock Hotels & Casinos the Seminole Tribe owns and operates the five Seminole Casinos; in Coconut Creek and Hollywood on the Southeast coast in Immokalee near Naples on the Brighton Reservation north of Lake Okeechobee and on the Big Cypres...

Overview: TekWissen is a global workforce management provider headquartered in Ann Arbor Michigan that offers strategic talent solutions to our clients world-wide. Job Title: Medical Writer Location: Paramus NJ 07652 Job Type: Temporary Assignment Duration: 5 Months...

About the team: The Analytical Development group within the Targeted LNP (tLNP) CMC Team at AbbVie is dedicated to advancing state-of-the-art analytical capabilities for mRNA-lipid nanoparticle therapeutics. Our team provides critical support across drug substance (DS) and drug product (DP) manufact...

Erascais a clinical-stage precision oncology company focused on discovering developing and commercializing medicines for the benefit of patients with cancer. Our programs take novel approaches to shutting down one of cancersmost commonly mutated signaling cascades the RAS/MAPK pathway which affects...

Erascais a clinical-stage precision oncology company focused on discovering developing and commercializing medicines for the benefit of patients with cancer. Our programs take novel approaches to shutting down one of cancersmost commonly mutated signaling cascades the RAS/MAPK pathway which affects...

Please note that this position can be based inSan Diego CA OR San Francisco CA OR Princeton NJ. Acadias hybrid model requires this role to work in our office three days per week on average.Position SummaryResponsible for the oversight of Translational Medicine preclinical safety assessment/toxicolo...

About Acadia PharmaceuticalsAcadia is committed to turning scientific promise into meaningful innovation that makes the difference for underserved neurological and rare disease communities around the world. Our commercial portfolio includes the first and only FDA-approved treatments for Parkinsons d...

The BSA/AML Director of Quality Assurance & Training plays a critical role in supporting the Wynn Resorts Anti-Money Laundering (AML) and Bank Secrecy Act (BSA) compliance program by overseeing quality assurance activities and AML training initiatives. This role oversees investigations customer due...

OverviewPOSITION SUMMARY: Under the direction of the Principal Investigator or designee the Research Nurse Coordinator is responsible to carry out all delegated tasks related to complex protocols testing investigational drugs devices or research interventions. The Research Nurse Coordinator is a pri...

The Regulatory Affairs Specialist role is responsible for preparing and submitting the appropriate documentation for FDA 510(k) submissions and documentation for other international regulatory bodies.Responsible for managing and preparing 510(k) submissions to obtain FDA clearance to commercially di...

The Regulatory Affairs Engineer role is responsible for preparing and submitting the appropriate documentation for FDA 510(k) submissions and documentation for other international regulatory bodies.Responsible for managing and preparing 510(k) submissions to obtain FDA clearance to commercially dist...

The Senior Division Order Analyst oversees and maintains a specific geographical area of responsibility for the Land team insofar as Division Orders. Responsible for reviewing title title opinions agreements and curative to create ownership decks. The ideal candidate will be experienced in handling...

Mylan Pharmaceuticals Inc.At VIATRIS we see healthcare not as it is but as it should be. We act courageously and are uniquely positioned to be a source of stability in a world of evolving healthcare needs.Viatris empowers people worldwide to live healthier at every stage of life.We do so via: Access...

Mylan Pharmaceuticals Inc.Viatris is a global healthcare company uniquely positioned to bridge the traditional divide between generics and brands combining the best of both to more holistically address healthcare needs globally. With a mission to empower people worldwide to live healthier at every s...

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