Regulatory affairs specialist jobs in United States

This position is eligible for the Education Debt Reduction Program (EDRP), a student loan payment reimbursement program. You must meet specific individual eligibility requirements in accordance with VHA policy and submit your EDRP application within four months of appointment. Program Approval, a...

Civica is a 501(c)(4) social welfare organization established in 2018 by health systems and philanthropies to reduce chronic generic drug shortages and related high prices in the United States. Civica is led by an experienced team of healthcare and pharmaceutical industry leaders. Today, more tha...

Our Company:   Gentiva Hospice is a member of the Gentiva family – an industry leader in hospice, palliative, home health, and personal home care. Our place is by the side of those who need us, offering physical, spiritual and emotional support to patients and their families so they may make the...

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The CMC Regulatory Technical Writer II authors high quality Module 2 and 3 regulatory submissions for both development and post-approval dossiers, change controls and technical reports. He/she defines and manages the compilation of the documentation, required for the authoring by reaching out to ...

Experience with Regulatory history, guidelines, policies, standards, practices, requirements and precedents; Regulatory agency structure, processes and key personnel; Principles and requirements of applicable product laws; Submission/registration types and requirements; GxPs (GCPs, GLPs, GMPs); P...

Summary As a Compliance Specialist in the consumer products industry, your primary responsibility is to ensure that the organization complies with relevant laws, regulations, and industry standards governing the manufacturing, labeling, and distribution of consumer goods. You will work closely w...

At Genworth, we empower families to navigate the aging journey with confidence. We are compassionate, experienced allies for those navigating care with guidance, products, and services that meet families where they are. Further, we are the spouses, children, siblings, friends, and neighbors of th...

About Civica Civica is a 501(c)(4) social welfare organization established in 2018 by health systems and philanthropies to reduce chronic generic drug shortages and related high prices in the United States. Civica is led by an experienced team of healthcare and pharmaceutical industry leaders. To...

About Civica Civica is a 501(c)(4) social welfare organization established in 2018 by health systems and philanthropies to reduce chronic generic drug shortages and related high prices in the United States. Civica is led by an experienced team of healthcare and pharmaceutical industry leaders. To...

The Regulatory Affairs Specialist will work in conjunction with the Quality and Regulatory team to create, maintain and approve regulatory technical documentation, licensing, registrations and inspections in compliance with local, state, national and international regulatory requirements.In this ...

Kelly Science & Clinical is seeking a. ...

Regulatory Affairs Specialist II – On-site in Alameda, CA.BS in Life Sciences or Medical Engineering/Technology.Medical device experience required.Needs to have the skill set and able to hit the ground running.Must be local candidates and 100% onsite.Chinese or Japanese bilingual preferred.Implem...

The Regulatory Affairs and Quality Assurance Specialist plays a critical role, ensuring in-market regulatory compliance of new and existing products and supports the Quality Management System.An experienced regulatory or quality professional, this person has a strong understanding of applicable r...

The primary responsibility of the Regulatory Affairs Specialist is to manage and perform regulatory submissions for local and worldwide regulatory agencies.The RAS is also responsible for ensuring products and procedures comply with regulatory agency specifications.Supports necessary regulatory a...

Consultant, GPV Case Management Product Specialist, Pharmaceuticals Summary Our growing, mid-sized pharmaceutical client has engaged GForce Life Sciences to provide a GPV Submission Specialist responsible for managing daily operational activities of the Global Submissions Team within Case process...

Regulatory Affairs Associate – Abbott Park, IL .As an individual contributor, the function of a Regulatory Affairs Specialist is to provide support for the regulatory department to ensure efficient and compliant business processes and environment.The individual may execute tasks and exercise infl...

Kelly Science & Clinical is seeking a. Bachelor’s degree in a science, mathematics, engineering or other technology field. ...

Immediate need for Regulatory Affairs Specialist with a Clinical Research Organization in Raleigh. Hybrid position - will work partly in office and partly remote. Looking for a Regulatory Affairs Specialist with at least 2 years of regulatory experience along with submissions. Will work on IND su...

Adecco Creative and Marketing is partnering with an American multinational beauty company.This person would be responsible for cosmetic regulatory compliance on the global team.Collection of the relevant documentation from our contract manufacturers .Review and assess completeness, consistency an...

Senior Regulatory Affairs Specialist (Medical Devices) - Hybrid (Bay Area). They are looking for a Senior Regulatory Affairs Specialist with a track record of bringing imaging devices to market. If you would like to learn more about this Senior Regulatory Affairs Specialist opportunity, apply tod...

Bachelor’s degree required in engineering or science, masters preferred. ...

Performs full-range of regulatory functions required for Global product registrations, new product development, and internal documentation review for assigned strategic business units serving as the Regulatory Affairs resource.This role manages assigned regulatory programs working towards success...

The Quality Specialist is responsible for organizing, planning, and directing activities related to the development, application and maintenance of quality standards for industrial processes, materials, and products. The Quality Specialist supports the Quality Assurance department by continuously...