A company is looking for a Regulatory Affairs Specialist. ...
Anticipate regulatory obstacles and emerging issues throughout the product submission cycle and develop solutions with other members of regulatory and related teams. Compile, prepare, and review regulatory submission to US and EU. Provide regulatory input for responsible countries/region for product...
A company is looking for a Senior Regulatory Compliance Specialist. ...
The Senior Regulatory Specialist responsible for Canadian legislation identifies, collects, and interprets science-based reports, data and regulations in order to prepare documents for government agencies, curate lists and/or develop Environment, Health, Safety, and Transportation (EHS&T) informatio...
A company is looking for a Principal Regulatory Affairs Specialist, US Regulatory Policy. FDA regulatory requirements and policyRegulatory experience within the medical device industry or a regulatory agencyExperience in advocacy related to healthcare policy and regulationsStrong research and analyt...
The Senior Regulatory Affairs Specialist provides hands-on regulatory affairs support for new product marketing approvals and renewals for existing products, including development of regulatory requirements and authoring submissions. The Sr Regulatory Affairs Specialist is the Subject Matter Expert ...
Regulatory & Compliance Specialist. Regulatory & Compliance Specialist in our Raleigh, NC or Denver, CO locations. Responsible for working with Project Managers and project teams to ensure successful project execution and delivery of telecommunications regulatory documents, reviews, and permitting. ...
Reporting to The State Regulatory Lead, the Specialist is responsible for the professional interaction with the US EPA, state and/or local regulatory authorities, trade associations, grower groups, customers and industrial partners, and competitors as required by job function. The Regulatory Special...
In this role, you will… Perform regulatory assessments for product changes including regulatory reportability decisions Work with cross functional team and international regulatory colleagues to develop and implement global regulatory strategy to support business global expansions Support regulatory...
Anticipate regulatory obstacles and emerging issues throughout the product submission cycle and develop solutions with other members of regulatory and related teams. Compile, prepare, and review regulatory submission to US and EU. Provide regulatory input for responsible countries/region for product...
Regulatory Data & Compliance Specialist. For those interested in Regulatory Data & Compliance Specialist role, then this is the perfect job for you. Perform high volume document control and technical writing activities to support regulatory data and compliance management. ...
We are seeking an ESG Regulatory & Product Material Compliance Counsel responsible for the North American region to be based in the US or NAM who will be a member of our Global Competency Center in our business function Legal and Integrity. This role will report to the Head of L&I Regulatory Affairs...
The Regulatory Affairs Senior Specialist - Medical Devices coordinates the regulatory activities for development projects including new products and life cycle management. This includes assisting with regulatory strategies and timelines as well as the development and implementation of submissions un...
The Regulatory Affairs Specialist coordinates the regulatory activities for life cycle management of marketed pharmaceutical products. Support the regulatory interactions with regulatory health agencies, contract manufacturers, affiliates and distributors as necessary. This includes assisting with r...
Anticipate regulatory obstacles and emerging issues throughout the product submission cycle and develop solutions with other members of regulatory and related teams. Compile, prepare, and review regulatory submission to US and EU. Provide regulatory input for responsible countries/region for product...
Consult with clients on regulatory topics and support regulatory inspections from health authorities. Experience with FDA, EMA, and knowledge of regulatory requirements with emphasis on regulatory requirements for biotechnology derived products. Responsible for regulatory compliance as it relates to...
Regulatory Affairs Specialist (SRA) will develop US, EU, and Canada strategies, assessments and submissions for complex projects and review issues related to regulatory documents, investigations, product development planning and regulatory agency interaction. The SRA will assist in mentoring and dev...
Do you have a keen eye for detail and a passion for ensuring quality? Are you a problem-solver who thrives in a fast-paced environment? If so, join our team as a Biopharma Quality Assurance Specialist and play a vital role in safeguarding the integrity of our life-changing products!. In this role, y...
A company is looking for a Senior JD Edwards IT Project Manager to lead and manage JDE-related projects remotely. ...
A company is looking for a Director of Regulatory Affairs, Lifecycle. ...
Key Responsibilities:Focus on clinical regulatory filings and providing strategic and operational leadership on project teamsContribute to IND/CTA and BLA submissions activities for products in developmentDevelop regulatory strategies for assigned programs and communicate with regulatory agenciesReq...
A company is looking for a CWR-Project Manager, HR to manage their Cornerstone OnDemand LMS and support various HR functions. ...
A company is looking for a Regulatory Manager to join their Corporate Counsel team. ...
A company is looking for a Senior Regulatory Affairs CMC Associate. ...
A company is looking for a Compliance Administrator / Specialist. ...