Researching and consolidating regulatory requirements to enable future development of regulatory strategies for all regions. Create Technical Files, Design Dossiers and Health Canada notifications of ...

As a Regulatory Affairs Specialist, you will play a pivotal role in monitoring regulatory developments, ensuring compliance, and driving regulatory excellence across multiple product categories, inclu...

As a Regulatory Affairs Specialist, you will play a pivotal role in monitoring regulatory developments, ensuring compliance, and driving regulatory excellence across multiple product categories, inclu...

Change Management Regulatory Impact Assessment: Provide regulatory assessments for post approval change proposals, filing strategies and timelines. Maintain regulatory information in accordance with p...

Maintain regulatory information in accordance with processes and procedures to support regulatory compliance. Change Management Regulatory Impact Assessment: Provide regulatory assessments for post ap...

Principal Regulatory Affairs Specialist,. Principal Regulatory Affairs Specialist,. This position requires extensive expertise in regulatory frameworks, strategic planning, and cross-functional collab...

As a Staff Regulatory Affairs Specialist in Advertising/Labeling, you will play a crucial role in supporting Medication Management Solutions (MMS) Dispensing products, including Medical Devices, Non-M...

Regulatory Affairs Specialist* This position assists the Director of Quality Operations (DQO) in maintaining an effective Quality Operations and Regulatory Program, which consistently delivers high qu...

The Principal, Specialist, Regulatory Affairs will provide expertise to the organization in the development of regulatory compliance strategies and in ensuring its conformance to Health Authority requ...

The Senior Regulatory Specialist must be experienced and thoughtful about the processes necessary for achieving domestic and regulatory approval. Perform regulatory assessment of product changes, deve...

The Senior Regulatory Specialist must be experienced and thoughtful about the processes necessary for achieving domestic and regulatory approval. Experience: 15+ years of experience in regulatory affa...

The Senior Regulatory Affairs Specialist is responsible for planning and executing regulatory submissions and ensuring regulatory compliance. Senior Regulatory Affairs Specialist. The individual combi...

The Senior Regulatory Affairs Specialist is responsible for planning and executing regulatory submissions and ensuring regulatory compliance. Senior Regulatory Affairs Specialist. The individual combi...

The Senior Specialist Regulatory Affairs executes on the pharmaceutical regulatory strategies for assigned brand products. Strong business acumen and ability to see the business drivers outside of Reg...

The Senior Specialist Regulatory Affairs executes on the pharmaceutical regulatory strategies for assigned brand products. Work with the Pharmaceutical Regulatory Brand Senior Manager to make certain ...

About the job Pesticide Regulatory Affairs Specialist. Pesticide Regulatory Affairs Specialist needs 5 years of experience in pesticide product registration; or equivalent combination of education and...

About the job Pesticide Regulatory Affairs Specialist. Pesticide Regulatory Affairs Specialist needs 5 years of experience in pesticide product registration; or equivalent combination of education and...

About the job Regulatory Affairs Specialist I. Regulatory Affairs Specialist I. The team partners closely with commercial leaders to define strategy and execute registrations, provides regulatory inte...

About the job Regulatory Affairs Specialist I. Regulatory Affairs Specialist I. The team partners closely with commercial leaders to define strategy and execute registrations, provides regulatory inte...

Stay abreast of Regulatory procedures and changes in the Regulatory climate. Support internal and external Regulatory agency audits, providing Regulatory input to minimize potential findings of non-co...

Support internal and external Regulatory agency audits, providing Regulatory input to minimize potential findings of non-compliance. Stay abreast of Regulatory procedures and changes in the Regulatory...

Technology Regulatory Affairs Specialist.

Technology Regulatory Affairs Specialist.

Familiarity with regulatory affairs and submission management tools, regulatory submission tracking, and compliance management. Proficiency in preparing regulatory submissions such as 510(k) (U. Globa...

Quality and Regulatory Affairs Specialist. Participates in the preparation, planning, coordination and oversight of planned and unplanned regulatory survey and reporting by The Joint Commission, New Y...

Quality and Regulatory Affairs Specialist. Participates in the preparation, planning, coordination and oversight of planned and unplanned regulatory survey and reporting by The Joint Commission, New Y...

Monitor regulatory trends and FDA guidance updates, proactively integrating these insights into product evolution. Demonstrated expertise in FDA regulatory requirements and promotional content complia...

Demonstrated expertise in FDA regulatory requirements and promotional content compliance. Proactive approach to identifying regulatory trends and implications for product innovation. We are an innovat...

The Regulatory Affairs Specialist will support the Director of Regulatory Affairs and collaborate with various departments to complete international product registrations (Canada, Southeast Asia, Midd...

The Regulatory Affairs Specialist will review and approve Dietary Supplement/Food labels for technical accuracy and compliance to all mandated regulatory requirements, provide information to rectify l...

The Regulatory Affairs Specialist will review and approve Dietary Supplement/Food labels for technical accuracy and compliance to all mandated regulatory requirements, provide information to rectify l...

Support daily Regulatory Affairs function eg; compliance to CFR ,, ISO requirements, Company policies, operating procedures, processes, promotional task assignments into windchill and assigned trainin...

Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society. Compile, prepare, and review regulatory submission to US and EU. Provide regulatory input for responsible countr...

Maintains advanced and current knowledge of relevant regulations, policies, and guidelines and acts as Regulatory Affairs Subject Matter Expert in assigned areas. Provides guidance/direction within th...

This position is responsible for the preparation of regulatory submissions required to market medical devices in both the and Europe, support of international product registrations and related regulat...

The Specialist Regulatory Affairs is responsible for ensuring that the assigned Brand products meet and follow all regulatory requirements necessary to conduct business globally. Assisting in gatherin...

The Specialist Regulatory Affairs is responsible for ensuring that the assigned Brand products meet and follow all regulatory requirements necessary to conduct business globally. Assisting in gatherin...

Regulatory Affairs Specialist Project Lead I (Scientific). At least - years of relevant pharmaceutical/biotechnology experience in R&D, including at least years of relevant Regulatory Affairs experien...

Regulatory Affairs Documentation Specialist. A Regulatory Affairs Documentation Specialist utilizes strong written communication skills to enhance the level of documentation maintained within the Depa...

At least 8-10 years of relevant pharmaceutical/biotechnology experience in R&D, including at least 5 years of relevant Regulatory Affairs experience (regionally and/or global), in early development. T...