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 ...

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

Principal Regulatory Affairs Specialist,. Principal Regulatory Affairs Specialist,. Contribute to the creation or revision of internal standard operating procedures (SOPs) related to regulatory affair...

Pesticide Regulatory Affairs Specialist requires:. Regulatory Affairs Specialist duties:. About the job Pesticide Regulatory Affairs Specialist.

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

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...

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...

Support regulatory impact assessments for change controls and other Regulatory Affairs/Quality Assurance items from a review and approval level. As a Staff Regulatory Affairs Specialist in Advertising...

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...

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...

Provide support in regulatory related product life-cycle review activities, preparation of regulatory documentation and ensuring compliance with all regulations of Hill's Pet Nutrition products. Provi...

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...

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. Regulatory Affairs experience or related experience in a regulated environment.

Provide support in regulatory related product life-cycle review activities, preparation of regulatory documentation and ensuring compliance with all regulations of Hill's Pet Nutrition products. Provi...

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...

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...

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...

Implements regulatory activities such as obtaining global regulatory clearances and/or approvals, preparing device listings, performing import/export requirements, fulfilling regulatory compliance obl...

Implements regulatory activities such as obtaining global regulatory clearances and/or approvals, preparing device listings, performing import/export requirements, fulfilling regulatory compliance obl...

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...

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. Knowledge in relevant Regulatory Affa...

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...

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...

Eligibilities & qualifications.

Working knowledge of relevant federal and state regulatory programs (e.

Working knowledge of relevant federal and state regulatory programs (e.

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 Specialist Project Lead I (Scientific). This role will be accountable for leading the development and execution of innovative and value-added global regulatory strategies and be res...

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

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...

Analyzes and communicate the adequacy of proposed regulatory pathways and strategy for initial product designs and recommend changes or refinements based on initial regulatory outcomes. Applicants wit...