Job Market Guide: Regulatory Affairs Specialist jobs in Hartford-New Haven

Competition
Desired Skills
Years of Experience
Years of Experience distribution graph for Regulatory Affairs Specialists in Hartford-New Haven. Regulatory Affairs Specialists in Hartford-New Haven have between ${} and ${} years of experience, averaging $${} years of experience.

17 Regulatory Affairs Specialist jobs in Hartford-New Haven

Franklin Lakes, NJ
Analyze and interpret current or proposed domestic and international regulations for impact to BD products and processes to help ensure continuous compliance.
industry
Medical Equipment
experience
5 - 7 years

$100K - $120K - Boston, MA
Draft, assemble, and file original documentation and submission materials for new or existing products to regulatory authorities to assure that all submissions are accurate, of high quality and well supported by literature and regulatory foundations, are presented in a manner to facilitate review, and are in conformance with appropriate statutes, regulations, and guidelines.
industry
Medical Devices & Diagnostics
experience
5 - 7 years

Franklin Lakes, NJ
This position will be responsible for all aspects of regulatory affairs including development and execution of global regulatory strategies and submissions for medical devices and drug/device combination products.
industry
Medical Equipment
experience
Less than 5 years

Franklin Lakes, NJ
This position will be responsible for all aspects of regulatory affairs including development and execution of global regulatory strategies and submissions for medical devices and drug/device combination products. The incumbent will perform essential duties and responsibilities with some supervision while providing guidance to more junior regulatory associates.
industry
Financial Services
experience
Less than 5 years

Andover, MA
Review and approve engineering changes, advertising, promotional items and labeling for regulatory compliance.
industry
Energy & Environmental Services
experience
Less than 5 years

New York, NY
Organize, manage and monitor the hospitals continual readiness for unannounced Joint Commission surveys and provide assistance as needed in interactions with onsite surveys, inspections and investigations from any/all federal, state and local regulatory authorities.
industry
Patient Care
experience
Not Specified

Mahwah, NJ
Develop EU technical documentation/design dossiers to meet the requirements of MDD93/42EEC and support granting the CE mark.
industry
Business Services
experience
8 - 10 years

Franklin Lakes, NJ
This position will be responsible for all aspects of regulatory affairs including development and execution of global regulatory strategies and submissions for medical devices and drug/device combination products. The incumbent will perform essential duties and responsibilities with some supervision while providing guidance to more junior regulatory associates.
industry
Financial Services
experience
Less than 5 years

Framingham, MA
Assist in the process for the development and release of labeling materials (Instructions for Use and patient materials) intended for users of HeartWare products. Assist in coordinating and executing all activities necessary.
industry
Medical Devices & Diagnostics
experience
8 - 10 years

Franklin Lakes, NJ
Analyze and interpret current or proposed domestic and international regulations for impact to BD products and processes to help ensure continuous compliance.
industry
Financial Services
experience
5 - 7 years

Mahwah, NJ
Participate in New Product Development Teams throughout all phases to ensure US, EU, and other international regulatory requirements are incorporated as part of the development process.
industry
Business Services
experience
Less than 5 years

Milford, MA
Participate as a core team member on new product development teams providing regulatory guidance.
industry
Healthcare IT
experience
5 - 7 years

Mahwah, NJ
Assisting in the establishment and maintenance of regulatory information systems both electronically and hard copy.
industry
Medical Devices & Diagnostics
experience
Less than 5 years

Woburn, MA
Communicate with regulatory agencies on administrative and routine matters in addition to pre-clinical, pre-submission, and submission discussions under the direction of management.
industry
Business Services
experience
5 - 7 years

Marlborough, MA
Reviews technical publications, articles and abstracts to stay abreast of regulatory developments in the industry.
industry
Healthcare IT
experience
5 - 7 years

Rensselaer, NY
Interact with other departments on site or at different locations, with customers and with suppliers for the preparation of regulatory submissions and responses to regulatory agencies questions.
industry
Information Services
experience
8 - 10 years