Senior Manager for Regulatory Affairs
Artech Information System LLC
Apply to this jobArtech Information Systems is the #1 Largest Women-Owned IT Staffing Company in the U.S. and an employer of choice for over 7,500 consultants. We recruit world-class talent for IT, engineering, and other professional jobs at 70+ Fortune and Global 500 companies coast-to-coast across the U.S., India, and China. We are one of the fastest-growing companies in the US.
At the forefront of the staffing industry, Artech is a minority and women-owned business enterprise (MWBE) committed to maximizing global workforce solutions on behalf of its clients. Artech's deep heritage, proven expertise and insightful market intelligence has secured long-term partnerships with Fortune 500 and government clients seeking world-class professional resources.
US Regulatory Advertising and Promotion (US Reg AD/Promo) is responsible for actively contributing to the implementation of regulatory strategy for promotional messaging. The contractor will serve as the regulatory representative on assigned review teams for promotional and non-promotional materials and contribute, as appropriate, to other assigned projects.
Essential functions:
• Responsible for accuracy and content of communications with FDA
• Extensive knowledge of advertising and promotion regulations and ability to interpret regulations to promotional materials and non-promotional materials
• Ability to influence teams
• Actively contribute to the development and implementation of regulatory strategy for promotional materials as well as any other assigned projects and programs.
• Decision maker in review meetings
• Responsible for coordinating all aspects of regulatory submissions relevant to assigned projects and programs. This includes promotional materials, including pre-use submissions for subpart E & H products.
• Provide regulatory guidance to cross-functional teams that establish strategy and vision for promotional materials, sales training materials, and other external communications.
• Work is performed under general direction. Capable of strategic thinking and risk assessment for area of responsibility. Demonstrate good communication skills (oral/written/listening).
Requires a minimum of 5+ yrs of direct regulatory promotional and non-promotional material review experience.
All your information will be kept confidential according to EEO guidelines.
Summary
Lead regulatory review for promotional and non-promotional materials, advise cross-functional teams, ensure FDA compliance.
Job title
Senior Manager for Regulatory Affairs
Experience level
5+ years
Industry
it staffing
Location requirements
On-site in Weston, MA, no remote work allowed
Salary
Not specified
Visa sponsorship
H-1B sponsor history
Management role
No
Required skills
Preferred skills
Specializations
Structured locations inferred from the posting.
Weston, MA 02493, USA