Sunquest Information Systems, Inc.
Sr Regulatory Affairs Specialist (Project Management)
At Sunquest Information Systems Inc., we use industry knowledge and focus to develop solutions and services that meet the changing needs of our customers and the marketplace. We combine this vision with the dream to make our company a phenomenal place to work. From our smart casual dress policy to our flexible work schedules, Sunquest promotes a balance of life for all our employees. We place emphasis on training plans for new and current staff, encourage promotion from within, and promote work on special projects and involvement with multi-functional teams. These activities foster a culture of professional growth and development for our employees to achieve their professional goals and reach their full potential.
PURPOSE (why this job exists):
The Senior Regulatory Affairs Specialist provides medical device Regulatory Affairs expertise by participating in the day to day operations of the Quality and Regulatory Affairs department as it relates to supporting business needs.
ESSENTIAL FUNCTIONS:
KNOWLEDGE, SKILLS, and ABILITIES
REQUIRED EDUCATION and EXPERIENCE
Preferred:
PHYSICAL REQUIREMENTS (any specific physical attributes or limiting factors to be accounted for):
Work is performed in a normal office setting with minimal exposure to health or safety hazards; substantial time is spent working at a computer.
Additional Information
Sunquest's policy is to provide equal opportunity to all people without regard to race, color, religion, national origin, ancestry, marital status, veteran status, age, disability, pregnancy, genetic information, citizenship status, sex, sexual orientation, gender identity or any other legally protected category. Applicants for U.S. based positions with Sunquest Information Systems must be legally authorized to work in the United States. Verification of employment eligibility will be required at the time of hire.