Regulatory Affairs-Tech Writer at Eden Prairie

Job Description

Job Classification: Contract The Regulatory Affairs & Compliance Associate is responsible for ensuring that policies, procedures and operating guidelines conform to laws and regulations as required by the FDAs Quality System Regulation. Will mainly be working with EU regulations and not FDA.Qualifications:-2+ of regulatory affairs experience in medical device or pharma company -Minimum of 6 months of EU experience -Effective communication skills -4 year degree preferred Will be expected to step in and have a strong working knowledge of EU regulatory guidelines, to coordinate, prepare, or review regulatory documents and submissions for international projects. Will also be expected to provide knowledge around EU guidelines since no on there currently has experience with it. Join Aerotek Scientific®LLC, one of the fastest growing providers of scientific and clinical research services in the nation. Due to our growth, were constantly on the lookout for qualified professionals to place in contract, contract-to-hire, and permanent placement positions across the scientific and clinical research communities. At Aerotek Scientific, we know its more than just your day-to-day responsibilities that can make or break a job. Its the support you get. Thats the reason Aerotek Scientific offers a variety of benefits including medical, dental, optical, 401k, and many more. Dont put your career in the hands of just anyone, put it in the hands of a specialist. Join the Aerotek Scientific team! Allegis Group and its subsidiaries are equal opportunity employers and will consider all applications without regard to race, marital status, sex, age, color, religion, national origin, veteran status, disability or any other characteristic protected by law.

Job Requirements

• Regulatory Affai-Uncategorized, EU experience, Medical Device

Country: USA, State: Minnesota, City: Eden Prairie, Company: Aerotek.