BD (Becton, Dickinson and Company) Regulatory Affairs Specialist I in Covington, Georgia
Job Description SummaryThe Regulatory Affairs Specialist I is responsible for implementation of regulatory strategies including domestic and international submissions and other support of product project team.
Must have knowledge of the U.S. and European medical device regulations
Must have excellent written and verbal communication skills
Must be self-motivated by working independently and having the ability to take ownership of her/his responsibilities
Must be able to prioritize and handle several projects concurrently
Must have technical writing skills and be proficient at compiling successful submissions for the appropriate audience
Must be able to provide leadership and mentoring skills to less experienced regulatory personnel.
Must be able to maintain confidentiality in dealing with regulatory and clinical documentation
Education and/or Experience:
BS in a scientific discipline with 1-3 years employment in the areas of project registration, compliance or quality systems; or
Combination of education and experience determined to be equivalent
Regulatory Affairs Certification (RAC) desired
Primary Work LocationUSA GA - Covington BMD
Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status