Regulatory Affairs Specialist Position Available In Hillsborough, Florida
Tallo's Job Summary: The Regulatory Affairs Specialist position at Katalyst Healthcares & Life Sciences in Tampa, FL offers a contract with an estimated salary range of $78.8K - $94K a year. The role requires 5 years of experience, a bachelor's degree, strong writing and communication skills, and knowledge of FDA regulations. Responsibilities include contributing to FDA regulatory submissions, developing regulatory strategies, and evaluating risk. Requirements include a US bachelor's degree in life sciences and advanced experience in Regulatory Affairs. Regulatory Affairs Certification is preferred.
Job Description
Regulatory Affairs Specialist Katalyst Healthcares & Life Sciences – 4.0
Tampa, FL Job Details Contract Estimated:
$78.8K – $94K a year 21 hours ago Qualifications 5 years Writing skills Microsoft Office Bachelor’s degree Computer skills Senior level Communication skills FDA regulations
Full Job Description Responsibilities:
Contributes to the FDA regulatory submission process; may aid in authoring and/or publishing electronic submissions. Leader in the development of dossiers for registration of products in countries outside the US; including authoring and/or publishing electronic submissions. Provides regulatory direction to development project teams as a core team member; develops regulatory strategy for new products. Evaluate risk of proposed regulatory strategies; may offer solutions. Reviews proposed labeling for compliance with applicable US and international regulations. Writes/manages the development of package inserts. Reviews and evaluates promotion and advertising material for compliance with applicable regulations. Reviews proposed product changes for impact on regulatory status of the product. Contributes to the FDA regulatory submission process; may aid in authoring and/or publishing electronic submissions. Leader in the development of dossiers for registration of products in countries outside the US; including authoring and/or publishing electronic submissions. Provides regulatory direction to development project teams as a core team member; develops regulatory strategy for new products. Expected Areas of Competence. Demonstrated strong writing and communication skills. Strong attention to detail, ability to multi-task. Knowledge of overall business environment, the orthopedic industry, and the marketplace. Ability to learn and stay abreast of regulations pertinent to medical devices, biologics, drugs, and combination products. Ability to function well as a member of the team and build relationships between RA and other areas of the organization. Able to identify risk in Regulatory strategies. Knowledge of FDA regulations (including labeling regulations) and regulations outside the US preferred. Basic computer skills, including Microsoft Office Suite.
Requirements:
US bachelor’s degree in life sciences, technical (engineering) or related field (or non-US equivalent). A minimum of 5 years’ experience in Regulatory Affairs. Advanced experience in the areas that may include preparation of dossiers for product registrations outside the US; preparation of submissions to the FDA strongly preferred. Regulatory Affairs Certification (US or EU) preferred. A combination of education and experience may be considered.
