Katalyst Healthcares and Life Sciences
Regulatory Affairs Manager
Katalyst Healthcares and Life Sciences - Miami, Florida, us, 33222
Work at Katalyst Healthcares and Life Sciences
Overview
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Overview
Responsibilities:
The delivery of regulatory guidance to project teams and external partners is a key activity that assists the company in achieving its business goals. The incumbent will serve as a member of the Global Regulatory department. Serve as the regulatory core team lead and provide active and ongoing regulatory guidance to project teams. Responsible for providing guidance to ensure that all regulatory submissions are planned, communicated, and performed per regulatory and business requirements. In addition, this position serves as a subject matter expert on various regulations, coordinating regulatory issue resolution through the use of internal resources, regulatory agencies, and outside consultants as needed. Document regulatory strategies for product submissions. Facilitate and prepare U.S. regulatory Pre-Submission documents for Next Generation Sequencing and/or PCR assays. Facilitate FDA pre-submission meetings. Prepare U.S. regulatory submissions (PMA, PMA supplement, and 510(k)) for Next Generation Sequencing and/or PCR assays. Support EU representatives in their creation of CE/IVD Technical Files. Support global regulatory registration representatives for product registration activities. Perform regulatory assessment of new and changed products. Stay on top of new or revised regulations, guidelines, points to consider, compliance guides, inspection reports, journals, meetings, etc. Conduct training and/or communicate appropriate materials, as needed, to improve the team's knowledge of working in a regulated environment. Participate in business meetings with potential new external partners. ssist the Regulatory department in updating, improving, and crafting internal policies and procedures. Requirements:
B.Sc. or equivalent experience in Biology, Chemistry, bioengineering, or related science at least 5 years of IVD Regulatory Affairs experience. Hands-on experience with 510(k), PMA, and PMA supplement submissions. Knowledge of regulatory strategy creation, design control, cGMP/Quality Systems, and import/export requirements. bility to lead multiple projects and meet deadlines. Strong communication and teamwork skills. Capacity to communicate regulations to technical functions within the company. Experience as the RA representative on project core teams.
The delivery of regulatory guidance to project teams and external partners is a key activity that assists the company in achieving its business goals. The incumbent will serve as a member of the Global Regulatory department. Serve as the regulatory core team lead and provide active and ongoing regulatory guidance to project teams. Responsible for providing guidance to ensure that all regulatory submissions are planned, communicated, and performed per regulatory and business requirements. In addition, this position serves as a subject matter expert on various regulations, coordinating regulatory issue resolution through the use of internal resources, regulatory agencies, and outside consultants as needed. Document regulatory strategies for product submissions. Facilitate and prepare U.S. regulatory Pre-Submission documents for Next Generation Sequencing and/or PCR assays. Facilitate FDA pre-submission meetings. Prepare U.S. regulatory submissions (PMA, PMA supplement, and 510(k)) for Next Generation Sequencing and/or PCR assays. Support EU representatives in their creation of CE/IVD Technical Files. Support global regulatory registration representatives for product registration activities. Perform regulatory assessment of new and changed products. Stay on top of new or revised regulations, guidelines, points to consider, compliance guides, inspection reports, journals, meetings, etc. Conduct training and/or communicate appropriate materials, as needed, to improve the team's knowledge of working in a regulated environment. Participate in business meetings with potential new external partners. ssist the Regulatory department in updating, improving, and crafting internal policies and procedures. Requirements:
B.Sc. or equivalent experience in Biology, Chemistry, bioengineering, or related science at least 5 years of IVD Regulatory Affairs experience. Hands-on experience with 510(k), PMA, and PMA supplement submissions. Knowledge of regulatory strategy creation, design control, cGMP/Quality Systems, and import/export requirements. bility to lead multiple projects and meet deadlines. Strong communication and teamwork skills. Capacity to communicate regulations to technical functions within the company. Experience as the RA representative on project core teams.