Katalyst CRO
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Katalyst CRO
as a
Regulatory Affairs Manager
in Charlotte, NC.
Salary: $91,000.00 - $145,600.00 (3 days ago).
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 ensuring all regulatory submissions are planned, communicated, and performed per regulatory and business requirements; serve as a subject matter expert, coordinate regulatory issue resolution.
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 to improve the team's knowledge of working in a regulated environment.
Participate in business meetings with potential new external partners.
Assist 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 with 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.
Ability 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.
Seniority Level Mid‑Senior level
Employment Type Contract
Job Function Legal
Industries Pharmaceutical Manufacturing
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Katalyst CRO
as a
Regulatory Affairs Manager
in Charlotte, NC.
Salary: $91,000.00 - $145,600.00 (3 days ago).
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 ensuring all regulatory submissions are planned, communicated, and performed per regulatory and business requirements; serve as a subject matter expert, coordinate regulatory issue resolution.
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 to improve the team's knowledge of working in a regulated environment.
Participate in business meetings with potential new external partners.
Assist 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 with 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.
Ability 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.
Seniority Level Mid‑Senior level
Employment Type Contract
Job Function Legal
Industries Pharmaceutical Manufacturing
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