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Regulatory affairs specialist Jobs in Knoxville, TN
- Promoted
Director of Regulatory Affairs
THOR CompaniesKnoxville, TN, United StatesMedical Affairs Executive Director (MED), TN / KY / WV
Genentech, IncTennessee- Promoted
Payroll Specialist
TeamHealthKnoxville, TN, United States- Promoted
Contract Specialist
Axle LogisticsKnoxville, TN, US- Promoted
- New!
CONCRETE SPECIALIST
SkillitTN, United States- Promoted
- New!
Technical Specialist
International UTC of ColumbusKnoxville, TN, United States- Promoted
Activity Specialist
Knoxville's Community Development CorporationKnoxville, TN, United States- Promoted
Senior Manager Regulatory Affairs CMC
VirtualVocationsKnoxville, Tennessee, United StatesPrincipal Medical Affairs Specialist.
MedtronicTennessee, USSenior Regulatory Implementation & Assurance Analyst
Highmark HealthTN, Working at Home, TennesseeRegulatory & Quality Compliance Manager (m / f / d)
LifelancerKnoxville, Tennessee, United States- Promoted
Leasing Specialist
AAMCIKnoxville, TN, US- Promoted
- New!
Authorization Specialist
Elevate ENT PartnersPowell, TN, US- Promoted
Scholarship Specialist
Pellissippi State Community CollegeKnoxville, TN, United States- Promoted
Training Specialist
UT Federal Credit UnionKnoxville, TN, USRegulatory Licensing Specialist
Siemens Medical Solutions USA, Inc.Knoxville, Tennessee, Estados Unidos de AméricaExecutive Director, Legislative and Regulatory Policy
001_BCBSA Blue Cross and Blue Shield AssociationUS Tennessee Remote- Promoted
Compliance & Regulatory Specialist
SedgwickKnoxville, TN, United States- Promoted
Registration Specialist
GrahamKnoxville, TNDirector of Regulatory Affairs
THOR CompaniesKnoxville, TN, United States- Full-time
Company Overview :
Thor Life Sciences has partnered with a leading [biotechnology / pharmaceutical] company dedicated to developing innovative therapies to address unmet medical needs. We are committed to excellence in research, development, and regulatory compliance to bring life-changing products to patients worldwide.
Position Overview :
We are seeking a highly experienced Director of Regulatory Affairs - CMC to lead the development and execution of CMC regulatory strategies. This role will be responsible for ensuring compliance with global regulatory requirements, supporting product development and lifecycle management, and liaising with regulatory authorities. The ideal candidate will have a strong background in CMC regulatory affairs, with expertise in [biologics / small molecules / cell and gene therapy] and experience managing regulatory submissions across multiple markets.
Key Responsibilities :
- Develop and implement global CMC regulatory strategies to support product development, registration, and post-approval changes.
- Lead the preparation, review, and submission of high-quality CMC sections of regulatory filings (IND / CTA, BLA / NDA / MAA, variations, supplements, annual reports, etc.).
- Provide strategic regulatory guidance to cross-functional teams, including R&D, Quality, Manufacturing, and Clinical, to ensure alignment with regulatory expectations.
- Serve as the primary point of contact with health authorities for CMC-related matters, including meetings, queries, and negotiations.
- Monitor and interpret global CMC regulatory requirements, trends, and guidelines to ensure compliance and assess potential impact on company projects.
- Lead interactions with external partners, CMOs, and contract laboratories to ensure regulatory compliance of outsourced activities.
- Support due diligence and business development activities by assessing regulatory risks and opportunities.
- Mentor and develop junior regulatory professionals within the organization.
Qualifications & Experience :