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Regulatory affairs specialist Jobs in Knoxville, TN

Last updated: 6 hours ago
  • Promoted
Director of Regulatory Affairs

Director of Regulatory Affairs

THOR CompaniesKnoxville, TN, United States
Full-time
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 ...Show moreLast updated: 6 days ago
Medical Affairs Executive Director (MED), TN / KY / WV

Medical Affairs Executive Director (MED), TN / KY / WV

Genentech, IncTennessee
Full-time
It’s what drives us to innovate.To continuously advance science and ensure everyone has access to the healthcare they need today and for generations to come. Creating a world where we all have more ...Show moreLast updated: 3 days ago
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Payroll Specialist

Payroll Specialist

TeamHealthKnoxville, TN, United States
Full-time
TeamHealth is named among the "150 Top Places to Work in Healthcare" by Becker's Hospital Review.The World's Most Admired Companies" by Fortune Magazine and one of America's 100 Most Trustworthy Co...Show moreLast updated: 1 day ago
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Contract Specialist

Contract Specialist

Axle LogisticsKnoxville, TN, US
Full-time
The Contract Specialist is responsible for managing the lifecycle of contracts critical to our 3PL operations.This role focuses on agreements with carriers, shippers, and other service providers.It...Show moreLast updated: 2 days ago
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CONCRETE SPECIALIST

CONCRETE SPECIALIST

SkillitTN, United States
$20.50–$26.50 hourly
Full-time
We are actively seeking skilled and experienced.As a Concrete Worker, your primary responsibility will be to assist in the preparation, placement, and finishing of concrete and / or a focus on formwo...Show moreLast updated: 14 hours ago
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Technical Specialist

Technical Specialist

International UTC of ColumbusKnoxville, TN, United States
Full-time
WE'RE INTERNATIONAL COMMITTED TO THE ROAD AHEADWe are seeking a Technical Specialist - Power Architecture , who will be responsible for developing system requirements documentation for a given area...Show moreLast updated: 6 hours ago
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Activity Specialist

Activity Specialist

Knoxville's Community Development CorporationKnoxville, TN, United States
$15.00 hourly
Full-time
The Activity Specialist is responsible for planning, organizing, and facilitating daily activities at an assigned KCDC residential property. The incumbent plans and supervises daily activities and m...Show moreLast updated: 1 day ago
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Senior Manager Regulatory Affairs CMC

Senior Manager Regulatory Affairs CMC

VirtualVocationsKnoxville, Tennessee, United States
Full-time
A company is looking for a Senior Manager / Associate Director in Regulatory Affairs CMC.Key ResponsibilitiesContribute regulatory CMC expertise to product development and registration for small mole...Show moreLast updated: 2 days ago
Principal Medical Affairs Specialist.

Principal Medical Affairs Specialist.

MedtronicTennessee, US
This position, Principal Medical Affairs Specialist, will have two primary responsibilities : .To interact with patients, investigate complaints that adverse health outcomes resulted from the use of ...Show moreLast updated: 30+ days ago
Senior Regulatory Implementation & Assurance Analyst

Senior Regulatory Implementation & Assurance Analyst

Highmark HealthTN, Working at Home, Tennessee
$124,800.00 yearly
Full-time
This job is responsible for leading large projects and initiatives related to the risk case management and intake activities of Highmark Health in support of a broad range of frameworks and oversig...Show moreLast updated: 30+ days ago
Regulatory & Quality Compliance Manager (m / f / d)

Regulatory & Quality Compliance Manager (m / f / d)

LifelancerKnoxville, Tennessee, United States
Remote
Full-time
Quick Apply
Regulatory & Quality Compliance Manager (m / f / d).The internal Job Title is called.Global Product Center Manager (m / f / d) - Sterile Fluids (Medicinal Products). Support as regulatory expert development...Show moreLast updated: 30+ days ago
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Leasing Specialist

Leasing Specialist

AAMCIKnoxville, TN, US
$16.00 hourly
Full-time
AAMCI is seeking a dynamic person to join our team as a Leasing Agent / Receptionist at a 199-unit Section 8 / Tax Credit community in Knoxville, TN. Full time : Monday thru Friday 8am to 5pm.The communi...Show moreLast updated: 2 days ago
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Authorization Specialist

Authorization Specialist

Elevate ENT PartnersPowell, TN, US
Full-time
The Authorization Specialist will be responsible for obtaining prior authorizations for medical services, procedures, and tests for patients in the ENT (Ear, Nose, and Throat) practice.This role en...Show moreLast updated: 17 hours ago
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Scholarship Specialist

Scholarship Specialist

Pellissippi State Community CollegeKnoxville, TN, United States
$36,270.00–$44,390.00 yearly
Full-time +1
Pay will be determined based on related work experience above required.To be considered in determining pay, all related work experience must be listed on the application. Required Documents Needed t...Show moreLast updated: 16 days ago
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Training Specialist

Training Specialist

UT Federal Credit UnionKnoxville, TN, US
Full-time
Responsible for assisting in the improvement of the productivity of the credit union's.Assists in the assessment of developmental needs that will drive training initiatives.Actively searches, c...Show moreLast updated: 30+ days ago
Regulatory Licensing Specialist

Regulatory Licensing Specialist

Siemens Medical Solutions USA, Inc.Knoxville, Tennessee, Estados Unidos de América
Permanent
Do you want to join us in helping to fight the world’smost threatening diseases and enabling access to care for more people aroundthe world? At Siemens Healthineers, we pioneer breakthroughs in hea...Show moreLast updated: 30+ days ago
Executive Director, Legislative and Regulatory Policy

Executive Director, Legislative and Regulatory Policy

001_BCBSA Blue Cross and Blue Shield AssociationUS Tennessee Remote
Remote
Full-time
Senior leader to advance BCBSA’s legislative and regulatory policy solutions and market positioning in Medicare, Medicaid, Duals, and Children's Health Insurance Program, impacting the tens of mill...Show moreLast updated: 30+ days ago
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Compliance & Regulatory Specialist

Compliance & Regulatory Specialist

SedgwickKnoxville, TN, United States
Full-time
Taking care of people is at the heart of everything we do, and we start by taking care of you, our valued colleague.A career at Sedgwick means experiencing our culture of caring.It means having fle...Show moreLast updated: 12 days ago
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Registration Specialist

Registration Specialist

GrahamKnoxville, TN
Quick Apply
REMOTE – Registration Specialist.Contract Position, 5 days per week, from 9am-6pm EDT with one-hour lunch.Registration Specialist opportunity with the possibility of becoming a permanent posi...Show moreLast updated: 30+ days ago
Director of Regulatory Affairs

Director of Regulatory Affairs

THOR CompaniesKnoxville, TN, United States
6 days ago
Job type
  • Full-time
Job description

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 :

  • Advanced degree (Ph.D., Pharm.D., or M.S.) in chemistry, pharmaceutical sciences, or related field preferred.
  • Minimum of [10+] years of experience in Regulatory Affairs, with a strong focus on CMC.
  • Proven track record of successful regulatory submissions and interactions with global health authorities (FDA, EMA, MHRA, PMDA, etc.).
  • In-depth knowledge of CMC regulatory requirements, ICH guidelines, and global regulations.
  • Experience with [biologics / small molecules / cell and gene therapy] CMC development and lifecycle management.
  • Strong leadership, strategic thinking, and problem-solving skills.
  • Excellent communication, negotiation, and interpersonal skills.
  • Ability to work collaboratively in a fast-paced, dynamic environment.