Full-Time

Regulatory Affairs Manager

Updated on 1/31/2025

Pegasus Laboratories

Pegasus Laboratories

51-200 employees

Pharmaceutical products for veterinary industry

Industrial & Manufacturing

Senior, Expert

Pensacola, FL, USA

Category
Risk & Compliance
Legal & Compliance
Required Skills
Sales
Marketing

You match the following Pegasus Laboratories's candidate preferences

Employers are more likely to interview you if you match these preferences:

Degree
Experience
Requirements
  • B.S. or M.S. with 8+ years’ experience in pharmaceutical or FDA/CVM related industry; DVM or PhD with 5+ years’ experience in pharmaceutical or FDA/CVM related industry
  • Proficient in Microsoft Office Suite (Word, PowerPoint, Excel, Outlook)
  • Experience using eSubmitter, Microsoft Dynamics 365 or related ERP, and Master Control preferred.
Responsibilities
  • Work with product development managers to prepare and submit major and minor pre-approval technical sections, process project related invoices, track project budgets, and assist with in-life study activities as needed.
  • Prepare and submit electronic submissions, review associated technical documentation, and ensure all post-approval regulatory requirements and commitments are met (MCSR, DER, 2301). Engage with CVM on submissions when necessary, and track through full submission process to approval.
  • Evaluate pre- and post-approval change controls, labels, manufacturing changes, etc. to determine impact and submission requirements to align with regulatory strategies.
  • Partner with marketing as subject matter expert to provide guidance and perform annual review of all approved and unapproved product labels, promotional materials, and website content.
  • Work cross-functionally across Quality, Marketing, and Sales as a subject matter expert on regulatory requirements on department-specific deliverables. Shapes submission decisions, anticipates regulatory challenges, and reduces risk.
  • Manage the FDA Structured Product Labeling (SPL) database: create new listings, submit updates, perform annual review and certification.
  • Actively engage with internal stakeholders, external stakeholders, and industry alliances to remain knowledgeable of industry changes and regulatory environment.
  • All tasks as requested or assigned.
Desired Qualifications
  • Preferred experience in animal health industry, new product development, and FDA/CVM regulatory affairs.

Pegasus Laboratories, Inc. specializes in innovative pharmaceutical and medical products for the veterinary industry, including solutions for behavior, urinary incontinence, and seizure management. They operate in a cGMP facility with DEA approval and utilize state-of-the-art manufacturing and laboratory facilities to support their services.

Company Stage

N/A

Total Funding

N/A

Headquarters

Pensacola, Florida

Founded

1986

Growth & Insights
Headcount

6 month growth

10%

1 year growth

3%

2 year growth

10%