Full-Time

Sr. Manager

Validations and Engineering

Updated on 2/11/2025

Pegasus Laboratories

Pegasus Laboratories

51-200 employees

Pharmaceutical products for veterinary industry

Industrial & Manufacturing

Senior

Pensacola, FL, USA

Category
Quality Assurance Management
Engineering Management

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Degree
Experience
Requirements
  • Bachelor’s degree in Engineering, Chemistry, Pharmaceutical Science, or related disciple. Advance degree preferred.
  • 7+ years’ experience with cGMP/FDA regulated pharmaceutical process development and validations experience including process validations, cleaning validations, scale-up, equipment qualifications, statistical process performance, and knowledgeable about SUPAC, USP, ICH, AND VICH guidelines.
  • 5+ years’ experience in People Leadership and Project Management required.
  • cGMP FDA regulated facility experience required with a background in budgeting, documentation (i.e., cGMP protocols, reports, system investigations, lab notebooks), and technical writing.
  • Proficient with Microsoft Office Suite (Outlook, Word, Excel, PowerPoint)
Responsibilities
  • Manages the Site Validation Master Plan and Product Validation Master Plans for assigned projects and/or products in cGMP facility.
  • Manages technical transfer projects, from formulations scale-up to approval and launch.
  • Oversees implementation of capital equipment projects supporting new product launches including budgets, design qualification, user requirement specifications, and qualification. Develop project plans, timelines, and reporting.
  • Oversees design and execution of sampling and sample preparation for cleaning validation, process, and packaging validation protocols.
  • Manages and monitors ongoing product validation activities including cleaning and manufacturing processes, utilizing a risk-based approach to establish and maintain the product-specific validation program.
  • Provides resources, support, and oversight to qualify new equipment lines and technical transfer projects and works cross-functionality to manage timelines.
  • Provides technical support and training to the production team, new employees and advises EH&S on equipment, cleaning procedures, and manufacturing processes.
  • Coordinates with CMC team to provide supporting documentation for FDA submissions including process validation protocols, process development reports, FMEA reports, process flow diagrams, and SUPAC supporting documents.
  • All other tasks as requested or assigned.

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%