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Posted 2 weeks agoSr. GMP Quality Specialist - Daytona Beach, FL
at Fortrea
On-site
Responsibilities
- Promote awareness of the applicable regulations and associated quality management system and lead the development / delivery of regulatory based training including quality management principles and risk management practices.
- responsibilities include ensuring local compliance with QMS requirements, overseeing and approving various quality-related issue resolutions and improvement actions, and managing vendor relationships and complaint handling.
Requirements
- experience Excellent leadership and interpersonal skills, e.g. communication, decision making, problem solving, data analysis, auditing, negotiating Bachelor’s Degree, e.g.
- Fortrea may consider relevant and equivalent
- experience in lieu of educational requirements. What do you get? Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive
Experience
- What you will need to bring: 5+ years of
Benefits
- benefits including but not limited to: Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers) 401(K) Flexible Time Off Employee recognition awards Multiple ERG’s (employee resource groups) Pay Range: $80,000 – $110,000 USD
- Benefits: All job offers will be based on a candidate’s skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data.
- benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(K), ESPP, Paid time off (PTO) or Flexible time off (FTO), and Company bonus where applicable. Physical Demands / Work Environment:
Additional details
- As one of the largest Clinical Research Organizations in the world, we have four Early Phase Clinical Research Units in the UK and US. We are currently seeking a Sr. GMP Quality Specialist, to lead and support our Clinical Pharmacology Start-up team in initiating Early Phase clinical trials for our clients with maximum speed and efficiency.