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Training Supervisor

Job in Methuen, Essex County, Massachusetts, 01844, USA
Listing for: Biolife Plasma Services
Full Time, Apprenticeship/Internship position
Listed on 2026-08-24
Job specializations:
  • Business
    Regulatory Compliance Specialist
Salary/Wage Range or Industry Benchmark: 75000 - 96500 USD Yearly USD 75000.00 96500.00 YEAR
Job Description & How to Apply Below

Bio Life Plasma Services is seeking a Training Supervisor to lead staff training in our plasma collection center. In this onsite role, you will coordinate and deliver new-hire and ongoing training for clinical, donor care, and lab teams, ensuring adherence to SOPs, FDA and quality standards, and site-specific procedures. You will observe performance, conduct competency checks, track training completion, and partner with center management to close skill gaps.

The Training Supervisor promotes a strong safety culture, supports inspections and audits, and helps maintain a mission-driven, patient-focused environment where ethical donor care and regulatory compliance are paramount.

Responsibilities

  • Coordinate, deliver, and track new-hire and ongoing training for center staff across donor care, lab, and operations.
  • Ensure all training aligns with FDA regulations, internal SOPs, GMP standards, and safety protocols.
  • Conduct competency assessments, skills check-offs, and refresher training to maintain high performance and compliance.
  • Monitor training records, maintain accurate documentation, and prepare for audits and inspections.
  • Coach and mentor staff, providing feedback to improve donor experience, quality, and safety outcomes.
  • Collaborate with center management to identify training needs and implement targeted development plans.
  • Support incident investigations and corrective actions through training interventions.
  • Promote a mission-driven, patient-focused culture with emphasis on ethical plasma collection and donor care.

Required Skills

  • Clinical training delivery
  • Adult learning principles
  • SOP development and documentation
  • Quality and compliance monitoring
  • FDA/GMP/GCP familiarity
  • Incident and deviation reporting
  • Electronic learning systems (LMS)
  • Data tracking and reporting (Excel/Sheets)
  • Coaching and performance feedback
  • Schedule and resource planning
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