QC Sample Management Group Leader - 2nd Shift (Wed-Sat)

About the role

At Eurofins PSS, we work with leading international companies across the pharma, medical device, food, cosmetic & consumer products industries - who all trust us with their mission-critical testing. For 20 years, our international network of teams have served clients at their sites, across 20 countries. PSS® is part of Eurofins Scientific, an international life sciences company, providing a unique range of analytical testing services across multiple industries, through a network of over 950 laboratories in 60 countries, and approximately 63,000 employees.

Responsibilities

• Verification of sample submissions to Quality Control
• Documentation of sample transactions in Laboratory Information Management System (LIMS)
• Handling, storage, and organization of samples
• Delivering samples to QC laboratories for testing as required
• Interacting with outside customers and functional peer groups
• Fulfilling sample pull requests
• Compliance with all pertinent regulatory agency requirements
• Conducting temperature, environmental, and/or CO₂ monitoring
• Preparation of samples for shipment
• Performing sample inventory and disposal
• Ensuring compliance with SOPs; reports any quality or other anomalies through the Deviation Notification and Resolution system
• Lead a team of Sample Management Specialists in a regulated facility
• Coordinates, supports, and monitors performance of team through quality metrics while ensuring client deadlines are met
• Coordinates with client contacts to communicate status of deliverables, determine priorities, and set timelines
• Set individual and team goals to develop the scope of work and responsibilities of the team
• Manage time off and payroll entries of the team
• May participate in new hire interviews
• Supports the on‑boarding process of new employees
• Participates in training of other employees

Requirements

• Bachelor's or Master's degree in Life Sciences or related concentration
• Minimum 2 years of relevant industry experience
• Leadership experience
• Ability to thrive in a fast‑paced environment with the ability to multitask
• Authorization to work in the United States indefinitely without restriction or sponsorship

Qualifications

• cGMP experience

Skills

• Strong computer, scientific,