QC Raw Materials Supervisor

Eurofins USA PSS Insourcing Solutions•Rensselaer, NY

2d•Onsite

About The Position

Eurofins PSS works with leading international companies in the pharma, medical device, food, cosmetic & consumer products industries, providing mission-critical testing. As part of Eurofins Scientific, a global life sciences company with over 950 laboratories worldwide, Eurofins PSS serves clients at their sites across 20 countries. This role involves delivering excellent customer service in a client-facing environment, performing testing of pharmaceutical utilities (air, gas, water), and managing samples. The position requires accurate recording and reporting of sampling and testing activities, instrument calibration, use of sterile gowning and aseptic techniques in cleanroom environments, and maintaining laboratory supplies. The role also includes investigating quality deviations, communicating findings, participating in cross-functional teams, and reviewing/revising controlled documents (batch records, logbooks, SOPs) in accordance with cGMP. Method validation assistance and compliance with regulatory and cGMP requirements are also key aspects. The leadership responsibilities include managing direct reports, training employees, documenting training, communicating updates, promoting company values, planning workloads, monitoring team performance, and developing team-building initiatives.

Requirements

Bachelor’s degree in Life Sciences, or other science related degree concentration, or equivalent directly-related experience
Authorization to work in the United States indefinitely without restriction or sponsorship
2+ years of GMP experience
5+ years of industry leadership experience

Nice To Haves

ISO 8 cleanroom experience preferred

Responsibilities

Delivers excellent customer service in a client-facing environment.
Collects, receives, handles, and disposes of samples.
Performs testing of pharmaceutical utilities, including air, gas, and water.
Records sampling and testing activities accurately and reports quality anomalies.
Calibrates instruments or verifies calibration before use.
Uses sterile gowning and aseptic techniques in cleanroom environments.
Maintains laboratory supplies and performs routine laboratory housekeeping.
Investigates quality deviations and implements measures to prevent recurrence.
Communicates findings and recommendations during group meetings.
Participates in or leads cross-functional teams to support client needs.
Reviews and revises controlled documents, including batch records, logbooks, and SOPs, in accordance with cGMP requirements.
Assists with method validation, as needed.
Complies with applicable regulatory and cGMP requirements.
Leads direct reports, group leaders, and their teams in laboratory or manufacturing environments.
Trains employees and coordinates required training activities.
Documents training and supports onboarding for GMP-related responsibilities.
Communicates administrative and organizational updates.
Promotes the company’s vision, values, and expectations.
Plans workloads and allocates resources to maximize productivity.
Monitors team performance against quality and productivity metrics.
Develops and implements team-building and employee engagement initiatives.