QC Raw Materials Wet Chemistry Analyst

Eurofins•Rensselaer, NY

7d•$23 - $24•Onsite

About The Position

At Eurofins PSS, teams provide mission-critical testing services to companies in the pharmaceutical, medical device, food, cosmetic, and consumer products industries. Eurofins PSS is part of Eurofins Scientific, an international life sciences company providing analytical testing services through a network of laboratories around the world. The QC Raw Materials Wet Chemistry Analyst performs raw material sampling and testing using wet chemistry techniques, and conducts visual and analytical testing to support the release of pharmaceutical packaging and medical device components. The role documents test results, maintains laboratory records, reviews related documentation, and writes, reviews, and updates SOPs, specifications, and other laboratory documents. It also involves calibration, verification, and maintenance of laboratory equipment, supplies, and instrumentation; compliance with cGMP, regulatory, and quality requirements; participation in training; collaboration with clients and cross-functional partners; and continuous improvement using Lean and 5S principles. This is a full-time, first-shift position, 8:00 a.m.–4:30 p.m., Monday through Friday. Candidates within commuting distance of Rensselaer, New York, and surrounding areas are encouraged to apply. The pay range is $22.50–$23.50 per hour.

Requirements

Bachelor’s degree in Life Sciences or a related field.
Hands-on laboratory testing experience with wet chemistry techniques.
Basic working knowledge of Microsoft Suite, including Word, Excel, and PowerPoint.
Authorization to work in the United States indefinitely without restriction or sponsorship.

Nice To Haves

Experience working in a fast-paced GMP environment.

Responsibilities

Perform raw material sampling and testing using wet chemistry techniques.
Conduct visual and analytical testing to support release of pharmaceutical packaging and medical device components.
Document test results, maintain laboratory records, and review associated documentation.
Write, review, and update SOPs, specifications, and related laboratory documents.
Calibrate, verify, and maintain laboratory equipment, supplies, and instrumentation.
Ensure compliance with cGMP, regulatory, and quality requirements.
Participate in training and collaborate with clients, team members, and cross-functional partners.
Drive continuous improvement initiatives using Lean and 5S principles.