Job Title: QC Scientist I
Job Description

Join our team and play a crucial role in ensuring the production of quality products. As a QC Scientist I, you will support the manufacturing at the STL site through tasks such as raw material sampling, inspections, and dispositions. You will also draft and revise procedures and specifications, conduct deviation investigations, and manage chemical sampling inventory. This fast-paced role requires the ability to switch tasks quickly and work efficiently in a clean room environment.

ResponsibilitiesPerform inspections and sampling on incoming materials, including bulk gasses and cell banks.Review and disposition raw materials.Gown into a clean room environment and maintain sterile techniques for raw material sampling.Order and stock sampling supplies, maintain chemical retain inventory, and manage hazardous waste disposal.Draft and revise standard operating procedures (SOPs) and other department-owned documentation.Conduct or assist in deviation investigations to ensure timely closure.Complete preventative maintenance tasks for the department.Essential SkillsExperience with HPLC, GMP, and chemistry.Proficiency with EMPOWER software.Strong aseptic technique.Ability to work with GMP standards.Additional Skills & QualificationsBachelor’s Degree in Biology, Chemistry, or another science field or 4 years of relevant experience.Quality control incoming material and/or raw material experience preferred.Minimum 1 year of cGMP experience preferred.Basic technical writing skills (i.e., SOPs, training documents, etc.).Proficiency in MS Excel, Word, and Access.Detail-oriented and results-driven.Ability to work weekends as required.Ability to read, write, and communicate in English.Ability to work independently on routine tasks and seek support for complex issues.Strong communication (verbal and written) and organizational skills.Ability to identify issues, brainstorm solutions, and utilize the Practical Process Improvements (PPI) Business System.High attention to detail and integrity.Work Environment

Monday to Friday, 8:00 AM to 4:30 PM (flexible start time up to 9:00 AM). Tasks involve bench work in a cleanroom environment. Must adhere to all GMP Safety Standards, including restrictions on hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair, etc. May require working in cold rooms/freezers at 22 degrees and using PPE (safety glasses, gowning, gloves, lab coat, ear plugs, etc.). Will work with hazardous/toxic materials. Must be able to lift 40 lbs. without assistance and handle inconsistent heavy lifting up to 50 lbs.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

Hiring diverse talent Maintaining an inclusive environment through persistent self-reflection Building a culture of care, engagement, and recognition with clear outcomes Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.