Job Description Join a dynamic team dedicated to ensuring the production of quality products at the STL site. In this role, you will perform a variety of duties including raw material sampling, inspections, and dispositions. You will also draft and revise procedures and specifications, manage chemical sampling inventory, and author deviation investigations. This role is fast-paced and requires the ability to switch tasks quickly. Responsibilities
- Conduct inspections and sampling on incoming materials, including bulk gases and cell banks.
- Review and disposition raw materials.
- Support general sampling functions such as ordering and stocking supplies, maintaining chemical retain inventory, and managing hazardous waste disposal.
- Draft and revise standard operating procedures (SOPs) and other department-owned documents.
- Assist in deviation investigations to ensure timely closure.
- Complete preventative maintenance tasks for the department.
- Bachelor's Degree in Biology, Chemistry, or another science field or 4 years of relevant experience.
- Minimum 1 year of cGMP experience preferred.
- Experience with quality control of incoming materials or raw materials is preferred.
- Basic technical writing skills for SOPs and training documents.
- Proficiency in MS Excel, Word, and Access.
- Attention to detail and results-driven attitude.
- Experience with aseptic technique.
- Ability to perform heavy lifting up to 50 lbs.
- 0-1 years of experience with a degree or 4 years of GMP industry experience without a degree.
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following: Medical, dental & vision
Critical Illness, Accident, and Hospital
401(k) Retirement Plan Pre-tax and Roth post-tax contributions available
Life Insurance (Voluntary Life & AD&D for the employee and dependents)
Short and long-term disability
Health Spending Account (HSA)
Transportation benefits
Employee Assistance Program
Time Off/Leave (PTO, Vacation or Sick Leave) Workplace Type This is a fully onsite position in Saint Louis,MO. Application Deadline This position is anticipated to close on Aug 25, 2025. 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.
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 due to a disability, please email ... for other accommodation options.