QC Laboratory Support Technician

Qc Laboratory Support Technician

As a QC Laboratory Support Technician, you will be part of a dedicated team focused on supporting QC Laboratory Operations. Your role will involve managing analytical testing samples, backups, standards, assay controls, laboratory reagents, and other inventory management tasks. You will facilitate laboratory operations by providing essential support that enhances the efficiency and effectiveness of testing processes. Please note, this position does not involve hands-on testing of product samples.

Responsibilities:

• Collaborate with laboratory analysts to ensure all required supplies are available prior to testing initiation.
• Utilize various information management systems to manage inventory and logistics for samples, standards, assay controls, critical reagents, and consumables.
• Support laboratory analysts with non-billable activities including glassware handling, labeling, waste management, and laboratory inspections.
• Assist in creating and monitoring purchase requisitions and orders to fulfill laboratory inventory requirements.
• Collect, wash, and redistribute laboratory glassware.
• Manage transport of laboratory waste to designated EHS drop-off areas.
• Assist with preventative maintenance tasks within the laboratory as appropriate.
• Provide additional laboratory support duties as necessary to meet departmental goals.

Essential Skills:

• Quality assurance and quality control experience.
• Experience in GMP/GLP within a laboratory or pharmacy technician setting.
• Sample preparation and management skills.
• Lab preparation expertise.
• Attention to detail for cleaning glassware and documentation.

Additional Skills & Qualifications:

• Minimum of a High School Diploma; Associate's or STEM degree preferred.
• 0-3 years of experience in a GMP regulated environment.
• 1-3 years of experience in a GLP/GMP lab or GMP manufacturing facility in a lab or quality role.
• Experience in a cGMP Quality Control laboratory is a plus.
• Proficiency with sample labeling and inventory management systems is advantageous.
• Working knowledge of GMP regulations and cGMP practices.

Work Environment:

This position operates on a Monday-Friday schedule with hours from 8:00 am to 4:30 pm. The role requires comfort in using computers and various systems, including software and Excel. The environment supports a contract-to-hire opportunity contingent on performance.

Job Type & Location:

This is a Contract to Hire position based out of St. Louis, Missouri.

Pay and Benefits:

The pay range for this position is $25.00 - $25.00/hr. Eligibility requirements apply to some benefits and may depend on your job 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 St. Louis, MO.

Application Deadline:

This position is anticipated to close on Oct 24, 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 actalentaccommodation@actalentservices.com for other accommodation options.