Job Description
The QC Technician - Sample Management will join a team dedicated to supporting the site's QC sampling operations. This role involves the pickup of GMP manufacturing samples and their transport to various storage locations within QC. The technician is responsible for sub-aliquoting bulk samples into smaller aliquots as dictated by GMP documents and using the site's LIMS systems to generate sample print labels and record GMP transactions. The team collaborates closely with the QC Laboratory Support functional team.
ResponsibilitiesPickup and transport samples from manufacturing areas to quality control testing/storage areas, reporting sample issues as per procedures.Receive samples into analytical and microbiology laboratories and for storage into QC Sample Management units.Manage receipt of incoming and outgoing sample shipments.Work in a biological safety cabinet with appropriate gowning to sub-aliquot bulk samples into smaller aliquots, properly label aliquots, and receive them to final storage as required.Clearly and accurately communicate the status of samples picked up for testing or send-out to cross-functional area teams.Support the team by managing inventory supplies stock.Maintain up-to-date training records and effectively train department employees in Sample Management tasks.Perform all duties in strict compliance with Standard Operating Procedures, Good Manufacturing Practices, Good Laboratory Practices, and Safety guidelines, maintaining necessary compliance status.May author Sample Management documents in the electronic document management system.May investigate and complete investigations of minor sample management deviations.Assist with additional laboratory support duties as necessary to meet departmental goals.Essential SkillsQuality assuranceQuality controlSample preparationSample managementLab preparationAdditional Skills & QualificationsHigh school diploma3 years of experience at a GMP manufacturing facility, preferably in sample management operations or sampling roleWorking experience in a cGMP Quality Control laboratory is a plusExperience with sample labeling systems and inventory management systems is a plusWorking knowledge of GMP regulations in a GMP environmentKnowledge of cGMP practices and aseptic techniquesWork Environment
The position includes weekend work and rotating shifts during the week, with hours alternating between 6am-2:30pm or 8am-4:30pm. Candidates should be comfortable working with computers, different systems, software, and Excel. This role requires working in a biological safety cabinet with some level of gowning.
Pay and Benefits
The pay range for this position is $25.00 - $27.00/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 Aug 22, 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.