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Job Title: QC Technician - Sample ManagementJob Description

The QC Technician - Sample Management will join a dedicated team responsible for supporting the site's Quality Control (QC) sampling operations. This role involves the pickup of Good Manufacturing Practice (GMP) manufacturing samples and their transport to various storage locations within QC. The team is also tasked with sub-aliquoting bulk samples from production into smaller portions as required by GMP documentation. Additionally, they utilize the site's Laboratory Information Management System (LIMS) to generate samples, print labels, and record GMP transactions. This position works in tandem with the QC Laboratory Support functional team.

Responsibilities

+ Pickup and transport samples from the manufacturing areas to quality control testing/storage areas.

+ Report sample issues to the appropriate management as per procedures.

+ Receive samples into the analytical and microbiology laboratories.

+ Manage the receipt of incoming and outgoing sample shipments.

+ Work in a biological safety cabinet, requiring some level of gowning, to sub-aliquot bulk samples.

+ Login samples to the LIMS system, properly label aliquots, and receive them for final storage.

+ Communicate the status of samples picked up for testing to cross-functional area teams.

+ Support the team by managing inventory supplies and 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.

+ May author Sample Management documents in the site's electronic document management system.

+ May investigate and complete minor sample management deviations.

+ Assist with additional laboratory support duties as necessary to meet departmental goals.

Essential Skills

+ Quality assurance and quality control experience.

+ Experience with GMP/GLP standards and practices.

+ Proficiency in sample preparation and management.

+ Lab preparation skills.

Additional Skills & Qualifications

+ High school diploma or equivalent education.

+ 3 years of experience at a GMP manufacturing facility, preferably in sample management operations or a sampling role.

+ Experience in a cGMP Quality Control laboratory is advantageous.

+ Experience with sample labeling systems and inventory management systems is a plus.

+ Working knowledge of GMP regulations in a GMP environment.

+ Knowledge of cGMP practices and aseptic techniques.

Work Environment

The position operates on a rotating shift schedule, Monday through Friday, with shifts of either 6am-2:30pm or 8am-4:30pm. Initially, the shift will be Wednesday-Saturday with 10-hour shifts from 6am-4pm, but this may eventually rotate to an 8am start time. The role requires comfort with computer systems, including software and Excel. The work environment includes adherence to safety guidelines and the use of personal protective equipment while working in a biological safety cabinet.

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 - $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 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 [email protected] (%[email protected]) for other accommodation options.