QC Sample Management Technician

The Sr. QC Technician – Sample Management will join a dedicated team responsible for supporting QC sampling operations at our site. The role involves handling GMP manufacturing samples, transporting them to various storage locations, and sub-aliquoting bulk samples into smaller aliquots in compliance with GMP documents. The technician will also utilize the LIMS system for generating samples, printing labels, and recording GMP transactions.

• Pickup and transport samples from manufacturing areas to quality control testing/storage areas.
• Report sample issues to the appropriate management as per procedures.
• Receive samples into analytical and microbiology laboratories and manage their storage.
• Handle incoming and outgoing sample shipments.
• Work within a biological safety cabinet with appropriate gowning to sub-aliquot bulk samples.
• Login samples to the LIMS system, label aliquots, and store them as required.
• Communicate the status of samples clearly and accurately to cross-functional teams.
• Support inventory supplies management for the team.
• Maintain up-to-date training records and train department employees in Sample Management tasks.
• Perform duties in compliance with Standard Operating Procedures, GMP, GLP, and Safety guidelines.
• Author Sample Management documents and investigate minor sample management deviations.
• Assist with additional laboratory support duties to meet departmental goals.

• Quality assurance and quality control expertise.
• Experience in sample management within pharmaceuticals and GMP environments.
• Proficiency with LIMS and sample preparation.
• Minimum of 5 years’ experience at a GMP manufacturing facility with a high school diploma, or 2-3 years with a college background.
• Working knowledge of GMP regulations and cGMP practices.
• Accurate pipetting skills and proficiency in MS Office.
• Strong communication skills and ability to multi-task.

• College education in a Science or Engineering related field (Biology, Biochemistry, or Chemistry) is preferred.
• Experience in a cGMP Quality Control laboratory is advantageous.
• Familiarity with sample labeling systems and inventory management systems.
• Experience with electronic document systems, SAP, and electronic laboratory monitoring systems.
• Ability to recognize and address developing problems.

This position requires a flexible work schedule, working Wednesday to Saturday on a 10-hour day shift from 5:30 AM to 4:00 PM, with training on a Monday to Friday day shift for the first 60 days. The role involves physical activities such as lifting up to 40 lbs independently and occasionally heavier objects with assistance. Routine push/pull/lift activities with sample carts and freezer trays are involved, and the ability to stand for extended periods is necessary. The role requires wearing gloves and other PPE to handle samples. Familiarity with various computer systems and software is essential.

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

The pay range for this position is $23.14 - $26.44/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)

This is a fully onsite position in St. Louis,MO.

This position is anticipated to close on Mar 17, 2026.

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.

Salary : $23 - $26