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Job Title: Sr. QA Technician

Job Description

Perform assigned quality assurance activities to ensure compliance with applicable Standard Operating Procedures (SOPs) and current Good Manufacturing Practices (cGMPs). Ensure the timely release of materials and batches through completion of required training, document review, batch release, QA on-the-floor activities, and Acceptable Quality Levels (AQLs). Maintain operational compliance with US and international regulatory agencies and guidelines, such as FDA, EU, HC, TGA, PIC/S, ISO, USP, NRC, and cGMP.

PAY - $29

Responsibilities

+ Conduct thorough and efficient review and disposition of completed batch record documentation, ensuring adherence to Good Documentation Practices, cGMPs, and applicable local procedures.

+ Perform and oversee Quality Assurance On The Floor tasks, including AQL inspections, clearances for manufacturing areas, and providing Quality input and guidance to manufacturing personnel.

+ Manage dispositioning of finished products, raw materials/components, and intermediates through comprehensive documentation review and cross-reference of electronic quality systems.

+ Release incoming raw materials and components per applicable local procedures, including support for labeling with appropriate status indicator labels.

+ Ensure a safe and quality working environment through training, awareness, and compliance with safety/Quality guidelines and SOPs.

+ Maintain the department, premises, and equipment.

+ Complete assigned training to competently perform tasks confidently and consistently.

+ Perform all work in compliance with site safety and radiation protection guidelines.

+ Collaborate with team members to ensure timely completion of tasks, demonstrating flexibility in adjusting to changing priorities and schedules.

+ Attend mandatory trainings as required by site regulatory requirements and management.

+ Assist with quality investigations to determine root cause and perform other general duties as required by supervision.

Essential Skills

+ Proficiency in batch record review and sampling.

+ 3-5 years of quality/quality control/production experience in a cGMP facility.

+ Associate degree in life science or related field with completion of 4 college-level life science courses.

Additional Skills & Qualifications

+ Bachelor’s degree in life science or related field preferred.

Work Environment

The role operates on a shift schedule: Monday – Friday 8am – 4:30pm and Saturday - Tuesday 7 pm - 5:30 am. The position supports all areas within Hot Products manufacturing, requiring training to work with and around radioactive materials as well as gowning for aseptic areas. The work environment is approximately 50% on your feet on the floor and 50% at a desk reviewing batch records.

Job Type & Location

This is a Contract position based out of Maryland Heights, MO.

Pay and Benefits

The pay range for this position is $29.00 - $29.00/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 Maryland Heights,MO.

Application Deadline

This position is anticipated to close on Dec 19, 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.