Job Description
Perform assigned quality assurance activities in compliance with applicable SOPs and cGMPs. Ensure timely completion of required training, work (including document review, batch release, QA on-the-floor, AQLs), and release of materials and batches. Maintain thorough and efficient review and disposition of completed batch record documentation to adhere to Good Documentation Practices/cGMPs and local procedures.
ResponsibilitiesPerform Quality Assurance On The Floor tasks including AQL inspections, manufacturing area clearances, and providing Quality input and guidance to manufacturing personnel.Disposition finished products, raw materials, components, and intermediates through comprehensive documentation review and cross-referencing of electronic quality systems.Release incoming raw materials and components per applicable local procedures, which may include 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 department premises and equipment.Complete all assigned training to competently perform tasks confidently and consistently.Perform work in compliance with site safety and radiation protection guidelines.Collaborate with team members to ensure timely completion of assigned 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 applicable CAPAs.Perform other general duties as required by supervision.Essential SkillsThorough understanding of batch record review and sampling.Associate degree in life science or a related field with completion of 4 college-level life science courses required.3-5 years of general quality/quality control/production experience in a cGMP facility.Additional Skills & QualificationsBachelor’s degree in life science or a related field preferred.Work Environment
Shift: Sunday - Wednesday 8:00AM - 6:30PM. Support all areas within Hot Products manufacturing, including work with and around radioactive materials and gowning for aseptic areas. The role involves 50% on-floor activities and 50% desk work reviewing batch records.
Pay and Benefits
The pay range for this position is $29.00 - $30.00/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 Mar 10, 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.
Diversity, Equity & InclusionAt Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
Hiring diverse talent Maintaining an inclusive environment through persistent self-reflection Building a culture of care, engagement, and recognition with clear outcomes Ensuring growth opportunities for our peopleThe 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 process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.