As a Quality Analyst, you’ll play a key role in ensuring products meet the highest standards of safety and quality. You’ll perform inspections, manage quality events, and support compliance with FDA, OSHA, and ISO regulations—all while working with medical devices and human tissue-based products.
Key Responsibilities:Review batch and manufacturing records for lot release.Conduct inspections of incoming materials, in-process items, and finished products using appropriate tools and methods.Maintain accurate QC documentation following Good Documentation Practices.Track and support CAPA, NCR, and Deviation records to ensure timely resolution.Coordinate environmental monitoring (EM) testing and reporting, highlighting significant trends.Assist with root cause analysis and corrective actions for quality events.Support equipment qualification, calibration, and maintenance reviews.Ensure timely review and approval of microbiology and EM testing results.Provide QMS support across CGMP departments and assist with regulatory audits.Contribute to gowning qualification and training efforts.Qualifications:
• Bachelor’s Degree in a Life Science discipline and/or in a related field
• Minimum of 0-2 years of relevant industry experience within a Medical Device, Pharmaceutical, or Tissue commercial organization preferred.
Pay and Benefits
The pay range for this position is $22.00 - $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 Vandalia,OH.
Application Deadline
This position is anticipated to close on Aug 21, 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.