QA Tech

We are seeking a dedicated QA Tech to join our team. You will support our quality department by contributing to and maintaining environmental monitoring compliance, regulatory protocols and ensuring the integrity of our environmental controls.

• Support the quality department with building qualifications and testing equipment.
• Author reports to document and communicate results.
• Conduct laboratory analysis and monitor microbial cultures and samples.
• Investigate growth and characteristics of microscopic organisms such as bacteria, algae, and fungi.
• Supervise and conduct research on microbiological activities.
• Maintain knowledge of research methods and perform manual operations on supplies, surfaces, and materials.
• Develop and maintain validation protocols for environmental controls.
• Perform laboratory analysis on materials after sterilization.
• Test component samples, identify contamination, and initiate corrective measures.
• Study cultures of microorganisms and ensure control over moisture and temperature.
• Monitor physiological and morphological characteristics to identify microorganisms.
• Perform tests on incoming ingredients and document results.
• Prepare research papers and documents for protocols.
• Conduct audits on environmental programs and perform reviews.
• Develop testing processes for raw materials and equipment.
• Monitor finished products and investigate issues to prevent GMP problems.
• Maintain accurate records and perform tests in the laboratory.
• Develop and document microbiology laboratory processes and prepare final reports.
• Maintain purchase orders for laboratory processes and monitor inventory.
• Review product batch records and communicate issues with supervisors.
• Prepare paperwork for shipping.
• Implement new requirements and ensure compliance with the quality management system.
• Maintain professional and technical knowledge through educational workshops and networking.
• Contribute to team efforts by accomplishing related results as needed.
• Take on additional responsibilities as directed by management.

• Quality control in-process and finished products
• Process QC and document control
• FDA and Tissue Processing
• Cleanroom and aseptic technique
• Environmental Monitoring
• Microbiology and GMP knowledge

• High School Diploma or equivalent
• Minimum 2+ years of GMP experience in an aseptic environment (medical device/pharma)
• Preferred:
  Quality control experience in ISO medical device manufacturing

The position is based in a biomedical manufacturing environment. You will work in a clean room laboratory and office setting. The role requires adherence to clean room protocols and a professional dress code.

This is a Permanent position based out of Gainesville, FL.

The pay range for this position is $20.00 - $20.00/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 Gainesville, FL.

Final date to receive applications This position is anticipated to close on Mar 4, 2026.

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 actalentaccom for other accommodation options.