Associate Quality Assurance

The Associate Quality Assurance position is a vital role responsible for inspecting raw materials, components, and labels, as well as sampling raw materials, labels, and sanitary utilities. This role involves generating and compiling quality data and reports, such as lot track/trace and incidents, assisting with document review, initiating incidents, coordinating and compiling general documents, and overseeing room clearance inspection. Additionally, the role provides daily guidance and support to manufacturing staff to ensure compliance with Standard Operating Procedures and Work Instructions.

Responsibilities

• Ensure regular presence on the packaging area to provide oversight to GMP operations and quality systems.
• Act as the first point of contact for production staff inquiries related to quality during operations.
• Review and approve batch record documentation and assist in sampling and inspections as required.
• Support daily operations by owning, reviewing, and approving controlled documents, including Standard Operating Procedures, Work Instructions, and Forms.
• Review and approve minor deviations.
• Adhere to safety rules and maintain a safe work environment, supporting Environmental Health and Safety corporate and site goals.

• Proficiency in GMP and quality assurance practices.
• Experience in GMP Manufacturing.
• Effective verbal and written communication skills.
• Strong interpersonal skills.
• Meticulous attention to detail and high degree of accuracy in task execution and GMP documentation.
• Ability to complete tasks autonomously and provide updates to senior management.
• Strong organizational skills, including the ability to follow assignments through to completion.

• Scientific degree in Life Sciences, Physical Sciences, Applied Engineering, or Manufacturing Technologies.
• Experience in and knowledge of GMP/GCP operations or similarly regulated industry.

This role is based in an on-site manufacturing facility equipped with a new state-of-the-art infrastructure. The work environment supports GMP operations and quality systems, requiring regular presence in the packaging area.

Pay and Benefits

The pay range for this position is $20.00 - $22.00/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 New Albany,OH.

Application Deadline

This position is anticipated to close on Jun 27, 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 ... for other accommodation options.