Actalent
Job Title: Associate Quality Assurance
Job Description
This role involves inspecting raw materials, components, and labels, sampling raw materials and sanitary utilities, and generating quality data and reports. You will assist with document review, coordinate general documents, and oversee room clearance inspections. Provide guidance to manufacturing staff on compliance with Standard Operating Procedures and Work Instructions.
Responsibilities
Ensure regular presence in the packaging area to oversee GMP operations and quality systems.
Act as a first point of contact for production staff inquiries related to quality during operations.
Review and approve batch record documentation, assist in sampling and inspections as required, and manage GMP documentation in support of daily operations.
Own, review, and approve controlled documents including Standard Operating Procedures (SOPs), Work Instructions, and Forms.
Review and approve minor deviations.
Adhere to safety rules and maintain a safe work environment by supporting Environmental Health and Safety goals.
Essential Skills
Proficiency in GMP and Quality Assurance.
Experience in GMP Manufacturing.
Effective verbal and written communication skills.
Strong interpersonal skills.
Attention to detail and accuracy in task execution and GMP documentation.
Ability to complete tasks autonomously and update management.
Strong organizational skills to follow assignments through to completion.
Additional Skills & Qualifications
Scientific degree in Life Sciences, Physical Sciences, Applied Engineering, or Manufacturing Technologies.
Experience in GMP/GCP operations or similarly regulated industry is beneficial.
Work Environment
This position is based at a brand new, state-of-the-art manufacturing facility. The role requires working on a swing shift with 12-hour shifts from 10 PM to 6:30 AM, and flexibility with shifts is necessary as they may fluctuate over the duration of the contract.
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 Aug 22, 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 (%20actalentaccommodation@actalentservices.com) for other accommodation options.
Job Description
This role involves inspecting raw materials, components, and labels, sampling raw materials and sanitary utilities, and generating quality data and reports. You will assist with document review, coordinate general documents, and oversee room clearance inspections. Provide guidance to manufacturing staff on compliance with Standard Operating Procedures and Work Instructions.
Responsibilities
Ensure regular presence in the packaging area to oversee GMP operations and quality systems.
Act as a first point of contact for production staff inquiries related to quality during operations.
Review and approve batch record documentation, assist in sampling and inspections as required, and manage GMP documentation in support of daily operations.
Own, review, and approve controlled documents including Standard Operating Procedures (SOPs), Work Instructions, and Forms.
Review and approve minor deviations.
Adhere to safety rules and maintain a safe work environment by supporting Environmental Health and Safety goals.
Essential Skills
Proficiency in GMP and Quality Assurance.
Experience in GMP Manufacturing.
Effective verbal and written communication skills.
Strong interpersonal skills.
Attention to detail and accuracy in task execution and GMP documentation.
Ability to complete tasks autonomously and update management.
Strong organizational skills to follow assignments through to completion.
Additional Skills & Qualifications
Scientific degree in Life Sciences, Physical Sciences, Applied Engineering, or Manufacturing Technologies.
Experience in GMP/GCP operations or similarly regulated industry is beneficial.
Work Environment
This position is based at a brand new, state-of-the-art manufacturing facility. The role requires working on a swing shift with 12-hour shifts from 10 PM to 6:30 AM, and flexibility with shifts is necessary as they may fluctuate over the duration of the contract.
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 Aug 22, 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 (%20actalentaccommodation@actalentservices.com) for other accommodation options.