Quality Line Auditor

Actalent; Chaska (MN); On-site; USD 60,000 - 80,000; Full time

Job summary

Actalent, a leader in engineering and sciences services, is seeking a Quality Line Auditor in Chaska, MN. This role involves auditing production lines to ensure compliance with industry standards, recording results, and making necessary corrections to improve processes. Ideal candidates will have a High School Diploma and exposure to quality environments, with plenty of growth opportunities in the field.

Benefits

Medical, dental & vision benefits

401(k) Retirement Plan

Life Insurance

Short and long-term disability

Employee Assistance Program

Qualifications

• Experience or exposure to working within Quality.
• GMP experience from food, cosmetics, or pharma industries.

Responsibilities

• Conduct audits on production lines for compliance with standards.
• Record audit results accurately and initiate corrective actions.
• Support investigations of quality events.

Skills

Attention to detail

Auditing

Education

High School Diploma

Bachelor's or Associate's degree in chemistry, biology, or related science

Job description

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Job Description

As a Quality Line Auditor, you will audit production lines to ensure conformance to Batch Record requirements, product specifications, and cGMP standards. This role requires attention to detail and accurate recording of audit results, as well as initiating corrective adjustments to manufacturing processes and supporting quality event investigations. Lots of room for growth!

Job Description

As a Quality Line Auditor, you will audit production lines to ensure conformance to Batch Record requirements, product specifications, and cGMP standards. This role requires attention to detail and accurate recording of audit results, as well as initiating corrective adjustments to manufacturing processes and supporting quality event investigations. Lots of room for growth!

Responsibilities

• Conduct audits on production lines, ensuring compliance with Batch Record requirements, product specifications, and cGMP standards.
• Record audit results accurately in Batch Records.
• Initiate and document corrective adjustments to manufacturing processes and verify successful adjustments through rechecks.
• Escalate issues according to established procedures to ensure correction and containment.
• Report non-conformances immediately to the Quality Unit.
• Support investigations of quality events to resolve issues.
• Comply with Standard Work, cGMP, SOPs, and Work Instructions at all times.
• Implement and maintain standards and processes to eliminate waste within the department.
• Apply and utilize lean tools to implement improvements permanently.
• Institutionalize 5-S in all aspects of the department (Sort, Straighten, Shine, Standardize, and Sustain).
  
  

Additional Skills & Qualifications

• High School Diploma required.
• Experience or exposure to working within Quality.
• GMP experience from food, cosmetics, chemical manufacturing, pharma, or medical device industries.
• Bachelor's or Associate's degree in chemistry, biology, or related science discipline is a plus.
  
  

Pay and Benefits

The pay range for this position is $21.00 - $21.00/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 Chaska,MN.

Application Deadline

This position is anticipated to close on Jun 12, 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 [e-mail] for other accommodation options.

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Quality Assurance

• Industries

  Business Consulting and Services

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