Quality Manager III

Manpower Group (USA)

Swiftwater (Monroe County)

On-site

USD 106,000 - 146,000

Full time

6 days ago
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Benefits offered by this job

Competitive pay
Professional growth opportunities
Dynamic and innovative environment

Job summary

Manpower Group (USA) is seeking a USA-Quality Manager III (Engineering) to join our client’s Quality Assurance team in Swiftwater, PA. You will lead quality validation activities across manufacturing and engineering, ensuring compliance with GxP, FDA, GMP and QSR.

The ideal candidate has a Bachelor's in Engineering or Life Sciences, 6–9 years in regulated environments, and strong CAPA leadership. This role offers a dynamic, impactful environment with opportunities for professional growth and

Qualifications

  • Bachelor's degree in Engineering, Life Sciences, or related technical discipline; Master’s degree preferred.
  • 6-9 years of experience in pharmaceutical, biopharmaceutical, or highly regulated manufacturing environments.
  • Strong background in quality validation, quality systems, and regulatory compliance within the life sciences industry.

Responsibilities

  • Lead and manage quality validation activities across manufacturing and engineering teams to ensure compliance with industry standards and regulations.
  • Support validation efforts for equipment, processes, facilities, and computerized systems, including documentation review and approval.
  • Oversee and investigate CAPA activities, ensuring root cause analysis and effective corrective actions are implemented.
  • Collaborate with cross-functional teams such as Quality, Manufacturing, Engineering, Validation, and Regulatory Affairs to drive continuous improvement initiatives.
  • Maintain comprehensive knowledge of GxP, FDA, GMP, and QSR regulations to ensure ongoing compliance and best practices.

Skills

Quality validation
Regulatory compliance
CAPA investigations
Communication
Project management

Education

Bachelor's degree in Engineering/Life Sciences
Master’s degree

Job description

Our client, a leader in the life sciences industry, is seeking a USA-Quality Manager III (Engineering) to join their team. As a USA-Quality Manager III (Engineering), you will be part of the Quality Assurance Department supporting cross-functional teams. The ideal candidate will demonstrate strong leadership, excellent communication skills, and a proactive approach to quality management, which will align successfully in the organization.

Job Title: USA-Quality Manager III (Engineering)

Location: Swiftwater, PA

Pay Range:$90.92

What's the Job?

  • Lead and manage quality validation activities across manufacturing and engineering teams to ensure compliance with industry standards and regulations.
  • Support validation efforts for equipment, processes, facilities, and computerized systems, including documentation review and approval.
  • Oversee and investigate CAPA activities, ensuring root cause analysis and effective corrective actions are implemented.
  • Collaborate with cross-functional teams such as Quality, Manufacturing, Engineering, Validation, and Regulatory Affairs to drive continuous improvement initiatives.
  • Maintain comprehensive knowledge of GxP, FDA, GMP, and QSR regulations to ensure ongoing compliance and best practices.

What's Needed?

  • Bachelor's degree in Engineering, Life Sciences, or a related technical discipline; Master’s degree preferred.
  • 6-9 years of experience in pharmaceutical, biopharmaceutical, or highly regulated manufacturing environments.
  • Strong background in quality validation, quality systems, and regulatory compliance within the life sciences industry.
  • Proven experience leading CAPA investigations and activities with a focus on root cause analysis and corrective actions.
  • Excellent communication, analytical, and problem-solving skills with the ability to manage multiple projects effectively.

What's in it for me?

  • Opportunity to work in a dynamic and innovative environment dedicated to advancing healthcare products.
  • Engage in meaningful projects that impact patient safety and product quality.
  • Collaborate with a diverse and talented team committed to excellence.
  • Develop your expertise in a regulated industry with ongoing professional growth opportunities.
  • Competitive pay rate aligned with industry standards and experience.
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