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64 Kpmg Qa Manager Jobs Hiring Near You

Filtration Group

Quality Assurance Manager

Louisville, CO · On-site

$120 - $140/hr

The QA Manager will be part of Operations, reporting directly to the Business Unit Leader; any conflicts between Operations and Quality will be addressed through the Group Business Unit Leader. * All ...

FullSteam

QA Manager

Bloomfield, CT · On-site

$57K - $64K/yr

Job Title: Quality Assurance (QA) Manager Cheese Department Industry: Food Distribution Center ... Comfortable working in refrigerated or cold storage environments Why Join Us * Competitive salary

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Relevante, Inc.

Quality Assurance Manager

Clifton, NJ · On-site

$107K/yr

Please review the description below and let us know if you are interested. Prioritized Must Have Skills for the Quality Assurance Manager: #1. 8+ years of quality leadership experience in ...

TFC Poultry

Quality Assurance Manager

Winchester, VA

$75K - $85K/yr

The Quality Assurance Manager will report to the Corporate Quality Assurance Manager and is responsible for managing quality assurance and quality control systems to ensure proper execution of ...

Life Signs

Quality Assurance Manager

Roanoke, TX · Remote

$56 - $62/hr

As a Quality Assurance Manager, you will play a critical role in developing and implementing ... Join us in our mission to deliver exceptional healthcare services and make a significant impact on ...

Robert Half

Quality Assurance Manager

Los Angeles, CA · On-site

$44.34 - $56.33/hr

The Medical Quality Assurance Manager coordinates the Quality Assurance and Performance Improvement (QA/QI) program, risk management activities, policy administration, and regulatory compliance ...

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JRG Partners

Quality Assurance Manager

Mobile, AL · On-site

$90K/yr

Quality Assurance Manager - Job D escription The Quality Assurance Manager ensures all regulatory, customer, and internal quality standards are met. This role leads the QA and Sanitation teams ...

Frey Consulting Group

Quality Assurance Manager

Aiken, SC · On-site

$110 - $160/hr

Quality Assurance Manager- Quality Assurance Manager will support a multi-year construction project involving significant civil, mechanical, and electrical construction, including grading, storm ...

Crescent Foods

Quality Assurance Manager

Chicago, IL

$80K - $100K/yr

ABOUT US Friendly work environment, amazing clients, and great opportunity for professional growth ... ABOUT THE ROLE The role of the Quality Assurance Manager is to be responsible for maintaining all ...

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Kelly Services

QA Manager

Randolph, MA

$100K - $120K/yr

Apply to be QA Manager today! As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Please note: The following ...

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Infographic showing various Qa Manager job openings at Kpmg in the United States as of August 2026, with employment types broken down into 95% Full Time, 4% Temporary, and 1% Contract. Highlights an 90% Physical, 5% Hybrid, and 5% Remote job distribution.

Head of US Quality Assurance

GenScript/ProBio

Pennington, NJ • On-site

$190K - $250K/yr

Full-time

Posted 13 days ago

Job description

About ProBio:

ProBio, a subsidiary of GenScript, is a global CDMO offering end-to-end services from discovery to GMP for plasmids, antibodies, and cell & gene therapies. We bring together multidisciplinary expertise to accelerate development and manufacturing through customized, and comprehensive services. ProBio has established companies in the United States, the Netherlands, South Korea, and China (Hong Kong, Shanghai, and Nanjing) and other regions to serve global customers, and has helped customers in the United States, Europe, Asia Pacific and other regions obtain more than 150 IND approvals since October 2017.

Job Scope:

The Head of Quality Assurance (QA) is responsible for leading the US Quality Assurance organization to ensure compliance with FDA, EMA, ICH, and GMP regulations. This role oversees Quality Systems, GMP Quality Assurance, regulatory compliance, inspection readiness, and quality oversight across all CDMO manufacturing operations while partnering closely with cross-functional teams to support business growth and successful customer project delivery.

Key responsibilities:

  • Lead the US Quality Assurance organization and provide strategic leadership to ensure compliance with FDA, EMA, ICH, and GMP regulations.
  • Develop, implement, and continuously improve the Quality Management System (QMS), including deviations, CAPA, change control, document control, quality risk management, and training compliance.
  • Provide QA oversight for GMP manufacturing, process development, technology transfer, validation, qualification, batch record review, and product release activities.
  • Ensure continuous regulatory compliance and maintain inspection readiness for FDA, customer, and other regulatory inspections and audits.
  • Lead customer quality activities, including Quality Agreements, customer audits, quality investigations, and issue resolution.
  • Partner with Manufacturing, Process Development, Engineering, Validation, Supply Chain, Project Management, and Commercial teams to ensure successful execution of CDMO projects while maintaining quality and compliance.
  • Drive continuous improvement initiatives to strengthen quality systems, operational excellence, and organizational effectiveness.
  • Develop, coach, and lead a high-performing Quality Assurance team by fostering talent development, succession planning, and a culture of quality and accountability.
  • Monitor quality metrics, identify risks, and implement proactive actions to continuously improve quality performance and compliance.

Qualifications:

  • Bachelor's degree in Life Sciences, Biotechnology, Pharmacy, Chemistry, or a related scientific discipline. Advanced degree (M.S. or Ph.D.) preferred.
  • 10+ years of progressive Quality leadership experience in biotechnology, pharmaceutical, or CDMO environments.
  • Demonstrated experience in Quality Management Systems (QMS), Quality Operations, and Quality Risk Management.
  • Strong experience supporting biologics, plasmid DNA, viral vectors, cell & gene therapy, or other GMP manufacturing operations.
  • Extensive knowledge of FDA, EMA, ICH, and global GMP regulations.
  • Proven experience leading regulatory inspections and customer audits.
  • Excellent leadership, communication, strategic thinking, and stakeholder management skills with the ability to influence cross-functional teams and drive continuous improvement.

The estimated pay range for the role is between $190K - $250K depending on experience and skill set

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