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Full Time Quality Assurance Operations Manager Jobs

Alphazyme

Manager, QA Operations

Jupiter, FL · On-site

The Manager, QA Operations is responsible for the implementation of policies and procedures to ensure adherence to production quality standards and oversight of the Company's electronic ISO 13485 ...

Abzena Inc.

QA Operations Supervisor

San Diego, CA · On-site

$100K - $120K/yr

The Quality Assurance Operations Supervisor is responsible for leading Quality oversight activities ... The supervisor serves as a key operational leader, managing shift resources, supporting technology ...

Simos

Quality Assurance Manager

Grand Rapids, MI · On-site

$40.75 - $43.25/hr

... QA operations, ensuring regulatory compliance, and driving continuous improvement initiatives ... Flexible Spending Accounts * $40.75 - $43.25/hour Employment Type & Shifts * Full Time * Direct ...

BakeMark

Be Seen First

Quality Assurance Supervisor

Elyria, OH · On-site

$65K/yr

This role involves supervising daily QA operations, implementing quality management systems, and driving continuous improvement initiatives across the organization. ESSENTIAL DUTIES AND ...

Axogen

Manager, Quality Assurance

Vandalia, OH · On-site

The Manager, Quality Assurance collaborates closely with Operations to provide Quality Assurance (QA) support, ensuring that the organization maintains high standards of compliance and fosters a ...

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How much do full time quality assurance operations manager jobs pay per year?

As of Sep 11, 2026, the average yearly pay for full time quality assurance operations manager in the United States is $118,074.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,000.00 and $144,500.00 per year, depending on experience, location, and employer.

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Manager, QA Operations

Jupiter, FL • On-site

Alphazyme
Biotechnology Research and Development • 11 - 50 employees
Learn more about Alphazymeexternal

Full-time

Re-posted 17 days ago

Job description

Your next role as a Miracle Maker 

Maravai LifeSciences is seeking a #MiracleMaker to join our Quality Assurance team as a Manager, QA Operations. The Manager, QA Operations is responsible for the implementation of policies and procedures to ensure adherence to production quality standards and oversight of the Company's electronic ISO 13485:2016 Quality Management System.  The Quality Assurance Manager is expected to ensure compliance with operational, statutory, and regulatory requirements in support of the Company's business objectives. 

How you will make an impact: 

  • Manage Quality Assurance department day to day operations, including implementing training and performance management activities for direct reports 
  • Implement and periodically evaluate documentation and policies to ensure continuous compliance to the quality, integrity, and efficiency standards set by the organization, the ISO 13485:2016 standard, and other statutory and regulatory requirements.  
  • Collaborate with management to identify and fill documentation and process gaps required to maintain QMS compliance and address CAPAs, NCs, and audit findings 
  • Author and maintain quality documentation, oversee timely reviews of all work instructions associated with production and quality control activities 
  • Support Quality Control with customer complaints and Out of Specification (OOS) investigations 
  • Actively participate on core teams and provide deliverables from QA on quality processes and required documentation practices from production through testing and shipment  
  • Implement and track metrics to monitor performance associated with Quality management 
  • Identify and implement efficiency improvement initiatives in support of Continuous Improvement 
  • Facilitate proactive solutions by collecting and analyzing quality data 
  • Manage Internal Audit Program 
  • Perform other functions and duties as required  

 The skills and experience that you will bring: 

  • Bachelor's Degree in Life Science, Biology, Chemistry or Pharmaceutical or related discipline 
  • 3-5 years of managerial experience in non-academic biotechnology related industry 
  • 1-3 years of supervisory experience 
  • Proven experience with: ISO 13485 certification, federal regulations 21 CFR 820 and 21 CFR Part 11 
  • Industry experience in a Good Manufacturing Practice (GMP) environment is preferred 
  • Thorough knowledge of analytical testing industry standards and quality assurance methodologies 
  • Excellent communication and presentation skills are required 
  • Demonstrated scientific "problem solving" skills, translated into consultative selling process where the "win" is for both the client and the company 
  • Ability to participate with others as a member of the team to ensure that demanding and difficult projects are handled smoothly and cooperatively to enhance success of project and maintain strong relationships within all parts of company  
  • Proven ability to thrive in a start-up/change oriented environment 
  • Great attention to detail and results driven approach 
  • Self-starter with ability to organize and prioritize a diverse set of responsibilities to ensure that focus on growth and success of company is achieved 
  • Proven coaching, mentoring, team building and leadership skills 

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