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Quality Assurance Operations Manager Jobs in Spring, TX

Lonza

Quality Assurance Specialist IV

Houston, TX

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Quality Assurance Specialist IV Location: This is an on-site position located in Pearland, TX. ... resolve operational issues. Support deviation management, CAPA development, investigation ...

Lonza

Quality Assurance Specialist IV

Houston, TX · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... operational issues. • Support deviation management, CAPA development, investigation activities, and change control processes as either record owner or QA approver. • Review and approve GMP ...

Houston Precision Fasteners

Be Seen First

Quality Assurance Engineer

Houston, TX · On-site

$80K - $90K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • PTO

... operations. · Participate in New Product Introduction meetings with internal personnel and ... Present to Top Management results of data analysis, corrective actions and improvement ...

Houston Precision Fasteners

Be Seen First

Quality Assurance Engineer

Houston, TX · On-site

$80K - $90K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • PTO

... operations. · Participate in New Product Introduction meetings with internal personnel and ... Present to Top Management results of data analysis, corrective actions and improvement ...

KBR, Inc.

Quality Assurance Engineer

Houston, TX · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Quality Assurance Engineer is responsible for developing, improving, and maintaining quality systems and processes to ensure aerospace products and operations meet customer, regulatory, and internal ...

Relative Dynamics

Quality Assurance Engineer

Houston, TX · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Support supplier quality management operations, requirements flow down, compliance verification ... Experience in manufacturing, assembly, and/or quality assurance of space flight hardware * Familiar ...

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Quality Assurance Operations Manager information

See Spring, TX salary details

$33.8K

$105.1K

$159.3K

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

As of Aug 16, 2026, the average yearly pay for quality assurance operations manager in Spring, TX is $105,073.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,900.00 and $128,600.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a quality assurance operations manager, and why are they important?

A Quality Assurance Operations Manager needs expertise in quality control principles, regulatory compliance, and process improvement, often supported by a degree in a relevant field and experience in quality management systems. Familiarity with tools like ISO standards, Six Sigma, CAPA systems, and audit software is typically required. Strong leadership, attention to detail, and effective communication enable success in managing teams and driving quality initiatives. These skills ensure products consistently meet standards, minimize risk, and enhance organizational efficiency.

What is quality assurance in operations management?

Quality assurance in operations management involves systematic processes to ensure products or services meet specified standards and customer expectations. It includes activities like process audits, defect prevention, and continuous improvement, often supported by tools such as quality management systems (QMS) and certifications like ISO 9001. The role of a Quality Assurance Operations Manager is to oversee these activities to maintain consistent quality across operations.

What does a quality assurance operations manager do?

A Quality Assurance Operations Manager oversees the quality assurance processes within an organization to ensure that products or services meet established standards of quality, reliability, and performance. They develop and implement quality control policies, lead a team of QA specialists, and coordinate with other departments to address quality issues. Their responsibilities also include conducting audits, analyzing quality data, and driving continuous improvement initiatives to enhance product or service quality.

What is the difference between Quality Assurance Operations Manager vs Quality Assurance Specialist?

AspectQuality Assurance Operations ManagerQuality Assurance Specialist
CredentialsTypically requires a bachelor's degree in quality management, engineering, or related field; certifications like ASQ CQE or CQA are commonUsually holds a bachelor's degree in quality assurance, engineering, or related area; certifications like ASQ CQA are beneficial
Work EnvironmentOversees QA teams, manages processes, and ensures compliance across departments in manufacturing or service industriesPerforms testing, inspections, and audits to ensure product or service quality, often working hands-on with products or data
Employer & Industry UsageFound in manufacturing, healthcare, and tech companies, focusing on operational quality managementCommon in manufacturing, software, and healthcare sectors, focusing on quality testing and compliance

The main difference is that the Quality Assurance Operations Manager oversees QA processes and teams, focusing on operational management, while the Quality Assurance Specialist performs hands-on testing and inspections to ensure quality standards are met.

What are some common challenges a quality assurance operations manager faces when implementing new quality protocols across teams?

One of the main challenges Quality Assurance Operations Managers encounter is ensuring consistent adoption of new protocols across multiple departments. Resistance to change, varying levels of quality awareness, and differences in team workflows can make standardization difficult. Effective communication, comprehensive training, and continuous monitoring are essential to address these challenges. Collaborating closely with production, engineering, and regulatory teams helps to preempt potential issues and foster a culture of quality throughout the organization.

What job categories do people searching Quality Assurance Operations Manager jobs in Spring, TX look for?

The top searched job categories for Quality Assurance Operations Manager jobs in Spring, TX are:

What cities near Spring, TX are hiring for Quality Assurance Operations Manager jobs?

Cities near Spring, TX with the most Quality Assurance Operations Manager job openings:

Quality Assurance Operations Manager jobs near you

Quality Assurance Specialist IV

Lonza

Houston, TX

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 4 days ago

Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

25th of 86 rated pharmaceutical

Job description

Quality Assurance Specialist IV
Location: This is an on-site position located in Pearland, TX.
Available shift: 8:00 am to 5:00 pm Monday through Friday.
The Quality Assurance Specialist IV serves as a senior quality representative supporting Cell Therapy manufacturing operations and associated support functions. This role provides Quality Assurance oversight for GMP manufacturing activities, quality systems, investigations, and documentation while ensuring compliance with cGMP regulations and company procedures. The position partners closely with Manufacturing, Quality Control, and Quality Systems teams to support production activities, review and approve quality records, drive issue resolution, and maintain a state of inspection readiness. The role also serves as a key quality resource for internal and external stakeholders while supporting continuous improvement initiatives and product quality objectives.
What you will get:
This is a competitive, salary position. In addition, below you will find a comprehensive summary of the benefits package we offer:
Performance-related bonus.
Medical, dental and vision insurance.
401(k) matching plan.
Life insurance, as well as short-term and long-term disability insurance.
Employee assistance programs.
Paid time off (PTO).
Compensation for this role will be determined by the candidate's qualifications, skills, experience, and relevant knowledge.
What you will do:
Perform Quality Assurance review and approval of GMP documents, including master documents, executed production records, deviations, investigations, CAPAs, change controls, and controlled documents.
Provide QA support and oversight for Cell Therapy manufacturing operations to ensure compliance with cGMP requirements and site procedures.
Conduct QA walkthroughs and on-the-floor quality oversight activities; partner with manufacturing and support groups to identify, investigate, and resolve operational issues.
Support deviation management, CAPA development, investigation activities, and change control processes as either record owner or QA approver.
Review and approve GMP documentation generated by Manufacturing, QC, Material Management, Facilities & Engineering, and other supporting departments.
Perform material release and lot disposition activities in accordance with approved procedures and quality requirements.
Represent Quality Assurance in internal and external client meetings to ensure quality expectations and regulatory requirements are met.
Track and manage quality system records to support timely closure and compliance objectives.
Support internal audits, customer audits, regulatory inspections, and inspection readiness initiatives.
Provide QA support regarding aseptic manufacturing activities, including gowning, cleanroom operations, and aseptic processing requirements as needed.
Collaborate cross-functionally with Manufacturing, QC, and Quality Systems teams to drive compliance, process improvements, and operational excellence.
Perform other duties as assigned.
What we are looking for:
Experience from 5+ years in Quality Assurance within a GMP-regulated biopharmaceutical, cell therapy, or related manufacturing environment.
Bachelor's degree in Biology, Biotechnology, Life Sciences, Engineering, or a related scientific discipline is required.
Experience supporting GMP manufacturing operations is required.
Experience in Cell Therapy manufacturing is strongly preferred.
Demonstrated experience with deviations, investigations, CAPAs, and change controls is required.
Knowledge of aseptic processing, cleanroom operations, and gowning requirements is required.
Experience with TrackWise and electronic quality management systems is preferred.
Strong understanding of cGMP requirements, FDA regulations, quality systems, and compliance expectations.
Experience reviewing and approving GMP documentation and quality records.
Strong technical writing, root cause analysis, risk management, and problem-solving skills.
Ability to work independently, prioritize multiple activities, and make sound quality decisions in a fast-paced manufacturing environment.
Strong communication and collaboration skills with the ability to effectively partner across multiple departments.
Proficiency in Microsoft Office applications and quality-related systems such as Documentum, SAP, and LIMS is preferred.
About Lonza:
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now.

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