1

Quality Control Operations Manager Jobs in Spring, TX

This position is responsible for the receipt, storage, tracking, and management of QC samples and materials that support manufacturing, product release, stability programs, and laboratory operations.

This position is responsible for the receipt, storage, tracking, and management of QC samples and materials that support manufacturing, product release, stability programs, and laboratory operations.

... operations. Qualifications * 5+ years of QC/QA leadership experience within fabrication, oil amp ... Experience managing turnover packages and quality documentation for customer deliverables.

Quality Control Apprentice

Humble, TX · On-site

$15.75 - $20/hr

Provides verbal and/or written test results to management and production staff in a timely manner ... Teamwork with QC, operations and drivers. * Self motivated. * Positive communication with customers ...

Quality Control Manager

Houston, TX · On-site

$95K - $115K/yr

Manage and oversee all quality control functions for fabrication operations. * Ensure compliance with customer specifications, company standards, and applicable industry codes. * Develop, implement ...

This role directs daily Quality Control operations on the Range 3 threading line, ensures compliance with API, ISO 9001:2015, and connection-licensor requirements, and manages the QC inspection ...

next page

Showing results 1-20

Quality Control Operations Manager information

See Spring, TX salary details

$27.1K

$72.4K

$115.2K

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

As of Aug 10, 2026, the average yearly pay for quality control operations manager in Spring, TX is $72,369.00, according to ZipRecruiter salary data. Most workers in this role earn between $53,800.00 and $89,000.00 per year, depending on experience, location, and employer.

What is the role of a quality control operations manager?

A quality control operations manager oversees the inspection and testing of products or services to ensure they meet quality standards and regulatory requirements. They develop and implement quality assurance procedures, analyze data to identify issues, and coordinate with production teams to improve processes. Strong leadership, attention to detail, and knowledge of quality management tools like Six Sigma are essential in this role.
What are popular job titles related to Quality Control Operations Manager jobs in Spring, TX? For Quality Control Operations Manager jobs in Spring, TX, the most frequently searched job titles are:
What job categories do people searching Quality Control Operations Manager jobs in Spring, TX look for? The top searched job categories for Quality Control Operations Manager jobs in Spring, TX are:
What cities near Spring, TX are hiring for Quality Control Operations Manager jobs? Cities near Spring, TX with the most Quality Control Operations Manager job openings:
Infographic showing various Quality Control Operations Manager job openings in Spring, TX as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $72,369 per year, or $34.8 per hour.

Quality Control Supervisor - Cell Therapy

Lonza

Houston, TX • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 12 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 Supervisor - Cell Therapy
Location: This is an on-site position located in Pearland, TX.
Available shift: AM Shift, Wednesday - Saturday, 6:00 AM - 4:30 PM, supporting Quality Control operations with weekend shift differentials included.
The purpose of this role is to supervise Quality Control (QC) operations within the Cell Therapy laboratory, including oversight of personnel, assays, and equipment that support the production, release, and distribution of cell therapy products. This position ensures testing activities are executed in compliance with cGMP requirements and works closely with Quality Assurance and Operations teams to successfully implement client methods and maintain regulatory standards.
What you will get:
This is a competitive, salaried 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:
  • Supervise daily operations of the QC Cell Therapy laboratory, including oversight of personnel, assays, and equipment.

  • Review laboratory testing and records to ensure accuracy, compliance with cGMP, and adherence to company procedures.

  • Lead, coach, and mentor laboratory staff, managing performance, development, and team objectives.

  • Develop and monitor QC resource capacity and communicate constraints to management and production planning teams.

  • Write, review, and approve SOPs, protocols, sampling plans, and specifications.

  • Support and respond to audits, deviations, investigations, CAPAs, and customer complaints, ensuring timely resolution.

  • Lead technical investigations and provide guidance to team members in resolving complex quality or operational issues.

  • Collaborate cross-functionally with Quality Assurance, Program Management, and Operations teams.

What we are looking for:
  • Bachelor's degree in a scientific/STEM field required; Master's degree preferred, with 5-10 years of relevant experience in cell therapy or related industry.

  • Demonstrated knowledge of biological and cell-based assays, ddPCR, ELISA, cell count and viability, complete blood count, and potency/culture assays.

  • Experience with assay qualification, validation, and technology transfer strongly preferred.

  • Experience with document management systems, technical writing, and QC systems such as LIMS, TrackWise, and SAP.

  • Proven leadership or supervisory experience overseeing full laboratory operations in a regulated environment.

  • Strong understanding of cGMP practices and quality systems in a QC laboratory setting.

  • Ability to manage complex tasks, prioritize effectively, and lead teams in a fast-paced environment.

  • Strong communication, problem-solving, and cross-functional collaboration skills.

  • Prior audit support experience (front room/back room) 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.

What Lonza employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom