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Quality Control Manager Jobs in Freeport, TX (NOW HIRING)

Completes QC Inspection Form for all completed installs. Ensure no damage happened during the installation. Reports all damage found. Equal Opportunity Employer This employer is required to notify ...

Performs Quality Control/Assurance and Field Inspections, as well as preparations of Inspection Reports and Sketches. * Complete and document inspection results by completing reports and logs ...

QAQC Manager

Clute, TX · On-site

$72K - $96K/yr

This position involves developing and implementing quality assurance and quality control processes that align with industry regulations and company policies. The QAQC Manager will lead a team of ...

... Control (product-focused) activities. Essential Functions • Internal Audits: Plan, execute, and report on internal audits of the Quality Management System (QMS) and operational processes (e.g ...

CWI

Alvin, TX · On-site

... QC programs across field and shop environments. This role demands a strong knowledge of welding ... management or leadership roles. • A performance-driven, safety-first culture built on trust ...

CWI

Alvin, TX · On-site

... QC programs across field and shop environments. This role demands a strong knowledge of welding ... management or leadership roles. • A performance-driven, safety-first culture built on trust ...

... QC programs across field and shop environments. This role demands a strong knowledge of welding ... management or leadership roles. · A performance-driven, safety-first culture built on trust ...

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Quality Control Manager information

See Freeport, TX salary details

$27.9K

$74.3K

$118.4K

How much do quality control manager jobs pay per year?

As of Aug 14, 2026, the average yearly pay for quality control manager in Freeport, TX is $74,335.00, according to ZipRecruiter salary data. Most workers in this role earn between $55,300.00 and $91,400.00 per year, depending on experience, location, and employer.

What does a quality control manager do?

A Quality Control Manager is responsible for overseeing and ensuring the quality of products or services within an organization. They develop and implement quality control procedures, inspect products, and monitor operations to ensure compliance with industry standards and regulations. Additionally, they analyze quality data, identify areas for improvement, and work closely with other departments to resolve quality issues. Their goal is to maintain high standards and minimize defects or errors in the final output.

What is the difference between Quality Control Manager vs Quality Assurance Supervisor?

AspectQuality Control ManagerQuality Assurance Supervisor
Primary FocusInspecting products and processes to identify defectsDeveloping and implementing quality systems and procedures
CertificationsISO 9001, Six Sigma, CQEISO 9001, Six Sigma, CQE
Work EnvironmentManufacturing, production lines, labsQuality departments, process improvement teams
Employer UsageManufacturers, factories, production facilitiesCompanies with formal quality management systems

Both roles focus on quality but differ in scope. The Quality Control Manager primarily inspects products to catch defects, while the Quality Assurance Supervisor develops systems to prevent defects. Understanding these differences helps in choosing the right career path or hiring focus.

What are the biggest challenges a quality control manager typically faces when implementing new quality standards?

One of the main challenges Quality Control Managers encounter is ensuring that all team members understand and consistently adhere to newly implemented quality standards. This often involves extensive training, clear documentation, and continuous monitoring to address resistance to change or misunderstandings. Additionally, balancing the need for thorough quality checks with production deadlines can be demanding, requiring strong communication and problem-solving skills to align quality goals with operational efficiency. Collaborative efforts with production, engineering, and compliance teams are essential to successfully integrate new standards while maintaining workflow.

What does a quality control manager do?

As a quality control manager, your responsibilities are to ensure that your company’s products are up to industry standards by inspecting items and overseeing the efficiency of production and manufacturing processes. Your job duties as a quality control manager include coordinating between company management and production departments, implementing strategies to maximize employee efforts, and evaluating processes on manufacturing and production lines. Your focus is on quality assurance of both processes and output to minimize the number of problems that inspectors might identify when visiting the company.

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

To thrive as a Quality Control Manager, you need expertise in quality assurance processes, analytical skills, and a background in science or engineering, often supported by a relevant degree. Familiarity with quality management systems (such as ISO 9001), statistical analysis software, and internal auditing tools is typically required. Strong leadership, problem-solving abilities, and excellent communication help drive team performance and foster a culture of continuous improvement. These skills ensure that products meet strict standards, reduce defects, and maintain customer satisfaction in a competitive market.

What are the most commonly searched types of Quality Control jobs in Freeport, TX?

The most popular types of Quality Control jobs in Freeport, TX are:

What job categories do people searching Quality Control Manager jobs in Freeport, TX look for?

The top searched job categories for Quality Control Manager jobs in Freeport, TX are:

What cities near Freeport, TX are hiring for Quality Control Manager jobs?

Cities near Freeport, TX with the most Quality Control Manager job openings:

Infographic showing various Quality Control Manager job openings in Freeport, TX as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 14% Part Time, 4% Contract, and 1% Nights. Highlights an 95% Physical, 2% Hybrid, and 3% Remote job distribution, with an average salary of $74,335 per year, or $35.7 per hour.

Full-time

Re-posted 6 days ago


Job description

See Yourself at Telix

 We are seeking a highly motivated and detailed oriented QC Specialist to join our team. The QC Specialist will execute analytical and biological testing in support of GMP manufacturing operations at our radiopharmaceutical facility. In this role you must be able to execute test methods as written, escalate any issues or deviations to management, and follow all GDP/GMP/GLP principles as applicable.

Key Accountabilities:

  • Execute lab operations to ensure compliance with GMP principles, data integrity, and good lab practices as applicable.
  • Ensure timely escalation to management for all quality events and investigations. Lab activities cover QC testing on radioactive material.
  • Experience in specific QC techniques such as HPLC, GC, TLC or Elisa, CE-SDS.
  • Continually identify areas of improvement for the lab and testing processes.
  • Independently completes all routine documentation in compliance with GDP.
  • Execute method validation activities including method development and qualification.
  • Perform review of QC testing data for accuracy to support the batch release process (including mAb and small molecule).
  • Participate / Perform laboratory investigations (OOS), deviations, Change control and implement the associated corrective/preventive actions.
  • Participation in management of QC material (consumables and chemicals)
  • Participation in management of laboratory equipment (maintenance, calibration, qualification, requalification, installation).
  • Participate in writing and updating Quality Control procedures.
  • Ensure compliance of site personnel and application of aseptic techniques and GMP principles.
  • Support FDA/Regulatory interactions for the Angleton site activities and products to ensure successful regulatory submissions and inspections.
  • Assist QA and other departments with investigations and the timely closure of investigations.
  • Understand and adhere to GMP policies and Procedures.
  • Other related duties as assigned.

Education and Experience:

  • Minimum of a Bachelor's degree in chemistry, biochemistry, biology, or related field.
  • 3+ years of experience in a laboratory role within a GMP environment.
  • Experience in GxP manufacturing operations is preferred.
  • Experience performing proper aseptic technique in controlled areas is preferred.
  • Cross functional collaboration is a requirement for the position.
  • Ability to work in a team environment and communicate effectively with diverse groups.
  • Willingness to work with radioactive materials and follow strict safety protocols.

Key Capabilities:

  • Inclusive mindset: Demonstrate an understanding and appreciation for diversity, and actively work to create an inclusive environment where everyone feels valued and respected
  • Creativity and innovation: Possess a willingness to think outside the box and come up with unique and creative solutions to challenges
  • Commitment to excellence: Take pride in your work and consistently strive for excellence in everything you do
  • Results-oriented: Driven to achieve goals and objectives, with a strong focus on delivering measurable results
  • Ethical behavior: Act with integrity and demonstrate a commitment to ethical behavior in all interactions with colleagues and stakeholders
  • Adaptability: Comfortable working in a dynamic environment, able to adjust to changing priorities, and willing to take on new challenges
  • Strong communication skills: Able to communicate effectively with colleagues and stakeholders at all levels, using clear and concise language
  • Collaboration: Work effectively as part of a team, actively sharing knowledge and expertise to achieve common goals
  • Resilience: Demonstrate the ability to bounce back from setbacks and persevere in the face of challenges
  • Continuous learning: Show a commitment to ongoing learning and professional development, continually seeking out opportunities to expand your knowledge and skills