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Medical Device Quality Control Jobs in Texas (NOW HIRING)

Quality Control Analyst II

Fort Worth, TX · On-site

$23 - $31/hr

The largest device company in the world - with complementary businesses in Surgical and Vision Care ... Medical, Dental, Holiday, PTO 401K matching Location: Fort Worth, TX Job Summary: Seeking a Quality ...

QC Inspector

Midlothian, TX · On-site

$19.25/hr

Oversees logs and procedures and ensures Q.C. and Production are abiding by GMP and GLP company ... medical device field (regulated industry). Experience with batch record keeping, CAPA initiation ...

QC Inspector

Midlothian, TX · On-site

$19.25/hr

Oversees logs and procedures and ensures Q.C. and Production are abiding by GMP and GLP company ... medical device field (regulated industry). Experience with batch record keeping, CAPA initiation ...

Quality Engineer

El Paso, TX · On-site

$34 - $35/hr

Medical Device Manufacturing domain Location: El Paso, TX 79912 Duration: 12 months (Possibility of ... Develop, change, and supervise Quality inspections to ensure the greatest value in quality control ...

As a Quality Control Associate, the role centers on evaluating incoming deliveries and ensuring ... Medical, Dental, 401k and more!) · Vacation / Paid Time Off Our Values · We put people first. · ...

As a Quality Control Associate, the role centers on evaluating incoming deliveries and ensuring ... Medical, Dental, 401k and more!) • Vacation / Paid Time Off Our Values • We put people first ...

As a Quality Control Associate, the role centers on evaluating incoming deliveries and ensuring ... Health and welfare benefits for eligible employees (Medical, Dental, 401k and more!) Vacation ...

Showing results 21-40

Medical Device Quality Control information

See Texas salary details

$10

$20

$31

How much do medical device quality control jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for medical device quality control in Texas is $20.01, according to ZipRecruiter salary data. Most workers in this role earn between $16.11 and $22.40 per hour, depending on experience, location, and employer.

What are some common challenges faced in a medical device quality control role, and how can I prepare for them?

Professionals in Medical Device Quality Control often face challenges such as keeping up with evolving regulatory standards, managing documentation for audits, and ensuring consistent product quality across batches. To prepare, it's helpful to develop strong attention to detail, stay updated on FDA and ISO guidelines, and build effective communication skills to collaborate with cross-functional teams like manufacturing and R&D. Being proactive in identifying potential risks and participating in continuous improvement initiatives can also help you succeed in this role.

What is the difference between Medical Device Quality Control vs Medical Device Quality Assurance?

AspectMedical Device Quality ControlMedical Device Quality Assurance
FocusInspecting and testing products to identify defectsDeveloping and maintaining quality systems and processes
ActivitiesProduct testing, inspection, samplingAudits, process validation, compliance management
CertificationsISO 13485, GMP trainingISO 13485, regulatory standards
Work EnvironmentLaboratories, manufacturing floorsQuality departments, regulatory offices

Medical Device Quality Control focuses on testing and inspecting products to ensure they meet quality standards, while Medical Device Quality Assurance emphasizes establishing systems and processes to prevent defects and ensure compliance. Both roles are essential in maintaining high-quality medical devices and often work closely within the industry.

What is medical device quality control?

Medical Device Quality Control refers to the processes and procedures used to ensure that medical devices meet safety, quality, and regulatory standards before they reach the market. This involves rigorous inspection, testing, and documentation throughout the manufacturing process to prevent defects and ensure consistent product performance. Quality control professionals work to identify issues, monitor compliance with industry regulations like ISO 13485 and FDA requirements, and help maintain the integrity of healthcare products. Their role is crucial in protecting patient safety and upholding the reputation of medical device manufacturers.

Is medical device quality control a good career?

Medical device quality control involves inspecting and testing devices to ensure they meet safety and regulatory standards, often requiring knowledge of quality management systems and industry regulations. It offers stable employment opportunities with potential for advancement and typically requires attention to detail and relevant certifications. The field is essential for patient safety and is considered a reliable career path within the healthcare manufacturing industry.

What are the key skills and qualifications needed to thrive as a medical device quality control professional?

To thrive in Medical Device Quality Control, you need a solid understanding of quality assurance principles, regulatory standards (such as ISO 13485 or FDA 21 CFR Part 820), and experience with inspection techniques, often supported by a degree in engineering or life sciences. Familiarity with tools like statistical process control (SPC) software, electronic quality management systems (eQMS), and documentation protocols is typical. Attention to detail, problem-solving abilities, and strong communication skills are essential soft skills for excelling in this role. These competencies are crucial for ensuring product safety, regulatory compliance, and maintaining the reputation of the medical device manufacturer.
What job categories do people searching Medical Device Quality Control jobs in Texas look for? The top searched job categories for Medical Device Quality Control jobs in Texas are:
What cities in Texas are hiring for Medical Device Quality Control jobs? Cities in Texas with the most Medical Device Quality Control job openings:
Infographic showing various Medical Device Quality Control job openings in Texas as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 13% Part Time, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $41,615 per year, or $20 per hour.

Quality Control Inspector

Carie Boyd Pharmaceuticals

Irving, TX • On-site

Full-time

Medical, Dental, Vision, Retirement

Re-posted 7 days ago


Job description

Company Overview
Carie Boyd Pharmaceuticals is a national 503B FDA outsourcing registered facility, enabling us to meet the needs of our patients and prescribers through a variety of office use products including but not limited to injectables, pellets, and topicals. Being a member of the Carie Boyd team means prioritizing patient needs, dedication to quality, and the drive to continue to scale our innovative business in new and diverse ways.

Responsibilities

· Perform routine tasks including:

· Sampling: personnel monitoring (PM) and environmental monitoring (EM)

· Incubate and read sample plates (TSA and SDA) per standard operating procedures

· Send off PM & EM samples to contract laboratory for identification

· Confirm growth promotion test results

· Documenting actions

· Start-Up and In-Process Checks

· Label Verification

· Assist production to verify steps critical to quality of final product

· Perform visual inspections

· Enforce good hygiene practices and aseptic techniques in GMP areas

· Successfully pass garbing qualification to enter clean rooms

· Perform aseptic processing media fill simulations for personnel certifications and garb qualifications for personnel monitoring

· Clearly communicate and enforce the company’s quality expectations outlined in standard operating procedures in a productive manner

· Prepare product to be shipped to contract testing laboratories, select appropriate testing on portals, and correspond with laboratories, as needed

· Perform GDP review of documents, as needed

· Assist production with reconciliation, as needed

· Assist Quality Management with other Quality Control duties, as needed

Has the decision-making authority for the following:

· Start-up and shut down of compounding suites

Qualifications:

· Minimum 3 years combined GMP experience in any of the following: contract manufacturing, food packaging or manufacturing, medical device, and / or 503B outsourcing facility.

· Strong documentation skills

· Cleanroom experience preferred, but not required

· Aseptic Processing and Aseptic Technique skills preferred

Confidentiality

· The employee must maintain the confidentiality of company information and, pursuant to State and Federal Law (including the Health Insurance Portability and Accountability (HIPAA) Act of 1996), protected health information.

EOE/ADA

· Carie Boyd Pharmaceuticals is an Equal Opportunity Employer. In compliance with the Americans with Disabilities Act, Carie Boyd Pharmaceuticals will provide reasonable accommodations to qualified individuals with disabilities and encourages both prospective and current employees to discuss potential accommodations with the employer.

Company Description

We specialize in compounding office-use and personalized prescription medications.