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Medical Device Labeling Jobs in Texas (NOW HIRING)

Axogen

Quality Analyst

Burleson, TX · On-site

Experience in an FDA-regulated environment, particularly medical device, human tissue or ... and labeling materials. * The Quality Analyst will maintain accurate and complete records of ...

Resource Label Group

Senior Staff Accountant

Plano, TX · On-site

$66K - $81K/yr

Resource Label provides products and services for the food, beverage, chemical, household products, personal care, nutraceutical, pharmaceutical, medical device, and technology industries. With ...

Resource Label Group

Be Seen First

Flexo Press Operator (1st Shift or 2nd Shift availabilities)

Dallas, TX · On-site

$21.25 - $28.25/hr

Resource Label provides products and services for the food, beverage, chemical, household products, personal care, nutraceutical, pharmaceutical, medical device, and technology industries. With ...

Resource Label Group

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Finishing Operator (Rewinder, Slitter, Seamer, etc...)

Plano, TX · On-site

$17 - $20.25/hr

Resource Label provides products and services for the food, beverage, chemical, household products, personal care, nutraceutical, pharmaceutical, medical device, and technology industries. With ...

CEDENT

Regulatory Affairs Specialist 3

Addison, TX · On-site

Provides feedback / approval of compliant labeling e.g., IFUs, marketing materials, package labels ... Qualifications * 5+ years of regulatory experience in medical device industry (equivalent industry ...

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Medical Device Labeling information

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How much do medical device labeling jobs pay per hour?

As of Aug 7, 2026, the average hourly pay for medical device labeling in Texas is $28.44, according to ZipRecruiter salary data. Most workers in this role earn between $16.11 and $36.49 per hour, depending on experience, location, and employer.

What is a medical device labeling?

A Medical Device Labeling job involves creating, reviewing, and managing labeling content for medical devices to ensure compliance with regulatory requirements. This includes instructions for use, packaging labels, and safety information for healthcare professionals and patients. Professionals in this role collaborate with regulatory, quality, and engineering teams to meet industry standards and country-specific regulations. Their work ensures that medical devices are used safely and effectively, reducing risks associated with improper usage.

What are the key skills and qualifications needed to thrive in medical device labeling?

To thrive in Medical Device Labeling, you need a strong understanding of regulatory requirements (such as FDA and EU MDR), attention to detail, and experience with technical writing or documentation, often supported by a degree in life sciences or a related field. Familiarity with labeling management systems, document control tools, and knowledge of ISO standards are key technical qualifications, and certifications like RAC can be advantageous. Strong communication, collaboration, and organizational skills set candidates apart, as these roles often involve coordinating with cross-functional teams such as regulatory, engineering, and quality assurance. These capabilities ensure labeling materials meet strict compliance standards, avoid costly errors or recalls, and support timely product launch and patient safety.

What does a medical device labeling do?

Professionals in Medical Device Labeling are responsible for creating, reviewing, and updating product labels, instructions for use, and packaging materials to ensure compliance with regulatory standards. They often collaborate closely with regulatory affairs, engineering, and quality assurance teams to gather technical product information and incorporate feedback. Daily activities may also include managing document control processes, implementing labeling changes driven by new regulations or product updates, and preparing submissions for global markets. Attention to detail and the ability to manage multiple projects simultaneously are crucial for success in this role.

What are popular job titles related to Medical Device Labeling jobs in Texas? For Medical Device Labeling jobs in Texas, the most frequently searched job titles are:
What job categories do people searching Medical Device Labeling jobs in Texas look for? The top searched job categories for Medical Device Labeling jobs in Texas are:
Medical Device Labeling jobs near you
Infographic showing various Medical Device Labeling job openings in Texas as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $59,154 per year, or $28.4 per hour.

Quality Analyst

Axogen

Burleson, TX • On-site

Other

Posted 23 days ago

Job description

Job Summary of the Quality Analyst

The Quality Analyst performs quality control (QC) inspections and dispositions of materials and products according to specifications. This role will perform QC inspection using measuring instruments (when applicable) and inspection methods. The role ensures any non-conforming materials or products that are identified are managed according to Axogen's Quality System. The Quality Analyst is responsible for following all Axogen policies and procedures to ensure compliance with applicable with FDA, state OSHA and ISO regs and standards. Employees within this role will performs a variety of tasks under limited supervision.

Requirements of the Quality Analyst

  • Bachelor's Degree in a Life Science discipline, engineering, or in a related field preferred.
  • High School Diploma and minimum of 0-2 years of relevant industry experience within a Medical Device, Pharmaceutical, or Tissue commercial organization.
  • Familiarity with ANSI/ASQ Z1.4-2003, c=0 and AQL methodologies preferred
  • Experience in an FDA-regulated environment, particularly medical device, human tissue or pharmaceutical manufacturing preferred.
  • Experience with Microsoft Excel
  • Experience writing Standard Operating Procedures and Work Instructions
  • Experience with Quality System elements for CAPA, Non-Conforming Reports (NCRs) and Deviations.

Responsibilities of the Quality Analyst

The specific duties of the Quality Analyst include but are not limited to:

  • Performs reviews of batch production records and manufacturing records as part of lot release activities.
  • Coordinates and tracks CAPA, NCR and Deviation records, ensuring tasks are completed on time.
  • Assists teams in coordination of problem solving and root cause analysis for associated quality events.
  • Provides input based on knowledge and experience with batch release requirements.
  • Provides QMS Operations related support to all CGMP departments.
  • Performs Quality Control activities at Axogen's processing or distribution sites. The Quality Analyst will be responsible for incoming material inspections, in-process inspections and finished product inspections.
  • Products include Medical Devices, sterile processed Human Tissue-Based Products, unprocessed human tissue, components supplies and labeling materials.
  • The Quality Analyst will maintain accurate and complete records of Quality Control activities, following Good Documentation Practices.
  • Provides support related to gowning qualification and training.
  • Interfaces with colleagues to ensure effective corrective and preventive actions are implemented for any recurring product/process discrepancies.
  • Assists in the review and approval of equipment qualifications.
  • Assists in the review of Calibration and Preventative Maintenance reviews.
  • Assists in hosing of onsite regulatory audits and inspections.

Location

300 Boone Road, Suites A2 & A3, Burleson, TX 76028

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