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Process Engineer Medical Device Jobs in Texas (NOW HIRING)

Viant

Process Engineer

San Antonio, TX · On-site

Viant is a global medical device partner providing design, development, manufacturing, and assembly services through capabilities in materials, plastics, metals, extrusion, and automation. With ...

medplast

Process Engineer

San Antonio, TX · On-site

Viant is a global medical device partner providing design, development, manufacturing, and assembly services through capabilities in materials, plastics, metals, extrusion, and automation. With ...

medplast

Process Engineer

San Antonio, TX · On-site

Viant is a global medical device partner providing design, development, manufacturing, and assembly services through capabilities in materials, plastics, metals, extrusion, and automation. With ...

medplast

Process Engineer

San Antonio, TX

Viant is a global medical device partner providing design, development, manufacturing, and assembly services through capabilities in materials, plastics, metals, extrusion, and automation. With ...

CooperCompanies

Senior Process Engineer

Stafford, TX · On-site

$90K - $117K/yr

The Senior Process Engineer is a key individual contributor responsible for the development ... supporting medical device products. This role partners cross-functionally with Quality ...

Cooper Companies

Senior Process Engineer

Stafford, TX

$90K - $117K/yr

The Senior Process Engineer is a key individual contributor responsible for the development, optimization, validation, and sustainment of manufacturing processes supporting medical device products.

Wood Plc

Process Engineer

Bishop, TX

In this role you will help lead in the management of the site's pressure relieving device systems and will provide other process engineering support of operating units in an active chemical ...

BSI Prof Serv EHS West

Medical Device Tutor

Italy, TX · On-site

About The Role As a Medical Device Tutor, you will work closely with numerous industry sectors ... Knowledge of the creation of technical files, process validation, and post-market surveillance and ...

BSI Group

Medical Device Tutor

Italy, TX · On-site

About The Role As a Medical Device Tutor, you will work closely with numerous industry sectors ... Knowledge of the creation of technical files, process validation, and post-market surveillance and ...

Aerotek

Medical Device Assembler

Dallas, TX

$22 - $24/hr

Job Title: Medical Device Assembler Join a dynamic team dedicated to assembling revolutionary ... We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing ...

Creation

Senior Process Engineer

Dallas, TX

$102K - $133K/yr

The Senior Process Engineer (SME) is a critical member of Creation's Customer Focused Team ... AS9100 and /or medical device manufacturing experience is an asset. * Ability to interpret an ...

Creation Technologies LP

Senior Process Engineer

Dallas, TX · On-site

$102K - $133K/yr

The Senior Process Engineer (SME) is a critical member of Creation's Customer Focused Team ... AS9100 and /or medical device manufacturing experience is an asset. * Ability to interpret an ...

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See Texas salary details

$46.1K

$85.7K

$132.8K

How much do process engineer medical device jobs pay per year?

As of Jul 7, 2026, the average yearly pay for process engineer medical device in Texas is $85,729.00, according to ZipRecruiter salary data. Most workers in this role earn between $69,400.00 and $96,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Process Engineer Medical Device position, and why are they important?

A Process Engineer in Medical Devices typically requires a degree in engineering (such as chemical, biomedical, or mechanical engineering) and experience with manufacturing processes, quality systems, and regulatory compliance. Familiarity with tools like CAD software, statistical analysis programs, lean manufacturing techniques, and knowledge of standards such as ISO 13485 are common requirements. Strong problem-solving abilities, project management skills, and excellent communication facilitate successful interactions with cross-functional teams. These skills ensure efficient, high-quality, and compliant manufacturing processes critical to patient safety and company success.

What are some common projects or responsibilities I might take on as a Process Engineer in the medical device industry?

As a Process Engineer in the medical device industry, you'll commonly work on projects such as optimizing manufacturing processes, implementing new technologies, and ensuring compliance with strict quality and regulatory standards. Your daily tasks may include designing and validating production methods, troubleshooting process issues, and collaborating closely with quality assurance, R&D, and production teams. You may also be involved in documentation, process scale-up for new products, and continuous improvement initiatives. The role is highly collaborative, requiring you to coordinate with both technical and non-technical staff to meet quality, efficiency, and regulatory goals.

What is a Process Engineer Medical Device job?

A Process Engineer in the medical device industry is responsible for designing, implementing, and optimizing manufacturing processes to ensure efficiency, quality, and compliance with regulatory standards. They work to improve production procedures, troubleshoot issues, and develop new process technologies. Their role involves collaborating with cross-functional teams, such as design, quality, and regulatory, to ensure medical devices meet industry requirements. Additionally, they analyze data, validate processes, and support continuous improvement initiatives to enhance product reliability and manufacturing scalability.

What are popular job titles related to Process Engineer Medical Device jobs in Texas? For Process Engineer Medical Device jobs in Texas, the most frequently searched job titles are:
What job categories do people searching Process Engineer Medical Device jobs in Texas look for? The top searched job categories for Process Engineer Medical Device jobs in Texas are:
Process Engineer Medical Device jobs near you
Infographic showing various Process Engineer Medical Device job openings in Texas as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $85,729 per year, or $41.2 per hour.
Process Engineer

Process Engineer

Viant

San Antonio, TX • On-site

Full-time

Re-posted 11 days ago

Job description

About the company:
Viant is a global medical device partner providing design, development, manufacturing, and assembly services through capabilities in materials, plastics, metals, extrusion, and automation. With nearly 6,000 employees across 24 locations worldwide, it delivers high-quality, life-enhancing products with the scale and expertise to bring devices to market efficiently. Learn more at Viant Medical's website or on LinkedIn.
About the role:
The Process Engineer is responsible for leading advanced process development across the full lifecycle of molding and manufacturing programs, applying expert scientific molding and cavity pressure control principles to deliver robust, optimized processes. This role provides hands-on technical leadership for tooling design, process validation (IQ, OQ, PQ), and DOE execution, while supporting NPI, sustaining engineering, and business development initiatives. The Principal Process Engineer serves as a key technical interface between Viant, customers, tool shops, and internal teams to ensure regulatory compliance and best-in-class production outcomes.
  • Work Model: Remote
  • Travel Requirement: 75% travel across Viant locations in the US but mainly to Costa Rica, Tijuana, BC, and Vega Baja, PR sites.

What you'll do:
  • Lead the process development cycle
  • Evaluate processes for robustness, accuracy, and optimization
  • Initiate improvement projects
  • Quality/Metrology support: Assist site QE on KPI/KPO impacting part quality and process control
  • Partner with GTS/Site Tooling Engineer on design requirements
  • Partner with Tool Engineer on design and development requirements
  • Support business development by selling tooling solutions and resolving processing issues
  • Support corrective actions, re-validations, and tool/process optimization
  • Oversee process development through I.Q. and O.Q. runs; report required
  • Complete other related projects and tasks assigned
  • Demonstrate expert knowledge and performance
  • Apply scientific molding (Decoupled 2 and Decoupled 3)
  • Expert in cavity pressure monitoring and control (RJG)
  • Join technical reviews with customers and mold shops
  • Support DFM and tool design reviews with Tool Engineers
  • Support molding cell development and execution
  • Support EOAT design and fabrication
  • Manage mold shop deliverables and expectations (SIM reports)
  • Confirm receiving-site requirements (press/shot size/tonnage/special sequence) and machine capability studies
  • Develop processes, review Moldflow data for start-up and debug
  • Travel to customer sites, tool shops, and Viant facilities as needed; trip report required
  • Prepare, track, and communicate Process DOEs, report results and recommendations
  • Manage multiple concurrent projects (minimum 20 active)

Requirements:
Education:
  • Bachelor of Science Degree in Engineering or related plastics discipline or 4-year engineering degree or equivalent completion of a 4,000 hour or 2-year process engineering apprenticeship.
  • Certification from a school in advanced molding or RJG Master Molder 2 (or equivalent).
  • Certification in Basic Mold Flow (or equivalent) is a plus.
  • Certification in Master Molding 3 is a plus.

Years of Experience:
  • 10+ years of experience in processing and in a molding environment, process development, qualification, validation of molds, etc.

Job Knowledge :
  • Extensive knowledge and able to train in: processing and process development techniques in scientific molding principles (MM2 skill level)
  • Plastics-Injection Molding; LSR (preferred)
  • Excel, PowerPoint, Word, and general computer skills; SolidWorks (drawing); 3D printing/3D software (preferred)
  • Some knowledge in FDA, QSR, and ISO 13485 medical device regulations and standards.
  • Understanding of statistics, Cp & Cpk studies for process. I.Q., O.Q. and P.Q. requirements
  • Strong understanding of DOE methods and implementation
  • Expert knowledge of cavity pressure technologies and advanced control principles
  • Familiarity with the various engineering grade thermoplastic resins and Mold Flow analysis."

Additional Requirements:
  • Authorized to work in the U.S.
  • Spanish proficiency
  • Ability to travel up to 75% to Viant sites (U.S., Costa Rica, Tijuana, and Vega Baja, PR)

Viant is a global medical device design and manufacturing services provider that partners and innovates with customers to provide the highest quality, life enhancing medical devices. We do this through our depth and breadth of capabilities, end-to-end integration, technical expertise, and relentless focus on our customers and on operational excellence. With nearly 6,000 associates across 24 locations worldwide, we offer a unique combination of small-company service and attention with big-company resources. For more information, visit viantmedical.com or follow us on LinkedIn.
Viant provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, gender, sexual orientation, national origin, age, disability, marital status, amnesty, or status as a covered veteran in accordance with applicable federal, state, and local laws. Viant complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities.

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