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Contract Medical Device Jobs in Spring, TX (NOW HIRING)

Varsity Tutors

Biomedical Engineering Tutor

Houston, TX · Remote

$18 - $40/hr

Skilled at breaking down physiological system modeling, biomechanical analysis, and medical device ... Varsity Tutors does not contract in: Alaska, California, Colorado, Delaware, Hawaii, Maine, New ...

BPM Micosystems

Shipping Clerk

Houston, TX · On-site

$15.75 - $18.50/hr

... industrial and medical device suppliers, as well as component distributors and independent ... contract manufacturers and semiconductor manufacturers in over 42 countries. BPM programmers ...

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All JobsContract Medical Device JobsContract Medical Device Jobs in Spring, TX

Contract Medical Device information

See Spring, TX salary details

$19

$44

$85

How much do contract medical device jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for contract medical device in Spring, TX is $44.35, according to ZipRecruiter salary data. Most workers in this role earn between $31.25 and $53.03 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a contract medical device engineer?

To thrive as a Contract Medical Device Engineer, you need strong expertise in biomedical engineering, regulatory standards (like ISO 13485 or FDA 21 CFR Part 820), and product development processes, typically supported by a relevant engineering degree. Familiarity with CAD software, risk management tools, and quality management systems is essential, and certifications such as Six Sigma or PMP can be advantageous. Excellent problem-solving, project management, and communication skills help you collaborate effectively with cross-functional teams and clients. These skills and qualifications ensure devices are developed safely, efficiently, and in full compliance with industry regulations.

What is a contract medical device professional?

A Contract Medical Device professional is a specialist who works on a temporary or project-based basis within the medical device industry. These professionals may be hired by companies to assist with tasks such as regulatory compliance, product development, quality assurance, or clinical trials. Their expertise helps organizations meet regulatory requirements, ensure product safety, and bring new medical devices to market efficiently. Contract roles are ideal for companies needing specialized knowledge for a specific project or limited time frame.

What are some common challenges faced by contract medical device professionals and how can they be addressed?

Contract medical device professionals often navigate challenges such as adjusting quickly to different company cultures, learning new product lines rapidly, and staying up-to-date with evolving regulatory standards. To address these, it's helpful to maintain strong communication with team members, proactively seek clarification on project expectations, and invest time in ongoing professional development. Being adaptable and building a network of industry contacts can also support success in various contract assignments.
What are the most commonly searched types of Medical Device jobs in Spring, TX? The most popular types of Medical Device jobs in Spring, TX are:
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What cities near Spring, TX are hiring for Contract Medical Device jobs? Cities near Spring, TX with the most Contract Medical Device job openings:
Contract Medical Device jobs near you

Sr. Quality Engineer-Metrology

BioPharma Consulting JAD Group

Houston, TX • On-site

Full-time

This job post has expired 1 day ago. Applications are no longer accepted.

Job description

We are seeking a highly experienced Senior Quality Engineer with 5+ years of expertise in metrology and calibration systems within a regulated manufacturing environment. The ideal candidate will be capable of assessing the current state of the calibration program, identifying compliance and technical gaps, performing risk‑based impact assessments, and leading a comprehensive remediation effort that withstands internal audits, customer audits, and regulatory inspections.

Key Responsibilities

  • Lead or support remediation of metrology and calibration programs in regulated industries (medical device, pharmaceutical, aerospace, etc.).
  • Conduct gap assessments, identify compliance deficiencies, and develop sustainable remediation plans.
  • Address audit observations, CAPAs, and regulatory findings related to calibration systems.
  • Improve calibration compliance, reduce overdue calibrations, and strengthen calibration governance.
  • Apply deep knowledge of dimensional metrology, measurement system analysis, and calibration principles.
  • Demonstrate strong understanding of measurement uncertainty, tolerance analysis, traceability, guard banding, and calibration intervals.
  • Perform fitness‑for‑use evaluations and apply decision rules (PAR, TMU, Z%, RSS guardbanding).
  • Support calibration and troubleshooting of equipment such as:
    • Ultrasonic welders
    • Pneumatic presses
    • Vision systems
    • Automated assembly cells
    • Injection molding equipment
    • Packaging equipment (FFS, band sealers, shuttle sealers)
    • CMMs
    • Force/torque systems
    • Leak and flow instruments
    • Environmental monitoring equipment
  • Evaluate out‑of‑tolerance (OOT) conditions and determine product/validation impact.
  • Ensure compliance with applicable standards and regulations, including:
    • ISO 13485
    • 21 CFR Part 820 / QMSR
    • ISO 17025 principles
    • 21 CFR Part 11 (as applicable)
    • Gage R&R and MSA methodologies
  • Author and revise calibration procedures, deviations, CAPAs, impact assessments, and risk assessments.
  • Support internal, customer, and regulatory audits.
  • Independently assess calibration events using risk‑based methodologies.
  • Conduct OOT/OOC impact assessments and analyze historical calibration data.
  • Apply statistical tools (Minitab or equivalent) to evaluate measurement trends and equipment performance.
  • Justify disposition decisions using objective evidence and scientific rationale.
  • Lead remediation and improvement initiatives across Engineering, Manufacturing, Validation, Laboratory Operations, and Quality.
  • Manage project timelines, prioritize activities, and ensure deliverables are met.
  • Train personnel, influence stakeholders, and implement lasting improvements to metrology processes and procedures.

Requirements

Qualifications

  • Bachelor’s degree in Engineering, Quality, Metrology, or a related technical discipline.
  • 5+ years of experience in metrology, calibration systems, or equipment quality engineering within a regulated industry (medical device, pharmaceutical, biotech, aerospace, or similar).
  • Demonstrated experience leading calibration program remediation, including gap assessments, CAPA execution, and audit response.
  • Strong technical expertise in dimensional metrology, measurement system analysis (MSA), and calibration principles.
  • Advanced understanding of:
    • Measurement uncertainty
    • Tolerance analysis
    • Traceability
    • Guard banding
    • Calibration intervals
    • Fitness‑for‑use decision rules (PAR, TMU, Z%, RSS)
  • Hands-on experience with a wide range of manufacturing and inspection equipment, including:
    • Ultrasonic welders
    • Pneumatic presses
    • Vision systems
    • Automated assembly cells
    • Injection molding equipment
    • Packaging equipment (FFS, band sealers, shuttle sealers)
    • CMMs
    • Force/torque systems
    • Leak and flow instruments
    • Environmental monitoring equipment
  • Strong knowledge of quality system regulations and standards, including:
    • ISO 13485
    • 21 CFR Part 820 / QMSR
    • ISO 17025 principles
    • 21 CFR Part 11 (as applicable)
    • Gage R&R and MSA methodologies
  • Proven ability to author and revise calibration procedures, deviations, CAPAs, impact assessments, and risk assessments.
  • Experience supporting internal, customer, and regulatory audits.
  • Strong analytical and statistical skills; proficiency with Minitab or equivalent tools.
  • Demonstrated ability to perform OOT/OOC impact assessments and data‑driven decision making.
  • Strong project management skills with the ability to lead remediation efforts, prioritize tasks, and meet aggressive timelines.

Preferred Qualifications

  • Experience working in medical device metrology programs.
  • Familiarity with cleanroom environments and standards:
    • ISO 9001
    • ISO 13485
    • ISO 17025
    • ISO 10012
    • ANSI/NCSL Z540
  • Working knowledge of:
    • ProCal V5
    • Siemens Teamcenter

Benefits

  • Shift: Administrative
  • Contract Duration: 12 months
  • Location: Onsite