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Manager Medical Device Operations Jobs in Texas (NOW HIRING)

Crown Medical, Inc.

Medical Device Rep

Austin, TX · On-site

$82K - $113K/yr

Medical Sales Territory Representative - Entry Level We are a leading Medical Device and Equipment ... Ability to effectively manage a physician-based customer base * Skills to communicate clinically ...

Vitrolife Group

Houston, TX (Preferred) Territory: TX, OK, KS, NM, CO, UT, NV, AR Travel: 70%+ Position Summary Vitrolife is seeking a highly motivated Medical Device & Equipment Account Manager to join our North ...

Houston Dose

Medical Device Integration Analyst

Houston, TX · On-site

$80 - $110/hr

... enhance operational efficiencies. Responsibilities may include creating, documentation and ... Demonstrated project management skills * Ability to problem solve and generate innovative solutions ...

Astura Medical

Medical Device Audit Inspector

Irving, TX · On-site

$20 - $21/hr

As a Medical Device Audit Inspector, you will support various inventory activities within the ... This position works from the direction of the Receiving Manager to process inventory. Your work ...

Astura Medical

Medical Device Audit Inspector

Irving, TX · On-site

$20 - $21/hr

This position works from the direction of the Receiving Manager to process inventory. Your work ... Familiarity with medical device handling, sterilization, or reprocessing workflows * Strong ...

Astura Medical

Medical Device Audit Inspector

Irving, TX · On-site

$20 - $21/hr

This position works from the direction of the Receiving Manager to process inventory. Your work ... Familiarity with medical device handling, sterilization, or reprocessing workflows * Strong ...

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Manager Medical Device Operations information

What is a manager medical device operations?

A Manager Medical Device Operations oversees the daily activities and processes involved in manufacturing, distributing, and maintaining medical devices. They ensure that operations comply with regulatory standards, manage teams, and work to optimize efficiency, quality, and safety. This role often involves coordinating with other departments, handling audits, and implementing process improvements to meet organizational goals. They play a critical role in ensuring that medical devices reach healthcare providers and patients safely and on time.

What are the key skills and qualifications needed to thrive as a manager medical device operations?

To excel as a Manager Medical Device Operations, you need expertise in supply chain management, regulatory compliance (such as FDA and ISO standards), and operational leadership, typically supported by a bachelor’s degree in engineering, life sciences, or business. Familiarity with ERP systems, quality management software, and relevant certifications like Six Sigma or PMP are commonly required. Strong communication, problem-solving, and team leadership skills help drive cross-functional collaboration and continuous improvement. These competencies are essential for ensuring product quality, regulatory adherence, and efficient operations in a highly regulated industry.

What are some common challenges faced by a manager medical device operations, and how can they be addressed?

Managers in Medical Device Operations often face challenges such as ensuring compliance with strict regulatory standards, coordinating cross-functional teams, and managing supply chain complexities. Staying proactive with regulatory updates, fostering open communication among departments, and implementing robust quality management systems can help address these issues. Additionally, investing in staff training and process improvement initiatives can streamline operations and minimize delays or compliance risks.

What are popular job titles related to Manager Medical Device Operations jobs in Texas?

For Manager Medical Device Operations jobs in Texas, the most frequently searched job titles are:

What job categories do people searching Manager Medical Device Operations jobs in Texas look for?

The top searched job categories for Manager Medical Device Operations jobs in Texas are:

What cities in Texas are hiring for Manager Medical Device Operations jobs?

Cities in Texas with the most Manager Medical Device Operations job openings:

Manager Medical Device Operations jobs near you
Infographic showing various Manager Medical Device Operations 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 92% Physical, 1% Hybrid, and 7% Remote job distribution.

Clinical Study Manager Medical Device

Kelly Services

Plano, TX

$134K - $145K/yr

Full-time, Part-time

Medical, Dental, Vision, Life, Retirement

Posted 29 days ago

Job description

Clinical Study Manager
  • Pay: $134,000-$145,000
  • FT or PT: Full-Time
  • Location: Plano, Texas (Hybrid)

Kelly® Science & Clinical is seeking a Clinical Study Manager for a direct-hire position at our innovative medical device client. If you’re passionate about leading clinical investigations for novel medical technologies and ready to take the next step in your career, trust The Experts at Hiring Experts.

As the Clinical Study Manager, you will lead the planning, execution, and oversight of clinical studies spanning the full medical device product lifecycle, including premarket and postmarket initiatives. This high-impact role ensures studies are conducted in alignment with ISO 14155, FDA regulations, EU MDR, and Good Clinical Practice (GCP). You will serve as the primary operational lead for assigned research projects, managing study timelines, budgets, site performance, vendor relationships, and data integrity. You’ll collaborate cross-functionally with Regulatory Affairs, Quality, Medical Affairs, and Product Development teams to support robust clinical evidence generation.

Key Responsibilities:

  • Lead and coordinate all aspects of clinical research, from study start-up to closeout (IDE, post-market, PMCF, registries, and observational studies)
  • Develop and manage project plans, study timelines, milestones, and budgets
  • Oversee clinical study documentation including protocols, informed consent forms, CRFs, statistical plans, and agreements
  • Manage site selection, qualification, initiation, monitoring, and performance oversight
  • Ensure compliance with regulatory and GCP requirements, supporting audits and inspections
  • Supervise vendors (CROs, labs) and monitor resource allocation and expenditures
  • Guide Clinical Research Associates and study team members with operational leadership
  • Drive risk management, data quality, and continuous process improvement

Requirements:

  • Bachelor’s degree in Life Sciences, Engineering, or related field; Master’s or PhD preferred
  • 3–8+ years of clinical research experience, including 2+ years in medical device study management
  • Strong knowledge of ISO 14155, FDA regulations, EU MDR, and GCP
  • Experience with EDC, CTMS, and eTMF systems
  • Exceptional project management, organizational, and communication skills
  • Certification (ACRP, SOCRA) and experience with interventional/procedural studies (IR, vascular, cardiology) preferred
  • Ability to travel up to 40% to clinical sites and industry meetings

Ready to make an impact in medical device innovation? Apply today!


As part of our promise to talent, Kelly supports those who work with us through a variety of benefits, perks, and work-related resources. Kelly offers eligible employees voluntary benefit plans including medical, dental, vision, telemedicine, term life, whole life, accident insurance, critical illness, a legal plan, and short-term disability. As a Kelly employee, you will have access to a retirement savings plan, service bonus and holiday pay plans (earn up to eight paid holidays per benefit year), and a transit spending account. In addition, employees are entitled to earn paid sick leave under the applicable state or local plan. Click here for more information on benefits and perks that may be available to you as a member of the Kelly Talent Community.

Why Kelly® Science & Clinical?

Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals-it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.

About Kelly

Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life-just ask the 300,000 people we employ each year.
Kelly is committed to providing equal employment opportunities to all qualified employees and applicants regardless of race, color, sex, sexual orientation, gender identity, religion, national origin, disability, veteran status, age, marital status, pregnancy, genetic information, or any other legally protected status, and we take affirmative action to recruit, employ, and advance qualified individuals with disabilities and protected veterans in the workforce. Requests for accommodation related to our application process can be directed to the Kelly Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.
Kelly may use AI-powered tools during the recruitment and hiring process. For full details, including how Kelly uses AI, your rights, and how to request a reasonable accommodation, visit the Recruitment Artificial Intelligence Notice.