Post-Market R&D Engineer II

CardioQuip; College Station (TX); On-site; USD 70,000 - 95,000; Full time

Benefits offered by this job

Relocation stipend

Health, dental, and vision insurance

Retirement savings plan with company/3

Job summary

CardioQuip, LLC is seeking a Post-Market R&D Engineer to support released cardiovascular products through the life cycle. You will perform engineering investigations, product improvements, design changes, and CAPA activities while maintaining compliant documentation.

Responsibilities include coordinating design transfers, validating changes, and ensuring manufacturing readiness, with exposure to post-market data analysis, risk assessment, and cross-functional collaboration.

Qualifications

• Bachelor's degree in an engineering field required.
• 1+ year of relevant industry experience preferred (medical device).
• PM experience or CAPM certification preferred.

Responsibilities

• Execute lifecycle-management and post-market maintenance for released CardioQuip products, including design changes with justification, risk assessment, validation, and documentation.
• Lead or coordinate routine design transfer activities for new products and changes, including manufacturing readiness, drawings, BOMs, work instructions, and production docs.
• Analyze post-market data, service, and customer feedback to identify trends and improvement opportunities, and recommend actions.

Skills

Project management

CAPA

Design controls

RCA

FMEAs

Design verification

Process validation

Risk management

Technical writing

Education

Bachelor's degree in engineering

Tools

DFM/DFA/DFS

FDA QMSR

ISO 13485

Job description

Post-Market R&D Engineers collaborate with cross-functional teams to support released CardioQuip products throughout the post-market lifecycle. Responsibilities include engineering investigations, product and process improvements, design changes, design transfer, complaint investigations, manufacturing support, post-market data review, and maintenance of compliant engineering and quality documentation.

*This position offers a one-time relocation stipend if relocation is required.*

What you’ll do

• Independently execute routine lifecycle-management and post-market maintenance activities for released CardioQuip products, including controlled product and process changes from problem definition through technical justification, risk assessment, verification and validation, documentation, and implementation.
• Lead or coordinate routine design transfer activities for new products and product changes, including manufacturing readiness, drawings and bills of material, work instructions, inspection and test methods, training support, and production documentation.
• Analyze post-market, service, manufacturing, complaint, and customer feedback data to identify trends, technical issues, product performance concerns, and opportunities for improvement, and recommend appropriate actions.
• Lead routine engineering investigations and root cause analyses for product, manufacturing, service, and complaint issues through technical troubleshooting and evaluation and implement or coordinate corrective actions.
• Perform complaint handling activities assigned to Engineering, including customer communication, device investigations, complaint determinations and documentation, risk assessments, corrective-action or CAPA evaluations, and domestic and international reportability determinations, regulatory reporting documentation, and approvals, as assigned, authorized, and qualified.
• Plan, draft, execute, and document verification, validation, and process validation activities supporting product design changes, technical investigations, and engineering improvements.
• Conduct routine engineering manufacturing-line audits and observations to verify personnel adherence to approved procedures, work instructions, and manufacturing practices; document findings and coordinate appropriate follow-up.
• Maintain design, manufacturing, risk-management, and change-control records for assigned products in accordance with applicable standards, regulations, and CardioQuip quality requirements.
• Work directly with contract manufacturers, suppliers, Service, distributors, and customers to resolve technical issues, evaluate changes, and support product and supply continuity.
• Coordinate cross-functional sustaining activities and update management and stakeholders regarding project progress, risks, budgets, and timelines.
• Participate in continuous improvement of engineering and sustaining processes and in outreach for prospective engineering talent.
• Other duties as assigned.

What we’re looking for

Requirements and Qualifications

• Completed a bachelor's degree in a relevant engineering field.
• At least 1 year of relevant industry experience, preferably in the medical device industry.
• Project management experience or CAPM certification preferred.

Preferred Knowledge & Skills

• Experience with medical device design controls, design history and technical documentation, change control, risk management, RCA, FMEAs, CAPA, design verification and validation, process validation, statistical methods, and risk-based design.
• Experience supporting released medical device products through design changes, manufacturing investigations, supplier changes, design transfer, or other post-market R&D engineering activities.
• Knowledge of manufacturing processes, engineering drawings and bills of material, DFM/DFA/DFS, and production problem solving.
• Knowledge of and experience with medical-device regulations and standards, such as FDA QMSR, 21 CFR Part 803, ISO 13485, ISO 14971, EU MDR, IEC 60601, IEC 62304, and IEC 62366, as applicable.
• Ability to analyze technical and post-market data, exercise sound engineering judgment, and translate findings into appropriate recommendations.
• Ability to lead routine project planning, scheduling, budgeting, and tracking efforts; excellent organizational, technical writing, oral, and interpersonal skills.

What We Offer

• Competitive Compensation
  • A fair salary commensurate with experience and qualifications.
  • One-time relocation stipend if relocation is required.
• Comprehensive Benefits
  • Health, dental, and vision insurance.
  • Retirement savings plan with company contribution.
• Dynamic Work Environment
  • A supportive team culture that values innovation, improvement, and empowerment.
• Work-Life Balance
  • Paid time off, including vacation days and holidays.
• Fun and Engaging Culture
  • We believe in working hard and celebrating our successes together, fostering a sense of camaraderie and enjoyment in our work.

Why Join?

At CardioQuip, we are dedicated to empowering people towards better healthcare. As a leading company in the medical device industry, we design and manufacture advanced cardiovascular devices that make a real difference in patients' lives. Our humble beginnings started with just two founders in a small office, and we've grown into a dynamic team that values every member's contribution. We believe in fostering an environment where our team is empowered, customer-focused, and continually striving for improvement—all while having fun along the way.