Design Quality Engineer

CONMED Corporation; Denver (CO); On-site; USD 74,000 - 95,000; Full time

Benefits offered by this job

Competitive compensation

Excellent healthcare including medical

401K with company match

Employee Stock Purchase Plan

Tuition assistance for undergraduate &

Job summary

CONMED Corporation in Colorado is seeking a Design Quality Engineer to support quality engineering activities across the new product lifecycle, from concept to commercialization, and sustaining activities. You will ensure compliance with ISO, FDA QSR, and EU MDR, and lead quality initiatives with cross-functional teams.

You will review design controls, risk management, verification and validation, and support audits and process improvements while focusing on patient safety and device efficacy.

Qualifications

• BS in Engineering with 2+ years medical device experience (MS with 1+ year acceptable).
• Experience interpreting/applying Quality Systems Regulations and ISO standards OR design controls (21 CFR 820, ISO 13485, ISO 14971, EU MDR).

Responsibilities

• Support and provide direction to product development teams for quality deliverables.
• Ensure product designs meet regulatory requirements and customer expectations; pursue continuous improvement.
• Review and approve design documentation and changes for quality, reliability, and manufacturability.
• Lead risk management activities prioritizing clinician and patient safety.
• Support verification/validation activities and design reports to address inputs and needs.
• Assist in quality investigations, trend analysis, and CAPA activities; participate in audits.

Skills

Quality engineering

Regulatory compliance

Risk management

Analytical skills

Education

Bachelor's degree in Engineering (Electrical, Mechanical, or Biomedical)

Master's degree in Engineering

Job description

The Design Quality Engineer is responsible for supporting all quality engineering activities to support the new product life cycle, from concept to commercialization, and sustaining activities. The Design Quality Engineer will serve as the quality engineering contact and be a key member of the cross-functional development and sustaining teams. The Design Quality Engineer serves as the key resource for ensuring compliance to ISO, EU MDR, and FDA QSR requirements for Medical Devices. The Design Quality Engineer takes the lead with quality initiatives with inter-organizational impact following QSR, CONMED Policies, standards and regulations. Works under direction from Quality Management.

Key Duties and Responsibilities

• Supports and provides direction to product development teams for the required quality deliverables.
• Ensures that product design meets customer expectations, regulatory requirements, appropriate voluntary standards, and all corporate requirements. Shows focus toward continuous improvement.
• Review, assess, and approve product design documentation to ensure compliance throughout product development cycle. Review and approve engineering designs/changes for adequate quality, reliability, maintainability, risk management, modeling, systems design, assessment tools, reporting, and manufacturability.
• Troubleshoot and direct the resolution of quality issues by fostering effective interdepartmental and cross-functional partnerships.
• A relentless focus on the safety and the efficacy of the medical device.
• Review and approve engineering designs/changes for adequate quality, reliability, maintainability, risk management, modeling, systems design, assessment tools, reporting, and manufacturability.
• Review and approve design verification and design validation protocols and reports. Ensure design activities prove design inputs and user needs are adequately addressed.
• Leads and provides support on risk management activities with a focus on clinician and patient safety.
• Support product development through capability assessment, analyzing performance data, facilitating problem-solving activities, developing quality tools, and quality techniques.
• Support sustaining activities such as complaint investigation and complaint trending. Monitor and analyze manufacturing and service trends. Perform Predicate Device reviews and surveillance reports. Able to perform data mining, analyze data and create trend reports.
• Demonstrate quality assertiveness and be able to represent the Quality function in various roles such as product support and lifecycle management.
• Investigates process and product issues identified through complaints and trend analysis of other conformance data. Works with other functional groups to resolve difficult quality problems on products, processes, or materials used in manufacturing operations.
• Direct and facilitate investigations and the corresponding preventative actions and corrective actions that result from abnormal results, customer complaints, quality inquiries, and other quality performance indicators.
• Travel Requirements (including international): 0-5%
• Support internal and external audits. Provide support for audit preparation activities. Participate in the back-room as needed.

In addition to the main responsibilities listed above the manager is allowed to USE discretion TO add further duties and tasks based on the business needs which are not explicitly listed here.

MINIMUM REQUIREMENTS

Education and Experience

• B.S. degree in Engineering such as Electrical, Mechanical, or Biomedical Engineering and 2+ years of medical device experience (or equivalent work experience), or M.S. and 1+ years of medical device experience.
• 1 year of experience in interpreting and applying Quality Systems Regulations and ISO quality requirements OR 1 year of experience in design controls, 21 CFR 820, ISO 13485, ISO 14971, EU MDR, and applicable medical device regulations.

PREFERRED REQUIREMENTS

• Professional certifications (CQE, CQA, CMQ/OE, Lead Auditor) are desirable.
• Design for Six Sigma training is desired along with knowledge of statistical methodologies.
• Involvement in back-room support process during external audits and/or inspections.
• Experience reviewing design verification and design validation protocols.

Other Attributes

• Excellent communication, problem solving, organizational, and interpersonal skills are required.
• Must be capable to plan schedules and to manage multiple projects simultaneously.
• Strong technical writing skills.
• Works independently with minimal direction or supervision.
• Decision intelligence.

Physical Requirements

• Ability to sit/stand for 8 hours.
• Ability to sit at a computer terminal for an extended period.
• N/A

Disclosure as required by applicablelaw, the annual salary range for this position is $74,200 to $94,600. The actual compensation may vary based on geographic location, work experience, education and skill level. The salary range is CONMED’s good faith belief at the time of this posting.

Coloradoresidents: In any materials you submit, you may redact or remove age identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

In addition to the main responsibilities listed above the manager is allowed to USE discretion TO add further duties and tasks based on the business needs which are not explicitly listed here.

No visa sponsorship will be provided. Relocation assistance will be considered

Benefits:

CONMED offers a wide array of benefits to fit your unique needs. Visit our Benefits Page for more information.

• Competitive compensation
• Excellent healthcare including medical, dental, vision and prescription coverage
• Short & long term disability plus life insurance – cost paid fully by CONMED
• Retirement Savings Plan (401K) – CONMED matches your contributions dollar for dollar, with the potential for up to 7% per pay period
• Employee Stock Purchase Plan – allows stock purchases at discounted price
• Tuition assistance for undergraduate and graduate level courses

CONMED is an equal opportunity employer and does not discriminate on the basis of any legally protected status or characteristic. Protected veterans and individuals with disabilities are encouraged to apply. Know Your Rights: Workplace Discrimination is Illegal Poster reaffirms this commitment.

Colorado Residents: In any materials you submit, you may redact or remove age-identifying information such as age, date of birth, or dates of school attendance or graduation. You will not be penalized for redacting or removing this information.

If you feel you need a reasonable accommodation pursuant to the ADA, you are encouraged to contact us at 800-929-7176 option #5.