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Manager, Engineering - Quality - Design ControlICU Medical • Lake Forest, California, United States
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Manager, Engineering - Quality - Design Control

ICU Medical
  • US
    Lake Forest, California, United States
  • US
    Lake Forest, California, United States
Postuler Maintenant

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Manager, Engineering - Quality
role at
ICU Medical
JOB DESCRIPTION Under the general guidance of the Senior Director, Quality Engineering, this position ensures new product development Quality Engineers and their associated project teams utilize appropriate engineering and scientific analyses and processes during the product development/qualification and commercialization process for ICU Medical electromechanical products, including Infusion Pumps and Temperature Management devices. He/She will work directly with Quality Engineers to provide guidance and direction relating to pipeline and on‑market product development teams. This individual will be responsible for planning and implementing the Quality System and Medical Device standards related to product development and on‑market devices, to ensure compliant, safe and effective products. The role will manage new product offerings and product life‑cycle management by assuring adequate completion of qualification activities, compliance with ICU Medical’s quality system and overall strong product documentation record.
Essential Duties & Responsibilities
Provide effective tactical Quality leadership for Quality Engineers.
Interact and communicate with Senior Leadership across ICU Medical regarding program status, risks, mitigation plans and business objectives.
Effectively deploy and assure compliance with ICU Medical’s Quality System such as Design Controls, risk analysis/management tools, design verification, design validation, investigations, CA/PA data, etc. to assure product quality.
Support design and manufacturing site inspections/audits, representing and defending Design Control compliance for medical device products.
Assure systems conform to all applicable US and international regulatory requirements and coordinate development of data and responses for regulators.
Understand medical device regulations and assure ICU Medical Quality Systems and documentation remain compliant.
Ensure all Quality attributes for design changes and fixes are met; work with cross‑functional teams to coordinate product changes.
Provide design quality support, guidance and direction for all manufacturing facilities, including driving/managing on‑market product issues to closure and escalating to senior management for support as necessary.
Define, evaluate, prioritize and correct potential product and process risks to drive continuous quality improvements.
Represent the Quality organization as the core team member on Platform/Business teams.
Work with on‑market teams regarding product life‑cycle management and change management.
Knowledge, Skills & Qualifications
Demonstrated leadership capabilities with strong inter‑personal communication capabilities.
Ability to communicate at all levels of the organization regarding project and business objective status, risks and recommendations/mitigations.
Demonstrated knowledge of Quality Management Systems and experience linking risk management to all elements of the Quality System (Design Controls, CAPA, Complaints, Document Control, etc).
Systems‑level product development experience with an appreciation for interactions of the design and risk of components, materials, drugs and manufacturing processes, inclusive of the interaction of user needs, requirements and how they link to specific test cases and design inputs/outputs.
Excellent knowledge of the philosophy and principles of quality engineering, design verification, design validation, risk management and quality management.
Demonstrated problem‑solving and decision‑making skills.
Strong understanding of failure analysis, test method validation and engineering tolerances.
Broad knowledge of manufacturing operations and quality system practices.
Education & Experience
Must be at least 18 years of age.
Bachelor’s degree from an accredited college or university is required in Mechanical Engineering, Bio Engineering, Materials Science, or Physics.
8 years of regulated industry experience required, preferably in a quality or compliance position of technical quality assurance experience in a related field.
2–4 years of management or supervisory experience.
Physical Requirements & Work Environment
This is largely a sedentary role.
This job operates in a professional office environment and routinely uses standard office equipment.
While performing the duties of this job, the employee is regularly required to talk or hear.
While performing the duties of this job, the employee may be required to sit or stand for long periods of time.
Employees are required to use a computer.
Typically requires travel 20% of the time.
About Us ICU Medical has consistently provided you with clinical innovations that help solve real‑world challenges. With the acquisition of Hospira Infusion Systems in 2017 and Smiths Medical in 2022, we are now a global market leader with a complete line of clinically‑essential IV therapy and high‑value critical care products for hospital, alternate site, and home care settings. We’re ready to bring you consistent quality, innovation, and value in more areas than ever. Our focus allows us to bring you dedicated and non‑dedicated IV sets and needle‑free connectors clinically proven to provide an effective barrier against bacterial transfer and colonization; the industry’s broadest IV smart pump offering covering large volume, pain management, and ambulatory needs; IV medication safety software providing full IV‑EHR interoperability with the highest customer satisfaction and compatibility with more EHR systems than any other company; plus significant US IV solutions manufacturing and supply capabilities.
ICU Medical EEO Statement ICU Medical is committed to being an Equal Opportunity Employer. We ensure that all qualified applicants receive fair consideration for employment regardless of race, color, nationality or national origin, ethnicity, sex, gender, religion or belief, marital or civil partnership status, sexual orientation, pregnancy or maternity, age, disability, or protected veteran status. If you are an individual with a disability and need reasonable accommodation to participate in the employment selection process, please contact us at humanresources@icumed.com. We are committed to providing equal access and opportunities for all candidates.
Seniority level
Mid‑Senior level
Employment type
Full‑time
Job function
Engineering and Information Technology
Industries
Medical Equipment Manufacturing
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  • Lake Forest, California, United States

Compétences linguistiques

  • English
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