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Fresenius Kabi

Sr Engineer, Quality

Posted 15 Days Ago
In-Office or Remote
3 Locations
145K-155K Annually
Senior level
In-Office or Remote
3 Locations
145K-155K Annually
Senior level
The Senior Engineer, Quality ensures product excellence by developing and implementing quality assurance processes, validating medical devices, and collaborating with teams on quality metrics and compliance.
The summary above was generated by AI
Job SummaryThe Senior Engineer, Quality will play a key role in ensuring product excellence by analyzing, developing, implementing, and executing processes that uphold the highest standards of quality. This position provides technical project leadership and guidance across the validation, verification, commercialization, and life-cycle management of BU-INS-IVX infusion systems and related disposable products.
Salary Range: $145,000-$155,000
• Position is eligible to participate in a bonus plan with a target of 10% of the base salary (include only if applicable to the grade level)
• Final pay determinations will depend on various factors, including, but not limited to experience level, education, knowledge, skills, and abilities.
• Our benefits and programs are comprehensive and thoughtfully crafted to ensure our colleagues live healthy lives and have support when it matters most. Benefits offered include a 401(k) plan with company contributions, paid vacation, holiday and personal days, employee assistance program, and health benefits to include medical, prescription drug, dental and vision coverage.
Hybrid role: Onsite Tues, Wed, Thurs
Applicants must be authorized to work for ANY employer in the United States. Fresenius Kabi is unable to sponsor or take over sponsorship of an employment visa either now or in the future.

Responsibilities

Develop and implement quality assurance processes for medical devices in compliance with industry standards and regulations, including: IEC/ISO 62304: Medical Device Software Lifecycle, 21 CFR 820.30: Design Controls, ISO 14971: Medical Device Risk Management, IEC 60601: Medical Device Electrical Safety, ISO 10993: Biological Evaluation of Medical Devices, IEC 62366-1: Application of Usability Engineering to Medical Devices
Assure thorough testing and validation of software and hardware systems to ensure they meet specified requirements and are free from defects.
Collaborate with cross-functional teams to define quality metrics, standards, and procedures throughout the software and product development life cycle.
Assist with cross-functional risk assessments and contribute to the creation of risk management plans related to software and product quality.

Review and assure that verification test plans, test cases, and validation protocols are complete and provide meaningful results to confirm design outputs meet design inputs.
Stay updated on industry trends, regulatory changes, and best practices in medical device software and product quality.
Participate in audits and inspections to ensure compliance with relevant quality standards and regulations.
Investigate and analyze reported product defects, providing detailed and accurate reports to support corrective and preventive actions (CAPAs).
Facilitate communication between development teams and regulatory affairs to address quality-related issues.
Contribute to continuous improvement initiatives by leading complaint investigations, CAPAs, and other corrective actions.

Review design specifications for clarity, testability, and regulatory compliance.
Participate in design reviews for new products and establish quality plans.
Facilitate pre- and post-market risk management activities.
Maintain accurate records to assure regulatory compliance throughout the product lifecycle

All employees are responsible for ensuring the compliance to company documents, programs and activities related to the Health, Safety, Environment, Energy, and Quality Management Systems, as per your roles and responsibilities
 

Requirements

•    B.S. degree in Engineering (materials, biomedical, or mechanical)
•     Minimum 8 years of specialized experience in a medical disposables/device products field or advance technical degree.
•     Experience in compliant practices of design control and medical device risk management. 
•     Excellent verbal and written communication skills. 
•     Strong leadership and project management skills.
•     Strong analytical capability and attention to detail.
•     Ability to operate independently and exercise good judgment.
•     Able to use electronic systems including IT equipment to carry out duties
 

Additional Information

We offer an excellent salary and benefits package including medical, dental and vision coverage, as well as life insurance, disability, 401K with company contribution, and wellness program.

Fresenius Kabi is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, citizenship, immigration status, disabilities, or protected veteran status.

Top Skills

Design Controls
Iec/Iso Standards
Medical Device Software Lifecycle
Risk Management
Usability Engineering

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