Sr Engineer, Quality at Fresenius Kabi USA

North Andover, Massachusetts, United States -

Full Time

Start Date

Immediate

Expiry Date

30 May, 26

Salary

155000.0

Posted On

02 Mar, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Quality Assurance, Product Excellence, Validation, Verification, Commercialization, Life-Cycle Management, Risk Management, Software Testing, Hardware Testing, Quality Metrics, CAPAs, Regulatory Compliance, Design Controls, Project Leadership, Analytical Capability, Judgment

Industry

Pharmaceutical Manufacturing

Description

Job Summary The 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. Fresenius Kabi (www.CaringForLife.us) is a global health care company that specializes in injectable medicines, biosimilars, and technologies for infusion, transfusion, and clinical nutrition. Our expansive portfolio of products and global network of science and manufacturing centers provide essential support for the care of critical and chronically ill patients. With more than 41,000 employees worldwide, our dedicated team is united by our shared purpose: to put lifesaving medicines and technologies in the hands of people who care for patients – and to find answers to the challenges they face. We call this purpose caring for life. Our U.S. headquarters is in Lake Zurich, Illinois and the company’s global headquarters is in Bad Homburg, Germany. Follow us on LinkedIn to learn more: http://bit.ly/3KdaGJr Fresenius Kabi is aware that scammers may attempt to impersonate our recruiters. While we have limited ability to stop these illegitimate efforts, there are some things you can do to protect yourself and not waste time communicating with an imposter. Check the email address – messages from our recruiters will always come from a company account with the Fresenius-kabi.com domain. We have seen imposters send emails using “Fresenius-kaabi.com” which of course includes an extra “a” in “Kabi.” Check our website to see if the position you were contacted about is actually posted. Be wary if someone asks you for personal information. We do not need your driver’s license, social security number, or bank account information before we have made you a conditional offer of employment. Refuse to pay any upfront fees. Fresenius Kabi never charges you a fee to apply for a job at Fresenius Kabi. We will not send you an invoice for equipment (such as a laptop) that we promise to order and reimburse you for once you start working. If you have any questions at any stage of the process, contact us at Careers@fresenius-kabi.com. Do not use any contact information in an unsolicited email. We look forward to talking to you about joining our team.

Responsibilities

The Senior Engineer, Quality will ensure product excellence by analyzing, developing, and executing processes for infusion systems and related disposable products, providing technical project leadership across validation, verification, and life-cycle management. Responsibilities include developing quality assurance processes compliant with standards like IEC/ISO 62304 and 21 CFR 820.30, assuring testing, investigating defects, and contributing to continuous improvement initiatives.