Job Purpose
As an experienced Quality Engineer you demonstrate commitment to the Quality Policy (patient safety and product quality) through daily execution of sound quality practices and the maintenance of an effective quality system. Understand and comply with all the regulations governing the quality systems. Ensure others are aware of their commitment to patient safety and product quality, are current with training requirements and that they understand and comply with all other regulations governing their work.
Key Responsibilities
Identifies and resolves complex exceptions to work assignments.
Summarizes, analyses, draws conclusions and makes appropriate decisions from test results or other process related findings.
Has the responsibility and independent authority to make decisions related to product quality, including the disposition of non-conforming product.
Participates in Customer Complaints investigation for areas under their control.
Continually seeks to drive improvements in product and process quality.
Knowledgeable on QSR and ISO/MDD standards, constantly promoting awareness of best industry practices, making appropriate decision on a daily basis utilizing the quality engineering manager/site QA Director as the final arbitrator on critical quality decisions.
Fully conversant with validation techniques and associated regulatory requirements including analysis of customer feedback and complaints.
Evaluates in conjunction with EHS new equipment/processes/chemicals for environmental impact/effect to eliminate or lessen such impacts/effects.
Knowledgeable on Risk Management, BSEN 14971 requirements.
Compiles and analyses operational, test and validation data to establish technical specifications and performance standards for newly designed or modified products and processes.
May participate directly in a new product/technology transfer to ensure compliance to all internal and regulatory requirements.
Uses knowledge of Six Sigma, Statistical Analysis and Lean principles to investigate and solve problems and improve quality.
Gives technical guidance to Associate Quality Engineer, Technician and Inspection staff.
Is a good team member, fully motivated to achieve and demonstrate best practices in line with the department and Site objectives.
Deals with suppliers, other engineering disciplines within and outside of the Site and customers should the need arise.
Is familiar with the internal auditing process.
Education & Experience
Level 8 Hons Bachelor Degree in Engineering, Science or equivalent in a STEM related discipline.
A minimum of 3-5 years experience working at Engineering level, ideally within the Medical Device industry or another highly regulated environment.
Experience in Validations is desirable.
Team player and someone who is fully motivated to achieve and demonstrate best practices in line with the department and site objectives.
Equal Employment Opportunity Statement
At Boston Scientific, we recognise that nurturing a diverse and inclusive workplace helps us be more innovative. It is essential in advancing science for life and improving patient health. We stand for inclusion, equality, and opportunity for all. By embracing the richness of our unique backgrounds and perspectives, we create a better, more rewarding place for our employees to work and reflect the patients, customers, and communities we serve. Boston Scientific is proud to be an equal opportunity and affirmative action employer. Boston Scientific is committed to providing reasonable accommodations for applicants and employees with a disability. Should you require a reasonable accommodation during the recruitment process, please email TalentAcquisitionIre@bsci.com
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