Job description
Quality Systems Engineer II
Boston Scientific's hybrid workplace includes remote and onsite roles. By applying to this position, you will have the opportunity to discuss your preferred working location with your Talent Acquisition Specialist.
Additional Location(s): N/A
Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance
At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.
About the role:
The focus of this Quality Systems Engineer II position will be supporting the Corrective and Preventive Action (CAPA) process at Maple Grove, including nonconforming events, and ensuring compliance to CAPA processes, Medical Device regulations, and BSC Quality System requirements. As a member of the Quality Systems team, this individual will support department, site, and global level initiatives and will maintain a strong collaborative partnership with multi-functional teams while contributing to the overall health, including the suitability, adequacy, and effectiveness, of the CAPA process.
This is a hybrid work mode position located in Maple Grove, MN with the expectation to be in the office 2 days per week.
- Mentoring cross-functional CAPA teams on:
- root cause analysis, corrective action plans, and effectiveness verifications
- using project management best practices to effectively coordinate activities, communicate progress, collaborate on key deliverables, and meet critical CAPA phase timelines
- creating robust, compliant, and timely records, using the electronic CAPA database system
- Providing continuous and rigorous assessment of CAPA activities and review of documentation throughout the CAPA lifecycle to ensure compliance with global BSC CAPA processes, FDA regulations, ISO 13485, and Medical Device Requirements
- Applying sound, systematic problem-solving methodologies to identify, prioritize, communicate, and resolve systemic quality issues
- Acts as an effective team member and/or leader in supporting quality disciplines, decisions, and practices
- Being part of a team of subject matter experts in matters relating to CAPA at the Maple Grove site and providing guidance on how to best apply the processes efficiently, effectively, and compliantly
- Determining and tracking actionable CAPA metrics and trends to ensure proper execution and effectiveness of the site CAPA program
- Supporting both site and global scale CAPA initiatives, continuous improvement opportunities and/or projects
- Bachelor's degree and 2+ years of experience in a medical device manufacturing setting, within quality or regulatory/compliance environment
- Knowledge of basic Quality System Requirements and Good Documentation Practices
- Experience working with nonconforming material and/or CAPA methodologies/systems
- Attention to detail, strong technical writing and documentation skills, and the ability to prioritize tasks effectively in a deadline-driven environment
- Strong communication skills (written and verbal), e.g. comfortable speaking and presenting to different levels of management and cross-functional stakeholders
- Degree(s) in Science or Engineering
- 2+ years of experience in Quality Systems and/or CAPA management
- Detailed understanding of quality system requirements as stated within FDA Quality System Regulation 21 CFR Part 820 and ISO 13485
- Hands-on Project Management experience
- Able to work independently and as a contributing team member
- Continuous improvement mindset with a passion for Quality
#LI-Hybrid
Requisition ID: 559734
As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most – united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do – as a global business and as a global corporate citizen.
So, choosing a career with Boston Scientific (NYSE: BSX) isn’t just business, it’s personal. And if you’re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!
At Boston Scientific, we recognize that nurturing a diverse and inclusive workplace helps us be more innovative and it is important in our work of advancing science for life and improving patient health. That is why 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 maintains a drug-free workplace. Pursuant to Va. Code § 2.2-4312 (2000), Boston Scientific is providing notification that the unlawful manufacture, sale, distribution, dispensation, possession, or use of a controlled substance or marijuana is prohibited in the workplace and that violations will result in disciplinary action up to and including termination.
Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination.
Nearest Major Market: Minneapolis
Job Segment: Medical Device Engineer, Compliance, Medical Device, Systems Engineer, Technical Writer, Engineering, Legal, Healthcare, Technology
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