Spécialiste de la qualité II/Quality Specialist II

Additional Locations: Canada-QC-Montreal

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 Quality Specialist II will provide Quality Engineering support to R&D activities and assisting in site improvement efforts. This includes generation, analysis and compilation of required metrics and presentations to support Quality Systems and Engineering requirements. In addition, the successful candidate will assist in the execution of projects designed to improve the compliance, efficiency, and effectiveness of assigned quality systems.

Your responsibilities will include:

• Coordinate and maintain Quality system data to assist senior leaders in making critical assessment of the health of the quality system.
• Create summary presentations of the analysis for review by a variety of key stakeholders.
• Work with QA and R&D to identify areas within the quality system and design assurance in need of improvement and execute NCEPs and Corrective and Preventive Actions as appropriate.
• Assist in the Quality Systems and Design Assurance portfolio management by monitoring, tracking, and providing data to management around the quality system for review in templates and presentations.
• Provide data to project/department managers on status of project metrics for their assigned project including tracking milestones, budget attainment, and other relevant metrics.
• Prepares new and revised documents for routing per the local document approval process. Tracks progress in obtaining approvals to for document change notices to aid in timely approvals.
• Incorporates documentation edits and updates all logs associated with documentation status. Releases approved documents and notifies affected personnel of changes impacting functional areas.
• Suggests changes to processes documentation and training programs in the spirit of continuous improvement.
• Supports teams in implementation of quality systems upgrades.
• Monitors and documents compliance with the local training program to ensure training compliance.
• Manages the biennial review of documentation system to ensure compliance to standards.
• Conducts internal audits as needed and supports regulatory, notified body and corporate external audits.
• Interacts between functional groups regard Document Change Notices.
• Facilitates Document Review meeting and makes recommendations as needed to functional areas.
• Support quality related needs of various departments and processes, including Design & Development and Non-Device Software & Equipment Controls. This includes validation documentation, and quality planning support.
• Root Cause Analysis of system/product non-conformances as discovered by Manufacturing, Customers, and Internal and External audits.
• Support the implementation of assurances, process controls, and CAPA systems designed to meet or exceed internal and external requirements.
• May actively participate in New Product Development, Design Review, and Design Control Activities.

Required qualifications:

• Undergraduate or master's degree in a science, business or related field.
• 2-4 years of relevant experience in a quality-related role.
• Experience in a regulated industry (i.e., pharmaceutical, automobile, aerospace, etc.).
• Strong documentation and writing skills.
• Excellent attention to detail.
• Requires minimal supervision.
• Willingness to learn and grow within the Quality Organization.

Preferred Qualifications:

• Engineering or Health Science related degree.
• Experience with ISO 13485.
• Internal Auditor Certification.
• Quality Management Certification.

Requisition ID:604312

Minimum Salary: $57200

Maximum Salary: $113700

The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) will vary based on actual location of the position and other pertinent factors considered in determining actual compensation for the role. Compensation will be commensurate with demonstrable level of experience and training, pertinent education including licensure and certifications, among other relevant business or organizational needs. At BSC, it is not typical for an individual to be hired near the bottom or top of the anticipated salary range listed above.

Compensation for hourly, non-sales roles may also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).

Compensation for salaried, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).

Compensation for sales roles is governed by Sales Incentive Compensation Plan (which includes certain annual non-discretionary incentives based on predetermined objectives).

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.

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!