Principal Design Quality Engineer - Cardiac Rhythm Management & Diagnostics (CRM

Boston, Inc.
Arden Hills, MN, United States
10 days ago

Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Experience level
Expert
Experience required
9 years minimum
Compensation
$102,100.0 - $194,000.0
Working hours
Regular working hours

Tech stack

Adobe InDesign Failure Mode Effects Analysis

Job description

This Principal Design Quality Engineer position will support active implantable medical devices. This position collaborates with cross functional teams including R&D, process development, manufacturing, and regulatory affairs to help ensure that the product and processes remain safe, of high quality, and compliant with BSC and regulatoryrequirements throughout the product lifecycle process., * Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues.

  • Acts as an effective team member in supporting quality disciplines, decisions, and practices.
  • Work within a cross-functional team to identify and implement effective controls for new technology in complex medical devices.
  • Write various technical documentation for procedure execution, technical rationale, and evidence of the development process.
  • Support Design Assurance activities as related to Risk Management, Design Controls, and other DA related priorities.
  • Support Post Market activities, as necessary, of risk based on post-market signals.
  • Actively participate in the Design Change process to ensure the proposed changes to the products are systemically and thoroughly analyzed and assessed.
  • Demonstrate good working knowledge and application of validation and statistical techniques in compliance with associated regulatoryrequirements and internal standards.
  • Support the verification, validation, and usability testing to meet or exceed internal and externalrequirements.
  • Develop, update, and maintain Design History File and Design Input / Output documentation (Product Specification, Component Specifications, and Prints).
  • Generate, update, and maintain product risk management tools (e.g., Hazard Analysis, Fault Tree, FMEAs).
  • Partner with R&D to determine and implement Design Controls based on Risk Management, Customer Needs, and Manufacturing Input.
  • Partner cross-functionally to identify and support value improvement efforts to support business goals.

Requirements

  • Minimum of a bachelor’s degree in mechanical, electrical, or biomedical engineering (or other related technical discipline).
  • 9+ yearsof experience in design assurance, new product development or related medical device / regulated industry experience.
  • Self-motivated with a passion for solving problems and a bias for action.
  • Strong communication skills (verbal & written).
  • Demonstrated use of Quality tools/methodologies.
  • Ability to effectively work and collaborate in a mixed onsite + remote environment.
  • Demonstrated experience creating detailed technical documents.

Preferred qualifications:

  • Experience working with medical electrical equipment and/or active implantables.
  • ISO 13485, ISO 14971 and Quality System Regulations understanding with a focus on Design Controls and Risk Analysis.
  • Experienced problem solver, capable of facilitating the problem-solving process.
  • Adaptable and effective collaborator in a team environment or in self-directed work.
  • Experience with design changes, complaint reduction, and corrective action.

About the company

The anticipated compensation listed above and the value of core and optional employee benefits offered by Boston Scientific (BSC) - see www.bscbenefitsconnect.com-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 non-exempt (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 exempt, non-sales roles may also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).

For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.

Boston Scientific transforms lives through innovative medical technologies that improve the health of patients around the world. As a global medical technology leader for more than 45 years, we advance science for life byprovidinga broad range of high-performance solutions that address unmet patient needs and reduce the cost of healthcare. Our portfolio of devices and therapies helps physicians diagnose and treat complex cardiovascular, respiratory, digestive, oncological,neurologicaland urological diseases and conditions. Learn more atwww.bostonscientific.comand follow us onLinkedIn.

Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.

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.

Among other requirements, Boston Scientific maintains specificprohibited substancetest requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement. The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law. Boston Scientific is an Equal Opportunity Employer - Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Disability, Veteran

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