Quality Eng - P2

Boston Scientific Gruppe

Dorado (PR)

On-site

USD 52,000 - 99,000

Full time

10 days ago

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Benefits offered by this job

Health insurance

Job summary

Boston Scientific in Puerto Rico is hiring a Quality Engineer II to provide process/quality engineering support for manufacturing and development teams, ensuring the highest quality products reach customers.

Responsibilities include defect control, quality planning, risk analysis, and process monitoring to reduce variation. The role requires a bachelor’s in engineering and strong knowledge of quality systems, with bilingual capabilities as a plus.

Qualifications

  • Identifies and controls manufacturing process defects through root-cause analysis and corrective actions.
  • Develops product quality plans and quality specifications with the development team.
  • Creates risk analyses and FMEAs to support product releases.
  • Identifies methods to capture quality metrics and perform data analysis.

Responsibilities

  • Provide process/quality engineering support to manufacturing and development teams.
  • Monitor processes to reduce variation and prevent defects.
  • Lead process improvement initiatives and quality tooling development.
  • Ensure compliance of systems and operations with regulations and company standards.

Job description

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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.


Quality Eng - P2 ( Quality Engineer II)


Provide Process/Quality Engineering support to manufacturing, helping to ensure delivery of highest quality product to the customer. Provide Process/Quality Engineering support to product development teams, helping to ensure development of highest quality new products.


Key Responsibilities


  • Identifies and controls Manufacturing process defects (scrap, nonconforming material, customer complaints) by participating in efforts/teams focused on identifying the primary root causes and implementing corrective and preventative actions. May be responsible for querying & bounding data to support implementation of complex & documenting release criteria.

  • Develops product quality plans, documents and systems by creating product specifications, quality specifications and quality plans in conjunction with other product development team members. May be responsible for creating risk analyses and FMEAs.

  • Develops Process Monitoring Systems by identifying critical process steps applying methods to reduce process variation in order to reduce/eliminate the cause of defects.

  • Leads process improvement efforts by identifying methods to capture quality metric data and by performing appropriate analysis methods to enhance sustaining product design and new product development.

  • Assists in creation of Quality Tools & Training Materials by understanding the limitations of existing quality tools and training materials, and by helping to identify more effective tools & materials.

  • Evaluates the adequacy and compliance of systems, operations, and practices against regulation and company documentation. Could serve as auditor of areas of the BSC quality system, such as development and manufacturing, as assigned.

  • Responsible for the final Process Monitor Release for products prior to distribution.


Management Requirements


  • Bachelor’s degree in engineering with at least3 years of experience or an equivalent combination of education and work experience

  • Knowledge of Quality System Mfg Process

  • General Knowledge of industry practices, techniques, and standards

  • knowledge of standard statistical analysis techniques and problem-solving methodologies, including capability studies

  • Medical Device Manufacturing Process expertise

  • Knowledge of Quality and Traceability Systems (MESS/SAP/eCAPA/Windchill)

  • General knowledge of quality metrics

  • Flexibility to work other shifts as needed

  • Fully Bilingual


Requisition ID:631505


Minimum Salary:$52300


Maximum Salary: $99400


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 at www.bostonscientific.com and follow us on LinkedIn .


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.



Nearest Major Market: Puerto Rico
Nearest Secondary Market: San Juan
Job Segment: Quality Engineer, Statistics, Business Process, Oncology, Neurology, Engineering, Data, Management, Healthcare

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