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Supervisor, Quality

Work mode:  Hybrid
Onsite Location(s): 

Global Park, La Aurora de Here, H, CR

Additional Locations:  N/A

 

Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance

At our company, we value diversity and believe it is our greatest strength. We are committed to empowering women, supporting the LGBTQ+ community, and creating opportunities for individuals with disabilities. Our belief is that your diversity enriches our work environment. As an equal opportunity employer, we wholeheartedly welcome applications from all qualified candidates, regardless of their background. Additionally, we have a Gender Equality Policy that reflects our commitment to fairness and equality in the workplace.

Hybrid Roles:

Boston Scientific's hybrid workplace includes WFH and onsite. You will have the opportunity to discuss details in the interview. 

 

About the role:

This position operates during night shift hours, supervising Engineering and/or Technician activities that directly or indirectly support production operations or test laboratories. Develops, establishes and maintains quality methodologies, systems, and practices which meet BSC, customer, and regulatory requirements. Identifies, coordinates, and assigns project priorities based on business and department objectives. Ensures implementation of assurances, process controls, and CAPA systems designed to meet or exceed internal and external requirements.

 

You're Responsibilities include:

  • Oversees daily functions and work flow to meet operational objectives, comply with all policies and procedures, assure safety, and achieve effective core metrics performance. 
  • Supervises the management of staff, including workforce planning, recruitment, shift schedules, skill and performance assessments, workload distribution, training, corrective action, recognition, and daily direction on work assignments and priorities. 
  • Identifies and resolves operational issues and manages addressing non-conformance matters. Recommends and implements process improvements. 
  • Serves as internal liaison for team operations, including preparing reports and presentations on functions and performance. 
  • Ensures that special projects are completed following established schedules and procedures. Interfaces with cross-functional teams on special projects. 
  • Performs other responsibilities as required. 

 

What We’re Looking For:

  • Bachelor’s degree in engineering (ie: materials, chemical, industrial or similar) could be in process. 
  • English Level desired: Intermediate.  
  • Experience: 3 years and 1 year in Incoming areas as coordinator or area lead.  
  • Or an equivalent combination of education and experience.

 

Desired knowledge

Technical & Quality Systems Knowledge 

  • SAP Quality Module: Deep understanding of inspection planning, material master data, and quality notifications. 
  • CAPA & Non-Conformity Management: Root cause analysis methodologies (e.g., 5 Whys, Fishbone Diagram), CAPA effectiveness checks. 
  • Validation Protocols: IQ/OQ/PQ processes, statistical tools for correlation studies, GAMP 5 principles. 
  • Measurement Systems Analysis (MSA): Gauge R&R, calibration techniques, and metrology fundamentals. 
  • Document Control Systems: Proficiency in Agile, Trackwise, and document lifecycle management. 

Shape 

Operational & Strategic Skills 

  • Area Metrics & KPI Development: Designing dashboards, trend analysis, and continuous improvement tracking. 
  • Lean Six Sigma: Application of DMAIC, waste reduction, and process optimization. 
  • Purchasing & Budgeting: Vendor evaluation, cost-benefit analysis, and procurement processes for lab equipment. 
  • Payroll & Personnel Management: Basic HR systems knowledge, timekeeping, and performance evaluation. 

Shape 

Leadership & Training 

  • Team Supervision: Conflict resolution, delegation, and performance coaching. 
  • Training Program Development: Creating competency matrices, onboarding plans, and technical training materials. 
  • Cross-functional Collaboration: Working with R&D, manufacturing, and regulatory teams. 

Shape 

Regulatory & Compliance Knowledge 

  • ISO 13485 / FDA 21 CFR Part 820: Understanding of medical device regulations and audit readiness. 
  • Risk Management: FMEA, hazard analysis, and risk mitigation strategies. 
  • Document Creation (WI/SOP): Writing clear, compliant procedures and work instructions. 

 

Requisition ID: 615428

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!

 

Benefits • Life-Work Integration • Community • Career Growth

 

At Boston Scientific, you will find a collaborative culture driven by a passion for innovation that keeps us connected on the most essential level. With determination, imagination, and a deep caring for human life, we’re solving some of the most important healthcare industry challenges. Together, we’re one global team committed to making a difference in people’s lives around the world. This is a place where you can find a career with meaningful purpose—improving lives through your life’s work.

#CRTA #HRDTA


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