Intern - (Design Compl Engineer) Job

hace 1 semana

San Francisco, Heredia, Costa Rica Boston Scientific Corporation A tiempo completo

**Intern - (Design Compl Engineer) Job**:

- Remote Eligible: Hybrid- Onsite Location(s): Heredia, H, CR**Additional Locations**: N/A

**Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - Caring - 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**:
Guarantee compliance with Quality System Regulations, Corporate Quality Manual and corporate and local standard operating procedures during the development and implementation of new processes, components or product

**You're Responsabilities include**:

- Support process with requirements and procedures that govern medical device Design Control, Risk Management and Post Market Surveillance.
- Support in complaints investigation, NCEPs, VIPs, and regulatory requirement changes from a design quality perspective.
- Works cooperatively with R&D, Regulatory Affairs, Clinical Risk, Medical Safety, Complaints Management Centre and Post Market Quality Assurance team environments to provide technical and quality systems input.
- Evaluate trending and product performance to ensure product/technology complies with all internal and regulatory requirements.
- Participate in analytical and problem-solving processes.
Analyze and draw conclusions making appropriate decisions concerning risk management activities.
- Collaborate with the maintenance of regulatory compliance with appropriate guidance documents - company SOP/WIs, EU/FDA/Global guidelines.
- Applies knowledge of Six Sigma, Statistical Analysis and Lean principles to investigate and solve problems and improve quality.
- Establishes and promotes a work environment that supports the Quality Policy and Quality System.
**What we're looking for**
- Academic background: Chemical, Industrial, Mechanical, Materials, Biomedical or related field
- Active student certification.
- At least 80% of the career approved (Bachelor´s or Licentiate degree).
- English level: 80% or above.
- Availability of 38 - 40 hours per week in site

**Requisition ID**:539158

**Job Segment**:Compliance, Regulatory Affairs, Statistics, Medical Device Engineer, Biomedical Engineering, Legal, Data, Engineering

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