Spencer Gregory Hale
Your key responsibilities will include:
- Influence key stakeholders through collaborative community engagement. Help to connect the key SMEs across divisions and capitalize on networking skills to promote best practice sharing and efficient problem solving
- Support internal and external audits and audit responses to existing products.
- Manage quality systems core within an integration project.
- Monitor clinical product flow and device tracking.
- Oversee product approval for distribution.
- Support CAPA (Corrective and Preventive Actions) and nonconformance processes.
- Provide PMPC (Product Manufacturing Process Control) support.
- Maintain docket records and data control.
- Partner with cross-functional teams to achieve integration goals.
What We’re Looking for in You:
Minimum Qualifications
- Minimum of 7 years of experience in medical device quality systems.
- Bachelor's degree in science, health, or engineering
- Understanding of design control and risk management.
- Understanding of US and International regulations including 21 CFR, 820, and ISO 13485 is required, as well as the Medical Device Directive, EUMDR, and EN ISO 14971.
- Familiarity with US and international regulations.
- Strong communication and presentation skills.
- Strong project management skills (preferred but not mandatory).
- Proficiency in Microsoft Office suite and Windchill.
- Ability to work with internal systems and external candidates.
Preferred Qualifications:
- Experience in managing quality systems within integration projects.
- Ability to work independently and as part of a team.
- Strong problem-solving skills and attention to detail.
Maximum Salary: $ 188300
Compensation fornon-exempt (hourly), non-sales rolesmay 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 forexempt, non-sales rolesmay 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.
Among other requirements, Boston Scientific maintains specific prohibited substance test 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.