
Quality Systems Engineer III
- Marlborough, MA
- $79,700 per year
- Permanent
- Full-time
- Communicate and document internal and external compliance-related information including changes in regulations, new guidelines and guidance documents and other information from regulatory authorities
- Apply effective, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues
- Assure the development and execution of streamlined business systems, which effectively identify and resolve quality issues
- Document and communicate non-conformances, evaluates impact, and makes recommendations for corrective actions
- Supports departmental, functional, divisional, and corporate quality goals and priorities
- Act as team member in supporting quality disciplines, decisions, and practices
- Builds quality into all aspects of work by maintaining compliance to all quality requirements
- Participate in CAPA and Continuous Improvement project teams as appropriate
- Other duties as necessary or required by the department or organization
- Bachelor's degree and 4+ years of experience in a medical device manufacturing, quality or regulatory/compliance environment
- Previous experience in Quality Systems or Country/Distribution QA or having experience in working in the Commercial/Supply Chain organisation
- Understanding of quality system requirements as stated within 21 CFR Part 820 and ISO 13485
- Technical writing and documentation skills
- Project management skills
- Fluent in English language
- Good knowledge of Microsoft Excel
- Strong communication, presentation, facilitation skills
- Organizational skills with good attention to detail
- Good working knowledge of SAP and non-device software validation would be beneficial