Staff Advanced Quality Engineer
Location: Allendale, NJ or Leesburg, VA (hybrid)
Company: VB Spine
Looking for a career where your work truly matters? At VB Spine, you’ll be part of a mission-focused team that supports surgeons during life-changing spinal procedures. We’re looking for driven individuals ready to learn quickly, adapt under pressure, and grow in a dynamic, fast-paced environment. As a Staff Advanced Quality Engineer, you’ll play a leading role in ensuring design and manufacturing excellence for new product development. This is a highly collaborative and technical position that drives quality throughout the product lifecycle—through risk management, verification and validation, and advanced quality planning. Candidates may be located in Allendale, NJ or Leesburg, VA, with flexibility for hybrid work environment.
What You’ll Do:
- Collaborate with Engineering and Advanced Operations to define design requirements and develop manufacturing processes for new product development
- Lead risk management activities and develop risk management plans and reports for product and process quality
- Create and maintain quality assurance documentation to support product development and regulatory submissions
- Identify and address gaps in design control processes and procedures
- Participate in design reviews to evaluate product risks and mitigation strategies
- Define and support design verification and validation test requirements and reports
- Promote efficient and statistically valid testing practices
- Develop, review, and approve inspection plans, routers, and drawings
- Support the definition of critical quality attributes and risk-based product evaluations
- Facilitate product design transfers to internal or external manufacturing
- Analyze feedback from early product launches and address quality issues
- Perform health risk assessments for post-market events
- Use tools such as FMEA, Root Cause Analysis, and GD&T for continuous improvement
- Interact with regulatory agencies and support audits and submissions
What You Bring:
- Bachelor’s degree in science, engineering, or related discipline required
- MS, Certified Quality Engineer (CQE), or Certified Reliability Engineer (CRE) preferred
- Six Sigma Green or Black Belt preferred
- Minimum 5 years of experience in medical device or other regulated industries
- Knowledge of design and process verification and validation in product development
- Expertise with quality tools such as FMEA, GD&T, Root Cause Analysis, and Mistake Proofing
- Proficiency in reading and interpreting CAD drawings
- Experience with US and international medical device regulations and agency interactions (e.g., FDA, TUV, MoH)
- Strong foundation in quality concepts such as CAPA, audits, and statistics
- Ability to manage multiple projects in a matrixed organization
- Strong problem-solving, critical thinking, and communication skills
- Experience working in compliance and risk assessment scenarios
- Proficiency with Microsoft Office and statistical analysis tools (e.g., Minitab)
- <20% travel required
Why VB Spine?
We believe in growing talent from within. At VB Spine, join a high-performing team, benefit from peer and executive mentorship, and shape strategy in the dynamic field of medical sales—positioning yourself to influence growth and innovation across the organization.
Compensation:
Pay for this role is competitive and based on experience, with additional factors like territory requirements, qualifications, and performance taken into account. The typical pay range for this position is $105,000.00 - $135,000.00 annually, with potential for bonuses and incentives plus benefits. Final compensation is determined on a case-by-case basis and considers a variety of factors including experience level, skillset, and market conditions.
Benefits include:
- Comprehensive health, dental, and vision insurance
- 401(k) with company match
- Paid time off (PTO) and holidays
- Ongoing training and professional development opportunities
- Opportunity to grow within a fast-paced, dynamic company