Senior QA Engineer, Medical Devices | CAPA & Compliance

Nextern; Maple Grove (MN); In loco; USD 100.000 - 135.000; Tempo pieno

Vantaggi offerti da questo lavoro

Health care plan

Retirement plan with company match

Paid time off, personal days, and a生日

Birthday holiday

Lifetime membership subsidy and wellnе

Life insurance

Family leave

Disability (short-term & long-term)

Taco Thursdays!!

Descrizione del lavoro

Nextern in Minnesota is seeking a Senior Quality Assurance Engineer to own quality input for manufacturing programs across the product lifecycle. You will support development activities, ensure readiness for commercial manufacturing, and collaborate with customers as needed.

The role emphasizes compliance with 21 CFR 820 and ISO 13485, CAPAs and root-cause analysis, and use of PLM tools such as Windchill, Agile, or Propel. Strong communication and detail orientation are essential.

Competenze

• Bachelor's Degree (BS) in life science discipline or equivalent combination of education and experience.
• 5+ years of experience in Quality Assurance role in a medical device development environment
• Experience working in quality systems as defined in 21 CFR 820 and ISO 13485.
• Development project team member on complex medical device development programs, including systems
• Understanding of ISO 14971 and application of risk management to product development and processes.
• Demonstrated technical expertise and leadership in quality.
• High attention to detail, organization, and accuracy.
• Instinctual capability for creative thinking and proposing novel solutions
• Strong ability to communicate (written and verbally) within and across disciplines and organization structures.
• Demonstrated use of quality tools and methodologies (e.g. nonconformance, CAPAs, root cause analysis, etc..).
• Experience with Product Lifecycle Management (PLM) software (e.g Windchill, Agile, Propel)
• Intermediate to advanced proficiency with MS Office Suit (Word, Excel, PowerPoint, Project, Outlook).

Mansioni

• Author and approve SOPs, work instructions, and forms. Support internal audits and maintain inspection readiness across the quality system.
• Compile and trend quality metrics to identify systemic issues. Present actionable insights to leadership and drive implementation of corrective and preventive actions.
• Oversee incoming inspection per approved sampling plans. Disposition nonconforming materials and coordinate supplier corrective actions to address recurring quality issues.
• Provide quality oversight for IQ/OQ/PQ qualification activities. Review and approve protocols, reports, and change orders.
• Manage nonconformances and CAPAs from initiation through effectiveness verification. Lead root cause analysis using structured methods (5-Why, fishbone).
• Act as the quality point of contact for production.
• Review batch records and travelers for GMP compliance.
• Support line clearances, first-article inspections, and process change reviews.
• Draft, collaborate, and approve product and engineering work orders.
• Create and maintain up-to-date product Design History Files (DHF).
• Advise project teams and lead by example in best-practices for Quality and Regulatory Compliance.
• Own, review, and approve changes ensuring impacts and resulting action/implementation (or lack thereof) are properly documented and executed.
• Receive, investigate, and document product complaints, interacting with customers as applicable.
• Support audits as Subject Matter Expert (SME) for QMS processes and product DHFs.
• Drive Product Lifecycle Management (PLM) architecture and changes, as needed.

Conoscenze

Quality assurance

Regulatory compliance

CAPA

Root cause analysis

Communication

Leadership in quality

Attention to detail

Formazione

Bachelor's Degree (BS) in life science

Strumenti

Windchill

Agile

Propel

Minitab

MS Office Suite

Descrizione del lavoro

Nextern in Minnesota is seeking a Senior Quality Assurance Engineer to own quality input for manufacturing programs across the product lifecycle. You will support development activities, ensure readiness for commercial manufacturing, and collaborate with customers as needed.

The role emphasizes compliance with 21 CFR 820 and ISO 13485, CAPAs and root-cause analysis, and use of PLM tools such as Windchill, Agile, or Propel. Strong communication and detail orientation are essential.