Manager, Validation & Verification (Hybrid, Boston)
- Compensation
- Not disclosed
- Location
- Boston, MA, US
- Work setup
- Not specified
- Seniority
- Not specified
- Employment
- Not specified
- Experience
- 8+ years
- Category
- Not specified
- Posted
Skills
Nice to have
- Training or certification in medical device quality systems, software validation, risk management, Agile development and test, project management, or related engineering leadership disciplines.
- People leadership, coaching, performance management, and team development
- Verification and validation strategy, planning, execution, and documentation
- Design controls, requirements traceability, risk management, and quality system compliance
- Medical device and software lifecycle knowledge, including regulated product development practices
- Cross-functional collaboration, stakeholder management, and executive communication
- Problem solving, decision making, prioritization, and risk-based planning
- Test management, requirements management, defect management, and engineering change control tools
- Continuous improvement, process standardization, metrics, and operational excellence
Full description
We are constantly looking to add to our core talent. If you are seeking a career that is challenging and rewarding, a work environment that is diverse and dynamic, look no further — Haemonetics is your employer of choice.
Job Details:
The Manager, Validation & Verification is responsible for leading validation and verification activities for medical device, software, and system-level product development programs. This role provides people leadership, technical direction, and execution oversight to ensure test strategies, protocols, methods, and objective evidence meet product requirements, design control expectations, quality system procedures, and applicable regulatory standards. The manager partners cross-functionally with Systems Engineering, Software, Hardware, Quality, Regulatory, Project Management, and Operations to plan and execute verification and validation work, resolve technical and compliance risks, improve test processes, and develop a high-performing team.
Essential Duties:
- Develop team capability through coaching, performance management, workload balancing, hiring support, training, and professional development planning.
- Lead and manage the Validation & Verification team responsible for planning, developing, executing, and documenting verification and validation activities for medical device and software-enabled products.
- Establish and maintain V&V strategies, schedules, resource plans, and deliverables aligned with product development milestones, regulatory expectations, and business priorities.
- Provide technical and compliance oversight for test plans, requirements traceability, protocols, test methods, test reports, defect investigations, and objective evidence supporting design verification and validation.
- Drive consistent application of design controls, risk management, test method validation, software validation, and quality system procedures across assigned programs.
- Partner with cross-functional leaders to identify verification and validation risks, remove execution barriers, support issue resolution, and communicate impacts to project scope, schedule, quality, and compliance.
- Review and approve verification and validation documentation, including test protocols, reports, traceability matrices, deviations, nonconformances, and change impact assessments.
- Promote continuous improvement in V&V processes, tools, templates, metrics, automation practices, and test management approaches to improve quality, efficiency, and predictability.
- Prepare and present clear status updates, technical summaries, resource needs, risks, and recommendations to functional leadership and program stakeholders.
- Ensure team deliverables support regulatory submissions, audit readiness, design history files,and product release decisions as applicable.
- Other duties as assigned