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Quality Engineering Director - Devens, United States - VulcanForms Inc.
1 month ago
Description
Job DescriptionJob Description Salary:
About us
VulcanForms builds and operates advanced digital infrastructure enabling the world's critical industries to innovate, grow, and deliver sustainable impact.
Founded in 2015, VulcanForms invented and commercialized the world's first industrially scalable laser metal additive manufacturing (AM) solution and pioneered integrated digital production systems.
We are a team of leading technology and operational experts with decades of experience in advanced manufacturing, materials, automation, and robotics.
We continuously seek contributors who demonstrate outstanding integrity, intelligence, accountability, and a passion for learning. We celebrate diversity and are committed to creating an inclusive environment for all employees.VulcanForms Inc. seeks a Quality Engineering Director for our Devens, MA location.
Job Purpose
As the
Quality Engineering Director
at VulcanForms Inc.,
Devens, MA , you will be responsible for the product quality engineering team, process quality engineering team, and software quality engineering team.
Provide Quality Engineering support to ensure compliance with the Quality System regulatory requirements and the business strategy of the company
Lead a team of product quality engineers, process quality engineers, and software quality engineers.
Represents Quality as a team member to support new product
development/introduction
activities
Supports the manufacturing line to address quality issues and resolution. Investigate and troubleshoot product or production issues.
Promotes awareness of Quality and Regulatory requirements
Leads or participates in the development of process and procedure
development/changes
Develops process control methods and, as applicable, applies statistical process control (SPC) methods to evaluate current processes and process changes
Supports validation and verification strategy for new and existing products and processes as assigned
Leads the development and maintenance of Master Validation Plans
Participates in the CAPA process as required as an assignee or project team member
Investigates escalated product complaints to root cause to ensure timely customer response and correction
Monitors product and process performance metrics and acts upon trends (positive or negative)
Authors, reviews, and approves Quality System documentation including change orders, DHF documents, DMRs, and DHRs
Interfaces with suppliers and customers to resolve Quality issues
Develops sampling plans
Develops and drives measurable Quality improvements relating to products and processes
Create test and inspection method and develop and execute test method validations
Collaborate to develop and implement quality and process controls and improvements.
Assure the QMS conforms to the customer, internal, industry (i.e., AS9100, ISO 9001, ISO 13485), and regulatory/legal requirements.
Qualifications
Minimum of 10 years of experience in quality in the medical device industry with demonstrated leadership of teams
Knowledge of GMP, FDA QSR, and ISO 13485 requirements
Knowledge of Root Cause Analysis, Data analysis, and Statistical Process Control concepts
Strong organizational, analytical, and problem-solving skills
Proficient in MS Office Suite (Outlook, Word, Excel, PowerPoint)
Strong sense of ownership
Team player with excellent communication skills
Excited about taking on new challenges in the metal additive manufacturing industry and working in a fast-paced startup environment
Self-motivated, agile, hands-on, with a practical mindset
Benefits
Medical, dental, vision, and life insurance are available to you starting on your first day of employment
Generous time off package, including vacation PTO, sick PTO, and 14 company-paid federal holidays
401(k) with company match and stock options
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