Bachelor's degree in Engineering or Scientific field (4+ years experience) or Master's degree (3+ years experience)
Proficient understanding of medical device operations and manufacturing processes
Experience in product development, quality assurance, or related fields
Knowledge of Engineering and Quality principles
Familiarity with ISO 13485 and risk management files
Basic understanding of statistical techniques; experience with Minitab is a plus
Experience in test method development and validation
Responsibilities
Perform Quality Engineering activities for product development and cleanroom support
Ensure compliance of NPD processes with quality systems and regulations
Maintain and update risk management and design control documentation
Develop and implement test method validations and qualification plans
Support design verification and assist in process validation for multi-site transfer
Collaborate with teams in R&D, manufacturing, regulatory, clinical, and marketing
Complete additional tasks as directed by Leadership
Full Job Description
Job Description:
The Senior Quality Engineer will perform Quality Engineering activities supporting product development and ongoing cleanroom build efforts, ensuring New Product Development (NPD) processes comply with quality systems and applicable regulatory standards.
The role works cross-functionally to support design verification, process validation, and commercialization activities.
Roles & Responsibilities:
Perform Quality Engineering activities related to product development and ongoing cleanroom build support.
Ensure NPD processes comply with quality system and applicable regulatory standards.
Update risk management and design control files and maintain relevant quality documentation.
Develop and execute test method validations and qualification plans.
Support design verification and facilitate process validation and commercialization activities related to multi-site transfer.
Work collaboratively with cross-functional teams including R&D, manufacturing, regulatory, clinical, and marketing.
Perform other duties as assigned by Leadership.
Requirements:
Bachelor's degree in Engineering or Scientific field with 4+ years of experience OR Master's degree or equivalent in Engineering or Scientific field with 3+ years of experience.
Proficient understanding of medical device operations and/or manufacturing processes (medical device experience strongly preferred).
Relevant experience in product development, quality assurance, and/or related fields.
Knowledge and understanding of Engineering and Quality principles, theories, and concepts.
Understanding of ISO 13485Experience developing, updating, and maintaining technical content of risk management files.
Basic understanding of statistical techniques; experience using statistical software (e.g., Minitab) is a plus.
Experience in test method development including validation and/or fixture development.
Solid problem-solving, organizational, analytical, and critical thinking skills.
Strong documentation and communication skills with attention to detail.
bility to build productive working relationships across all organizational levels.
bility to manage competing priorities in a fast-paced environment.
