Vp, Quality Assurance

Company Description
We seek extraordinarily capable and committed people to help shape and develop our Company. We offer competitive benefits to all levels of employees and provide free shuttles to and from nearby BART and Caltrain stations. If this seems like an exciting role, then apply today!
We design, develop, manufacture, and market medical instruments used in dermatology for advanced energy-based medical aesthetic solutions. Founded in 1998, the corporate headquarters for the Company is located in Brisbane, CA (just outside of San Francisco) and we are proud to manufacture all of our systems and accessories at our headquarters.
Please visit www.cutera.com for more information about Cutera.
Job Description
The individual is responsible for activities which lead to, and maintain compliance to/with Cutera's Quality Management System and maintains regulatory approval to market devices. Additionally, the individual is responsible for assessment of device changes for quality and regulatory implications and develop strategies for submissions and maintenance of documentation within the framework of regulatory requirements in an efficient manner.
Duties and Responsibilities:

• Manage and maintain Cutera's Quality System to ensure continued compliance with global regulatory and customer requirements.
• Lead and manage Cutera's Quality Assurance department and employees to achieve organizational goals and employee development and growth.
• Promote the recognition of quality programs within the company to create a shared continuous improvement mindset across functional departments.
• Prepare and maintain organizational readiness for FDA, ISO and other agency audits of our quality system.
• Lead and manage compliance processes (CAPA, Internal Audit, Material Review board, Supplier Quality) and implement improvements
• Formulate, document and maintain quality metrics and on-going objectives.
• Serve as a Lead Auditor, develop and manage internal audit systems, address non-conformities from internal and external audits.
• Oversee calibration and testing systems.
• Participate and provide input into the design and development of new products, including: risk analysis and quality planning to transition new products to production.
• Participate in supplier qualification and oversight, including perform supplier audits.
• Train and support manufacturing personnel on quality system requirements, and safety and hazardous material handling processes.
• Maintain compliance with FDA, GMP/QSR, Manufacturing process/Work Instructions and ISO 13485.
• Other duties as assigned.

Qualifications
Position Requirements:

• Master's or Bachelor's Degree in a technical field, or equivalent experience, with a minimum of 10-Plus years of experience with Quality System Management for an ISO certified Technology Company (medical device or electronics devices preferred).
• ISO 9000/2000 or ISO 13485 auditor training.
• Experience in quality planning, project management, verification, validation, and process validation
• Strong organizational skills and high quality standards
• Hands on ability to lead a group of individuals and various cross-functional project teams on collaborative projects and the ability to work as a member of a team.
• Ability to link functional responsibilities to overall business goals, and to manage and prioritize multiple projects simultaneously. Previous experience mentoring and training staff is Preferred.
• Proficient in use of MSWord, Excel, PowerPoint and other technical tools for QMS / PLM management is required.
• Good writing skills and formatting skills.
• Ability to work well under pressure and handle multiple projects and meet deadlines.
• Provide detailed reports to Senior Management on critical projects as well as provide quarterly updates to the BoD.
• Ability to read and understand regulations, standards and procedures.
• Good leadership, analytical and interpersonal skills.
• Travel of 5 to 10% possible

Additional Information
All your information will be kept confidential according to EEO guidelines.
If you are ready to become part of our spectacular, growing, and FUN company, then apply today!
We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, perform essential job functions, and receive other benefits and privileges of employment. Please contact us to request accommodation.
Applicants responding to this posting must be able to provide proof of eligibility to work in the United States. Competitive salary, benefits, ESPP and stock options. Cutera is an Equal Employment Opportunity Employer.
If you are ready to become part of our spectacular, growing, and FUN company, then apply today!
We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, sex, gender, gender expression, sexual orientation, age, marital status, veteran status, or disability status.
We will ensure that individuals with disabilities are provided reasonable accommodation to participate in the job application or interview process, perform essential job functions, and receive other benefits and privileges of employment. Please contact us to request accommodation.
Applicants responding to this posting must be able to provide proof of eligibility to work in the United States. Competitive salary, benefits, ESPP and stock options. Cutera is an Equal Employment Opportunity Employer.