Director, Quality Assurance – QMS & Customer Quality
The Director, Quality Assurance - QMS will lead our Quality Assurance team in maintaining and enhancing our ISO 13485-certified QMS. The ideal candidate will have a proven track record of success in managing and executing QMS activities, ensuring compliance with regulatory requirements, and resolving customer complaints. They will also have deep expertise in ISO 13485, genomics, and hands-on experience in conducting internal and external audits. The Director of Quality Management System at Twist is responsible for building and maintaining the Twist Quality Management System (QMS). This individual designs quality programs that will satisfy customer requirements for each individual product line. The QA Director is responsible for achieving and maintaining the appropriate ISO and/or regulatory certifications for each business unit.
What You’ll Be Doing
Lead and manage a team of Quality Assurance specialists responsible for all aspects of the QMS, including corrective and preventive actions (CAPA), and audits.
Develop and implement comprehensive QMS procedures to ensure compliance with ISO 13485 and other applicable regulatory requirements.
Conduct internal and external audits to identify and address potential QMS non-conformities.
Investigate and resolve customer complaints in a timely and effective manner.
Manage the CAPA process to ensure that all non-conformities are identified, investigated, and resolved promptly.
Stay up-to-date on the latest industry trends and regulatory changes in the genomics field.
Provide training and mentorship to Quality Assurance team members on QMS principles, ISO 13485, and regulatory compliance.
Manage local and global Complaint Handling and Audit Team
Ensure maintenance of job descriptions
Build and maintain a CAPA system
Achieve and maintain 13485:2016 certification as appropriate per product line
Achieve and maintain 9001:2015 certification as appropriate per product line
Oversee QMS compliance for all personnel and disciplines
Ensure supplier quality objectives are met
Establish and maintain an internal audit schedule
Conduct internal audits
Establish product development lifecycle with appropriate design controls
Establish SW development lifecycle with appropriate design controls
Build and maintain a change control system
Establish monitoring and measuring systems
Create customer complaint and feedback tracking
Implement continuous improvement
What You’ll Bring to the Team
Master's degree in Quality Assurance, Regulatory Affairs, or a related field.
Minimum of 10 years of experience in the medical device or biotechnology industry, with a strong focus on QMS and ISO 13485 compliance.
Proven experience in developing and implementing QMS procedures and conducting internal and external audits.
Deep expertise in ISO 13485, genomics, and regulatory compliance.
Experience in resolving customer complaints and managing the CAPA process.
Excellent communication, collaboration, and leadership skills.
Ability to work independently and as part of a team in a fast-paced environment.
Hands-on experience with QMS management software.
S. in Biochemistry, Molecular Biology, Microbiology, Bioengineering, or related field and fifteen years of experience in the area of technology transfer
At least 10 years GxP experience
Ability to communicate effectively both verbally and in writing
Demonstrated knowledge of product development lifecycle, including the ability to guide large-scale programs toward commercialization goals
Strong supervisory and organizational abilities
Demonstrated experience in product commercializing
About Twist Bioscience
Twist Bioscience synthesizes genes from scratch, known as “writing” DNA. Just as children learn to both read and write, the next phase of development for the genomics revolution is the ability to write DNA.
At Twist Bioscience, we work in service of people who are changing the world for the better. In fields such as health care, agriculture, industrial chemicals and data storage, our unique silicon-based DNA Synthesis Platform provides precision at a scale that is otherwise unavailable to our customers.
Twist Bioscience Corporation is an Equal Opportunity Employer. Twist Bioscience Corporation provides equal employment opportunities to all employees and applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, disability, genetic characteristics, or any other category protected by law.
The base cash compensation for this California-based role is below. In addition to base salary, this role is eligible for bonus, equity, and a generous benefits package. Final compensation amounts are determined by multiple factors, including candidate skill, experience, expertise, and location and may vary from the amount listed above. Compensation may be different in other locations. San Francisco Bay Area Pay Range $201,000 — $230,000 USD
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