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Ginkgo Bioworks

Senior Director, Quality Assurance

Ginkgo Bioworks, Boston, Massachusetts, us, 02298


The Corporate Quality Team is responsible for the overall Quality across Ginkgo. We focus on defining and measuring Quality, QMS (Quality Management System) implementation, training, maintenance, and continuous improvement. The QMS is the foundation of Ginkgo’s quality culture as it includes the quality issues escalation process, internal and external audits, and risk assessment programs. Generally, we ensure Ginkgo is executing high-quality science and is in compliance with all required regulations. We deliver on this by providing centralized quality leadership and resources and partnering with all functions across the organization. A high standard of quality is critical to the services and products Ginkgo provides as we are revolutionizing how biology can be engineered.Job Description:Design, develop, and implement a Quality Management System through which quality at Ginkgo will be managed.Implement a system that assures the organization complies with the QMS and all required quality standards and regulations. Maintain the company's quality system and issue updates.Drive, promote, and embed a culture of ethics, integrity, and continuous improvement that focuses on delivering efficiencies.Responsible for annual audit plans including supplier/vendor qualification audits and inspection management.Ensure that the Quality System meets standards expected by US and global regulatory authorities for research, development, and ultimately commercial activity.Communicate significant quality risks that may impact product suitability or regulatory compliance in a timely manner to Executive Management.Provide regulatory and quality support for cross-functional activities as needed.Provide strategic and technical leadership of quality assurance activities, including cross-functional efforts to develop policies, processes, and SOPs on both N-GXP and GXP and ensure compliance with global and regional regulations and ICH guidelines.Ensure quality metrics comply with best industry standards and practices.Demonstrate Quality leadership to the site providing guidance and interpretation on the regulatory requirements.Lead the assigned Quality Assurance organization to generate a strong quality culture of engaged and motivated staff maintaining strong working relationships with external customers and internal customers: Quality Operations QC, manufacturing, engineering, supply chain, and R&D. Implement and maintain a compliant QMS that is simple to understand and follow.This role will partner with our EHS function but will not be directly responsible for EHS functions.This is a new role for Ginkgo as we expand our Quality function and will include the creation of many of the processes to effectively implement all of the above.This role may develop into the direct management of 2-4 QA professionals that will align with various functions across the organization.This position will be hybrid based out of our Drydock (Boston, MA) Location.Responsibilities:Provide proactive strategic regulatory and compliance guidance in support of Ginkgo’s current and potential future funnel of work and work locations (including various states and countries).Provide regulatory guidance at the project level to ensure we are prepared to execute individual projects in compliance with all applicable regulatory guidance.Partner with our EHS function to ensure compliance with all applicable regulatory, environmental, and safety requirements that effectively provide Ginkgo with a “license to operate.”Coordinate, facilitate, and lead all (non-EHS) compliance external audits performed by customers and regulatory bodies.Partnering across operations teams, develop and implement internal process audit plans across key functions.Track and report on all internal and external audit findings.Provide regular communication and educational opportunities across Ginkgo to objectively improve our awareness and knowledge of applicable regulatory requirements.Support the development of Quality-related SOPs across operational teams.Minimum Requirements:Master's degree (or equivalent experience with a Bachelor's) in Science or Quality-related discipline plus 11-13+ years of related experience.Experience building and leading teams.Preferred Capabilities and Experience:Familiarity with applicable regulatory bodies overseeing the Biotechnology and Genetic Engineering space.Knowledge of Quality development and execution within scientific Discovery laboratories.Proven ability to successfully manage both audit preparedness and inspection activities in lab-based functions.Ability to collaborate with senior management to drive Quality compliance, execution, and improvement.Proven ability to measure complex quality goals that positively impact both our compliance and our achievement of business goals.

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