Associate Director, Quality Management System

requirements; implementing corrective actions to resolve audit findings Ensuring that the company is inspection ready and provide guidance and support during regulatory inspections Collaborate with functional leads and/or stakeholders on conducting routine risk assessments for clinical development and manufacturing activities including service provider oversight and trial conduct Facilitating training on Quality systems, policies and SOPs for employees and GxP contractors

Requirements: BS degree in (Biological) Science, Engineering, or Operations Management; Advanced Degree (s) preferred Position requires a seasoned Quality professional with a minimum of eight [8] years of experience in biopharmaceutical companies with strong working knowledge in all GxP disciplines. Must have successful track record of implementing EQMS, preferred Veeva Quality Docs and QMS or other electronic systems. Working knowledge of Veeva workflows and configurations to enable efficient and compliant Veeva improvement projects. Must have a track record of success and a broad understanding of contemporary quality practices as they apply to product development, clinical manufacturing and commercial operations Knowledge of and ability to apply GxP, FDA, EU and ICH regulations and guidelines Proven expertise in the design and implementation of quality processes Experience in development of an organizational culture that promotes and sustains quality as an element of superior business performance Ability to effectively relate the quality functions to the business as a whole. Results-oriented team player; enjoys working collaboratively with colleagues and building positive relationships Demonstrated ability to work independently and flexibly in a fast-paced, high growth environment Excellent verbal & written communication skills. All employees are expected to act with integrity and in full compliance with applicable laws, regulations, and IDEAYA policies, including IDEAYA’s Code of Conduct. Employees must demonstrate good judgement and ethical behavior in all business activities, maintain patient and product safety as a top priority, and report any suspected violations of law or Company policy through appropriate channels Total Rewards Along with our inspiring mission, and highly collaborative and inclusive environment, IDEAYA offers a competitive total rewards package that reflects our pay-for-performance philosophy where employees are eligible to be considered for merit-based salary increases, company discretionary short-term incentive plan participation, and company discretionary stock option awards (based on board approval). Our comprehensive

benefits package includes, but is not limited to, medical/dental/vision coverage (100% company paid for employees and 90% company paid for dependents), 401k, ESPP, and wellness programs. The expected salary range for

the role of Associate Director, Quality Management Systems (QMS) is $171,000 - $211,000. The final salary offered to a successful candidate will depend on several factors that may include but are not limited to the office location where this open position is located, the final candidates’ experience within their profession, experience in the disease areas we are striving to make an impact in as a company, length of time within the industry, educational background, and performance during the interview process. The Company complies with all laws respecting equal employment opportunities and does not discriminate against applicants with regard to any protected characteristic as defined by federal, state, and local law. This position requires you to work onsite in the office at the Company’s facilities for training & meetings, with work-from-home flexibility, and the Company requires that all employees working in its facilities be fully vaccinated (except as required by applicable law). Therefore, this position requires you to be fully vaccinated from COVID-19, subject to reasonable accommodations for medical or religious reasons, and/or as otherwise required by applicable law. The Company considers you fully vaccinated once 14 days have passed since you received either the second dose in a two-dose COVID-19 vaccine series or a single-dose COVID-19 vaccine. The vaccine must have been FDA approved, have emergency use authorization from the FDA, or, for persons fully vaccinated outside of the U.S., be listed for emergency use by the World Health Organization. IDEAYA is an equal opportunity employer. In accordance with applicable law, IDEAYA does not discriminate in hiring or otherwise in employment based on race, color, religion, sex, national origin, age, marital or veteran status, disability, sexual orientation, or any other legally protected status. EOE/AA/Vets. We are committed to providing reasonable accommodations to qualified individuals with disabilities. If you need assistance or an accommodation due to a disability, please get in touch with us at [email protected]. At IDEAYA we believe in the importance of on-site presence by all team members as an essential ingredient to effective collaboration. Our hybrid approach to work at IDEAYA includes all staff being on-site four days per week in the office, and one day per week working from home. IDEAYA Company Values: Passionate Commitment Fearless Innovation Courageous Integrity Respectful Teamwork Objective Decision-Making Empowered Accountability For more information, please see www.ideayabio.com California Job Applicant Privacy Notice

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