This description is a summary of our understanding of the job description. Click on 'Apply' button to find out more. Role Description Syndax Pharmaceuticals is looking for a Contractor, GMP Quality Assurance - Investigational. At Syndax, we are determined to realize a future in which people with cancer live longer and better than ever before. Syndax Pharmaceuticals is a commercial stage biopharmaceutical company developing an innovative pipeline of cancer therapies. The Role: - Responsible for lot review/release activities for drug substances, drug products, and finished goods by Contract Manufacturing Organizations (CMOs). - Ensure compliance with cGMPs and standards established by the company as well as regulations of applicable authorities. Key Responsibilities: - Support clinical product release activities for drug substance, drug product, and/or finished goods for all phases of development including review and approval of Master Batch Records along with executed batch records. - Effectively interact with external contract manufacturers and testing laboratories as well as work as part of an internal multidisciplinary team. - Manage and address associated investigations, CAPAs, change controls, OOS, etc. - Support investigations into quality issues with focus on product impact and patient safety. - Facilitate identification of root cause and development of appropriate corrective and preventive actions. - Track actions and confirm effectiveness; ensure reporting of potential or confirmed violations to regulatory authorities, as appropriate. - Identify and mitigate GMP activities and process improvement initiatives as requested by management. - Work closely with Quality Assurance team to ensure alignment and compliance with Syndax Quality Systems. - Self-motivating and independent. - Work independently with guidance from manager and senior staff. - Must be able to articulate complex issues clearly verbally and in writing. - Author, review, and/or approve documents including deviations, SOPs, and protocols. Qualifications - BS degree in scientific field required. - Minimum of 5 years of experience in the pharmaceutical industry, within GMP QA supporting contract manufacturing organizations. - Small molecule experience required (drug substance/API, drug product, packaging and labeling) including QC/analytical. - Experience supporting clinical labeling/packaging activities, including QP release. - Must have experience working in cross-functional teams including CMC, analytical, supply chain, and regulatory affairs. - Experience working with external vendors and suppliers including drug substance/API, drug product, analytical, and/or clinical packaging and labeling. - Strong technical writing skills. - Excellent communication skills. - Strong judgment, project management and decision-making skills; able to manage multiple projects and demanding timelines. - Ability to rapidly synthesize complex issues and identify risks in a pragmatic way. Location Syndax has an office in New York City and has a dispersed workforce across the United States. Company Description Syndax Pharmaceuticals is a commercial-stage biopharmaceutical company advancing innovative cancer therapies. Highlights of the Company’s pipeline include: - A menin inhibitor for R/R acute leukemia. - A monoclonal antibody that blocks the CSF-1 receptor for chronic graft-versus-host disease. Fueled by our commitment to reimagining cancer care, Syndax is working to unlock the full potential of its pipeline and is conducting several clinical trials across the continuum of treatment. For more information, please visit www.syndax.com or follow the Company on X and LinkedIn . Syndax Pharmaceuticals is an equal opportunity employer and will not discriminate against any employee or applicant on the basis of age, color, disability, gender, national origin, race, religion, sexual orientation, veteran status, or any classification protected by federal, state, or local law.

This description is a summary of our understanding of the job description. Click on 'Apply' button to find out more. Role Description The Director of Quality Assurance, AEMEA is responsible for overseeing the quality of Kao Group products and services in the designated market and ensuring they meet customer expectations. The role involves: - Continuously monitoring quality information from internal and external sources. - Identifying deviations from established quality criteria. - Requesting relevant departments to investigate root causes and implement corrective actions. - Evaluating the severity of quality problems and convening appropriate meetings. - Deciding on market actions to address issues. - Conducting or coordinating internal and external audits to verify compliance with quality standards and regulatory requirements. - Communicating with stakeholders to ensure consumer safety and maintain the company's reputation and stakeholder trust. - Determining the need for product recalls and leading recall projects in the designated market. - Serving as the Chief Quality Officer for the business region. - Reporting to the Global Chief Quality Officer (G‑CQO) at HQ. Qualifications - Bachelor's degree in a related field such as chemistry or pharmacy; advanced degrees are preferred. - Quality-related certifications such as ISO9001 Lead Auditor are highly desirable. - Strong knowledge of quality management systems and regulatory requirements in the cosmetics or consumer goods sector (e.g., GMP, ISO standards, FDA regulations). - Demonstrated leadership and communication skills to collaborate effectively with cross‑functional teams and senior management. - Exceptional capabilities in quality risk management, including risk identification, assessment, and mitigation. - Ability to provide constructive, and when necessary, critical feedback to stakeholders and functional teams. - Proven track record of driving quality improvement initiatives and implementing best practices to achieve measurable quality outcomes. Requirements - Experience in beauty care or cosmetics. Benefits - Amazing benefits available on the first day of employment (healthcare, 401(k) plus company match, etc.). - 41 total days off (vacation + holidays + sick). - Competitive salary range of $160,000 - $200,000 plus bonus. How we work Having been selected among the World's Most Ethical Companies for 19 consecutive years, we are a company with a purpose and strong corporate values. We never compromise on quality and craft our products with care for the consumer and the environment. At Kao, each employee can actively shape their job and their career. We work collaboratively to achieve our common goals, always aiming to deliver the best for our customers. What we offer A friendly and flexible work environment with great compensation packages, benefits package, ongoing development and the opportunity to enhance your skills and deliver tangible results. At Kao your voice will be heard. Your opinion really counts. We believe that change comes from taking opportunities into your own hands, so we value and reward entrepreneurial thinking and innovation. Hiring Process Kao embraces the diversity and the individual personalities of its people because we believe it is diversity that makes us strong. This is why we welcome applications from all areas of the global community. Want to learn more If you feel you are as unique as our products and want to find out why 33,000 people across the globe opted for a career with us please visit our Americas website ( https://www.kao.com/americas/en/ ). Kao is an Equal Opportunity Employer, including disability/vets.

• Test Planning: Collaborate with development teams and stakeholders to understand project requirements and specifications; Create comprehensive test plans and test cases to cover various scenarios and functionalities. • Manual Testing: Execute test cases and document test results, including defect tracking and reporting; Perform regression testing to ensure the stability of existing features; Conduct exploratory testing to identify potential issues not covered by test cases. • Bug Identification and Reporting: Identify, report, and prioritize software defects, providing detailed information to assist developers in resolving issues. • Collaboration: Collaborate with cross-functional teams, including developers, product managers, and business analysts, to ensure quality standards are met.

• Own Tier 2 validation: reproduce the issue, retest the fix, confirm acceptance criteria, and capture clear evidence. • Regression & impact checks: ensure fixes don’t break related workflows or dependencies. • Release validation: drive regression + smoke testing for patches, configuration changes, and maintenance releases; provide QA readiness input. • Defect management: log, track, retest, and communicate status/risk using client-standard tools (e.g., Azure DevOps/JIRA/TestRail or equivalent). • Operationalize QA: build and maintain lean, repeatable regression packs and incident-based test scenarios that improve speed and consistency over time.