QA Manager (GCP audit) - BEIJING / SHANGHAI
OBJECTIVE
The purpose of this position is to ensure that PDD clinical trial activities for all assigned projects are conducted in compliance with applicable regulations, Good Clinical Practice (GCP) guidelines, the International Conference on Harmonization (ICH) and corporate Policies and Procedures. In addition, this position is responsible for ensuring that investigator sites, external vendors and internal PDD processes meet corporate quality standards. The position’s incumbent is responsible for technically complex assignments, accurately identifying and communicating compliance risks, and developing action plans to mitigate risks.
ACCOUNTABILITIES
Responsible for developing and implementing a strategic audit plan for the development of assigned compounds. Ensure that activities are conducted and reports written according to applicable regulations and corporate SOPs.Lead domestic and international audits of clinical investigator sites, documents, databases, vendors (clinical, bioanalytical, and GLP) to assure compliance with applicable regulations, ICH and corporate policies and procedures. Audits conducted will require advanced auditing skills and will include the most technically complex assignments, including audits of potentially high risk to PDD. Assess impact of audit findings on subject safety, data integrity, and business operations.Obtain audit responses from PDD functional areas and/or vendors, and evaluate proposed corrections, corrective actions, and/or preventive actions for compliance with applicable regulations, guidelines, and corporate policies. Facilitate risk remediation. Escalate inadequate audit response to senior CQA management.Lead investigations into scientific misconduct and/or serious breach of GCP. Analyze investigation findings to identify root/probable cause. Propose, document, and track appropriate corrective actions. Assure reporting of potential or confirmed violations, as appropriate, to regulatory agencies.As assigned, review and approve audit reports submitted by Clinical Compound Support Compliance Specialists for content, format, regulatory risks, and compliance with SOPs. Promote consistent audit report writing standards across function.Participate in the development and implementation of a comprehensive training program for Clinical Compound Support Quality Assurance. As appropriate, monitor and document Compliance Specialist / Associate Compliance Specialist progress against the training program.Manage audit teams, including outside contractor auditors, to assure compliance with objectives of this position.Report metrics associated with assigned compounds to QA management, clinical development staff, and contract research organization staff. Evaluate if corrective and/or preventative actions are required, and ensure implementation.Identify potential systemic compliance risks, through audit activities and data analysis, and elevate to immediate manager for immediate and long-term resolution across PDD.Provide GCP compliance interpretation, consultation, training, and other supportive services necessary to maintain and improve the quality of PDD research for timely product applications to worldwide regulatory authorities. Independently analyze and interpret regulatory requirements as they apply to functional responsibilities.Develop and conduct GCP compliance presentations at internal and external R& D meetings, corporate facilities or investigator sites as needed.Provide GCP compliance technical support during regulatory inspections of investigator sites or corporate facilities worldwide to mitigate regulatory action.Provide on–the-job training to colleagues in areas of expertise.Contribute to the development, introduction and continuous improvement of CQA systems and processes.Provide QA input in cross-functional committees responsible for development or revision of corporate procedures.Demonstrate and maintains proficiency in the knowledge and application of industry standards.REQUIREMENTS
Bachelor’s degree required.Minimum 4 years in pharmaceutical R&D, most of which will have been gained in either a CRO or multinational pharmaceutical companyMinimum 2 years of experience in GxP Quality Assurance or equivalentMinimum 2 years of experience in the Asia Pacific regionIn-depth knowledge of the interpretation and application of FDA and international clinical trials regulations and guidance, and ICH Good Clinical Practice guidelines.Auditing Knowledge: Demonstrates advanced knowledge in the conduct and reporting of audits and the translation of findings into corrective action plans that mitigate risks to the company, to subject safety and data integrity.Negotiation Skills: Demonstrates proficiency in negotiation and conflict resolution.Clinical Development: Understands the phases, processes and techniques used to execute a clinical development program.Product Knowledge: Understands the medical/therapeutic impact of products.Scientific Knowledge: Possesses the necessary science education and knowledge to manage quality assurance oversight for clinical trials and to assure the ethical treatment of subjects. Understands medical terminology, standards of care, and disease states.Communication skills: Must communicate professionally, clearly, concisely and consistently to external and internal customers, both verbally and in writing. Must demonstrate professional presentation skills.Project Management: Must demonstrate proficiency in managing complex projects, delivering all expected deliverables in a timely manner, and proactively communicating changes in pre-established goals and deadlines.Organizational skills: Must be able to prioritize work effectively to meet timelines.Interpersonal: Must be able to adapt to other personalities in a respectful manner that is conducive to goal achievement and team building.Computer skills: Must be able to efficiently utilize the computer hardware and software programs provided to plan, manage, conduct and track deliverables and to communicate with internal and external team members. Must be proficient in use of the Quality Assurance Audit Database (QAAD).ASQ Certified Quality Auditor (CQA) or SQA Registered Quality Assurance Professional certification preferred.Requires up to 50 % travel.If you want to expand your skills set and take on a new challenging role with the opportunity, please don’t hesitate to send your CV to keith@barringtonjames.com or contact Keith at +65 6589 0589 for a confidential discussion.
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