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更新:2024-05-09
临床质量管理QA
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成都武侯区  | 5-10年  | 社招
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Job Description

Management/coordination/oversight of QA compliance GxP activities in a specific geographical and/or functional/specialist area :
Lead and work independently and as part of the QA team
Act as expert GxP consultant in relevant area to groups within the Parexel organization and Parexel clients.
Promote compliance within the company and represent QA, as required.
Review Parexel SOPs as assigned to ensure GxP compliance of processes
Proactively re/review and oversee QA SOPs and be able to speak to their contents
For area of specialization, work with internal customers and develop and execute strategic audit plans for the area.
Contribute to the information provided to QA management to summarize quality issues arising from audits and other related activities, as requested.
In liaison with the QA management matrix, manage tasks and initiatives, including teams of multifunctional personnel, as needed.
Review the work of the matrix team to ensure consistency and quality within the group.
Deputize for Sen Compliance Manager and QA management within area of specialization.
Work closely with Regulatory Authorities and Clients. Support regulatory inspections & client audits as needed.
Provide consultation and interpretation on regulatory compliance to internal/external clients, Parexel management, and staff with regards to the implementation of GxP and safety/PV requirements, and implementation of appropriate regulatory requirements.
Act as a contact with members of Regulatory Authorities and / or clients; lead their audits / inspections in agreement with QA management.
Act as key contributor for review of client audit/regulatory inspection findings.
Provide strategic feedback and trending for Regulatory Inspectorates and client audits.
Review and contribute to Requests for Information (RFI) as assigned.
Conduct mock office inspections in agreement with QA management.
May serve as a member of industry association boards, task forces, and committees and / or as chairperson or officer of one or more professional associations. Contributes expertise to professional societies, academic, or other similar groups influential in his / her area of expertise.
Develop and maintain network contacts with other QA professionals.
Act as QA Lead for billable audit programs or client account for which QA representation is needed (as applicable)
Oversee billable audit programs.
Create and maintain the Audit Process Plan (APP) for the program.
Coordinate billable audits across all regions.
Act as main QA contact for the client and the Parexel project teams
Request assignment of auditors by Parexel QA management.
Provide auditors with the information required to schedule their assigned audits.
Review audit reports and responses to ensure consistency in audit conduct, report writing and follow-up for the program.
Raise a Change in Scope (CIS) if QA services outside of the APP are requested by the client.
Maintain relationships with clients and ensure audits programs are managed to a high degree of client satisfaction.
Support client QA needs and identify areas where billable services may be offered.
Develop and optimize new and existing processes to maintain and improve quality within the billable group.
Lead and coordinate internal audits and audit programs (global and regional)
Plan and conduct complex/for cause audits as assigned across all phases of Clinical Research including, but not limited to project related audits, system audits, supplier qualification and re-qualification audits (including GMP & GLP, as well as GCLP accreditation audits), safety/pharmacovigilance (PV) audits in order to evaluate the quality system against the appropriate regulatory requirements, relevant procedures and applicable guidelines. Ensure required audits are performed and reported in accordance with Parexel QA requirements, and on time.
Coordinate internal global process/system audits across regions and develop all necessary tools such as report templates, checklists and standard emails. Report outcome and trends of audit program to the process owner, QA Senior Management. Resolve program related issues in a constructive and pro-active way.
Escalate quality and compliance issue trends to QA Senior Management and relevant operational functions
Review audit reports, responses and other audit and program deliverable to ensure consistent high quality
Review and, if necessary, identify improvements that enhance the quality and clarity of audit reports.
For area of specialization, work with internal customers and develop and execute strategic audit plans for the area.
Travel internationally for audits as required. Travel time could be up to approx. 60%.
Maintain QA records / systems
Manage tasks or initiatives as assigned, including teams of multifunctional personnel, as needed.
Maintain required QA tools and ensure Parexel and QA systems are regularly updated with accurate information for audits and other activities.
Maintain and / or develop records / documents for assigned areas.
Process Improvements
Optimize new and existing processes to maintain and improve quality standards including supporting quality initiatives as assigned
Assist QA Management in the development and implementation of audit plan, strategic procedures and working practices to ensure continuous quality improvement.
Ability to review and, if necessary, identify improvements that enhance the quality and clarity of audit reports.
Analyze audit activities and provide metrics to relevant parties (QA, Operations, Procurement).
Proactively recognize areas for process / procedural improvements, providing input to QA management and taking the initiative, as appropriate.
Provide Trainings and Mentoring
Develop and present training courses as needed.
Train new and existing less experienced QA personnel.
Train and educate operational staff by the development and presentation of training courses.
Mentor new QA staff as assigned.
Build and maintain relationships
Build, develop, and maintain good working relationships with internal and external customer groups.
Work well in team environment.
Liaise with clients and operational staff on quality aspects which may include attendance of meetings, presentations and audits
Perform other quality related task or initiatives as assigned
Perform other quality related tasks or initiatives as assigned.
Provide Quality representation on Serious Breach Assessments
Support and assist with Information Security Incidents and technology related policies and procedures
Other duties as assigned.

其他信息
语言要求:英语
行业要求:全部行业
工作地址
成都-武侯区来福士广场
公司介绍
As one of the world's global clinical research organizations (CRO), we provide the clinical development capabilities and integrated consulting expertise it takes to streamline development every step of the way — faster and more cost-effectively. Our over 18,000 employees have a deep conviction in what we do, and together with our customers, we are shaping the next generation of therapies, one patient at a time. What we do, we do.
工商信息
以下信息来自
企业类型
有限责任公司(港澳台法人独资)
经营状态
存续
行业类型
研究和试验发展
成立日期
2002年04月23日
注册地址
中国(上海)自由贸易试验区商城路506号新梅联合广场写字楼二期12层、14层
统一社会信用代码
91310115737470728W
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