(Associate) China Quality Manager

Purpose Statement (2-3 Sentences):
Describe the primary goals objectives or functions or outputs of this position:
This position is central to advancing the strategic vision and enforcing robust oversight of Quality Compliance in
affiliate serving as the critical link between regulatory excellence and operational integrity.
The role will be advocating for comprehensive support across all affiliate quality activities related to pharmaceutical
products medical devices combination products and biologics. With critical support on risk management agency
inspections internal audits CAPA and holistic Quality oversight this role ensures the organizations alignment with
the highest quality and compliance standards. She/he will provide strategic support for clinical operations
rigorously supervising quality control processes to ensure compliance with industry standards and regulatory
requirement. This role will lead collaboration with cross-functional teams driving continuous improvement
initiatives support quality activities on development roadmap for both pharmaceutical products and medical
devices. By embodying a catalyst for excellence she/he not only fosters transformative change but also instills a
culture of unwavering quality and compliance throughout the organization elevating its reputation and efficacy in
the global arena.
Major Responsibilities:
List up to 10 main responsibilities for the job. Include information about the accountability and scope.
Develop Affiliate Quality Strategy: Develop and offer affiliate quality execution strategy directions to
clinical operations teams to optimize quality and process for clinical trial execution ensuring effective
management between quality and study timeline.
Enhance Affiliate Quality Process: Collaborate with internal cross-functional stakeholders to develop and
optimize Quality related processes ensuring compliance and enabling smooth integration within local and
global requirements.
Collaborate on Quality Strategic Management & Planning: Work with CDO leadership and relevant
departments to formulate comprehensive strategic and operational plans for clinical trials guiding affiliate
CDO team in developing and executing specific quality oversight and execution plans.
Oversee Clinical Trial Quality in China: Regularly review study related risk and quality guiding operational
team in identifying issues and issuing risk warnings to ensure timely advancement.
Develop and Guide Risk identification & Mitigation Plans: Create risk identification and mitigation
strategies and instruct team in their execution to ensure health and continuity of clinical trials.
Ensure Regulatory Compliance: Proactively track regulatory requirements and updates coordinating
cross-departmental resources to align HGR applications with global standards thereby enhancing the
efficiency of study start-up processes.
Quality Knowledge Development: Conduct quality related training and knowledge-sharing to enhance team
expertise and optimize performance.
Facilitate Cross-Functional Communication: Organize cross-departmental meetings to foster
communication and collaboration among team members promoting the establishment and implementation
of standardized processes.
External intelligence: Develop and build relationships with industry quality platform and gain industry good
practice and taking back to AbbVie. Leverage industry experience to develop internal quality strategies to
support internal business enhancement.

Qualifications :

• Qualifications:
  List required and preferred qualifications (up to 10). Include education skills and experience.
  Bachelors Degree or Higher: A bachelors degree in life sciences medicine pharmacy biochemistry or
  related fields is required. Advanced degrees such as a masters or Ph.D. in clinical research public health
  or health administration are preferred.
  Quality Experience: at least 1 years experience in clinical quality management with good Quality
  Management System and GxP compliance concept.
  Project Management Experience: Strong project management skills. At least 2 years experiences in clinical
  trial management. Experience in clinical trials at global pharmaceutical company is required.
  Clinical Trial Operational Experience: at least 3-5 years clinical trial operational experiences
  Cross-Functional Collaboration Experience: Proven experience in cross-functional communication and
  coordination working effectively across multiple departments. Strong influencing motivational
  interpersonal and relationship-building skills.
  Strategic and Critical thinking: Good mindset and ability to analyze complex situations anticipate
  challenges and devise effective plans for achieving long-term objectives through informed and innovative
  decision-making skills.
  Leadership and Communication Skills: Strong leadership and communication skills to manage teams and
  engage with various stakeholders effectively.
  Excellent written and oral communication skills in English.
  Strong computer skills and knowledge of systems such as CTMS Vault SolTraqs etc.
  Key Stakeholders:
  Country COM COM RDQA QMTC CPC.

Additional Information :

AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. 

US & Puerto Rico only - to learn more visit  & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:

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