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QA SITE HEAD

QA SITE HEAD

WuXi AppTec
5-7 Years
  • Posted 18 hours ago
  • Be among the first 10 applicants

Job Description

Job Responsibility

  • Be responsible for site quality matters, ensure the product quality, and meet client's quality expectation. Be responsible for establishing, optimization and maintenance of the quality system, ensure that the site quality activities comply with quality management requirement, such as;
  • Review and approve quality procedures, quality manuals, annual/month quality review.
  • Establish, optimize and maintain the company quality system, ensure the regulator compliance and operability.
  • Define effective CAPAs, ensure the continuous improvement of the quality system by deviation investigation, quality incident handling, quality review, self-inspections and external inspections.
  • Ensure good communication with clients, maintain company quality imagination.
  • Follow client quality agreement, meet client's quality expectation.
  • Host client auditing, respond the audit report and follow up the actions.
  • Review and approve VMP and validation documents.
  • Organize quality training, promote employee quality awareness and company quality culture.
  • Notify top management and responsible management team in a timely manner regarding quality issues, quality trending etc.
  • Comply with national and local EHS laws and regulations, and strictly implement all EHS policies, SOPs and rules of the Company.
  • Participates in EHS working conference, EHS training, fire drill and other activities, continually learning EHS knowledge and improving skills, enhancing safety awareness, and actively participating in the establishment of EHS culture.
  • Build a highly efficient team.
  • Enable each team member's initiative, enthusiasm and creativity.
  • Energize the whole team.

Job Requirements

  • Education: Pharmacy or chemistry related major, university degree or above.
  • Major: Understand pharmaceutical production, testing and quality management, be familiar with GMP related regulations.
  • Language: Proficient in English.
  • Misc: Good computer skills.
  • Work Experience: More than 5 years of quality management related experience in pharmaceutical factory.
  • Work Capability: Have good coordination and communication skills; determine problems through scientific reasoning, collect information, understand facts, and draw correct and effective conclusions; preliminarily formulate research plans and specific implementation plans for each project, and track project progress.
  • Leadership: Guide and supervise subordinates; responsible for work assignment, assessment, and motivation of subordinate staff.

More Info

Job Type:
Industry:
Employment Type:

Key Skills

Client auditing

Deviation investigation

Quality incident handling

Quality manuals

Self-inspections

Quality training

External inspections

EHS laws and regulations

Quality review

About Company

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