QC Testing Supervisor

2 days ago

Tuas West Region, Singapore WuXi AppTec Full time $60,000 - $120,000 per year

Requirements:

  • Responsible for the daily operation and management of the analytical lab, ensuring smooth progress of release testing.
  • Organize lab events, deviations, and OOX investigations occurring during GMP testing.
  • Responsible for building the capability of the team, developing new business capabilities (such as oligonucleotide & peptide), and cultivate a talent echelon.
  • Responsible for the paperless construction and maintenance of analytical lab, such as ELN, LIMS, etc.
  • Ensure personnel are qualified through training and maintain continuous training and assessment.
  • Organize timely data review by personnel to ensure related deviation investigations are completed before product release.
  • Maintain good communication with same business laboratories of other sites, ensuring consistency in documentation systems and execution processes.
  • Participate in the maintenance and optimization of processes to ensure personnel are following the procedures.
  • Participate in customer audits and government inspections, promptly complete rectifications of findings, and ensure GMP compliance.
  • Timely track work progress, strengthen communication with internal and external customers, and establish stable and good relationships.
  • Ensure laboratory safety and personnel safety.
  • Responsible for other tasks temporarily assigned.
  • Assist department leaders in building a high-efficiency team.
  • Enhance the team's capabilities for new business to meet new business requirement.
  • Bring out the initiative, enthusiasm, and creativity in each team member.
  • Energize the entire team.
  • Any ad-hoc tasks assigned by supervisor.

Responsibilities:

  • Pharmacy or chemical related major, bachelor's degree or above.
  • Understand pharmaceutical production, microbiology, testing, and quality management; familiar with GMP regulations.
  • Proficient in English and Chinese, fluent in spoken English and Chinese, to communicate with internal stakeholders in China HQ.
  • Good computer skills.
  • Over 5 years of work experience, with more than 3 years in managing a GMP analytical team.
  • Good coordination and communication skills.
  • Ability to determine problems, gather information, understand facts, and draw correct and effective conclusions through scientific reasoning.
  • Project management and tracking skills.
  • Guide and supervise the work of subordinates.
  • Responsible for assigning work, assessing, and motivating subordinate employees.
  • Open for 3-6 months training in China Changzhou/Taixing.

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