Manufacturing Division Quality Control Associate Director

Merck & Co., Inc.

Not specified; not specified; not specified
Hybrid
Cgmp regulatory compliance
Analytical methodology knowledge
People management experience
The Associate Director will lead a team of analysts to ensure high standards of quality and compliance within the organization

Job Summary

  • The Associate Director will lead a team of analysts to ensure high standards of quality and compliance within the organization.
  • Responsibilities include managing analytical testing activities, leading investigations, and implementing corrective and preventive actions in accordance with cGMP requirements.
  • The role requires strong communication skills in both English and Japanese to effectively collaborate with stakeholders and manage cross-functional initiatives.

Matching Summary

The Associate Director will lead a team of analysts to ensure high standards of quality and compliance within the organization.

Salary

Not specified; Not specified; Not specified

Skills & Requirements

Must-have

  • cGMP regulatory compliance
  • analytical methodology knowledge
  • people management experience
  • cross-functional team leadership
  • CAPA and deviation management

Nice-to-have

  • Japanese language proficiency
  • continuous improvement mindset
  • strategic critical thinking
  • inclusive culture creation
  • budget forecasting skills

Key Requirements

  • Bachelor's degree in Life Science or related field
  • Minimum 8 years in pharmaceutical quality operations
  • At least 3 years of people management experience
  • Mandatory English and Japanese communication skills

Work Rights

Not specified

Tailored Resume

Cover Letter