Validation Supervisor

pfizer.de

Jakarta, Indonesia
**
Validation master plans
Validation protocols
Validation reports
** Pfizer is seeking a Validation Supervisor in Jakarta, Indonesia, to ensure compliance with quality standards in pharmaceutical processes. The role requires a strong technical background in validation, experience in the pharmaceutical industry, and the ability to manage multiple projects in a fast-paced environment. **

Job Summary

  • Evaluate, review, and approve validation master plans, protocols, and reports, ensuring compliance with company standards and regulatory requirements.
  • Manage routine quality systems such as Change Control, Documentation, and Investigations, and coordinate testing with functional groups.
  • Maintain and manage of Continued process verification (CPV) and Periodic Cleaning Monitoring (PCM).

Matching Summary

Match Score: 75

** Pfizer is seeking a Validation Supervisor in Jakarta, Indonesia, to ensure compliance with quality standards in pharmaceutical processes. The role requires a strong technical background in validation, experience in the pharmaceutical industry, and the ability to manage multiple projects in a fast-paced environment. **

Skills & Requirements

Must-have

  • validation master plans
  • validation protocols
  • validation reports
  • GMP
  • pharmaceutical development processes
  • validation/qualification of pharmaceutical processes
  • equipment
  • utilities
  • facilities
  • computer systems
  • statistical analysis
  • process anomalies
  • Quality Investigations
  • Change Control
  • Documentation
  • regulatory audits
  • Continued process verification
  • Periodic Cleaning Monitoring

Nice-to-have

  • innovative, flexible, customer-oriented culture
  • mentoring and guiding colleagues
  • Lean Six Sigma Yellow Belt or Green Belt certification

Key Requirements

  • Degree in pharmacy, pharmaceutical technology or comparable scientific discipline
  • Minimum two years of experience in pharmaceutical industries
  • Strong knowledge of regulatory requirements
  • Strong technical knowledge with validation/qualification
  • Excellent verbal and written communication skills
  • Ability to work independently and in a team environment
  • Ability to work under pressure and adapt to a fast-paced environment
  • Strong analytical and problem-solving skills
  • Strong organizational and time management skills
  • Willing to be placed in Jakarta

Work Rights

Not specified

Tailored Resume

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