Quality Associate (m/f)

Pfizer Com Ec

Savski Marof, Croatia
Quality assurance elements
Regulatory requirements
Pharmaceutical manufacturing
Monitoring and ensuring the implementation of Quality Assurance elements, regulatory requirements, and applicable standards in pharmaceutical manufacturing

Job Summary

  • Monitoring and ensuring the implementation of Quality Assurance elements, regulatory requirements, and applicable standards in pharmaceutical manufacturing.
  • Preparing and maintaining product specifications in accordance with cGMP guidelines and implementing quality requirements for new products.
  • Involvement in quality processes related to investigations, complaints, market actions, change controls, CAPA systems, regulatory inspections, internal audits, risk management, projects, and technology transfer.

Matching Summary

Monitoring and ensuring the implementation of Quality Assurance elements, regulatory requirements, and applicable standards in pharmaceutical manufacturing.

Skills & Requirements

Must-have

  • Quality Assurance elements
  • regulatory requirements
  • pharmaceutical manufacturing
  • product release procedure
  • cGMP requirements
  • quality processes

Nice-to-have

  • interpersonal and communication skills
  • teamwork and collaboration
  • accountable and adaptable
  • analytical thinking
  • problem-solving abilities

Key Requirements

  • University degree or 300 ECTS
  • Proficiency in Croatian and English
  • Competency in MS Office
  • At least 1 year of working experience

Work Rights

Not specified

Tailored Resume

Cover Letter