Quality Associate (m/f)

pfizer.ca

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.
  • This position offers organized transport, modern automated systems, a strong education program, bonuses, affordable meals, career enhancement opportunities, and free psychotherapy.

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
  • batch documentation review
  • cGMP requirements

Nice-to-have

  • Excellent interpersonal and communication skills
  • teamwork and collaboration
  • Accountable, adaptable, systematic
  • Strong attention to detail
  • 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
  • Experience in Quality Assurance or pharmaceutical manufacturing

Work Rights

Not specified

Tailored Resume

Cover Letter