Quality Associate (m/f)

Pf Health

Savski Marof, Croatia
Quality assurance elements
Regulatory requirements
Cgmp requirements
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
  • cGMP requirements
  • product release procedure
  • batch documentation review

Nice-to-have

  • interpersonal and communication skills
  • teamwork and collaboration
  • accountable and adaptable
  • attention to detail
  • analytical thinking

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