About this role
Work location: Savski Marof
Job Description/Responsibilities:
• Knowledge in GMP documentation practice • Conducting incident investigations. • Documenting the investigation of the cause of the incident. • Defining and documenting corrective and preventive actions resulting from the incident impact investigation. • Defining and documenting the verification of the effectiveness of corrective and preventive activities resulting from the investigation of the impact of the incident. • Monitoring and reporting on conducted incident investigations. • Initiating follow-up tasks defined during incident investigations. • Work in 1 shift.
Qualifications:
• University degree or 300 ECTS in Chemical Technology, Biotechnology, Animal Health, Pharmacy, Chemistry • Proficiency in Croatian and English language • Competency in MS Office applications and internet • At least 2 years in Pharmaceutical Industry
Candidate's profile:
• Accountable, adaptable, systematic and punctuate • Interpersonal and communication skills • Experience in teamwork • Experience in working with sterile product is preferred. • Experience in working with GQTS, pDOCS, SAP system, Veeva Vault (eQMS) is preferred.
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