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