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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Manufacturing