Job Description/Responsibilities:
- Main task - regular participation in manual and automated production activities on floor in 3 or 4 shifts.
- Execution of daily production activities.
- Participation in cleaning and disinfection of controlled classified production areas.
- Cleaning and sterilization of equipment, equipment parts, dishes and utensils per current procedures.
- Monitoring and filling of technical documentation during production.
- Responsibility for material and raw material status and inventory in production environment.
- Confirmation and tracking of material usage using current application (SAP).
- Application of relevant guidelines and procedures in the production.
- Creation of new Standard Operating Procedures (SOPs), revision of current SOPs and creation of new Job Aids.
- Training of employees according to current SOPs and Job Aids per Good Manufacturing Practice (GMP) guidelines.
- Participation in changes, amendments and improvements in the product quality requirements.
- Performing necessary actions, research and measures in case of deviations during production.
- Participation in improvement of the existing technological processes.
- Participation in creation of other documentation for the process according to the GMP standards.
- Implementation of validation activities.
- Participation in the transfer of technological processes.
- Implementation and improvement of environmental protection measures, safety at work and fire protection in accordance with the regulations and by-laws.
- Continuous professional development and monitoring of new technologies and equipment.
- Responsibility for department inventory, technical documentation and its storage.
- Participation in interdepartmental activities and active exchange of business and professional information and knowledge.
Qualifications:
- University degree or 300 ECTS in Biotechnology, Chemical Technology, Pharmacy, Chemistry, Animal Health, Technical Studies
- Proficiency in Croatian and English language
- Competency in MS Office applications and Internet
Candidate's profile:
- Accountable, adaptable, systematic and punctuate
- Skilled in teamwork and communication
- Ready to work in 3 or 4 shifts
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Manufacturing
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What We Do
Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.
Why Work With Us
We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.
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