Analyst in Group for stability and sample management (m/f)

Work location: Savski Marof

Job Description/Responsibilities:

• Coordinate stability testing activities within Quality Control, Biotech Quality Operations.
• Evaluate, trend, and report analytical results.
• Drive continuous improvement initiatives related to stability testing and sample management processes.
• Perform sampling and analysis of packaging materials.
• Collaborate with cross-functional teams to ensure timely execution of stability studies and sample management activities.
• Support compliance with GMP requirements, company procedures, and quality standards.

Qualifications:

• University degree in life science (Chemistry, Biotechnology or similar)
• At least 2 years of working experience in Bio/Pharmaceutical industry in GMP surrounding
• Croatian native speaker
• Proficiency in English language - Ability to communicate fluently in oral and written English
• Competency in MS Office applications

Candidate's profile:

• Demonstrated ability to be highly organized and detail oriented
• Adaptable, systematic and punctuate
• Skill in handling multiple tasks in an efficient manner and complete assigned duties within time frames
• Interpersonal communication skills
• Tendency for teamwork
• Ready to work in shifts

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.


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Quality Assurance and Control