Senior Stability Specialist (m/f)

About the role

JGL, a Croatian pharmaceutical company operating on 60 global markets, is looking for a Senior Stability Specialist in Rijeka. The role suits someone who understands GMP requirements, quality and regulatory compliance, enjoys analysing stability data and working with documentation, procedures and colleagues.

Key responsibilities

• Create, review and approve stability documentation in line with regulatory requirements and internal standards
• Analyse and interpret stability data and give expert opinions on product quality, trends and shelf life
• Take part in investigations into stability results and follow up corrective and preventive actions
• Oversee implementation of new equipment and software, including qualification, validation and data integrity
• Monitor regulatory requirements and support internal units and business partners

Required profile

• Higher education in biomedical or chemical fields (pharmacy, chemistry, sanitary, laboratory technician and similar)
• At least two years of experience in a pharmaceutical quality control or quality assurance department
• Knowledge of GMP, regulatory guidelines and registration documentation
• Active English at B2 level or higher
• Organised, proactive and team-oriented

Required skills

• Computer literacy, with emphasis on Excel
• Good time management and organisational skills

What we offer

• First shift work (8–16 hours) in clean rooms with mentorship and validated methods
• Onboarding, performance management, development plans, training and mentoring
• Flexible benefits package, annual bonus depending on company results
• Voluntary health insurance and accident insurance
• Christmas bonus, holiday allowance, tax-free reward, family support and official mobile phone

Candidates apply through the online application form by 16 November 2026; only those meeting the requirements will be shortlisted.