The Stability Program Coordinator position at a leading biopharmaceutical company requires expertise in stability protocols, regulatory compliance, and cross-functional collaboration. The candidate should possess a degree in a relevant field and have at least four years of industry experience, alongside strong organizational and communication skills
Job Summary
We aspire to be the premier research-intensive biopharmaceutical company delivering innovative health solutions that advance disease prevention and treatment for people and animals.
The role involves drafting and maintaining stability protocols, managing sample lifecycle and data integrity, supporting audits, and collaborating with global teams to ensure compliance and continuous improvement.
This position supports digitalisation efforts, KPI reporting, and harmonization with global standards while driving improvements in stability workflows and scheduling.
Matching Summary
Match Score: 85
The Stability Program Coordinator position at a leading biopharmaceutical company requires expertise in stability protocols, regulatory compliance, and cross-functional collaboration. The candidate should possess a degree in a relevant field and have at least four years of industry experience, alongside strong organizational and communication skills.
Skills & Requirements
Must-have
Stability protocol management
ICH guidelines compliance
GLIMS proficiency
GMP and GDP adherence
Stability chamber management
Data integrity and documentation control
Trend analysis and OOT detection
Nice-to-have
Lean Six Sigma experience
Cross-functional collaboration
Continuous quality improvement
Digitalisation and KPI reporting
Strong organizational skills
Flexible and self-motivated work style
Key Requirements
Degree in Science/Technical/Quality or related field
4 years’ experience in biotechnology or pharmaceutical industry
Understanding of cGMP requirements for laboratory operations
Knowledge of GMP, ICH, USP and global compendia regulations