This role contributes to global healthcare advancement by ensuring compliance, quality, and operational excellence across facilities
Job Summary
This role contributes to global healthcare advancement by ensuring compliance, quality, and operational excellence across facilities.
The Technical Transfer Engineering Lead is responsible for planning projects, defining budgets, and managing technical aspects for sterile departments.
Candidates must possess strong knowledge of GMP validation principles including IQ/OQ/PQ protocols and FDA/EMA regulatory requirements.
Matching Summary
This role contributes to global healthcare advancement by ensuring compliance, quality, and operational excellence across facilities.
Skills & Requirements
Must-have
Bachelor's Degree in Engineering
2-5 years GMP pharmaceutical experience
Sterile manufacturing and packaging knowledge
GMP validation IQ OQ PQ protocols
FDA/EMA regulatory compliance expertise
CAPEX budget management and forecasting
URS FAT SAT commissioning execution
Nice-to-have
Strong problem-solving analytical mindset
Excellent written verbal communication skills
Ability to work independently cross-functionally
Knowledge of data integrity requirements
Experience with risk assessment methodologies
Flexible schedule for time-sensitive activities
Key Requirements
Bachelor's Degree required
2-5 years pharmaceutical engineering experience
Experience in sterile pharmaceutical manufacturing