The role involves writing and reviewing qualification documents for new and existing production systems while supervising their execution
Job Summary
The role involves writing and reviewing qualification documents for new and existing production systems while supervising their execution.
Candidates will collaborate on laboratory service documentation including SOPs, validations, deviations, and CAPA files within a global pharmaceutical team.
The position requires managing equipment controls for critical systems such as purified water, HVAC, and compressed air in a large-scale production facility.
Matching Summary
The role involves writing and reviewing qualification documents for new and existing production systems while supervising their execution.
Skills & Requirements
Must-have
HVAC system knowledge
Purified water plant operations
Vacuum pump systems
Equipment qualification documentation
SOP and validation support
Preventive maintenance supervision
Nice-to-have
Intermediate English proficiency
Team training experience
Passive guard duty participation
Supplier management skills
Change control procedures
Key Requirements
Mechanical or Electromechanical Engineer/Technician degree
Minimum 3 years experience in large pharmaceutical manufacturing