The role involves executing and managing process validation activities including manufacturing, cleaning, and sterilization to ensure cGMP compliance
Job Summary
The role involves executing and managing process validation activities including manufacturing, cleaning, and sterilization to ensure cGMP compliance.
Candidates will be responsible for writing validation plans, protocols, and reports while facilitating quality risk assessments.
Siegfried offers a flexible schedule with two days of remote work per week along with comprehensive benefits including medical insurance and pension plans.
Matching Summary
Match Score: 85
The role involves executing and managing process validation activities including manufacturing, cleaning, and sterilization to ensure cGMP compliance.
Skills & Requirements
Must-have
2-3 years validation experience
cGMP regulatory compliance knowledge
Process validation planning and execution
Cleaning and sterilization process validation
Risk assessment tools application
Nice-to-have
Collaborative cross-functional teamwork
Flexible work schedule availability
Continuous process verification expertise
Master Batch Record review skills
Key Requirements
Degree in Pharmacy, Chemical Engineering, or Pharmaceutical Technology
Spanish and English First Certificate level proficiency
2-3 years prior experience in validation department