Strong Technical Writing (English and Spanish) mainly focuses
Strong knowledge of Microsoft Excel as a Tool for Data Analysis
Project Management
Sample Management
Ability to develop inspection or qualification protocols in a short timeframe period.
Strong negotiation skills
Knowledge in:
Computer System and Method Validation
Strong knowledge and experience with quality process management
Basic Knowledge on equipment preventive maintenance and troubleshooting
Agile on prioritization of critical tasks
Administrative shift 8:00am – 5:00pm (subject to changing business needs and project priorities).
Requirements
Doctorate or Master +2 years of directly related experience or
Bachelors +4 years of directly related experience or
Associates + 8 years of directly related experience
Preferable Scientific Background (Science or Engineering) with experience in the Pharmaceutical Industry, Quality Control, Laboratory Testing, Project Management Method Validation, Method Transfer and Quality processes. Preferable experience as Microbiologist, Chemist, Biochemistry, Molecular Sciences, or Chemical Engineering.
