Sterility assurance engineer
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CAI Overview: Are You Ready? CAI is a professional services company established in 1996 that has grown year over year to nearly 800 people worldwide. For Life Sciences and Mission Critical industries that need to deliver critical solutions in high-stakes environments, we provide accelerated operational readiness and unparalleled performance at the highest standard through our rigorous approach, field tested processes, and elite expertise developed over 30 years. Our approach is simple because our Purpose informs everything we do:
- We exist to be the trusted solution for our clients as they strive to build a better working world and improve the human experience.
- We act with integrity
- We serve each other
- We serve society
- We work for our future
- Experience with microbiological and biological methods, including method application and validation.
- Understanding of quality systems, GMP regulations, and Good Documentation Practices.
- Familiarity with Annex 1 requirements and sterile manufacturing principles.
- Experience with aseptic techniques and biological safety cabinets.
- Ability to work independently while managing multiple priorities.
- Strong attention to detail, organizational skills, and problem-solving capabilities.
- Intermediate level professional with hands-on experience in sterility assurance and aseptic process validation activities.
- Capable of independently managing documentation, coordinating assigned activities, and supporting field execution when required.
- Strong communication and stakeholder management skills.
- Comfortable working in cross-functional and project-based environments.
- Proficient in spoken and written English.
- Strong technical writing and documentation skills.
- Ability to work autonomously and proactively.