Sterility assurance engineer

ph3CAI Overview: /h3 pbAre You Ready? /b /p pCAI 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. /p h3Our approach is simple because our Purpose informs everything we do: /h3 pWe exist to be the trusted solution for our clients as they strive to build a better working world and improve the human experience. /p h3At CAI, we are committed to living our Foundational Principles, both professionally and personally: /h3 pWe act with integrity /p pWe serve each other /p pWe serve society /p pWe work for our future /p pAt CAI, we believe in a relentless dedication to excellence, pushing boundaries and surpassing /p pexpectations. From the beginning, we’ve challenged ourselves to do what others wouldn’t. Not just setting industry standards, but redefining them entirely. We are bold in our thinking and creative in our approach. We operate at the intersection of wisdom and technology and thrive when they come together with humanity. For us, operational readiness isn’t simply a goal. It’s a way of life. Because tomorrow demands to be at the forefront of today. We do this through tireless effort, precision, efficiency and an unwavering belief that there is always room for advancement. We’re not interested in how it used to be done. We’re obsessed with how it will be done. /p h3Key Responsibilities: /h3 ul liExperience with microbiological and biological methods, including method application and validation. /li liUnderstanding of quality systems, GMP regulations, and Good Documentation Practices. /li liFamiliarity with Annex 1 requirements and sterile manufacturing principles. /li liExperience with aseptic techniques and biological safety cabinets. /li liAbility to work independently while managing multiple priorities. /li liStrong attention to detail, organizational skills, and problem-solving capabilities. /li /ul h3Preferred Profile /h3 ul libIntermediate level professional with hands-on experience in sterility assurance and aseptic process validation activities. /b /li libCapable of independently managing documentation, coordinating assigned activities, and supporting field execution when required. /b /li libStrong communication and stakeholder management skills. /b /li libComfortable working in cross-functional and project-based environments. /b /li /ul h3Essential Requirements /h3 ul libProficient in spoken and written English. /b /li libStrong technical writing and documentation skills. /b /li libAbility to work autonomously and proactively. /b /li /ul pbWillingness to travel domestically and internationally if required. /b /p pbLa selezione rispetta il principio delle pari opportunità (l. 903/77) /b /p p€45,000 - €57,000 a year /p pbThe compensation package offered ranges from €45,000 to €57,000 gross per annum (Gross Annual Salary). The final salary within this range will be determined according to the candidate’s technical competencies and relevant professional experience. /b /p /p #J-18808-Ljbffr