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Sanitation Engineer
2 months ago
Overview
Are you ready to contribute to a pioneering global organization and engage in a groundbreaking initiative? If you have a passion for integrating innovative technologies with extensive expertise in biotech production, we invite you to consider the role of a Cleaning Engineer.
Role Summary
In the capacity of a Cleaning Engineer, your responsibilities will encompass participation in project endeavors aimed at assessing design feasibility, construction viability, scheduling, and budgeting for a new purification facility. The primary design objective will be to adopt industry-leading design standards derived from existing facilities.
You will be an integral part of a skilled user organization, collaborating with engineering partners and overseeing contractor activities. We anticipate your proactive management of project risks and your development of standards that promote clarity and structure. Your expertise will be vital in guiding the team towards implementing established solutions while also innovating new design approaches when necessary.
We are flexible in tailoring the responsibilities and level of the position to align with your professional background.
Key Responsibilities
Your main duties will include:
• Engaging in project activities such as design evaluations, risk assessments, Factory Acceptance Testing (FAT), and Site Acceptance Testing (SAT).
• Conducting tests and ensuring comprehensive documentation is maintained.
• Validating Cleaning-in-Place (CIP) processes for all operational equipment, with specific ownership of CIP-related procedures.
• Assuming professional accountability for pharmaceutical processes and equipment.
Desired Qualifications
We value candidates who possess:
• A minimum of a bachelor’s degree in a relevant field such as natural sciences or engineering.
• Significant experience in Good Manufacturing Practice (GMP) and preferably in Active Pharmaceutical Ingredients (API) production.
• A robust understanding of unit operations, pharmaceutical processes, and documentation practices.
• Familiarity with design reviews and CIP validation, which is considered advantageous.
• Proficiency in written and spoken English at a professional level.
On a personal level, you thrive in collaborative environments, demonstrate resilience, and inspire those around you. You possess the ability to balance teamwork with independent work effectively.
The ability to excel in a multicultural setting that requires independent decision-making is a crucial aspect of this position. We seek a colleague who naturally builds structure, appreciates simplicity, remains motivated to achieve success, and is eager to establish a clear direction.
About Novo Nordisk A/S
Novo Nordisk A/S is a leader in the production of biopharmaceuticals, with a commitment to improving the lives of individuals living with chronic diseases. Our dedicated workforce is integral to our mission, and we foster an inclusive environment that values diverse perspectives. Together, we strive to make a meaningful impact every day.