Process Engineer III
2 months ago
About the Role
We are seeking an experienced Process Engineer III to join our team at Novo Nordisk. The successful candidate will play a key role in ensuring production quality and compliance, preparing for audits, and executing validation and revalidation. As a Process Engineer III, you will be responsible for maintaining compliance between authorities and NN requirements, as well as global standards and local SOPs.
Main Responsibilities
- Ensure production quality and compliance by maintaining adherence to cGMP regulations and NN standards.
- Develop and maintain local procedures and standards within the process area, including training materials and documentation.
- Lead and drive process optimization and improvement, including event response and NC handling.
- Participate in validation, technology transfer, and process improvement initiatives.
- Ensure effective communication and collaboration with cross-functional teams.
Requirements
- 4-6 years of relevant working experience in aseptic process of cGMP regulated pharmaceutical industry or life science industry.
- Experience with cGMP or GMP manufacturing process validation/qualification.
- Strong documentation experience and ability to write high-quality validation documentation.
- Excellent communication and interpersonal skills.
What We Offer
At Novo Nordisk, we are committed to creating an inclusive culture that celebrates diversity and promotes equal opportunities for all employees. We believe that our employees are our greatest asset, and we strive to provide a work environment that is engaging, challenging, and rewarding.
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