Key Responsibilities:
Collaborate with the project team to support and align product and production-specific requirements.
Design, test, and modify recipes (under change control) during design, start-up, qualification, and production stages.
Ensure compliance with cGMP, including documenting electronic batch records (eBR), standard operating procedures (SOP), and operation reports.
Drive improvements in procedures and processes, adhering to safety, hygiene, environmental, and quality regulations within your area of responsibility.
Job Requirements:
Essential Skills:
Extensive experience with Emerson Syncade and DeltaV.
Strong background in Recipe Authoring and Troubleshooting in Syncade; experience with other MES is a plus.
Good experience in Bioprocess Automation.
Strong understanding of GMP.
Good experience in Commissioning and Qualification.
Fluent in English.
Nice to Have Skills: Experience in the Life Sciences Industries