מציאת משרת הייטק בחברות הטובות ביותר מעולם לא הייתה קלה יותר
This role is available anywhere in Europe
As the Associate Director, you will lead and manage the RFP process to ensure timely and accurate responses. You will coordinate cross-functional teams to deliver project results within established timelines and support the execution of specific CDMO projects, ensuring alignment with customer expectations and company goals.
You will have over 3 years of experience in the CDMO sector, focusing on managing RFPs and/or CDMO projects. You should have experience in peptides and small molecule development and manufacturing. You will bring a scientific background in (peptides) chemistry, chemical engineering, pharmaceutical sciences or related field. You will bring a scientific background in (peptides) chemistry, chemical engineering, pharmaceutical sciences or related field.
Head of CDMO Program Management TAPI
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