*QA MES Specialist** *Location**
: Schaffhausen (hybrid working 3 days onsite /2 days home office
*)
Duration of the contrac**
t: Until 31st December 20
*26
Hours per we**
ek: 40 ho
*urs
Essenti**
al: Both languages English & German, 3 years plus within a GMP environment and previous experience of batch record systems is mandatory,
MES
Imagine your next project supporting the digital transformation of life-saving medicine production. We are seeking a highly skilled and experienced QA MES specialist to strengthen the QA Parenterals Team. This role is at the heart of our challenging journey to digitalize batch records, offering the opportunity to work with cross-functional teams on exciting projects where quality is always the North
*Star.
roles and responsi**
bilities You will own compliance-relevant project tasks within the MES implementation, ensuring every digital step meets our rigorous st andards.
This wil
l involve:
Owning compliance relevant project tasks within the MES project, define framework conditions and approve relevan
t proceduresApprove and release MES relevant data in the frame of the project im plementationReview and approve MES relevant NC and CoC recordsTake over the QA MES role during Dry Run, Verification and Wet testingMaintain compliance with all company policies and procedures.Working in a hybrid model (3 days onsite in Schaffhausen, 2 days h *ome office).**
how to succeed You are a quality-minded professional who thrives at the intersection of traditional GMP standards and modern di gital systems.
You
**will also bring:
Professional experience in a GMP environment (Pharma, Bio-Tech,**
**or Food industry)Full professional proficiency in both German and E** **nglish (Mandatory)Proven experience with MES (Manufac