מציאת משרת הייטק בחברות הטובות ביותר מעולם לא הייתה קלה יותר
Job Description
Theat our Carlow Site will ensure compliance of vaccine and biologics manufacturing processes with cGMP and regulatory requirements. This role involves providing cross-functional support, facilitating compliance, and supporting quality systems, monitoring, and management. Ideal candidates will have 3-5 years of pharmaceutical/regulatory experience and a strong working knowledge of aseptic processing and environmental monitoring in a sterile manufacturing facility. The role also includes liaising with technical experts from other sites and providing technical expertise and training in various operational areas.
What you will do:
Bring energy, knowledge, innovation, and leadership to carry out the following:
What skills you will need:
In order to excel in this role, you will more than likely have:
Current Contingent Workers apply
*A job posting is effective until 11:59:59PM on the dayBEFOREthe listed job posting end date. Please ensure you apply to a job posting no later than the dayBEFOREthe job posting end date.
Job Posting End Date:09/24/2024
A job posting is effective until 11:59:59PM on the day BEFORE the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date.
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