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De missie van AbbVie is het ontdekken en leveren van innovatieve geneesmiddelen die vandaag een oplossing bieden voor ernstige gezondheidsproblemen en de medische uitdagingen van morgen aanpakken. We streven ernaar om een grote impact te hebben op het leven van mensen in verschillende belangrijke therapeutische domeinen: immunologie, oncologie, neurowetenschappen, oogzorg, virologie, vrouwengezondheid en gastro-enterologie, naast producten en diensten uit de portefeuille van Allergan Aesthetics. Bezoek www.abbvie.com voor meer informatie over AbbVie. Volg @abbvie op Twitter, Facebook, Instagram, YouTube en LinkedIn.

European Lead, Commissioning & Qualification

Dublin, Leinster, Ierland Job ID 2205896 Categorie Engineering Afdeling AbbVie

Want to make a global impact? We offer that
Be part of a high performing international team? We offer that too

Welcome to AbbVie!

At AbbVie, our strength lies in our team of experts who conduct ground-breaking science on a global scale every day. In choosing your career & life path, choose to be extraordinary!

We are excited to be recruiting a European Lead, Commissioning & Qualification (C&Q) to join our global Engineering team. In this role, you will be responsible for setting directions, providing guidance and managing the global commissioning and qualification (C&Q) program for the European and Singapore regions. 
 
You will collaborate with the R&D and manufacturing site leadership, and Site Quality teams to drive optimum and standardized C&Q approach across the global network while leading and providing directions and validation strategy for key capital projects.  In addition, you will benchmark with other bio-pharma companies to continue to enhance the overall C&Q program for achieving optimal program outcome.  

Are you intrigued? Do you want to learn more?             

A snapshot of your key responsibilities as European Lead, Commissioning & Qualification (C&Q) are:

•    Collaborate closely with the C&Q Manager in US to set Vision and Strategy for the corporate C&Q program.
•    Implement corporate C&Q strategies.
•    Identify and implement continuous improvement ideas to enhance the program.
•    Development and plan for C&Q budget/estimates and other financial planning.
•    Provide leadership and oversight on C&Q for all European and Singapore sites.
•    Drive global paperless C&Q initiative and deployment
•    Represent AbbVie in external industry committees and network as C&Q SME
 


So, what do you need to do this role? 
•    You will have a B.S degree in Chemical, Mechanical, or Electrical Engineering with a minimum 10 years of experience in Pharmaceutical/bio-pharmaceutical industry
•    Minimum 7 years of experience in leading C&Q programs, and experience with interfacing Regulatory/Quality or auditors with 5 years + supervisory, project management and budget management experience
•    Leadership of other technical professionals and experience in leading cross-functional teams with results-orientation.  Skilled in the strategy development, initiation, selection, coordination and management of projects and have ability to solve unique problems.
•    Knowledge of regulations and standards affecting devices, biologics and pharma products.  Strong working knowledge of ICH, ISO, US CFR and EU regulations.
•    Knowledgeable with latest industry standards and guidelines on C&Q, including ISPE/ASTM
•    Strong interpersonal and communication skills (verbal/written) with strong negotiation skills

So, are you ready to take on this role? Apply today!

It’s important to remember, AbbVie is an Equal Employment Opportunity Employer; we value bringing together individuals from diverse backgrounds to develop innovative solutions for patients and being part of an inclusive work environment

Travel: Yes, 20 % of the Time
Job Type: Experienced
Schedule: Full-time
ABBVIE

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