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Dev. Quality Lead, Biosciences - Belgium  

Company managed [?] Still accepting applications

Posted on : 04 August 2017

Project Description

Description:
To strengthen our Development Quality Assurance Department, based in our development & manufacturing site in  Belgium, we are looking to fill the position of: Leader, Development Quality Assurance, Biologic.

 
 As a  'ethiborative' person and Leader, Development Quality Assurance, Biologic you like to work in an environment where you can:  
  • Use your cultural empathy to facilitate the development and manufacturing of our company  products at partner organisations 
  • Work collaboratively with colleagues from QA, Development & Manufacturing in the delivery of the pipeline and the supply of clinical products to patients 
  • Utilize your quality mindset in the execution of activities  


 As a  'ethiborative' person and Leader, Development Quality Assurance, Biologic you will contribute by:   
  • Leading QA project related activities, including manufacturing and testing activities at partner sites, thereby ensuring that all activities are conducted that ensures product quality, meets regulatory requirements and delivers business performance 
  • You will be prepared to travel as the role may require periods of significant amount of travel 
  • You will be responsible for partnering with other company  departments in order to ensure Quality Assurance support for product development activities in order to identity, mitigate and resolve compliance and quality issues that may affect our company  activities 
  • You will be responsible for liaising with other company  departments and partners in order to ensure consistent approach globally to the management of Product Development activities in accordance with company's policies and procedures  


For this position you’ll need the following education, experience and skills:   
  • Minimum of 8 years experience in a pharmaceutical regulated environment 
  • Experience of a Biolgics manufacturing or testing environment 
  • Must be fluent in English, other languages are a bonus
  • Facilitator and planner, with excellent people skills and cultural awareness that is well organised with the ability to see the bigger picture 
  • Knowledge of cGMP and appropriate regulations (eg US, European, Japanese)  
    

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