משרות תוצאות חיפוש מתאימות לבקשתך:

The opportunity
Are you an experienced project manager looking for a new challenge in the pharmaceutical industry? Are you motivated by improvement and growth? Then the Investigation and Improvement team is the right fit for you! Join Teva Haarlem as a Senior Project Professional! Be part of this dynamic team, which is the brain of the company! Help us to execute improvement projects within production and work together with various teams to improve our processes. Initiate changes and execute CAPA’s in the Manufacturing department in response to production deviations, audit observations, or as part of continuous improvement. Make recommendations for working conditions ans assess current processes!
Your responsibilities
Responsible for the execution of improvement projects within production, including:
 
Ensure the execution of improvement project activities related to pharmaceutical manufacturing processes (bulk production and packaging):

•    Drawing up, initiating, and executing CAPA’s and Changes in the Manufacturing department in response to production deviations, (internal and external) audit observations, or as part of continuous improvement.
•    Executing updates of SOP’s and implementation of new working procedures and technical improvements. The projects may relate to Safety, Quality or Operational excellence. 
•    Performing Impact Assessments related to Changes. 
•    Writing test protocols and reports related to the CAPA’s and Changes. 
•    Representing the production department and providing production knowledge in project teams for introduction of Capex. 

Provide substantive and technical support to the Business Unit with regard to improvement processes:
 
•    Assess current processes and write justifications or initiate changes where applicable. 
•    Making recommendations for working conditions, (product) safety and the environment.
•    Support the production department in case of safety, process, or quality issues.
•    Make proposals to improve manufacturing methods and to implement developments in manufacturing technology.
•    Participate in various projects to improve quality aspects.

Implement and maintain the corporate quality and GMP instructions, ensure adequate protocolling:
 
•    Reviewing SOPs.
•    Support with Compliance investigations and Audit responses.
•    Knowledge transfer, training of manufacturing personnel or technicians.