GMP Supporter

at  Novo Nordisk

GMP Supporter
Category: Engineering & Technical
Location:Kalundborg, Region Zealand, DK
Do you want to be part of an organisation that makes a difference for thousands of people every day? Can you maintain an overview and ensure compliance in a dynamic environment? Are you good at problem solving and are a team player? Do you enjoy being able to use your analytical approach to optimise and improve processes?
If so, read more and apply today for a life-changing career as a GMP supporter at the warehouse within Finished Products Manufacturing (FPM) based in Kalundborg!

THE POSITION

As our new GMP Supporter, you will be welcomed into a team of 12, and will be involved in various daily tasks to support the warehouse and logistics departments with GMP Support. If you are looking for a varied role where you can apply your strong GMP experience to develop strategy, provide solutions and implement new processes through working closely with other departments, then this role could be for you!
In addition to documenting quality incidents within the warehouse and providing guidance to operators about the correct procedures for documenting events accurately, you will also be responsible for:

• 
  Handling quality issues in the warehouse
  
• 
  Investigating and reporting deviations
  
• 
  Supporting Warehouse and Logistics, in the processes
  
• 
  Participate in workshops, tests or fix issues with proposed improvements in our processes
  
• 
  Updating and improving SOPs
  
• 
  Training of operators in new tasks
  
• 
  Systematic problem-solving
  
• 
  Present cases at internal audits and authority inspections
  No two days are the same, the interface is very wide and there are often new issues to follow up. We are excited the warehouse is about to be automated! Therefore, our new colleague is willing to alter existing processes, utilise LEAN principles to optimise them and actively seeks to improve the entire department alongside the team.

  QUALIFICATIONS

  Your experiences include:
  

• 
  Degree or equivalent in Pharmacy, Chemistry, Engineering or related field.
  
• 
  The ideal candidate has 2-4 years of work experience within GMP in the pharmaceutical industry. Experience working in other highly regulated industries is also of interest.
  
• 
  Hands-on approach to executing processes and solving challenges amongst stakeholders within the department and cross functionally.
  
• 
  Fluency in spoken and written Danish and English.
  You see yourself as a fast learner with strong analytical skills to gain oversight of complex processes and issues. You thrive taking on challenges and able to take the lead, show initiative and prioritise to work systematically to resolve them within deadlines. Since you will be working closely in the team and cross functionally, great communication skills are important to support driving the strategy.

Please refer the Job description for details