QA for Drug Substance Production [Denmark]


 

Do you want to help secure products for the market from our Drug Product factory?
Are you motivated by a diverse everyday life characterized by new challenges and problem solving? Are you challenged by ensuring the quality of Batch documentation?

Then it might be you we are looking for, in our newly established Drug Substance Team in QA Operations.

We are looking for a candidate that:

  • Hold a Master of Science within Pharmacy, Biotechnology, Biology or similar
  • Have 1-3 years of work experience within the pharmaceutical industry, preferably within Quality Assurance within a Production environment
  • Have solid GMP/Good Documentation Practice (GDP) knowledge
  • Experience with releasing product
  • Master fluent English and Danish in writing and speech

The role as QA for Drug Substance Production

  • Participate in the core tasks of the team where your contribution matters

  • QA review and approval of SOPs, Change Control

  • Review and QA approval deviations, and guidance during root cause analysis
  • Batch Journal Review
  • Daily coordination and prioritization
  • Provide quality advice and ensure quality oversight & compliance
  • Participation in optimization projects within batch review and daily operations

As a person you are:

  • Structured and thrive on solving new challenges daily.
  • You manage to find pragmatic solutions without compromising on product quality.
  • Communication with collaborators is a big part of the job.
  • You got eye for details, but you are able to set things in perspective
  • Stakeholder management and adapting your communication to different partners.
  • Proactive and actively contribute to implementing improvements

Together we succeed - do you want to join?

The QA Operations organization will consist of approximately 46 employees based in Kvistgaard (36) and Munich (3) and four Managers.

It is a growing department which currently consists of these QA teams: Drug Substance (Building 1), Drug Substance (Building 8), Drug Product, EQ (Equipment Qualification), ENV (Environment), QC (Quality Control), RM (Raw Material), and Warehouse, OMCL, and the QA Operations Management Team.

You will join the newly establish DS Building 8 QA Team located in Kvistgaard Denmark, and become part of the QA Operations reporting to the QA Manager for the Team.

We offer

Besides focusing on saving lives every day – being a large-scale vaccine company, we also offer a great canteen, cold soft drinks, nice coffee, and a modern work environment.

In Bavarian Nordic, we believe in the power of the team, and you will be part of a global team of +1000 dedicated people with diverse backgrounds and viewpoints who are bound together by our commitment to protect lives every day. We believe in creating an inclusive and flexible workplace with a strong focus on personal and professional development because we need each other to take things further.

Do we have your attention? Ready-Set-Apply!

We are interviewing on an ongoing basis and look forward to receiving your application as soon as possible. We cannot wait to get to know you better!


 

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