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Specialist in Raw Material and Pharmaceutical Analysis – Fresenius Kabi

FRESENIUS KABI AB

Stockholms län, Upplands-Bro

Previous experience is desired

30 days left
to apply for the job

We are a growing company with approximately 1,000 employees in Sweden and over 40,000 employees worldwide. Our pride in our products permeates the entire company. In our employee surveys, colleagues, development opportunities, and the family-like atmosphere are highlighted as some of the best things about working at Fresenius Kabi.

Being part of Fresenius Kabi is synonymous with being part of an environment with future prospects. We believe in our staff and are passionate about developing all our employees. You have great opportunities to influence how this development looks. Fresenius Kabi has, for the fourth year in a row, been named a Career Company, making us an attractive employer in Sweden thanks to our unique career opportunities. Our global organization means there is a wide variety of paths to choose from as part of your future development.

1 position(s).

The section for analysis of self-manufactured and purchased raw materials at Fresenius Kabi is located at the facility in Brunna. Here, responsibility lies for the development, implementation, and execution of chemical analyses to ensure the quality of incoming and self-manufactured raw materials. The department plays a crucial role in the quality control of raw materials used in Fresenius Kabi's manufacturing of pharmaceuticals. QC Brunna has approximately 35 employees who work closely together in teams and enjoy their work.

Responsibilities

As a specialist, you are responsible for providing chemical expertise in the areas of; raw material analysis, finished pharmaceutical analysis, development and validation of analytical methods, instrument qualification, and handling regulatory issues regarding analytical methods. You plan your own work according to given priorities and timeframes, where short deadlines may occur during certain periods, requiring good ability to handle several ongoing activities simultaneously and make relevant prioritizations.

Responsibilities also include participating in deviation investigations, as well as drafting and maintaining the department's SOPs.

About You

We place great emphasis on personal qualities, analytical competence, and the ability to independently perform tasks within set timeframes. We are looking for someone who is meticulous, results-oriented, and flexible. In this role, you are expected to initiate and drive activities and tasks in parallel, which requires a structured approach to work.

We want you, the applicant, to have:

  • An academic education in analytical chemistry or equivalent competence.
  • At least 5 years of experience from one of the above areas that the group is responsible for, as well as experience in independently initiating and driving larger tasks.
  • Very good ability to express yourself in English and Swedish, both orally and in writing, as well as good knowledge of MS Word and MS Excel.

As a specialist, it is important that you enjoy independently planning, driving, and taking responsibility for your own work. You will also lead and support others and have close contact with different functions within quality control, tech transfer projects, and production. Many meetings take place in close collaboration with your colleagues, which requires good teamwork and communication skills.

To succeed in this role, you need to be curious, goal-oriented, and structured. You possess good problem-solving and reasoning skills and have an easy time seeing the big picture where you make correct checks and prioritizations in parallel tasks and projects. It is also important that you are self-reliant in your work, take initiative, and demonstrate good judgment.

Experience in independently driving own larger tasks/projects, authority inspections, and experience from GMP-regulated operations in one or more of the areas that the group is responsible for is meritorious. We place great emphasis on your personal qualities.

About the Position

The position is a fixed-term appointment on probation, which after 6 months converts to a permanent position after agreement between the parties. The location is in Brunna, Kungsängen.

Contact

If you want to know more about the position, you are welcome to contact the recruiting manager Reefat Rahman via email: [email protected] (mailto:[email protected]).

For union representatives, you can email [email protected] (mailto:[email protected]) for contact with Unionen and [email protected] (mailto:[email protected]) for contact with the Academic Association.

We warmly welcome your application via the link. Unfortunately, we do not accept applications via email or post. Selection and interviews are conducted on an ongoing basis. An appointment may be made before the last application date, so do not hesitate to send in your application today!

Our recruitment process includes tests, interviews, reference checks, and background checks. During the interview, we ask you to present your degree transcript and relevant certificates. For the final candidate, a pre-employment health examination is conducted at our occupational health service.

Employment Type: Permanent.
Duration: Permanent.

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