QC Specialist

We are reinforcing our Quality Control team! Quality Control team is responsible for in-process and release testing of the manufactured batches in order to prove they are acceptable for patient use. We are now looking for Specialist for HPLC analyses.

As a Specialist for HPLC you will be a contact person for HPLC in-house assays. Your main responsibility is to organize and control the routine HPLC-based assays. That includes participating in planning of the assays, ensuring they are performed as scheduled, and approving the final results. You may also be needed for practical laboratory work occasionally. Besides the routine analysis responsibilities, you will need to communicate with the analytical development team to support the establishment of new processes and improving the existing ones. Close communication with other department and teams will also be required. In addition, the related GMP documentation (standard operating procedures, specifications, CCs and CAPAs) as well as participating in various investigations will be under your responsibility.

You should have a degree in biochemistry, chemistry or equivalent with good knowledge on biochemical analyses and being familiar with chromatographic techniques. Previous working experience in the pharma industry or with HPLC is beneficial.  

You could be the person if…

  • You communicate and produce clear and accurate documentation in English.
  • Your work approach is precise and you achieve objectives set to you in a timely manner.
  • You apply your expertise, make rational decisions based on the data at hand and find new solutions to clear obstacles.
  • As a person, we would like you to be open-minded towards new challenges and self-development and spread good team spirit.
  • You can adjust to rapidly changing situations and timelines.

We offer you an active and lively work community with diverse staff. Furthermore, we will support your personal development and well-being.

Please apply by 30th Nov 2022. We will start interviewing suitable applicants during the application period.

For more information regarding this position, you can contact QC Team Lead Mikko Ylilauri on weekdays between 9-15 phone +358(0) 44 430 4609.

Apply between and

What we are looking for

  • suitable educational background and professional profile
  • English skills


  • ePassi wellbeing benefit
  • extensive occupational health-care
  • physical and cultural free-time activities


FinVector Oy is a growing pharmaceutical company authorized by FIMEA, following the procedure of Good Manufacturing Practice (GMP). FinVector is internationally recognized and is a pioneer in its operational field. FinVector works on the cutting-edge biopharmaceuticals and we’ve invested into building state-of-the-art development and GMP facilities for Viral Vector and Cell Therapy platforms including vaccines. Our research and development agenda is focused on the most commonly used gene therapy vectors: adenoviral, adeno-associated viral (AAV) and lentiviral vectors and innovative cell therapies. FinVector offers a versatile and responsible work environment and the work is done together with a group of professionals from various fields. FinVector is owned by Ferring Ventures and we are located in Kuopio, Finland.

Location: Microkatu 1, Kuopio

QC Specialist

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