Informacje o stanowisku

Client: Selvita

Location: Kraków, Poland

Job Category: Other

EU work permit required: Yes

Job Reference: 9594624bfe73

Job Views: 21

Posted: 23.01.2025

Expiry Date: 09.03.2025

Job Description:

Selvita is a global integrated drug discovery partner for the pharmaceutical and biotechnology industries with laboratories in Poland (Krakow & Poznan), Croatia (Zagreb), and offices in Cambridge, UK, Greater Boston Area & San Francisco Bay Area in the US. The company offers drug discovery support at every stage of the early discovery phase up to the preclinical research phase.

Continuous recruitment – that’s about Selvita! We are focused on constant team growth and we hire new employees on an ongoing basis. The team growth rate correlates with the growth of the project portfolio we perform for our clients. We are a stable employer with a clear perspective for the future.

Due to constant development, currently, we are seeking individuals with experience in the field of analytical chemistry, open for a variety of experiences, with a willingness to specialize in quality control assignments related to release testing.

As a Quality Control Specialist in the analytical chemistry team, you’ll play a vital role in the Drug Discovery processes for biotech and pharma companies from Europe, USA, and the rest of the world. Youll be working in a friendly and collaborative environment created by open-minded people, always ready for new challenges that new projects can bring, with an everyday opportunity to exchange knowledge with experienced members of the team. The variety of projects we run offers an opportunity to profile a career path in an interesting and diverse way.

At Selvita, we work knowing that the research we do makes an impact on human lives.

Key Responsibilities:

1. Performance of quality control tests of pharmaceutical and bioanalytical products and starting materials.
2. Development, analysis, interpretation of the results and registration of them in accordance with applicable procedures.
3. Planning and performing daily analysis.
4. Participation in the transfer of methods together with the preparation of related documentation.
5. Contact with clients.

Your Background:

1. Completed university degree in life sciences: chemistry, pharmacy, biotechnology or related fields.
2. Experience in chromatography techniques (HPLC, UHPLC, GC).
3. Experience in spectrophotometric techniques (UV-Vis, IR), dissolution, titration.
4. Experience in working with MS would be an asset.
5. Minimum 2 years of experience in laboratory work.
6. High motivation with excellent organization and planning skills.
7. Communication and team-working skills.
8. Fluency in English.

Your Benefits Package:

1. Extensive research facilities and modern laboratories.
2. Daily cooperation and know-how exchange with an experienced research team.
3. Long-term cooperation based on stable employment conditions and a clear career path.
4. Support of experienced mentors with international scientific experience.
5. Benefits: private medical care, on-site fitness zone & subsidized sports card, lunch benefits & fruits in the office, on-site subsidized kindergarten.
6. Support in legalization and relocation from abroad.
7. Language courses (English & Polish).
8. Complex training programs.
9. Support & incentive bonus for completing Ph.D.
10. Various sports initiatives.
11. Referral program.

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