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Quality Control Expert / Analytical Project Lead

Duchnice, PL

Boost your career with us

Polpharma Biologics is a biopharmaceutical company with state-of-the-art facilities across Europe. Operating across international centers of excellence specialized in cell line development, product and process development, clinical manufacturing, commercial scale production and regulatory affairs, allows us to work and partner on our in-house biosimilar pipeline and at the same time provide top-quality contract development and manufacturing services to the industry.

Together we develop medicines, offering a new hope to patients suffering from serious diseases. We create a passionate and friendly workplace environment. Join us!

Boost your career with us
Polpharma Biologics is a biopharmaceutical company with state-of-the-art facilities across Europe. Operating across international centers of excellence specialized in cell line development, product and process development, clinical manufacturing, commercial scale production and regulatory affairs, allows us to work and partner on our in-house biosimilar pipeline and at the same time provide top-quality contract development and manufacturing services to the industry.

Together we develop medicines, offering a new hope to patients suffering from serious diseases. We create a passionate and friendly workplace environment. Join us!

Your responsibilities include, but are not limited to:
Coordinating and implementing QC-related projects, including analytical method transfers and product testing
Monitoring project timelines and escalating risks when necessary
Supporting operational teams with project execution
Creating and approving quality system documentation
Acting as the main QC contact for cross-functional project teams
Collaborating with external partners on analytical matters
Preparing and managing project budgets within QC
Handling deviations, lab investigations, and CAPAs
Participating in audits and implementing post-audit actions
Ensuring full regulatory compliance (GMP, pharmacopeias, pharmaceutical law)

If you have:
A university degree in biotechnology, biology, chemistry or a related field
At least 5 years of experience in a pharmaceutical or biotech QC/analytical lab
Strong knowledge of analytical techniques and method validation
Familiarity with EMA guidelines, EU/US Pharmacopeia, GMP, and safety regulations
Proficiency in MS Office and fluency in English (written and spoken)

What we offer:

Competitive salary.
Private healthcare.
Life insurance.
Pension plan above national standards.
Additional free day.
and more..

Why you should work with us

Apply now »