Operational Quality Assurance Senior Specialist

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!

Scope of Duties:

 

  • Participating in the maintenance and continuous improvement of the pharmaceutical quality system in compliance with GMP, EMA, PIC/S, WHO, ISPE, PDA, and EU GMP guidelines.
  • Ensuring GMP areas comply with organizational policies and procedures appropriate to the manufacturing readiness stage.
  • Preparing and reviewing Quality Assurance documentation and verifying documentation provided by other departments.
  • Evaluating changes, conducting investigations, managing deviations, and performing risk assessments.
  • Reviewing documentation and audit trails related to manufacturing processes and equipment/installation qualification.
  • Participating in health authority inspections, customer audits, and internal audits as assigned.
  • Supporting change control, risk analysis, deviation and root cause analysis processes.
  • Verifying CAPAs in accordance with procedures.
  • Conducting regular checks of GMP areas to ensure compliance with requirements.
  • Interpreting and implementing quality assurance standards into internal procedures.
  • Collecting and compiling data for Annual Product Quality Review (APQR).
  • Analyzing quality data to identify improvement areas.
  • Identifying training needs and coordinating training programs to meet quality standards.
  • Assessing audit findings and implementing corrective actions.
  • Participating in additional projects assigned by the line manager within Polpharma Biologics S.A.
  • Working with digital systems such as TrackWise and SAP.

 

Our Expectations:

 

  • University degree in biotechnology, biology, chemistry, pharmacy or related field.
  • At least 4–5 years of experience in the pharmaceutical industry.
  • Solid understanding of GMP requirements, pharmaceutical regulations, and quality management systems.
  • Strong problem-solving and analytical thinking skills.
  • Knowledge of data integrity principles and experience with computerized systems.
  • Ability to work under pressure, manage multiple projects, and meet deadlines.
  • Excellent verbal and written communication skills in both Polish and English.
  • Proficiency in MS Office tools.

 

What we offer:

 

  • Employment at a company that is a leader in the Polish biotechnology sector, and contribute to life-changing medicines reaching patients globally.
  • Collaboration with experts from the world’s leading biotechnology companies.
  • Attractive benefits package, including:
    • Private healthcare.
    • Life insurance.
    • Employee Pension Program (EPP).
    • Annual and occasional bonuses.
    • Financial support for skills development.
    • Lunch card.
    • One additional day off per year (Polpharma Day).
  • And much more...
Why you should work with us