Porton PharmaTech, d.o.o.

Porton PharmaTech, d.o.o. is the first research and development and production unit of Porton Pharma Solutions Ltd. in Europe. As a contractual partner, we will provide CDMO services in the field of active pharmaceutical ingredients (small molecule area) for large and well-known pharmaceutical companies around the world.

Do you want to join a newly formed company, an expert, international team and build a success story with us? Connect with us! jobs@portonpharmatech.com

QC Analyst (m/f)

PLACE OF WORK

Mengeš

APPLICATION DEADLINE

31.10.2025

TYPE OF EMPLOYMENT

Full time, permanent

Porton PharmaTech, d.o.o. is the first research and development and production unit of Porton Pharma Solutions Ltd. in Europe. As a contractual partner, we will provide CDMO services in the field of active pharmaceutical ingredients (small molecule area) for large and well-known pharmaceutical companies around the world.

Do you want to join a newly formed company, an expert, international team and build a success story with us? Connect with us! jobs@portonpharmatech.com


Job responsibilities

  • Perform routine and non-routine analyses in the QC laboratory (e.g., HPLC, GC, GC-HS, IR, KF, LOD, ROI, titration, etc.);
  • Ensure compliance with GMP standards, SOPs, and internal quality requirements;
  • Maintain accurate and complete laboratory documentation to support audits and inspections;
  • Contribute to method validation, method transfer, stability studies, and cleaning validation;
  • Provide analytical support to cross-functional departments (R&D, Production, QA);
  • Ensure laboratory housekeeping, equipment maintenance, and safety compliance;
  • Use laboratory data systems (e.g., Empower 3®, MassHunter, MassLynx) for data processing and reporting.

What we expect

  • Perform routine and non-routine analyses in the QC laboratory (e.g., HPLC, GC, GC-HS, IR, KF, LOD, ROI, titration, etc.);
  • Ensure compliance with GMP standards, SOPs, and internal quality requirements;
  • Maintain accurate and complete laboratory documentation to support audits and inspections;
  • Contribute to method validation, method transfer, stability studies, and cleaning validation;
  • Provide analytical support to cross-functional departments (R&D, Production, QA);
  • Ensure laboratory housekeeping, equipment maintenance, and safety compliance;
  • Use laboratory data systems (e.g., Empower 3®, MassHunter, MassLynx) for data processing and reporting.

Our offer

  • A dynamic role in a growing international CDMO company.
  • Professional training and career development opportunities.
  • A collaborative, safe, and compliant working environment.

As a member of our growing team you will play a vital role in ensuring stable, secure, and efficient operations while supporting the needs of our business.

Is this job a challenge for you? You are invited to submit your application in Slovene and English using portal mojedelo.com.

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QC Analyst (m/f)

PLACE OF WORK

Mengeš

APPLICATION DEADLINE

31.10.2025

TYPE OF EMPLOYMENT

Full time, permanent

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