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

QA Specialist (m/f)

PLACE OF WORK

Mengeš

APPLICATION DEADLINE

30.09.2025

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

  • Prepare, review, and maintain quality system documentation in compliance with cGMP.
  • Review and approve deviations, CAPAs, quality events, qualification documentation and related tasks.
  • Support the batch release system for manufacturing and packaging.
  • Participate in preparation and review of procedures and batch documentation.
  • Conduct risk assessments and support investigations.
  • Perform audits of suppliers and service providers.
  • Work cross-functionally with other departments to ensure timely closure of quality actions.
  • Actively contribute to continuous improvement initiatives.
  • Ensure compliance with HSE (Health, Safety & Environment) standards.

What we expect

  • University degree in pharmaceutical, chemical, or other relevant natural sciences (e.g. biochemistry, biology, biotechnology).
  • Previous work experience in Quality Assurance within the pharmaceutical, chemical, or CDMO industry is essential).
  • Strong knowledge of GMP regulations and quality processes.
  • Excellent written and verbal communication skills.
  • Analytical mindset with problem-solving ability and attention to detail.
  • Ability to work under pressure and meet strict timelines.
  • Professional integrity and a proactive, collaborative approach.

Our offer

  • Permanent job contract with a trial period.
  • Dynamic and stimulating work environment that values expertise and innovation.
  • Opportunity to actively contribute to the development of a fast-growing international company.
  • Exposure to a regulated, science-driven, and international industry.
  • Professional growth and career development opportunities.

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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QA Specialist (m/f)

PLACE OF WORK

Mengeš

APPLICATION DEADLINE

30.09.2025

TYPE OF EMPLOYMENT

Full time, permanent

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