PhD Positions

Prepare, review, and maintain GMP documentation;

Ensure compliance with current good practices (GxP) and data integrity standards;

Contribute to the preparation of R&D project proposals;

Prepare and support for regulatory inspections;

Participate in deviation investigations and coordinate corrective and preventive actions (CAPA), including follow-up;

Train and supervise the work of technical staff, facilitate knowledge transfer within the team;

Contribute to scientific dissemination (reports, presentations, publications, and outreach activities);

Communicate with external regulatory bodies;

Maintain continuous professional development;

Perform additional duties as assigned in line with agreed objectives and performance indicators.

What we expect

Expected Qualifications: PhD; life sciences

Alternative qualifications: PhD in pharmaceutical, biotechnology, biological, chemical, microbiological or other relevant life sciences

Work experience: 4 years. Preferably work experience in production, bioprocess developmnet, sterile process development, quality assurance/quality control, or other professional quality experience.

What we offer

• Duration of employment: Fixed term for the duration of the project, until 31.8.2029
• Probationary period: 4 months
• Working time: 40 hours/week

More info: 00 386 1 4760 236
(dr. Darja Marolt Presen)

Requirements

• Research Field: All
• Education Level: PhD or equivalent
• Languages: ENGLISH
• Level: Good