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Gruppentreffen

Join our Team

Shape the future of pharma with us!

Are you passionate about science and innovation? Do you think ahead, connect ideas, and enjoy working in an international environment? Then you’ll fit right in with us.

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At our company, you can expect flexible working hours, flat hierarchies, a collaborative culture, and plenty of opportunities for personal and professional growth. We believe in open communication, modern workplaces, and a team spirit that values curiosity and initiative.

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Your opportunities:

We’re always looking for talented graduates and professionals in chemistry, pharmaceutics, biology, microbiology, medicine, and related fields who want to make an impact together with us and our clients.

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Currently, there are no open positions – but we’re always happy to receive unsolicited applications from motivated individuals who share our passion for science and quality.

Pharmacovigilance Specialist (m/f/d)

Part-time/Full-time

for the following areas of responsibility:

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  • EU Qualified Person for Pharmacovigilance (EU-QPPV)

  • Local pharmacovigilance contact person for our clients

  • Supporting and maintaining internal pharmacovigilance-related standard operating procedures and processes

  • Regular literature searches in defined journals and databases, reconciliation

  • Support during external pharmacovigilance audits/inspections

  • Support with ICSRs / CIOMS / XEVMPD

  • Shared responsibility for recording, documenting and following up on adverse reaction reports

  • Ensuring pharmacovigilance compliance in accordance with guidelines

  • Conducting pharmacovigilance training

  • Point of contact for internal and external enquiries regarding pharmacovigilance

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Required qualifications:

  • A university degree in a scientific discipline (preferably medicine, pharmacy, chemistry or biology)

  • You have knowledge of the creation and maintenance of pharmacovigilance-related documentation

  • You have experience of working with national and international clients and regulatory authorities

  • You have expertise in handling ADRs and conducting literature searches

  • You possess a team spirit and a structured, goal-oriented working style

  • Several years’ professional experience in the pharmaceutical industry and in the field of pharmacovigilance/regulatory affairs is an advantage

  • An independent, team-oriented, proactive, service-minded individual with a confident and pleasant manner

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We offer you a highly challenging role with scope for initiative and creativity right from the start. The comprehensive induction programme will help you settle in and provide you with the necessary know-how for a successful role. Within our open and dynamic structures, supported by continuous professional development, you will find the ideal conditions for your career with us. Salary on application and in accordance with the collective agreement, with a competitive salary above market rates provided depending on qualifications and professional experience.

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Location: Graz and/or remote

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If you are interested in joining a young, dynamic team at the interface between research/development and industry/business, please contact:

 

Mag. Lydia Morawetz

Ragnitzstraße 55, 8047 Graz

Tel. + 43 69 1313 9767; office@prsg.at

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