Life Sciences Operations Systems Senior Specialist

, Lausanne" /> Life Sciences Operations Systems Senior Specialist

,Emploi Life Sciences Operations Systems Senior Specialist,Lausanne,Agap2 is a European engineering and operational consulting group founded in 2005 and specialised in industry,We work in the pharmaceutical,biotechnology,medical devices" /> Life Sciences Operations Systems Senior Specialist

, Lausanne" /> Life Sciences Operations Systems Senior Specialist

,Emploi Life Sciences Operations Systems Senior Specialist,Lausanne,Agap2 is a European engineering and operational consulting group founded in 2005 and specialised in industry,We work in the pharmaceutical,biotechnology,medical devices" />
Description

Agap2 is a European engineering and operational consulting group founded in 2005 and specialised in industry. We work in the pharmaceutical, biotechnology, medical devices, watchmaking and precision mechanics sectors.

As a consultant, you will support our clients in carrying out their projects on site by bringing your expertise and skills. You are agile and eager to adapt to different working environments that will fuel your curiosity to see what lies behind the closed doors of the largest projects in our clients' portfolios.



Life Sciences Operations Systems Senior Specialist



?? Your missions

• Administer and develop the Veeva platforms (CRM, Vault MedComms, PromoMats, MedInquiry).

• Manage deployment, migration and system integration projects.

• Gather business requirements and translate them into effective technical solutions.

• Collaborate with international teams, IT partners and suppliers.

• Participate in innovative initiatives around AI applied to medical content and processes.

• Ensure support, governance and continuous improvement of the tools.

?? Your profile

• Minimum 2 to 5 years of experience in system administration and project management within the pharmaceutical, biotech or Life Sciences industry.

• Solid experience with Veeva solutions (CRM, Vault, MedInquiry).

• Good understanding of Medical Affairs processes and regulated environments (GxP/CSV).

• Experience with international projects and managing multiple stakeholders.

• Fluent English is essential. French is an advantage.

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