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New opportunities at Chiesi

Chiesi is an international research-focused pharmaceutical company with Nordic headquarters in central Stockholm.The Company has about 55 employees in the Nordic region and is in a strong expansion phase with several upcoming launches. The Company is growing and is now seeking specialists in Pharmacovigilacse and Regulatory Affairs.
Are you looking to work in an entrepreneurial organization that is part of a family-owned, research-driven and global company?
The team working with quality/pharmacovigilance/regulatory in the Nordics is under creation. The role includes being the expert in Pharmacovigilance and driving the developement in the pharmacovigilance area, including continous improvements.
Main tasks
• Handling of ICSRs
• Responsible for the company's training in pharmacovigilance
• Create local pharmacovigilance processes including local SOPs
• Actively work with continuous improvement of existing processes
• Participate in the local work with RMPs
• Participate in the local work with SDEA
• Providing local information to the global pharmacovigilance organisaion
• Work with quality monitoring and deviation management within the pharmacovigilance area.

The tasks also include some back-up to the other functions of the team (RA and QA).

Qualifications
• Degree in Science (medical or equivalent)
• Excellent language proficiency in English and Swedish or other Nordic language
• At least 2-3 years of experience of pharmacovigilance, preferably in an affiliate/marketing company

Additional experience in pharmacovigilance or related functions such as RA or QA are of interst, as well as experience from working with other Nordic cuntries.

Your profile
To be sutable for this role, you are quality focused and sees your role in a broader context. You like to be part of and build the team, take your own initiatives and work with continous improvements. You have good teamwork skills and want to dvelope in your role.

You will be located at the Nordic headquarters in Stockholm City and report to Quality/Regulatory/Pharmacovigilance Manager.
If you want to know more about the role, please contact Catharina Bergold at the recruitment specialist via bergold@rekryteringsspecialisten.se or 070-2179879.

Chiesi is an international research-focused pharmaceutical company with Nordic headquarters in central Stockholm.The Company has a about55 employees in the Nordic region and is in a strong expansion phase with several upcoming launches. The Company is growing and is now seeking specialists in pharmacovigilance and Regulatory Affairs.

Are you looking to work in an entrepreneurial organization that is part of a family-owned, research-driven and global company?

The team working with quality/pharmacovigilance/regulatory in the Nordics is under creation. The role includes nordic regulatory responsibility for an assigned product portfolio, in combination with the day-to-day work in the pharmacovigilance area.

Main tasks
• Regulatory responsibility including e.g. variations and line extensions for products approved via national, MRP/DCP and central procedure
• Acting as contact person with the Nordic authorities
• Artwork updates
• Provide regulatory support to other fuctions, acting as a regulatory expert
• Handling of ICSRs
• Act as back-up for Pharmacovigilance Specialist
• Continous improvements of the teams processes and procedures

Qualifications
• Degree in science, such as pharmaceutical or biomedicinal
• Excellent language proficiency in English and Swedish or other Nordic languages
• At least 2 years of work experience from Regulatory Affairs in the pharmaceutical industry

Language prificiency in Finnis, experience in pharmacovigilance or GDP and experience from working with other Nordic countries is an advantage.

Your profile
To fit into the role, you qualiy focused and sees your role in a broader context. You like be part of and build the team, take your own initiatives and work with continous improvements. You have good teamwork skills and want to develope in your role.

You will be located at the Nordic headquarters in Stockholm City and report to Quality/Regulatory/Pharmacovigilance Manager

If you want to know more about the role, please contact Catharina Bergold at the recruitment specialist via bergold@rekryteringsspecialisten.se or 070-2179879.

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