Regulatory Operations Intern: Data & Submissions

OM Pharma SA; Meyrin; In loco; CHF 17.000 - 23.000; Tempo pieno

Vantaggi offerti da questo lavoro

Paid internship

Mentorship by RA team

International exposure

Descrizione del lavoro

OM Pharma SA in Meyrin invites motivated students to join a paid 6 to 12-month internship at our headquarters. You will work under the supervision of the Regulatory Operations Team Lead and collaborate with the RA team and external partners to support regulatory data management, dossier maintenance and electronic submissions.

This internship offers hands-on regulatory operations experience within an international pharmaceutical environment, with exposure to health authority submissions and

Competenze

• Currently pursuing a Bachelor's or Master's degree in a life sciences field.
• Strong interest in pharmaceutical regulatory affairs and data management.
• Good command of English; French/Spanish is a plus.

Mansioni

• Support regulatory operations activities and projects with accurate documentation
• Maintain and update product and registration information in regulatory databases
• Review regulatory data for accuracy and completeness
• Archive regulatory documents and submission packages per internal procedures
• Assist with preparation and technical review of electronic submission packages for health authorities
• Contribute to management of regulatory data used for health authority submissions
• Collaborate with stakeholders and partners to collect and update regulatory data
• Track regulatory submissions and project progress using tracking tools
• Stay updated on regulatory requirements and best practices

Conoscenze

English proficiency B2

MS Office

Veeva familiarity

Formazione

Bachelor or Master in Life Sciences, Pharmacy, Regulatory Affairs, Health Sciences or related

Strumenti

Veeva

Regulatory databases / document management systems

MS Office

Descrizione del lavoro

OM Pharma SA in Meyrin invites motivated students to join a paid 6 to 12-month internship at our headquarters. You will work under the supervision of the Regulatory Operations Team Lead and collaborate with the RA team and external partners to support regulatory data management, dossier maintenance and electronic submissions.

This internship offers hands-on regulatory operations experience within an international pharmaceutical environment, with exposure to health authority submissions and