Regulatory Specialist - Temporary Contract

Are you passionate about regulatory affairs and ensuring compliance with local regulations? Do you have experience in the pharmaceutical industry and a deep understanding of the regulatory landscape in Algeria? Then you might be the regulatory specialist we are looking for! Read below to know more about the role.

The position 

As a regulatory specialist (temporary contract), you will be responsible for ensuring compliance with local regulations and guidelines in Algeria. You will work closely with the local regulatory authorities and Novo Nordisk's global regulatory team to ensure timely and successful registration of our products. Your main responsibilities will include: 

• Preparing and submitting regulatory applications for new products, variations, and renewals 

• Providing regulatory guidance to cross-functional teams 

• Handling adverse events and technical complaints 

• Maintaining regulatory documentation and databases 

• Participating in regulatory inspections and audits 

Qualifications 

To succeed in this role, you need to have: 

• Bachelor's or Master's degree in Pharmacy, Chemistry, or related field 

• At least 3 years of experience in regulatory affairs in the pharmaceutical industry 

• Deep understanding of the regulatory landscape in Algeria 

• Strong communication and interpersonal skills 

• Ability to work independently and as part of a team 

Working at Novo Nordisk 

Novo Nordisk is its people. We know that life is anything but linear and balancing what is im-portant at different stages of our career is never easy. That’s why we make room for diverse life situations, always putting people first. We value our employees for the unique skills they bring to the table, and we work continuously to bring out the best in them. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 63,400 employees. Together, we go further. Together, we’re life changing. 

About the department 

We are part of a big department named CMR which contains three departments:  

Clinical, Medical & Regulatory. CMR is headed by a Sr.Director. 

Regulatory & PV department is headed by a Head of department:  

The structure contains 4 peoples: 3 RA specialist & 1 RA specialist & PV responsible. 

Our Key Internal stakeholders:  

At Affiliate level : MA/PA, Marketing, Medical, Clinical affairs & PS 

At regional level : Regulatory Affairs & PV 

At global level : Regulatory Affairs & PV 

Our Key External stakeholders:  

Ministry of pharmaceutical production 

• Department of regulation & pharmaceutical affairs 

• Department of Pharmaco-economy 

• Department of promotion of the pharmaceutical production    

• National drug agency  

Ministry of Health 

• National center of Pharmacovigilance 

• Pharmacy department 

• Central Hospital pharmacy   

Contact 

If you believe you are qualified, and are willing to take the challenge, please send your CV directly via our online application tool. 

Application deadline  

Please apply before the 30th December

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. 

At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.