Vacant job

Are you looking for a role where you can influence, grow, and contribute to societal benefit, in a culture characterized by learning, humility, and supportive leadership? Bioglan's Regulatory Affairs and Pharmacovigilance department consists of six dedicated employees who work closely with development, production, and marketing. We are responsible for a broad product portfolio that includes pharmaceuticals, medical devices, cosmetics, and dietary supplements. 

We are now looking for a Regulatory Affairs (RA) Manager, a key person with drive, curiosity, and a desire to contribute both operationally and strategically. 

Why Bioglan? More than just an RA role!

At Bioglan, you work closely with the entire chain, from idea to finished product. Here, you not only manage, but you also get to develop, influence, and advance our products. 

Bioglan offers a genuine culture, close leadership, and great opportunities for professional development. Your manager gives you freedom, trust, and support when you need it and encourages you to try new things, develop, and sometimes make mistakes to learn. 

This is the role of RA Manager! 

As an RA Manager, you will have a broad and varied responsibility where you independently drive regulatory issues while working closely with colleagues in development, production, logistics, and quality. The role is both operational and strategic; you handle ongoing variations, renewals, and updates but are also expected to contribute to long-term planning and regulatory choices. 

Examples of tasks: 

• Be responsible for life cycle management for pharmaceuticals, primarily within module 3, in national procedures and DCP/MRP. 

• Drive regulatory projects and ensure that timelines are met. 

• Act as an internal advisor and contribute regulatory perspectives in development issues and in production. 

• Review and approve labeling and marketing materials. 

• Work on improving and developing internal processes and documentation. 

• Be responsible for ensuring updates are entered into national databases such as FASS. 

• Contribute to continuous learning within the team through knowledge sharing and environmental monitoring. 

What we are looking for in you! 

We are looking for someone who is analytical, structured, and self-driven, but who also appreciates close collaboration. You are pedagogical, enjoy sharing your knowledge, and have an easy time seeing issues from different perspectives. With a curious and solution-oriented approach, you take initiative and thrive in an environment where the pace can vary. We are looking for someone who has: 

• An academic degree in Life Science. 

• Is at the beginning of their career with about 2–3 years of experience in Regulatory Affairs focusing on life cycle management for pharmaceuticals (module 3). 

• Has a very good ability to express yourself in Swedish and English, both verbally and in writing. 

Who are we at Bioglan?

At Bioglan, we do a lot to ensure that you as an employee thrive and develop. Here, you will encounter a humble and helpful culture with a strong team spirit, great personal responsibility, and good opportunities to influence. You will receive continuous professional development, flexible working conditions, breakfast every day, and several great benefits, all in an environment where engaged colleagues and a well-planned introduction make you feel at home quickly.  

We develop, manufacture, and market pharmaceuticals, medical devices, dietary supplements, and cosmetics that help people around the world every day. In Malmö, we manufacture products for topical use in the form of creams, ointments, and gels. We are part of the Spanish pharmaceutical group Reig Jofré Group. The quality system follows GMP (Good Manufacturing Practice) and ISO 13485. We have just over 100 employees defined by a great diversity, considering age, nationality, and education at the facility in Malmö. The organization is affiliated with the IKEM unions. 

Read more about us at www.bioglan.se (http://www.bioglan.se/) 

Apply today!   

You are warmly welcome to upload your CV, or alternatively apply with your LinkedIn URL. Selection is ongoing, and the role may therefore be filled before the application deadline, which is 31/1 2026.    

We do not accept personal letters. Instead, relevant candidates will be asked to answer questions in writing to ensure equal opportunities to explain their experience related to the role.    

In this recruitment, Bioglan AB collaborates with Roi Rekrytering. For questions, please contact recruitment consultant Lina Friberg at [email protected] (mailto:[email protected])