Regulatory Affairs Specialist

buscojobs España; Alicante; Presencial; EUR 30.000 - 50.000; Jornada completa

Descripción de la vacante

An innovative international company is seeking a Regulatory Affairs specialist to join their dynamic team. This role offers the chance to work closely with an experienced Regulatory Manager, contributing to impactful projects in the pharmaceutical industry. You'll be responsible for preparing regulatory dossiers, managing lifecycle activities, and ensuring compliance across various product categories. With a focus on collaboration and professional growth, this position provides a hybrid work model, competitive salary, and additional perks like private health insurance and subsidized meals. If you are looking for a role where your contributions truly matter, this is the opportunity for you.

Servicios

Permanent contract

Hybrid model (2 days remote / 3 days on-site)

Continuous working hours with early Friday finish

Competitive salary + annual bonus

Private health insurance (after 6 months)

Subsidized lunch

Free fruit and coffee

Formación

• 1-2 years of experience in Regulatory Affairs, preferably in pharma or supplements.
• Strong English skills and a proactive, independent work style.

Responsabilidades

• Prepare and update regulatory dossiers for pharmaceutical products.
• Manage lifecycle activities and ensure compliance with regulations.

Conocimientos

Regulatory Affairs

Life Sciences

English (spoken and written)

Collaboration

Educación

Degree in Life Sciences (Pharmacy, Chemistry, or related fields)

Herramientas

Regulatory databases

Descripción del empleo

If you’ve spent the last couple of years building your expertise in Regulatory Affairs and you're now looking for a more technical, specialized role—with real impact in pharmaceuticals—this could be your next step.

You’ll work closely with an experienced Regulatory Manager in a growing international company that values stability, collaboration, and a hands-on approach. This isn’t just another large corporate team—you’ll have visibility, ownership, and the opportunity to truly contribute.

What you’ll do

• Prepare and update regulatory dossiers for pharmaceutical products across Spain and Europe.
• Manage lifecycle activities such as variations, renewals, and supporting documentation.
• Provide regulatory support for food supplements, cosmeceuticals, biocides, and medical devices.
• Collaborate with cross-functional teams : Quality, R&D, and Marketing.
• Review packaging materials and maintain regulatory databases.
• Ensure compliance with current regulations throughout the product lifecycle.

You’re a fit if you have...

• A degree in Life Sciences (Pharmacy, Chemistry, or related fields).
• 1–2 years of experience in Regulatory Affairs (pharma, supplements, or similar).
• Interest in transitioning further into pharmaceuticals, while keeping exposure to diverse categories.
• Strong English skills (spoken and written)—other languages are a plus.
• A proactive and independent work style, with a collaborative mindset.

What’s in it for you

• Permanent contract and long-term professional stability.
• Hybrid model : 2 days remote / 3 days on-site.
• Continuous working hours with early Friday finish.
• Competitive salary + annual bonus.
• Private health insurance (after 6 months).
• Subsidized lunch, free fruit and coffee.