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Regulatory Internship

On-site in Barcelona·Full-time·Added 2 days ago (last checked 6 Nov)

Agency

Randstad España

6006 open roles

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Our summary

Hours: Monday to Friday
Work mode: On-site, Barcelona
Contract: Internship, full-time hours
Spanish: Expected (ad in Spanish)
Education: University degree
Benefits: Meal vouchers

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Skills

This job advert was originally written in Spanish.

Pay & benefits

What you'll get

Financial aid: Monthly allowance of 900 — gross.

Extra benefits: Meal card for your daily meals, in addition to the monthly economic allowance.

Duration: Initial 6-month internship, with real possibility of extension depending on performance and the availability of the agreement.
Working day and hours: Full-time from Monday to Friday, from 9:00 to 17:00 h.
Modality: On-site, guaranteeing constant and close tutoring by the technical team.
Learning and development: Comprehensive and practical training in regulatory projects of local and global scope within a constantly growing Consumer Health pharmaceutical company.
Work environment: Dynamic, collaborative environment with high scientific rigor where you can boost your first experience in the industry.

The role

Do you want to be part of the scientific and regulatory engine that brings safe and effective health solutions to the market? At Cooper-Vemedia, we want to boost your career. If you are looking for a practical internship to apply your scientific knowledge in a real environment—from registration and labeling to the validation of promotional materials—we offer you the ideal space to learn and grow alongside a multidisciplinary team with a local and global presence.

What you'll do

Integrated into the company and with the direct mentorship of your assigned tutor, your main responsibilities will be:

Document management and archiving: Provide support in the review, periodic updating, and systematic archiving of the technical and regulatory documentation of the product portfolio.
Registration processes: Support the preparation, submission, and follow-up of dossiers and regulatory procedures before the corresponding health authorities.
Labeling and packaging review: Review packaging texts, leaflets, artworks, and claims, ensuring they strictly comply with the approved information and current regulations.
Supervision of promotional materials: Collaborate in the control and administrative processing before health authorities and self-regulation entities (such as Autocontrol) of the company's marketing/advertising materials and actions.
Cross-functional support: Assist from a technical and scientific perspective, under supervision, key areas such as Marketing, Quality, Sales, and Commercial.
Corporate projects: Participate in working groups and regulatory department initiatives at a local level and in coordination with the global headquarters.

Requirements

Academic training and agreement:

Student of a Bachelor's or Master's Degree in Pharmacy, Biotechnology, Biology, Chemistry, or related Health Sciences.
It is essential to be able to formalize an **internship agreement** with a university or study center for at least 6 months (not having finished the master's degree).

Languages and IT

Proficiency in the Office suite (Word, Excel, and PowerPoint).
Intermediate English level (B1-B2) is valued for the review of technical documentation.

Personal skills

High level of detail and thoroughness for document review and packaging texts.
Capacity for organization, order, and teamwork.

Availability:

Full-time on-site from 9:00 to 17:00 h, with incorporation planned for the month of December.

Hiring process

2 steps1 interview

Apply to the job
Under review · With a Randstad consultant
Shortlisted
Consultant contact
With a Randstad consultant
One of our consultants will review your application and contact you about the next steps.
Company decision
With a client company
Randstad acts as an intermediary connecting candidates with companies; in some cases final handling of profiles and the decision on whom to contact rest solely with the company.

The final stages are set by the client company: final handling of profiles and the decision on whom to contact rest solely with the company.
Randstad does not publish timescales; your application status may not change because of the high volume of applications or because the company manages its own timings.
The published statuses only go as far as shortlisting: Randstad does not detail later interviews or assessments.

About Randstad España

Randstad España is the Spanish branch of Randstad N.V., a global leader in human resources and staffing solutions. The company provides a wide range of workforce solutions, including temporary and permanent placement, recruitment process outsourcing, and HR consulting. With a strong presence in Spain, Randstad España connects thousands of professionals with job opportunities across various sectors, including industrial, technical, and customer service roles.

For international professionals, Randstad España offers a gateway to the Spanish job market, with numerous openings in technical maintenance, customer service, and administrative roles. The company values diversity and inclusion, and its extensive network of offices across Spain ensures support for candidates seeking employment in different regions. Randstad's global reach and local expertise make it a reliable partner for those looking to relocate and work in Spain.