Regulatory Affairs Associate - Temporary

Exeltis; Madrid; Presencial; EUR 42.000 - 65.000; Jornada completa

Descripción de la vacante

Exeltis is a pharmaceutical company seeking a Regulatory Affairs Associate to support regulatory development and lifecycle management of pharmaceutical products in Madrid on-site. You will prepare eCTD modules, manage submissions and renewals, archive documents, and collaborate with Clinical Operations in the US as needed.

3+ years of regulated industry experience and fluent English are required. Join a dynamic team and help ensure timely regulatory filings while staying up-to-date with ICH,

Formación

• Bachelor’s degree in Health Sciences, preferably Pharmacy.
• 3+ years of relevant experience in regulated/pharma industry.
• Fluent English, written and spoken.
• Knowledge of ICH, GCP, regulations and directives.
• Willingness to travel.
• Experience with or understanding of eCTD documentation.

Responsabilidades

• Prepare and validate eCTD modules for regulatory submissions.
• Archive Product Information per procedures.
• Provide documents for national submissions to local affiliates.
• Submit renewals on time and track timelines.
• Support regulatory activities related to US clinical trials.
• Track and archive regulatory submissions.

Conocimientos

Fluent English

Attention to detail

Autonomy

Educación

Bachelor's degree in Health Sciences (Pharmacy preferred)

Herramientas

eCTD documentation

Descripción del empleo

Position: Regulatory Affairs Associate – Temporary (maternity leave)

Location: Madrid (on-site)

Experience: 3+ years

Want to know more?

Exeltis is a pharmaceutical company committed to improving people’s health and well‑being through the development, manufacturing, and commercialization of innovative, high-quality products.

We are looking for a Regulatory Affairs Associate to support the regulatory development of pharmaceutical products and the lifecycle management of the portfolio, ensuring that submissions, variations, amendments, and renewals are filed on time and in full compliance with regulatory requirements. This role will also provide support, when needed, to Clinical Operations activities in the US.

What are we looking for?

The selected candidate will play a key role in regulatory activities, including:

• Support global and local teams in preparing eCTD modules for regulatory applications.
• Prepare eCTD documentation for regulatory submissions.
• Archive essential documents, such as Product Information, in line with company procedures.
• Provide local affiliates with the documentation required for national submissions.
• Ensure that essential post-approval dossier information is shared with the relevant departments according to applicable procedures.
• Prepare the documentation required for the submission of administrative variations, quality‑related variations, non‑clinical and/or clinical variations, as well as amendments.
• Compile and prepare the documentation needed for the submission of safety reports in collaboration with the Exeltis Pharmacovigilance department.
• Submit renewals on time and communicate timelines to all relevant partners.
• Track the qualification of clinical sites, including the collection, review, and preparation of regulatory documentation such as Form 1571, financial disclosure forms, and debarment/restricted list reviews.
• Perform visits, when needed, to sites involved in US clinical trials to verify compliance with regulatory requirements.
• Track service agreements.
• Track and archive regulatory submissions.
• Support Clinical Operations with public database disclosures such as clinicaltrials.gov.
• Ensure that the regulatory database for assigned projects in the region is always up to date.
• Stay up to date with the latest regulatory requirements in the region.
• Inform key stakeholders, such as Commercial, Business Development, and Top Management, about the regulatory status in the relevant area.

The challenge!

• Coordinate the preparation and review of regulatory documentation for international submissions.
• Manage regulatory lifecycle activities across the product portfolio.
• Ensure compliance with regulatory timelines for variations, renewals, and amendments.
• Work closely with internal teams and local affiliates to support national submissions.
• Oversee the archiving and traceability of essential regulatory documentation.
• Support regulatory activities related to US clinical trials.
• Verify the regulatory and documentary compliance of clinical sites when required.
• Maintain clear and proactive communication with internal stakeholders regarding the regulatory status of projects.

What do you need?

• Bachelor’s degree in Health Sciences, preferably Pharmacy, although degrees in Chemistry, Biology, Biochemistry, or related fields will also be considered.
• 3+ years of relevant experience, preferably in a regulated industry, ideally within the pharmaceutical industry.
• Fluent English, both written and spoken.
• Additional languages will be considered a plus.
• Basic knowledge of international standards related to drug registration and drug development, including ICH, GCPs, regulations, and directives.
• Knowledge of international markets and distribution business will be considered an asset.
• Experience with or understanding of eCTD documentation preparation.
• Knowledge of regulatory documentation related to clinical sites and clinical trials.
• Willingness to travel.
• A profile with initiative, proactivity, autonomy, decisiveness, and strong attention to detail.

Do you think this job is not for you?

We encourage you to stay tuned for future opportunities at Exeltis and to share this vacancy with people in your network who may be a great fit. Your next professional challenge—or someone else’s—might be closer than you think!

COMMITMENT TO EQUAL OPPORTUNITIES

At Exeltis, we are committed to equal opportunities and to building diverse and inclusive workplaces. All applications will be considered regardless of gender, gender identity or expression, sexual orientation, marital status, age, ethnicity, nationality, religion, beliefs, disability, or any other characteristic protected by applicable law.