GlaxoSmithKline Biologicals S.A.S. Posted June 25, 2026

Alternant(e) Affaires Réglementaires H/F

Saint-Amand-les-Eaux, France Full time
Regulatory Affairs

GlaxoSmithKline Biologicals S.A.S. is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Nous recherchons un(e) Alternant(e) Affaires Réglementaires H/F pour la rentrée de Septembre 2026 pour notre site de production basé à Saint-Amand les Eaux (59).

Durée : 1 an

VOS MISSIONS

Au sein de l'équipe Affaires Réglementaires, vous aurez pour principales missions :

Support aux activités réglementaires : rédaction de documents entrant dans le module 3 des dossiers d’AMM (Autorisation de Mise sur le Marché)

Autorisations d’importation de produits semi-finis (ANSM) : recueillir les besoins et effectuer les demandes auprès de l'ANSM après constitution des dossiers.

Participation à la mise à jour de l'Etat des lieux (EDL) annuel de l’établissement (ANSM)

Support aux activités quotidiennes du service affaires réglementaires

VOTRE PROFIL

Diplôme préparé : Bac+6 Pharmacie ou Ingénieur

Bonne maitrise de l'anglais à l'écrit et à l'oral

Bonne capacité rédactionnelle

Capacité d’analyse et de synthèse

Connaissance du cycle de vie d’un médicament et des bonnes pratiques de fabrication

Maîtrise du Pack Office

Cette opportunité vous intéresse ? Alors transmettez nous votre candidature !

A propos du site de Saint-Amand-Les-Eaux : 

Impliqué depuis plus de 60 ans en vaccinologie, GSK est un leader pharmaceutique dans ce domaine. Pour se consacrer à la découverte et à la production de vaccins à destination des enfants, des adolescents et des adultes dans plus d’une centaine de pays, et en particulier dans les régions les plus défavorisées, la division Vaccins de GSK compte 15 sites de production stratégiquement positionnés à travers le monde, et emploie plus de 16 000 personnes. Son portefeuille est de 30 vaccins commercialisés et de 16 vaccins en cours de développement. GSK Saint-Amand-les-Eaux (59), à proximité de Lille et Valenciennes, est un site entièrement dédié à la fabrication (formulation, remplissage aseptique et lyophilisation) et au conditionnement des vaccins GSK. Le rôle du site est de produire et fournir des vaccins répondant aux principaux enjeux de santé publique. L’ambition de Saint-Amand est de garantir les plus hauts standards de qualité grâce à ses technologies les plus en pointe au niveau mondial et à l’engagement de ses équipes. Le site de Saint-Amand-les-Eaux, qui emploie environ 800 personnes fabrique une large gamme de vaccins du portefeuille de GSK et connaît une forte expansion. La capacité de production du site est de 300 millions de doses par an, et ses perspectives de croissance sont très importantes dans les années à venir.

A propos de GSK :

La mission du Laboratoire GlaxoSmithKline est d'améliorer la qualité de vie pour que chaque être humain soit plus actif, se sente mieux et vive plus longtemps. Toutes les actions et les décisions de l'entreprise sont guidées par des valeurs fortes : placer le patient au cœur de nos priorités, le respect, la transparence et l’intégrité.

Le Laboratoire GlaxoSmithKline est présent dans un grand nombre de pays et de domaines thérapeutiques, afin de répondre aux attentes des professionnels de santé et des patients de toutes origines, de tous âges et de tous niveaux sociaux. Pour les maladies les plus fréquentes comme pour les maladies rares, il propose des solutions adaptées aux besoins médico économiques de chacun : l'accès aux traitements pour tous et partout dans le monde est une priorité.

Pour en savoir plus vous pouvez consulter les ressources suivantes :

www.GSK.fr

www.GSK.com

*LI-GSK

Why GSK?

Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

Should you require any adjustments to our process to assist you in demonstrating your strengths and capabilities contact us on [email protected]

Please note should your enquiry not relate to adjustments; we will not be able to support you through these channels.

GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information (including family medical history), military service or any basis prohibited under federal, state or local law.

Important notice to Employment businesses/ Agencies

GSK does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact GSK's commercial and general procurement/human resources department to obtain prior written authorization before referring any candidates to GSK. The obtaining of prior written authorization is a condition precedent to any agreement (verbal or written) between the employment business/ agency and GSK. In the absence of such written authorization being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of GSK. GSK shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.

Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment. This capture of applicable transfers of value is necessary to ensure GSK’s compliance to all federal and state US Transparency requirements. For more information, please visit the Centers for Medicare and Medicaid Services (CMS) website at https://openpaymentsdata.cms.gov/

Job details

Seniority
Not listed
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Saint-Amand-les-Eaux, France
Employment type
Full time

How this role compares

Computed from every other active Regulatory Affairs role in our database, not just this employer's listings.

We currently track 305 comparable Regulatory Affairs roles across 66 biopharma companies.

305Comparable roles tracked
275Currently active
66Companies hiring similar roles
37Countries represented

Salary context

85 of 305 peers report a salary range (USD, annualized)

Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.

This roleSubject Not listed on this posting
Highest disclosed · AVP, Therapeutic Area Head, Clinical Safety and Risk Management · Merck $378,100/yr – $595,100/yr
Peer group range $98,050 – $486,600 (median $205,000)

Where these roles are based

Top locations among the 305 comparable roles

United States124
Ireland25
India25
United Kingdom17
Poland16
Japan13

+ 31 more countries

Seniority mix

261 of 305 peers have a known seniority level

Manager112
Director61
Senior27
Associate Director26
Senior Director12
Executive/VP11
Associate8
Principal2
Intern/Fellow/Postdoc2

Therapeutic area mix

33 of 305 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology10
Dermatology & Aesthetics6
Neuroscience6
Immunology4
Cardiovascular / CVRM2
Rare Disease2
Respiratory2
Vaccines & Infectious Disease1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

40%similar
sanofi aventis Recherche et Développement Marcy-l'Etoile, France
Same function Same country
40%similar
Sanofi Winthrop Industrie Tours, France
Same function Same country
25%similar
Lilly Indianapolis, Indiana, United States of America
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

25%similar
Lilly Shanghai, Shanghai, China Manager
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

25%similar
Lilly Bracknell, United Kingdom Principal
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

25%similar
Lilly Indianapolis, Indiana, United States of America Senior Director
Same function

Matched on job function only -- seniority, specialty, and location weren't confirmed as aligned.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

40%
Submission Lead for Structured Data
sanofi aventis Recherche et Développement · Marcy-l'Etoile, France · Seniority not listed
Function Therapeutic area Seniority Country
25%
Sr Regulatory Affairs Manager- DIA
Lilly · Shanghai, Shanghai, China · Manager
Function Therapeutic area Seniority Country
25%
Associate Director/Director, GRA, Regulatory Affairs Head – Canada
Lilly · Ontario, Ontario, Canada · Associate Director
Function Therapeutic area Seniority Country
25%
Sr.Manager- Regulatory Delivery Excellence, China Regulatory Affairs
Lilly · Shanghai, Shanghai, China · Manager
Function Therapeutic area Seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.