Cookie-Hinweis

Wir verwenden Cookies auf dieser Website. Einige davon sind notwendig, damit die Website funktioniert, wie z. B. technische und funktionale Cookies. Andere Arten von Cookies, deren Verwendung Sie ablehnen können, sind Cookies von Drittanbietern oder Cookies zur Erstellung von Werbeprofilen. Wenn Sie auf "Alle akzeptieren" klicken, stimmen Sie der Verwendung aller Cookies auf der Website zu. Durch Klicken auf die Schaltfläche "Konfigurieren" können Sie Ihre Einstellungen wählen.

Alle akzeptieren
Konfigurieren
Nur notwendig
header backgorund
Suchen

Regulatory Affairs Associate (interim contract)  

Standort

Schweiz, Tessin, Lugano

Branche:

Pharma-Industrie

Funktion:

Anderes

Datum der letzten Aktualisierung: 09/03/2026

Aktivitäten 

Stellenbeschreibung

Überprüfen Sie Ihre Kompatibilität mit diesem Stellenangebot

header backgorund
? %
Bewerben

Gi Group – Life Sciences Division is seeking a:

Regulatory Affairs Associate

The candidate will be placed, on a temporary contract through Gi Group, at an international pharmaceutical and biotech company focused on specialty medicinal products, to cover an extended absence.

This position offers the opportunity to work in an international regulatory environment and contribute to the lifecycle management of medicinal products across multiple markets.

This role is ideal for candidates with initial regulatory experience who want to strengthen their expertise in eCTD submissions and regulatory documentation management.


Key Responsibilities

• Preparation and management of regulatory submissions in eCTD format

• Compilation and organization of submission documentation and sequences

• Support the Regulatory Affairs team in submission preparation and lifecycle activities

• Maintenance of regulatory documentation and internal databases

• Coordination of documentation for international regulatory submissions

• Interaction with internal teams to collect and organize required regulatory data


Requirements

• Degree in Life Sciences (Pharmacy, Biotechnology, Chemistry or related disciplines)

• Initial experience in Regulatory Affairs within the pharmaceutical sector

• Mandatory: familiarity with eCTD submission processes and regulatory documentation

• Good knowledge of regulatory requirements for medicinal products

• Professional English proficiency

• Strong organizational skills and attention to detail


What we offer

• Temporary contract via staffing agency

• Opportunity to gain experience in an international pharmaceutical environment

• Exposure to regulatory submission processes

• Collaborative and supportive team environment


Gi Life Science is part of Gi Group Holding, a global ecosystem of HR services and consulting that supports the development of the labour market and helps to change people's lives in 37 countries around the world. In Switzerland we operate with the brands Gi Life Sciences, Gi Group, Grafton and Bautech Personal. We are active in temporary, permanent and professional staffing as well as in a variety of complementary HR Services. With a direct presence in 40 locations across Switzerland and over 200 employees, we are one of the leading staffing companies in the Swiss recruitment market. Gi Life Sciences is specialist for Temporary and Permanent staffing in the Life Science sector, as well as a valuable partner for many other HR Solutions. We believe in experts talking to experts: all our professionals are certified in scientific sector, meaning that they are able to understand your needs and support you at 360°.

Details ansehen

Führungsperson: Nein

Vertragstyp: Temporäre Arbeit

Karriere: Angestellte/r

Karte

Bewerben
Oder
Teilen Sie dieses Stellenangebot
Powered by arca24.com logo
Weitere Stellenangebote von diesem Unternehmen: LOADING...

Ähnliche Stellenangebote

Regulatory Affairs Specialist

Schweiz, Tessin, Lugano - Gi Group SA empImg

For one of our esteemed clients, international pharmaceutical and biotech company focused on specialty medicinal products, we are looking for a Regulatory Affairs Specialist to strengthen its Regulatory team. This position offers the opportunity to work in an international regulatory environment and contribute to the lifecycle management of medicinal products across multiple markets.   Key Responsibilities • Preparation and management of regulatory submissions in eCTD format • Lifecycle management activities including variations, renewals and maintenance of Marketing Authorisations • Preparation and review of regulatory documentation and product information (SmPC, PIL, labeling) • Coordination of submission dossiers for international markets • Interaction with internal departments (QA, CMC, Clinical, Pharmacovigilance) • Ensure compliance with international regulatory requirements • Management and compilation of eCTD sequences using regulatory publishing tools   Requirements • Degree in Life Sciences (Pharmacy, Biotechnology, Chemistry or related fields) • 4–5 years of experience in Regulatory Affairs within the pharmaceutical industry • Proven experience with medicinal products regulatory dossiers • Mandatory experience working with eCTD tools (experience with EXTEDO is highly preferred) • Hands-on experience with international submissions, variations and lifecycle management • Ability to work independently on regulatory documentation and product information • Professional English language proficiency   What the company offers • Permanent contract • Opportunity to work in an international pharmaceutical environment • Exposure to global regulatory activities • Hybrid work model (1 day per week remote work) • Collaborative and scientifically driven working environment   Gi Life Science is part of Gi Group Holding, a global ecosystem of HR services and consulting that supports the development of the labour market and helps to change people's lives in 37 countries around the world. In Switzerland we operate with the brands Gi Life Sciences, Gi Group, Grafton and Bautech Personal. We are active in temporary, permanent and professional staffing as well as in a variety of complementary HR Services. With a direct presence in 40 locations across Switzerland and over 200 employees, we are one of the leading staffing companies in the Swiss recruitment market. Gi Life Sciences is specialist for Temporary and Permanent staffing in the Life Science sector, as well as a valuable partner for many other HR Solutions. We believe in experts talking to experts: all our professionals are certified in scientific sector, meaning that they are able to understand your needs and support you at 360°. 
...
companyImg
09/03/2026

Regulatory Affairs Specialist

Schweiz, Tessin, Lugano - Manpower empImg

​ Fondata nel 1948 a Milwaukee, Wisconsin, USA, Manpower è una società internazionale leader nel settore delle risorse umane. Presente a livello mondiale in 82 paesi con oltre 3'900 filiali risponde ai bisogni dei suoi 400'000 clienti. Specialisti nel reclutamento e nella selezione di personale fisso e temporaneo in diversi settori dell'economia, siamo presenti in Svizzera da oltre 60 anni con più di 260 collaboratori in più di 37 sedi.  Il nostro cliente ci ha incaricato di selezionare il seguente profilo professionale: Regulatory Affairs Specialist ​ Requisiti  - Esperienza minima di 3 anni nel ruolo di Regulatory Affairs Specialist in ambito farmaceutico - Esperienza comprovata di interazione diretta con Autorità Regolatorie internazionali quali: FDA, Swissmedic, Health Canada, SFDA - Pregressa esperienza nella preparazione del modulo 1, inclusi stampati e mock-ups - Buona conoscenza dei principali strumenti informatici e software di Regulatory Affairs - Must have: e-CTD Manager Extedo  Competenze tecniche  - Gestione di procedure di Lifecycle Management di una MA application (esempio: renewal, promotional review, compliance) - Gestione di procedure regolatorie quali: MAA, Variations, Scientific Advice, Orphan Designation, Paediatric Requirements - Gradita esperienza nella gestione delle sezioni pre-cliniche e cliniche dei dossier registrativi (Moduli 4 e 5) Formazione e competenze  - Laurea in discipline scientifiche (CTF, Farmacia, Biotecnologie o affini) - Ottima conoscenza della lingua inglese scritta e parlata - Precisione, autonomia organizzativa e capacità di interfacciarsi con stakeholder internazionali ​ SE RITIENE DI POSSEDERE TUTTI I REQUISITI RICHIESTI, NON ESITI AD ISCRIVERSI E A CANDIDARSI SUL NOSTRO SITO UFFICIALE: WWW.MANPOWER.CH, ALLEGANDO IL SUO CURRICULUM VITAE.
...
companyImg
27/02/2026

ANALISTA SENIOR CONTROLLO QUALITA'

Schweiz, Tessin, Lugano - ER Services Sagl empImg

ER Services Sagl ricerca ANALISTA SENIOR CONTROLLO QUALITA' per azienda farmaceutica con sede a Lugano, TI.  Il profilo prescelto sarà inserito nel Laboratorio Chimico di Controllo Qualità afferente al Reparto Produttivo Orali & Solidi.  Responsabilità  • Svolgere analisi per il rilascio del prodotto finito e per gli studi di stabilità, contribuendo direttamente alla sicurezza e alla qualità dei prodotti;  • Garantire la conformità con le normative GMP, le linee guida Data Integrity Compliance, Annex 11 EU GMP & 21 CFR Part 11;  • Cura e manutenzione delle strumentazioni di laboratorio;  • Collaborare in sinergia armoniosa con il team per il monitoraggio delle attività operative;  • Operare in conformità alle buone norme di laboratorio (GLP), mantenendo elevati standard di igiene, ordine e pulizia dei locali e delle apparecchiature.  Requisiti  • Laurea in Chimica / Chimica industriale o Diploma di Perito Chimico;  • Esperienza pregressa di almeno 10 anni in Laboratorio Chimico Controllo Qualità in ambito GMP;  • Ottima conoscenza della Lingua Inglese;  • Disponibilità a lavorare su giornata o su turni diurni a seconda delle esigenze aziendali.  Competenze richieste  Persona con un approccio analitico, precisa e orientata alla qualità, che si distingue per le seguenti competenze:  • Capacità di eseguire tecniche analitiche chimico – fisiche, titolazioni e analisi HPLC, GC e KF;  • Conoscenza degli applicativi LIMS, ELS e Software HLPC Chromeleon;  • Elevato orientamento al compito e attenzione al dettaglio;  • Capacità di svolgere le attività con ordine e metodo; • Dinamismo e ottima predisposizione all'analisi critica di trend e anomalie;  • Capacità di lavoro in team e comunicazione efficace.    Previsto inserimento a tempo indeterminato full time in un ambiente di lavoro stimolante e dinamico, con opportunità di formazione e buone prestazioni sociali e remunerative.
...
companyImg
23/02/2026

Projektleiter Heizung Lüftung Kälte Klima

Schweiz, Basel-Stadt, Basel - Manpower empImg

​ Bei Interesse und passender Qualifikation kannst du dich gerne direkt melden:  Alba Jansa alba.jansa(at)experis.ch +41 61 282 22 13 ​ Wir suchen einen erfahrenen Projektleiter (m/w/d) im Bereich Gebäudetechnik, der unser dynamisches Team in fester Anstellung verstärkt. In dieser Position haben Sie die Möglichkeit, vielfältige Projekte in der Pharma- und Life-Sciences-Branche an verschiedenen Standorten zu betreuen. DEIN PROFIL ? abgeschlossene Ausbildung und/oder Ausbildung/Weiterbildung als Techniker (HF)/Ingenieur (B.Sc/M.Sc.) der Gebäudetechnik ? Erfahrung als Projektleiter ? zuverlässig, kommunikativ und lösungsorientiert ? Teamplayer ​ UNSER ANGEBOT ? anspruchsvolle und interessante Projekte ? Mitgestaltung einer jungen Unternehmung ? moderne und gut ausgestattete Büroräumlichkeiten unmittelbar in Bahnhofsnähe ? junges und engagiertes Team ? flache Hierarchien und kurze Entscheidungswege ? jede Menge Freiheiten ? intensive Betreuung in Deiner Einarbeitungszeit ? ausgezeichnete Rahmenbedingungen  
...
companyImg
11/03/2026
  Zeigen Sie diese Nachricht nicht mehr an
Erstellen Sie Ihren kostenlosen digitalen Lebenslauf!
Erstellen Sie Ihren digitalen Lebenslauf: Bewerben Sie sich auf Stellen, indem Sie einen einfachen Link an die gewünschte Person senden. Der digitale Lebenslauf enthält: Videos, Prüfungen und Anhänge für eine effektivere und aktuellere Bewerbung. Verleihen Sie Ihrer Bewerbung einen Mehrwert!