Offres d'emploi Pharma Industrie - Suisse

Our client is seeking a Pharmaceutical Quality Assurance Specialist to ensure the procurement of safe, effective, and high-quality health products. You will play a key role in policy development, risk management, and cross-functional collaboration within a global supply environment.

The Pharmacovigilance (PV) Expert (a) will play a key role in ensuring compliance with pharmacovigilance processes and regulations within a biotech company. This temporary position requires a detail-oriented individual who can manage safety data and contribute to the overall safety of pharmaceutical products. Remote work possible but must be based in Switzerland. Start ASAP (latest July) for the next 12 months.

Support de 3 mois au département juridique d'une institution genevoise dans le domaine de la santé, notamment dans les domaines de la recherche clinique et non-clinique, gestion contractuelle et conformité réglementaire (LRH, OCLIN).

1. Du berätst Life‑Science‑ und MedTech‑Kunden technisch und entwickelst passende Lösungen.
2. Du identifizierst neue B2B‑Geschäftschancen und begleitest den gesamten Verkaufsprozess.

This role is responsible for ensuring quality oversight of internal and external GxP activities within a global environment. Acting as a key cross-functional partner, you will collaborate with Quality, Supply Chain, Manufacturing, Clinical Operations, and Regulatory teams to ensure compliance and continuous improvement across the value chain.

The (Senior) Manager REGULATORY AFFAIRS (a) will play a pivotal role in ensuring compliance with industry standards and regulatory requirements. Depending on the experience level of the candidate, this temporary position in Basel involves supporting/leading regulatory processes with national authorities in CH. Start is ASAP latest in July till end of the year. Remote work possible however the candidate has to be located in Switzerland. Extension is possible.

As Senior Legal & Compliance Counsel, you will provide expert legal advice and ensure regulatory compliance across Switzerland, Germany and Austria, with a primary focus on Switzerland, where you will act as the dedicated legal lead. This is a high‑impact, strategic role offering exposure to complex commercial and regulatory matters.

In this role, you lead quality investigations and CAPA processes to ensure product and process compliance. You play a key role in continuous improvement and proactive resolution of quality issues.

Our client is seeking afull-time Laboratory Technician for a 6 to 12‑month assignment to support a scientific research initiative. The role focuses on retrieving, organizing, and preparing a very large number of tissue samples for international shipment, ensuring full traceability and data accuracy.

Rattaché(e) au Responsable Maintenance, vous assurez la fiabilité et la performance des équipements de production dans un environnement pharmaceutique certifié. Vous intervenez sur l'ensemble du cycle de maintenance en respectant strictement les normes GMP et EHS.

Le Représentant Médical est responsable du développement commercial et de la croissance du marché en promouvant des solutions médicales auprès de ses clients, tout en construisant des partenariats durables en Suisse romande.

As a ASIC VERIFICATION ENGINEER (a) in this MedTech (microelectronics) company, you will play a crucial role in ensuring the reliability and accuracy of digital systems and processes. This temporary role offers an exciting opportunity to contribute to innovative projects within the R&D department. Start is ASAP. Latest in July. 12 months contract. Extension is a strong possibility.

Acting as the central coordination point of a growing ophthalmology practice, the Executive Assistant / Office Manager manages complex agendas, supervises the administrative team, and ensures a seamless experience for an international client base.

This role combines front office leadership with executive support responsibilities, requiring strong organizational skills, autonomy, and the ability to interact confidently with high-end clientele.

We are looking for a Quality Manager to oversee and develop a harmonized Quality Management System across two production sites in a regulated MedTech environment. This role combines operational leadership, regulatory compliance, and strategic quality oversight with direct team management responsibilities.

Unser Kunde ist eine der führenden Gesundheitseinrichtungen in der Schweiz. Für ihren Nebensitz im Raum Aargau suchen wir eine tatkräftige operative Unterstützung für die Beschaffungsadministration und Massendisposition mit SAP MM. Start ab sofort. 12-24 Monate. Übernahme möglich. Hybrides Arbeitsmodell 60:40.

We are looking for a GL Accountant immediately available for a 6-month assignment.

The CQV ENGINEER (a) will play a key role in overseeing the commissioning, qualification, and validation activities for systems and equipment in the LIFE SCIENCE sector. Based in Lucerne, this temporary position (18 months contract) offers an exciting opportunity to contribute to high-quality standards in a dynamic and regulated environment. Start is in July.

On behalf of our client, we are seeking an experienced HR Generalist to support its people operations during a temporary assignment and contribute to ongoing HR initiatives.

• 6-month assignment
• 40% for the first 2 months, increasing to 80% for the remaining 4 months

The HR Operations Senior Manager is responsible for driving the efficiency, compliance, and scalability of global HR operations across multiple geographies within a highly regulated biotech environment. The role combines payroll governance, HRIS leadership, compensation benchmarking, and process optimization to support business growth and strategic decision-making.

For our client, a leading international pharmaceutical company with modern offices in the canton of Lucerne, we are seeking a Batch Record Review Specialist (m/f/d). In this role, you will support clinical biologics manufacturing by reviewing completed batch records and ensuring all documentation meets ALCOA+ and GMP standards.