Offres d'emploi Pharmaceutique - 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.

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.

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.

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.

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.

Unser Mandant ist ein innovationsgetriebenes, international tätiges Unternehmen im Bereich Medizintechnik, das moderne Lösungen für den Gesundheitssektor entwickelt und vertreibt.

Für den Standort in der Schweiz, basiert im Kanton Aargau, suchen wir ab sofort eine engagierte Persönlichkeit, die Lust hat, aktiv zum Unternehmenserfolg beizutragen.

Unser Kunde ist eine der führenden Gesundheitseinrichtungen in der Schweiz. Für ihren Hauptsitz in Zürich suchen wir einen PMO Supply Chain Digitalisierung mit praktischer SAP MM Erfahrung (d/m/w) mit Start ab sofort (idealerweise Juli) für ein Try&Hire. Hybrides Arbeitsmodell (60:40).

You will support end-to-end procurement and supply operations for an international health-focused organisation, ensuring efficient demand planning, order management and delivery of critical products across multiple countries.

We are looking for a Senior Statutory Consolidation Analyst quickly available for a 7-month assignment starting early July.

Our client is a global, research-driven biopharmaceutical company specializing in innovative and specialty medicines. As Global Pricing Lead, you will support the launch of a key immunology asset by executing pricing strategy and ensuring alignment across global and local stakeholders.

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.

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.

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.

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