My client is an independent and international pharmaceutical company located in Basel. They are currently looking for a Quality Assurance Manager to straighten their QA Team.

• This role will be responsible for execution of daily activities associated with implementation and maintenance of the QMS and QA activities in relation to Trading Entity Support the establishment of procedures and processes only
  Ensure all requirements to maintain the Wholesale Distribution Authorisation and appropriate licenses are met

For our client, an international Pharmaceutical Company in the greater Zurich area, we are urgently looking for an Real World Evidence Senior Consultant to start ASAP for a 12 months contract which can be extended.

For our client, an international Pharmaceutical Company in the greater Zurich area, we are urgently looking for an Junior and Senior Quality Assurance Specialist Pharma to start ASAP for a 12 months contract which can be extended.

The QA Manager, GVP is responsible for:

Ensuring quality oversight and support of the PV activities

Build and develop the audit strategy, program and plans within the PV area

Perform and coordinate PV audits internally, Partners and externally at external service providers

Support and collaborate with Drug Safety,Medical Affairs, Regulatory Affairs and Affiliates as necessary

• Ensure local GxP software compliance with regulatory requirements.
• Project for at least 1 year

We are looking for a Director QA GCP/GVP.

You will be responsible to ensure quality oversight and support the Clinical research and Drug Safety activities. In this role you will work with relevant stakeholders across our clients organization: R&D (Clinical Dev/Drug Safety, RA), Medical Affairs, Commercial, Technical Operations and Global Quality.

• Main duties for the position is to focused around non-laboratory support of the QC functions.
• Data analysis, data trending, project and testing coordination, product and material specification management, inspection support, investigation leads, operational excellence leads, document revisions, initiating/completing quality systems, method/equipment validation and method projects activities.

Operational and regulatory support for submission and maintenance activities, including preparation and submission of regulatory dossiers, maintenance of regulatory databases and archives.

Head of Sales will lead the Sales Force team in Austria dn Switzerland. And will be responsible for development & implementation of the sales strategy and for achieving sales targets within the allocated markets.

Pour l'un de nos clients nous sommes à la recherche d'un(e) legal counsel ayant minimum 7 années d'expérience PQE en droit des affaires suisse et international.

Develop and implement CH local market access strategies for existing products and localize global value dossiers for launch products to achieve a commercially successful market access environment. Executing value-price strategies in affiliates. Tailoring global payer value proposition and access strategy to local needs

This a unique opportunity to join a very dynamic and innovative European pharmaceutical company.

The Key Account Manager will be a part of Field Sales Team, and will promote new product in allocated territory (Bern, Basel, Zurich and sub regions). Develop long term business relations through regular contact with relevant HCPs, clinical managers to maximise business opportunities.

Für unseren Kunden, einen internationalen key player im Bereich OTC, suchen wir per sofort oder nach Vereinbarung einen Account & Access Manager für die Zielgruppe Hospital/Spitäler in der deutschsprachigen Schweiz. Der Account und Access Manager ist ein fachlicher und kommerzieller Experte der die Spital-Strategie mit-entwickelt, anpasst und erfolgreich umsetzt.

MDR 2017/745 Project Manager.

Innovative medical devices.

Our client is an International Biotech company located in Basel. Thanks to their constant growth we are looking for a talented Senior CMC Dossier Specialist to complete its CMC team.

As the Head of Quality Control m/f, your role will be to lead the Quality Control Team for activities related to the manufacturing of kits as well as QC methods development. You will report directly to the COO and collaborate closely with the Head of Production, the Industrialization Manager. Position based in Lausanne.

As Verification & Validation engineer, you will conduct equipment systems or software validations (IQ/OQ/PQ) for manufacturing and QC processes/equipment in the plant. Position based next to Lausanne.