Le Superviseur Bulk Operations aura pour mission d'assurer les activités de fabrication des produits (capsules et/ou comprimés), dans le respect de la réglementation BPF/ cGMPs, des règles d'hygiène, et de sécurité. II devra s'assurer du respect du plan de production établi tout en se conformant aux procédures définies par le système qualité du site pharmaceutique. II aura également en charge la supervision des opérateurs et techniciens sur les étapes de fabrication.   Le superviseur bulk operations est en charge de la gestion et de la...

This position is responsible to perform all type of analytical testing that is required for release of packaging materials and all the environmental sampling. The position is responsible for the documentation management for the QC Laboratory, the sample management and the management of the consumable (Reagent & others) by purchasing, receptioning and providing the Couvet Laboratory in time with materials. The management of the standards for the analytical testing is under the responsibility of this position. Additional responsibilities can be the support of the analytical testing, handling of deviations and change controls likewise the follow up and performs of complaints.

The Quality Control laboratory at the Couvet site performs analytical & microbiological testing of incoming materials, packaging components, in-process testing, drug product & drug substance release testing and stability testing. Multiple method transfers and validations are performed to support new products. This position is responsible for the Quality Control support activities, including the setup and maintenance of master data within LIMS, Empower and analytical instruments, setup and qualification of new instruments, audit trail review, and adherence with data integrity principles. As a QC leader, you will be customer focused. Using your significant experience, you will mentor and coach your team, creating a strong team...

L'Operator Packaging Operations aura pour mission d'assurer les activites de conditionnement des produits (blister, bouteille, etui, wallet, inspection visuelle), dans le respect de la reglementation BPF / cGMPs, des regles d'hygiene, et de securite. II devra se conformer aux procedures definies par le systeme qualite du site pharmaceutique.

L'Operator Packaging Operations aura pour mission d'assurer les activites de conditionnement des produits (blister, bouteille, etui, wallet, inspection visuelle), dans le respect de la reglementation BPF / cGMPs, des regles d'hygiene, et de securite. II devra se conformer aux procedures definies par le systeme qualite du site pharmaceutique.

This position is a leadership role being responsible in direct management of individual contributors and/or supervisors and/or managers.   This position is a safeguard and role model for the WuXi values and competencies.   Job Summary:

This position is accountable for the Quality Control activities at the OSD drug product manufacturing site of Couvet, Switzerland, including method transfer / verification, the analytical & microbiological testing of incoming materials, packaging components, in-process testing, drug product & drug substance release testing and stability testing, as well as equipment cleaning residual testing and support the manufacturing related area operation such as environment monitoring.  You will ensure activities meet cGMP requirements and customers’ expectations.

The Senior Analyst is part of the Quality Control (QC) department of STA Pharmaceuticals Switzerland. He/She is responsible for executing protocols for method validations, verifications and transfers for the QC Laboratory. The position will also perform all testing of both material and finished product in support of the larger product introduction activities e.g. testing of samples for stability registration studies, process validation or cleaning validation. Additional duties includes participation to investigations in case of deviations, cleaning validation, preliminary testing, and preparation or review of documentation

Le Technician Bulk Manufacturing aura pour mission d’assurer les activités de fabrication des produits (capsules ou comprimés), dans le respect de la réglementation BPF / cGMPs, des règles d’hygiène, et de sécurité. Il devra se conformer aux procédures définies par le système qualité du site pharmaceutique.

The MS&T Senior Engineer is in accountable for the new introduction of oral solid dosage forms (capsules and tablets) in the site of Couvet. The Senior Engineer, MS&T authors, leads and updates of Technical Transfer Plan and Gap analysis. He/she trains the operational teams to the protocol/master batch record for the new product.

Le Technicien Packaging aura pour mission de supporter les activites de conditionnement dans le respect de la reglementation cGMPs*, des regles d'hygiene et de securite. II devra se conformer aux procedures definies par le systeme qualite du site pharmaceutique.    

Le Technician Bulk Manufacturing aura pour mission d’assurer les activités de fabrication des produits (capsules ou comprimés), dans le respect de la réglementation BPF / cGMPs, des règles d’hygiène, et de sécurité. Il devra se conformer aux procédures définies par le système qualité du site pharmaceutique.

The Senior Analyst is part of the Quality Control (QC) department of STA Pharmaceuticals Switzerland. He/She is responsible for executing protocols for method validations, verifications and transfers for the QC Laboratory. The position will also perform all testing of both material and finished product in support of the larger product introduction activities e.g. testing of samples for stability registration studies, process validation or cleaning validation. Additional duties includes participation to investigations in case of deviations, cleaning validation, preliminary testing, and preparation or review of documentation

Le Technician Bulk Operations aura pour mission d’assurer les activités de fabrication des produits (capsules ou comprimés), dans le respect de la réglementation BPF / cGMPs, des règles d’hygiène, et de sécurité. Il devra se conformer aux procédures définies par le système qualité du site pharmaceutique.   ***** Long Term Temporary position*****

The Project Manager II will manage and coordinate clinical and/or data project services for sponsors to assure project/program milestones are met according to contract and applicable regulations are followed. Preference for in-office over work from home with occasional travel depending on project.

WuXi Clinical, a wholly owned subsidiary of WuXi AppTec, is a global Contract Research Organization (CRO) providing a comprehensive range of services in clinical development. We provide Phase I to Phase IV clinical development services & BE (Bioequivalence), for products including pharmaceuticals, biologics, and medical devices. With expertise spanning all major therapeutic areas, we deliver the unique blend of an experienced team, combined with the creativity, responsiveness, and customer centric-focus of a highly nimble organization. This forward-thinking approach has allowed us to work on a variety of projects ranging from first-in-human products to marketed drugs and devices.

WuXi Clinical, a wholly owned subsidiary of WuXi AppTec, is a global Contract Research Organization (CRO) providing a comprehensive range of services in clinical development. We provide Phase I to Phase IV clinical development services & BE (Bioequivalence), for products including pharmaceuticals, biologics, and medical devices. With expertise spanning all major therapeutic areas, we deliver the unique blend of an experienced team, combined with the creativity, responsiveness, and customer centric-focus of a highly nimble organization. This forward-thinking approach has allowed us to work on a variety of projects ranging from first-in-human products to marketed drugs and devices.