Lead the material supply processes related to products manufactured at the Couvet site, from the procurement of the raw materials to the shipment of finished goods, as well as manufacturing master data management. As a strategic role and key player for the organization, this position will interact with the following departments: Bulk Operations, Packaging Operations, QC, Validation, QA, IT and Finance. This position oversees lead-times and the requested delivery date and ensures on time in full...

The MS&T Engineer is involved in the new introduction of oral solid dosage forms (capsules and tablets) in the site of Couvet. He/she is involved in all the technical activities related to Product transfer. He/she authors the technical transfer plan and the Gap analysis He/she trains the operational teams to the protocol/master batch record for the new product.

The MS&T Senior Engineer is in accountable for the new introduction of oral solid dosage forms (capsules and tablets) at our Couvet, Switzerland site. The MS&T Senior Engineer,  authors, leads and updates of Technical Transfer Plan and Gap analysis. 

The Continuous Improvement and Compliance Senior Specialist is responsible for driving process improvements and ensuring regulatory compliance within the pharmaceutical industry. This role involves analyzing existing processes, identifying areas for improvement, and implementing best practices to enhance operational efficiency while maintaining adherence to industry regulations.

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

L'Operator 1 Bulk Operations aura pour mission d'assurer les activites de fabrication des produits (capsules et (ou) comprimes), 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.

Quality Operation is responsible to support the entire Couvet site to ensure that each GxP-stakeholder operates in compliance with the site's Quality Management Systems (QMS), the cGMP and the applicable laws, regulations, and standards; and support client relationships by ensuring that TMA quality agreement is respected. The position holder is responsible to ensure the proper support of the GxP stakeholder, the proper application and use of the QMS, the proper control of all the GxP processes and the investigation and assessment of any issue, to review and...

The Senior Scientist is part of the the Quality Control (QC) department of STA Pharmaceuticals Switzerland. The Team is responsible for introducing new raw materials, drug substance (API), and drug product (Bulk) as well as new technologies at the site. The Senior Scientist provides technical and scientific expertise to support transfer/verification/validation of new methods and investigation and troubleshooting of analytical issues (commercial or not). Additional duties includes participating to registration stability studies, participating to supplier qualification & supplier Audit, participating to cleaning validation and validation processes, and leading QC risk...

The Specialist, Manufacturing Compliance authors, owns and leads updates of GMP documents related to Bulk and/or Packaging Operations. This includes batch record master creation and revision. He/she initiates and owns deviations related to Bulk and/or Packaging Operations and leads investigation tasks as required.  

As a Senior Quality Control Analyst, with a CDMO organization, you will perform a wide variety of chemical or biological analyses on products, in-process materials, or samples in support of the company’s quality assurance and quality control program.   (This is a 12-month temporary role, with huge probabilities of extension or turning into a permanent role)

The Senior Manager QA Projectis responsible to support the entire Couvet site to ensure that each product is continuously manufactured, packaged, and tested in compliance with the Marketing Authorisation Dossier managed by the Customer/Product Owner and also to represent the site in the Company Regulatory Surveillance initiatives. As a member of the Quality Leadership Team, the position holder is collaborating with the other members of the QLT to ensure that on the...

We are seeking a seasoned and dynamic Customer Service Manager to join our Supply team, playing a pivotal role in cultivating exceptional relationships with our commercial clients.   This newly created position offers a unique opportunity for you to leverage your extensive experience to shape and enhance our customer relationship strategy.  

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.

This position is responsible for leading the business development activities within STA, WuXi’s CMC small molecule development and manufacturing division. The position works closely with STA’s other BD team members and senior management team in China to develop and execute the most effective strategy to increase small molecule drug product, API and intermediate sales across US based key accounts both biotech and large pharma. This position manages sites for key accounts and is also responsible for business development for any new accounts.   This position works proactively with other BU team members, such as other BD team members, Marketing, Project Management,...

Mission: The Supervisor Packaging Operations will be responsible for overseeing product packaging activities (blister packs, bottles, boxes, wallets, visual inspection) in compliance with GMP/cGMP regulations, hygiene rules, and safety standards. They will ensure adherence to the established production plan while conforming to procedures defined by the site's quality system. They will also be in charge of supervising operators and technicians working in packaging.

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 Business Development Senior Manager drives sales growth in close coordination with WuXi Biology leadership. The Senior Business Development Manager will have an additional focus on penetrating certain assigned customers with significant growth opportunity, as assigned by management. Reporting to the Director, Business Development, the Senior Manager, Business Development closes and implements growth opportunities with Companies in their assigned territory. The Senior Business Development Manager’s most important means of interacting with customers and prospects is through face-to-face meetings and is responsible for achieving an assigned sales and profit...

This position is responsible for leading the business development activities in the EU within STA, WuXi’s CMC small molecule development and manufacturing division. The position works closely with STA’s other BD team members and senior management team in China to develop and execute the most effective strategy to increase small molecule Drug Substance, Drug Product, API and intermediate sales in their area of geographic responsibility. This position manages sites for key accounts and is also responsible for business development for any new accounts. This position works...

This position is responsible for leading the business development activities in The EU within STA, WuXi’s CMC small molecule development and manufacturing division. The position works closely with STA’s other BD team members and senior management team in China to develop and execute the most effective strategy to increase small molecule Drug Substance, Drug Product, API and intermediate sales in their area of geographic responsibility. This position manages sites for key accounts and is also responsible for business development for any new accounts. This position works...

The incumbent will uncover and cultivate business relationships and opportunities to generate revenue with prospective and existing clients for WuXi Tides and STA Pharmaceutical, a WuXi AppTec company, in particular to support the growth of emerging oligo and peptide (O&P) Contract Development and Manufacture (CDMO) business. The candidate will work within the US business development (BD) team to pursue new business leads; follows up on critical issues and aid in resolving customer inquiries. Assists marketing in raising the profile of WuXi Tides within US.