HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology Division. We are seeking highly skilled and motivated Research Associate to join the team.

L'Operator 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.

We are looking for a long-term, in-house teammate to join our Facilities team.Responsible to assist with the day-to-day maintenance activities associated with the WuXi AppTec San Diego facility.  This includes assisting with maintenance/repairs as well as working with various external contractors and service providers.

Job Summary:   This position is accountable for the integration of New Product Introductions, NPI, within QC at the site of STA Pharmaceutical Switzerland SA.   Accountable for the project management and on time delivery of NPI within QC, including method transfer / validation, analytical testing of incoming materials, packaging...

The Manager/ Senior Manager, Business Development East Coast drives sales growth in close coordination with Research Chemistry Services 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 VP, Business Development, the (Senior) Manager, Business Development closes and implements growth opportunities with Companies in the Eastern region. The Manager/ Senior Manager, Business Development’s most important means of interacting with customers and prospects is through face-to-face meetings, and is responsible for achieving an...

This position is accountable for the Quality Control activities at the OSD drug product manufacturing site of Couvet, Switzerland, including method transfer / verification / validation, 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. As the QC leader, you will be...

  Job Summary:   L'Associate Operator Packaging Operations aura pour mission d'assurer les activités de base de conditionnement des produits (blister, bouteille, étui, wallet, inspection visuelle), dans le respect de la réglementation BPF / cGMPs, des règles d'hygiène,...

The Analytical Scientist is part of the Quality Control (QC) department of STA Pharmaceuticals Switzerland. The Analytical Scientist provides technical and scientific expertise to manage transfer/verification/validation of new methods for introducing new raw materials, drug substance (API), and drug product (Bulk). He / She supports 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.

Job Summary:   The Validation Technician, performs validation and qualification activities. They assure compliance of these activities with cGMP as well as with internal policies and procedures. The Validation Technician is authorized to direct external vendors performing work in this field.

The incumbent will uncover and cultivate business relationships and opportunities to generate revenue with prospective and existing clients for WuXi TIDES in the EU, a WuXi AppTec company. To support the growth of emerging oligo and peptide CMC development and Manufacturing (CDMO) business. The candidate will work within the European TIDES business development team to pursue new business leads in addition to following up on critical issues and aid in resolving customer inquiries.  

The Senior Analyst is a key member of the Quality Control (QC) department at STA Pharmaceuticals Switzerland. This role is responsible for executing protocols related to analytical method validation, verification, and transfer in compliance with regulatory standards (cGMP, ICH, FDA, EMA). In addition to supporting method lifecycle activities, the position includes testing of raw materials, intermediates, and finished products, particularly in support of new product introductions, stability and registration studies, process validation, and cleaning validation.

Execute Business Development plans in close coordination with Research Chemistry Service (RCS) leadership, leading to identification, penetration, and growth of business and accounts in the assigned region. The Senior Director Business Development drives sales growth in close coordination with Research Chemistry Services leadership, penetrating certain assigned customers with significant growth opportunity, as assigned by management. The Senior Director Business Development closes and implements growth opportunities with companies in the territory by interacting with customers and prospects through face-to-face meetings, and is responsible for achieving an assigned purchase order (PO) goal....

The Senior Director, Business Development expand Biology Division business in US as part of the broader Business Development team, through proactively managing the sales process, following up on leads, filling the pipeline to meet the yearly revenue targets for the region whilst demonstrating WuXi AppTec’s core values and complying with Company Policies. Leading and managing a team to achieve Division targets, provide exceptional customer service and to build capabilities in the region Please note the location of this job is remote / work from home. Overnight travel requirement is approximately 50%.

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.