Support assigned departments by promoting, communicating and implementing human resources strategies and initiatives. Build and maintain influential relationships by being a strategic partner with management. Provide legal advice, coordinate performance management, and resolve employee relations issues. Act as experts on human resources policies and procedures such as Benefits, compensation, and employee development   ** Advanced Therapies is currently hiring for either an HRBP (Human Resources Business Partner) or an Associate Director role. These positions are being posted separately.**

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.

Pharmaceutical Manufacturing: The EHS Specialist will be responsible for supporting EHS compliance and risk management within the PHL Campus. The EHS specialist will monitor and improve processes to prevent and eliminate injury and illness to employees and assist the company to comply with safety laws.

Pharmaceutical Manufacturing: The EHS Specialist II will be responsible for supporting EHS compliance and risk management within the PHL Campus. The EHS specialist will monitor and improve processes to prevent and eliminate injury and illness to employees and assist the company to comply with safety laws.

The Training Associate II will have the responsibility for performing a variety of tasks related to learning and development in a Good Manufacturing Practices (GMPs) facility. The position requires providing classroom and laboratory training to site employees who produce and/or support Master and Working Cell Banks. The ideal candidate will have strong communication and leadership skills. The individual must be able to coach and mentor trainees and elevate issues to proper personnel timely.  

HD Biosciences Inc. a WuXi AppTec company, offers biology-focused preclinical drug discovery services to biotech and pharmaceuticals. We offer our clients comprehensive service platforms around target validation, plate-based pharmacology, hit identification and lead discovery, in vivo pharmacology, and other research and development services.   The Principal Scientist should have deep and broad expertise in...

Advanced Therapies is a Contract Testing, Development and Manufacturing Organization (CTDMO). We offer technology platforms and services that enable the discovery, development, testing, manufacturing, and commercialization of cell and gene therapies. Our services and solutions accelerate time to market and support patients around the world. Working at Advanced Therapies means being part of a dynamic, fast-paced, and innovative environment where you will have the opportunity to work on cutting-edge technology and make a real difference in the lives of patients. Our culture is collaborative and supportive, with a focus on teamwork and continuous learning. Our benefits...

This position will coordinate and manage WuXi AppTec’s presence with industry conventions and conferences, as well as local seminars/receptions in Europe. The Event Marketing Specialist will report to the Associate Director Marketing Europe and will support WuXi Discovery Services with event marketing planning, developing marketing materials, trade shows, and on-line and off-line events.

The Marketing Coordinator plays a vital role in supporting the marketing team by assisting in the coordination of marketing projects, events and digital campaigns.

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...

The Metrology Equipment Service Coordinator (ESC) schedules all equipment service events for testing and manufacturing departments. The ESC; after confirming with equipment owners, updates the CMMS to reflect scheduled dates and locations. The ESC is responsible for processing of vendor certificates and documents, uploads them into the CMMS and when applicable, reviews vendor work documents. The ESC will track and maintain equipment warranty information and service contracts. The ESC will be responsible for escorting vendors and assure vendor services are complete and accurate prior to them leaving site.

HD Biosciences-US, a WuXi AppTec Company, is seeking an experienced and dynamic Senior Project Manager to coordinate and lead project management team and support business development activities. This role will collaborate closely with the internal scientific leaders, the business development team and clients to propose research service quotations, manage client relationships and project workflows, collect and analyze business data, and contribute to the company’s business development and strategic planning. The ideal candidate will also work alongside senior management, R&D group leaders, BD, legal, finance, marketing, and logistics teams to provide comprehensive project and business management and ensure high-quality research services to the clients.

The Principal Scientist of Hit-Finding Platforms will lead the development and implementation of cutting-edge screening platforms and directly lead discovery projects for business partners. This role is critical to conducting high-quality research, fostering innovation across the teams, and driving business growth.   As a global company with operations across Asia, Europe, and North America, WuXi AppTec provides a broad portfolio of R&D and manufacturing services that enable the pharmaceutical and healthcare industry worldwide to advance discoveries...

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.

Responsible for the support activities and disinfection of GMP space, equipment and associated areas involved in the manufacture of Master and Working Cell Banks, within production facilities involved in the manufacture Cell & Gene Therapy products and final product fills according to current Good Manufacturing Practices (cGMPs).

Responsible for the support activities and disinfection of GMP space, equipment and associated areas involved in the manufacture of Master and Working Cell Banks, within production facilities involved in the manufacture Cell & Gene Therapy products and final product fills according to current Good Manufacturing Practices (cGMPs).

Responsible for the support activities and disinfection of GMP space, equipment and associated areas involved in the manufacture of Master and Working Cell Banks, within production facilities involved in the manufacture Cell & Gene Therapy products and final product fills according to current Good Manufacturing Practices (cGMPs).   3rd Shift Work Schedule:  6:00pm - 4:30am

STA is constructing new facilities to manufacture small molecule drug products. This will include capabilities for oral solid as well as sterile dosage forms manufacturing. As well as the supporting analytical, warehousing and other needed capabilities. The position will initially lead the team (including consultancy firms) responsible for the quality and compliance support during design, construction and qualification phases of these facilities. And will be responsible for the implementation of the quality system. After start of operations and manufacturing, this position will take...

Responsible for building and supervising a team of manufacturing trainers and training coordinator(s) who coordinate, schedule, design, provide, document, maintain and improve training for all manufacturing personnel on matters including but not limited to: new hire orientation, department and facility specific training.

The Training Associate II will have the responsibility for performing a variety of tasks related to learning and development in a Good Manufacturing Practices (GMPs) facility. The position requires providing classroom and laboratory training to site employees who produce and/or support Master and Working Cell Banks. The ideal candidate will have strong communication and leadership skills. The individual must be able to coach and mentor trainees and elevate issues to proper personnel timely.