This position is responsible for organizing, planning and managing the personnel, systems and resources critical to the daily operation of the department(s).  The Manager works cross functionally to ensure processes and procedures in place to align with regulatory requirements.

Research and analyze the synthesis and purification of novel chemical compounds for potential clinical drug development using chromatographic and analytical techniques, Scale up (multi-kg scale), Experimental design and planning; Design and synthesize molecular targets and execute multi-step synthetic sequences towards key target molecules using purification and compound characterization techniques; Research and recommend new methods and alternative synthetic sequence techniques to optimize existing processes (Process R&D); Perform job-specific tasks in compliance with FDA regulations, Safety Consciousness, internal standards, company policies, and standard operating procedures (SOPs).

WuXi AppTec is a leading global pharmaceutical, medical device open-access capability and technology platform company with global operations. We have an opening in our Media Prep department for an Associate Sterilization Technician.  This position will work to prepare various media in compliance with GLP, GMP and ISO standards.   Monday - Friday 8 AM to 5 PM This is a full-time, permanent position offering...

This position is a safeguard and role model for the WuXi values and competencies.   Job Summary: This position is 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 support...

This role provides HR and recruiting experience and expertise to the assigned Business Units. Performs various human resources duties in areas such as new hire orientation, talent acquisition, employee relations, benefits, payroll, and other special projects. Serves as contact for employees and managers and answers questions regarding HR and company policies and procedures. This position is a hybrid position with 3 days on-site in Munich.

HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology team. We’re seeking a highly motivated Research Associate I to support our in vivo pharmacology team for various projects.

WuXi AppTec is a leading global pharmaceutical, medical device open-access capability and technology platform company with global operations. We have an opening in our Sterility Department for an Associate Lab Technician.     Position Details: - Schedule: - Monday - Friday 10AM to 7:00 PM -

WuXi AppTec is a leading global pharmaceutical, medical device open-access capability and technology platform company with global operations. We have an opening in our Sterility Department for an Associate Lab Technician.     Position Details: - Schedule: - Monday - Friday 5AM to 2:00 PM -

Responsible for producing documents for sterility assurance related programs, providing aseptic processing oversight, and technical support to manufacturing operations to ensure contamination control. Acts as the Primary Sterility Assurance Representative and effectively collaborates with multi-disciplinary teams for designated projects.   Position Details: Monday to Friday Standard Business Hours

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.  

The activities associated with this role fall into four categories: 1. Support Business Development (BD) and IPM by providing close management of clients, coordinating across Business Units (BU’s) and promoting the integrated discovery services platform 2. Carry out marketing and BD activities as required 3. Support research into and the assessment of technical development initiatives for Discovery Services 4. Support the EU BD team as required  

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.

Responsible for coordinating the training for those who produce Master and Working Cell Banks and activities within production facilities to support manufacture of Cell & Gene Therapy products, and final product fills according to current Good Manufacturing Practices (cGMPs)   Monday to Friday Standard Business 100% Onsite at our Philadelphia, PA location

The Manager Facilities is responsible for providing construction, engineering oversight and maintenance services for a state-of-the-art, multi-product contract manufacturing and testing facility. General responsibilities include: developing operational requirements for equipment/systems, developing request for proposals (RFP’s) for Facilities’ projects and supervise overall corrective and preventative maintenance program for facility, equipment and systems to support operations. Specific responsibilities include: maintaining and operating mechanical and utility systems, troubleshooting equipment/processes, ensuring regulatory compliance, and supervising internal facilities technician staff, external contractors and writing...

The Quality Assurance Specialist - Testing reviews laboratory testing data/records in accordance with current Good Manufacturing Practices (cGMP), and Good Laboratory Practices (GLP) for Nonclinical Laboratory Studies, as applicable. Monitor processes for adherence to established procedures/regulatory compliance. Provides guidance for quality related issues and consults with QA Management to resolve complex quality issues in a timely manner.   Position Details: -

Introduction to Metrology and the scientific study of measurement. Metrology Technician I acquires training and the skills required for calibration of instrumentation & equipment. Metrology Technician I is introduced to the industry regulatory requirements and guidelines necessary for processing and creating documents. This individual will obtain detailed instruction and document all results consistent with all applicable quality standards and GXP requirements.  

This position will be responsible for managing projects within STA, WuXi’s API development and manufacturing division. Leads the orderly progression of projects from the proposal stage through project completion by interacting with the client, technical team and business development team. The incumbent will also participate in business development activities such as visiting existing or new clients and promoting STA’s services in conferences/trade shows.

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, as well as other research and development services. We are seeking a highly motivated and skilled Principal Scientist to lead our fast-growing bioanalysis platform. The AD will lead a team to achieve long-term research and business goals in a CRO setting. The position will independently design, execute, trouble shoot and deliver the projects with LCMS, including small molecules and biologics, as well as lipidomics, glycomics and proteomics.

The jobholder would lead the development of new bioanalytical studies and technologies, and implementing process improvements. Perform LC-MS method development, method validation/qualification, sample analysis, report writing, complex trouble-shooting and problem-solving in the field of drug discovery and development.   The Scientist III will join WuXi DMPK at Cranbury, New Jersey site to support in vitro ADME, in-vivo PK and bioanalytical assays in a dynamic environment. The...

Contribute to the completion of routine technical tasks by providing programming assistance as part of the Clinical and Statistical Programming (CSP) team to test, maintain, and document programs for clinical trials in drug development. Assist with the development of project-related database and statistical programming solutions under the direction of the CSP Lead.