WuXi AppTec

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Search Results Page 7 of 12

Job Locations US-CA-San Diego
HD Biosciences, a WuXi AppTec company, located in San Diego, CA is seeking a highly skilled and motivated scientist to join our Discovery Research team. The Senior Scientist will play a role in the fast-paced and dynamic R&D team. She/he will independently lead the projects including human iPSC/ESC culture, reprogramming, differentiation, and assay development using the iPSC derivatives. Extensive hands-on experience in working with human iPSCs is required.
External ID
WXHDB-1453
Job Locations US-CA-San Diego
Responsible for supporting the Database and Statistical Programming (DSP) efforts for specific projects/studies with SAS. Responsibilities include developing, testing, maintaining, validating, and documenting SAS programs to meet the project’s needs. Work within general programming standards and procedures to independently perform statistical programming tasks.
External ID
WXPAC-1128
Job Locations US
The Senior Project Manager will mainly support and manage Lab Testing Division’s WIND programs in the US to closely work with the project teams and scientists of relevant business units in China (Shanghai and Suzhou, etc.) This position has the ability to be on-site at our Cranbury, NJ Facility or remote within the US. Position level will be based on the individual experience and education background.
External ID
WXLLC-12490
Job Locations US-MN-St. Paul
The Quality Systems (QS) Validation Specialist serves as a key resource for providing oversight and guidance to ensuring equipment and computerized systems (CSV) compliance with applicable standard and regulatory requirements, along with site operations, policies, procedures, processes to mitigate process and/ or product risks at WuXi AppTec St. Paul.  This position will support multiple aspects within the Quality organization with focus on but not limited to: equipment and computerized systems validations, supplier quality functions, SOP writing and review, Quality event review, and auditing support.
External ID
WXINC-21328
Job Locations US-MN-St. Paul
Job Summary: This individual will be responsible for performing the technical aspects of assigned tests in compliance with GLP, USDA and AAALAC guidelines.
External ID
WXINC-1995
Job Locations US-MN-St. Paul
Job Summary: This individual will be responsible for performing the technical aspects of assigned tests in compliance with GLP, USDA and AAALAC guidelines.
External ID
WXINC-23212
Job Locations US-PA-Philadelphia
Designs and executes research & development studies, assay qualifications and test article validations under limited supervision. Drafts test methods and clearly documents all experiments according to SOPs and cGMP guidelines. Acts as a Technical Reviewer and assay trainer. Partners with Testing Operations during assay transfer and validation activities. Participates in client calls and face to face meetings with assistance by departmental senior staff.
External ID
WXATU-2809
Job Locations US-PA-Philadelphia
Designs and executes research & development studies, assay qualifications and test article validations under limited supervision. Drafts test methods and clearly documents all experiments according to SOPs and cGMP guidelines. Acts as a Technical Reviewer and assay trainer. Partners with Testing Operations during assay transfer and validation activities. Participates in client calls and face to face meetings with assistance by departmental senior staff.
External ID
WXATU-2808
Job Locations US-NJ-Cranbury
Lead Talent Acquisition strategy development and talent delivery in support of a growing global organization operating in the US UK, and EU, ensuring alignment with business strategy. Responsible for establishing the global talent acquisition processes and managing a dispersed team of Talent Acquisition Professionals. Providing expert level guidance toward the continuous improvement of the global Talent Acquisition function by developing recruiting competencies throughout the company that include short- and long-term recruitment planning, resource allocation and deployment, performance reporting and employer branding. Actively enhance and maintain all recruitment related systems and processes.
External ID
WXLLC-12489
Job Locations US-PA-Philadelphia
Designs, plans, authors, and executes research & development studies, assay qualifications and test article validations under very limited supervision. Leads method development projects. Acts as a Technical Reviewer and assay trainer. Partners with Testing Operations during assay transfer and validation activities. Participates in client calls and face to face meetings with limited assistance by departmental senior staff.
External ID
WXATU-1148
Job Locations US-PA-Philadelphia
Performs and directs assays according to and in compliance with Good Laboratory Practices (GLP), current Good Manufacturing Practices (cGMP), Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs). Sufficiently competent in science to initiate and carry out scientific development projects related to the development of new assays, initiation of new programs, assay validations and associated projects. Schedules and directs assays. Assists with training junior staff members. Performs Research & Development activities. Acts as Study Director as required. Assists supervisor with day-to-day lab management duties. Correctly analyzes scientific data with accuracy and precision.
External ID
WXATU-2802
Job Locations US-MN-St. Paul
The Associate Scientist will help develop and conduct qualitative and quantitative chemical analysis and experiments using the appropriate equipment and analytical techniques. The individual will perform a variety of analytical tests, prepare samples/standards/reagents, troubleshoot, maintain and run instruments (primarily GC-MS).
External ID
WXINC-23362
Job Locations US-PA-Philadelphia
Supervises the day to day molecular biology operations (employees, resources, and capacity) to ensure execution of testing support services
External ID
WXATU-2786
Job Locations US-CA-San Diego
The Operations Associate will be responsible for inventory control and management of all internal inventory items from across all departments that are supported by the Operations team. He/she will manage all invoicing. He/she will provide backup for procurement, Quality Assurance, and other operational support for our growing company. 
External ID
WXHDB-1451
Job Locations US-PA-Philadelphia
Associate Scientist in Molecular Biology acts as Independent Technical Reviewer and has ability to operate in a fast paced, rigorous cGMP testing environment. Responsible for technical review of GMP documents to ensure correct interpretation, analysis, documentation, and reporting of results. Generates R&D and validation reports, GMP documents and GMP Test Methods. Oversees assays and investigations according to and in compliance with current Good Manufacturing Practice (cGMP), Code of Federal Regulations (CFR) and Standard Operating Procedures (SOPs).   *Due to growth, we have multiple positions on the Molecular Biology Team.
External ID
WXATU-1988
Job Locations US-PA-Philadelphia
Independent scientist who demonstrates innovative technical knowledge and significantly contributes to the overall operations of the Virology Department. Demonstrates strong oral and written communication skills and actively contributes to training, report generation and documentation. Demonstrates strong supervisory skills and contributes to the achievement of company and departmental goals and objectives. Manages resources that support client facing Virology laboratory operations. Supports management of laboratory schedule with operations team. Performs and directs assays according to and in compliance with Good Laboratory Practice (GLP), current Good Manufacturing Practice (cGMP), Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs). Acts as Study Director as required.
External ID
WXATU-2126
Job Locations US-PA-Philadelphia
Independent scientist who demonstrates innovative technical knowledge and significantly contributes to the overall operations of the Virology Department. Demonstrates strong oral and written communication skills and actively contributes to training, report generation and documentation. Demonstrates strong supervisory skills and contributes to the achievement of company and departmental goals and objectives. Manages resources that support client facing Virology laboratory operations. Supports management of laboratory schedule with operations team. Performs and directs assays according to and in compliance with Good Laboratory Practice (GLP), current Good Manufacturing Practice (cGMP), Code of Federal Regulations (CFR) and/or Points to Consider (PTC) guidelines and Standard Operating Procedures (SOPs). Acts as Study Director as required.
External ID
WXATU-1769
Job Locations US-MN-St. Paul
Performs laboratory assays that demand a professional application of the principles, theories, and techniques of cell culture and media preparation.
External ID
WXINC-23357
Job Locations US
Job Summary: This person will be responsible for accomplishing results through the execution and delivery of the end to end, full-cycle recruitment process for a wide range of roles within the Business Development, Clinical Research, Data Management, Statistics and Project Management functions. This person will be supporting the WuXi Clinical team.
External ID
WXRPG-2302
Job Locations US
STA Pharmaceuticals, a WuXi AppTec Company, has an exciting opportunity for an Associate Director, US Project Management. 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. Due to offshore client engagements, the ideal candidate must be fluent in Mandarin and English.
External ID
WXSTA-11239

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