WuXi AppTec

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Search Results Page 4 of 10

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-2248
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 research & development activities and assay validations as required under direct supervision. Drafts test methods and clearly documents all experiments according to SOPs and cGMP guidelines. Performs laboratory maintenance duties. Works closely with Testing Operations during assay transfer and validation activities.
External ID
WXATU-2806
Job Locations US-PA-Philadelphia
Maintains current knowledge of compliance guidelines and requirements related to advanced therapy manufacturing and testing. Designs, plans, authors, and executes research & development studies, assay qualifications and test article validations. Leads method development projects. Acts as a Technical Reviewer and assay trainer. Partners with Testing Operations during assay transfer and qualification activities.
External ID
WXATU-2805
Job Locations US-TX-Austin
WuXi Clinical, a wholly owned subsidiary of WuXi AppTec, is a global Contract Research Organization (CRO) providing a comprehensive range of services in clinical development. We provide Phase I to Phase IV clinical development services & BE (Bioequivalence), for products including pharmaceuticals, biologics, and medical devices. With expertise spanning all major therapeutic areas, we deliver the unique blend of an experienced team, combined with the creativity, responsiveness, and customer centric-focus of a highly nimble organization. This forward-thinking approach has allowed us to work on a variety of projects ranging from first-in-human products to marketed drugs and devices. Founded in 2000, the WuXi AppTec is the leading global pharmaceutical, medical device open-access capability and technology platform company with more than 25,000 employees across 25 locations globally. The WuXi platform is enabling more than 3,000 innovative collaborators from more than 30 countries to bring innovative healthcare products to patients, and to fulfill WuXi AppTec’s dream that “every drug can be made and every disease can be treated.”
External ID
WXRPG-2304
Job Locations US-MN-St. Paul
The Project Manager develops, manages and tracks compliance programs crucial to the success of the organization.  Facilitates the resolution of all issues to ensure timely delivery of the project.
External ID
WXINC-22992
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-2804
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-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-2801
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
The Sample Coordinator will process incoming samples, assist with administrative duties relating to Central Sample Repository functions
External ID
WXATU-2316
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
STA is constructing new facilities to manufacture small molecule drug substances and drug products. In addition to small molecule active ingredient manufacturing, this will include capabilities for oligonucleotides, peptides and High Potent drug substances. From a drug product perspective this will include oral solid as well as sterile dosage forms. The position will lead the team responsible for the quality and compliance support during design, construction and qualification phases of these facilities. After start of operations, this position will take leadership responsibility for continuous quality improvement and will lead a Quality team to support ongoing maintenance, engineering and site expansion projects. The individual will keep close cooperation with the Site Leadership Team, and will develop the Quality assurance team to support the creation of a culture that aligns with the Company’s core values of integrity & dedication, working together, doing the right thing, and doing it right. The position will ensure compliance with all Company, local, state, and federal policies and procedures and international authority requirements for quality and compliance.
External ID
WXSTA-11241
Job Locations US-GA-Marietta, Georgia
WuXi AppTec is a leading global pharmaceutical, medical device open-access capability and technology platform company with global operations. We have an opening for an Equipment Validation Specialist.
External ID
WXINC-23360
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-2784

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