WuXi STA (stapharma.com), a subsidiary of WuXi AppTec, is a leading pharmaceutical development and manufacturing capability and technology platform company serving the life sciences industry, with global operations across Asia, North America, and Europe. As a premier Contract Research, Development, and Manufacturing Organization (CRDMO), WuXi STA offers its worldwide partners efficient, flexible and high-quality solutions for integrated chemical, manufacturing and controls (CMC) from preclinical to commercial uses.   WuXi TIDES is an integral part of WuXi STA, a subsidiary of WuXi AppTec. WuXi TIDES offers our worldwide partners efficient, flexible, and high-quality solutions for the drug development of oligonucleotides, peptides and related synthetic conjugates (“TIDES” drugs). We greatly simplify the TIDES drug development by providing all discovery, CMC development and the entire manufacturing supply chain under one roof.   We are looking for a Head of Marketing and Communications who’ll lead WuXi STA (including WuXi TIDES) global marketing and communication activities from social media and digital campaigns to advertising and creative projects. The Head of Marketing and Communications responsibilities include developing plans to help increase our brand value, allocating resources to different projects and setting short-term and long-term department goals. Ultimately, you will run our Marketing department in ways that promote higher profitability and competitiveness.

Under close regular supervision, the individual performs vivarium and animal care, maintenance, and sanitation; including running a cage washer and tunnel washer, keeping laboratory supplies filled and organized, pest control monitoring, and environmental monitoring.   **Please note that this is a contingent/temp position and not eligible for benefits.**   Schedule: Monday to Friday 8 AM - 4:30 PM (flexibility in start time available) Hours: 40 per week Anticipated assignment length: 6-9 months with opportunity to convert to permanent employee

We are seeking a highly skilled and dynamic individual to join our team as a Technical Content Director. The successful candidate will play a crucial role in bridging technical expertise with marketing initiatives to showcase WuXi STA's strengths in the industry.

Job Summary:   This position is responsible to perform all Super User activities for the laboratory computerized systems. This includes at least Audit Trail Reviews and Master Data Management, optimization and/or new method setup, in adherence with data integrity principles as well as end user training, on-the-job training and equipment troubleshooting. Additional responsibilities are selection, acquisition, and qualification of new analytical equipment by handling, writing and executing Change Control, User Requirement Specification and Performance Qualification protocol. Owns deviations, leads or supports laboratory investigations associated with equipment issues.   As a QC Team Member, the person filling this position supports all activities to continuously maintain the GMP status of the QC Laboratory. As a Senior QC Team Member this position acts as a centre of competence reflecting experience, transferring knowledge and supporting other QC team members in all aspects of their daily work.

Plans and carries out in vivo experiments and associated research assignments in rodents. Maintains the vivarium, labs, and program to AAALAC standards. Operates lab equipment including oxidizers, centrifuges, LS counters, and cage/tunnel washers.   **Please note that this is a contingent/temp position and not eligible for benefits.**   Schedule: Monday to Friday 6:30 AM - 3:00 PM (occasional weekend rotations)

WuXi Advanced Therapies is a leading global cell and gene therapy contract, testing, development, and manufacturing organization (CTDMO) that is dedicated to advancing the development and commercialization of cell and gene therapies. Our values include innovation, excellence, and collaboration, which are reflected in our mission to accelerate the development and availability of life-saving therapies for patients in need.    Working at WuXi 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 include: - 401K matching - PTO - Employee discount programs - Medical, dental and vision insurance - and much more As a Manufacturing Technical Writer, you will continually function as a subject matter expert support and provide input pertaining to the Manufacturing client proposal process to the Manufacturing Management team, the Manufacturing department, & other departments as needed.

WuXi Advanced Therapies is a leading global cell and gene therapy contract, testing, development, and manufacturing organization (CTDMO) that is dedicated to advancing the development and commercialization of cell and gene therapies. Our values include innovation, excellence, and collaboration, which are reflected in our mission to accelerate the development and availability of life-saving therapies for patients in need.    Working at WuXi 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 include: - 401K matching - PTO - Employee discount programs - Medical, dental and vision insurance - and much more Shift time:(Sun-Thurs- 2pm-10:30pm)   The Associate Scientist - QC Manufacturing 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

Responsible for driving the company’s continued growth and carrying the sales targets for Toxicology, DMPK, and Bioanalytical service offerings from the Laboratory Testing Division. These services encompass services at discovery, development and clinical stages.  Serves as the primary commercial point of contact for the Division with key Pharma & Biotech stakeholders and decision makers, as well as key opinion leaders.  This position will be located in the East Coast, preferably in the Boston area.

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.

This position fulfils the desire of Senior Management to increase the overall level of leadership capability at Bioanalytical Services (BAS), Plainsboro, New Jersey (NJ). The incumbent will provide leadership for the performance of the Small Molecule, Large Molecule and Central Lab functions at the WuXi NJ site, lead the team in bioanalytical sciences, GLP operations, and business aspects, and to collaborate with WuXi’s Bioanalytical and Central Labs in China to promote synergy in supporting global clinical and non-clinical studies.

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.

This position will primarily support the review and generation of quotations from queries. The candidate should have a biology background, be detailed oriented and well organized. This position requires someone who works well under supervision and within a team to ensure proposal deadlines are met.

The Director will provide planning, supervision, management, leadership, scheduling and financial oversight to the daily lab operation of the Analytical Chemistry Department in Germany. He/She will have a strong science background, the ability to manage laboratory workflow efficiently, good attention to detail and experience in Good Manufacturing Practices (cGMP) environments. In addition, this individual should have the ability to work effectively in a cross functional team-based environment and work independently. This position will have direct oversight of the technical operations group and dotted line oversight to the quality group and the business operations group. 

Shift time:(Sun - Thurs - 2nd shift - 3pm -11:30pm)   WuXi Advanced Therapies is a leading global cell and gene therapy contract, testing, development, and manufacturing organization (CTDMO) that is dedicated to advancing the development and commercialization of cell and gene therapies. Our values include innovation, excellence, and collaboration, which are reflected in our mission to accelerate the development and availability of life-saving therapies for patients in need.    Working at WuXi 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 include: - 401K matching - PTO - Employee discount programs - Medical, dental and vision insurance - and much more The Associate Scientist - Microbiology 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.

Job Summary:   Le Technician Bulk Operations 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.

The Sr. Manager, Business Development drives sales growth in close coordination with WuXi Biology leadership. The Sr. Business Development Manager will have an additional focus on penetrating certain assigned customers with significant growth opportunity, as assigned by management. The Sr. Business Development Manager’s most important means of interacting with customers and prospects is through face-to-face meetings and is responsible for achieving an assigned sales goal.

The primary responsibilities of this position are to provide statistical consulting to clients in the biotech/pharmaceutical industry in their drug development programs with a focus on protocol/study design, analysis planning, and regulatory submission strategies.    

The primary responsibilities of this position are to provide leadership in planning and conducting data analyses in clinical studies, and participate in planning and data analyses for regulatory submission.       

WuXi Advanced Therapies is a leading global cell and gene therapy contract, testing, development, and manufacturing organization (CTDMO) that is dedicated to advancing the development and commercialization of cell and gene therapies. Our values include innovation, excellence, and collaboration, which are reflected in our mission to accelerate the development and availability of life-saving therapies for patients in need. Working at WuXi 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 include: - 401K matching - PTO - Employee discount programs - Medical, dental and vision insurance - and much more   The Technical Operations Specialist II is responsible for generating and/or review manufacturing related technical documents and manage timely closure of these documents. This includes but is not limited to Non-Conforming Event (NCE) investigations, CAPAs, Change Controls (CC), Batch Records (BR), Technical Transfers (TT), Final Reports (FR), and Standard Operating Procedures (SOP).

WuXi Advanced Therapies is a leading global cell and gene therapy contract, testing, development, and manufacturing organization (CTDMO) that is dedicated to advancing the development and commercialization of cell and gene therapies. Our values include innovation, excellence, and collaboration, which are reflected in our mission to accelerate the development and availability of life-saving therapies for patients in need.    Working at WuXi 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 include: - 401K matching - PTO - Employee discount programs - Medical, dental and vision insurance - and much more The Technical Operations Specialist I is responsible for providing technical support to the manufacture of Master and Working Cell Banks and performing activities within production facilities to support manufacture of Cell and Gene Therapy products, and final products fills according to current Good Manufacturing Practices (cGMPS).