The Project Manager will be responsible for managing projects within STA, WuXi’s API and Drug Product 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. Please note this is a remote (work from home) position within the EU, and that English and Mandarin language skills are required.

The Specialist Material Management is responsible for indirect material activities at the site. They ensure supply continuity within agreed timelines, technical, cost and quality targets. Responsible for PO creation and follow-up with suppliers, as well as invoicing. They also act as backup within the purchasing team.   As a key player for the organization,...

Primary Quality Assurance Representative for review of GLP Final Reports, GMP Certificates of Analysis (CoA’s), Assay Validations, deviations, and CAPAs. Reviews laboratory testing data or manufacturing batch records in accordance with current Good Manufacturing Practices (cGMP consults with QA Management to resolve complex quality issues in a timely manner.

The Senior Manager QA Projectis 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 represent the site in the Company Regulatory Surveillance initiatives. As a member of the Quality Leadership Team, the position holder is collaborating with the other members of the QLT to ensure that on the...

This position is responsible for leading the business development activities in Scandinavia and key accounts in the European Union within the WuXi Discovery Chemistry Division. This position works closely with technical team, other BD team members and senior management team in China to develop and execute the most effective strategy to increase services along with project management in assigned area of geographic responsibility.    This position manages some key accounts and is also responsible for business development for new accounts.  This...

WuXi AppTec Pathologists contribute to a wide range of critical activities within Toxicology, Safety, and Biocompatibility. Testing including but not limited to study evaluation for nonclinical studies spanning all phases of drug development for pharmaceutical industries.

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 Aide.     Position Details: - Schedule: Tuesday - Saturday 9:00 AM - 6:00 PM (Saturday shift could start earlier) - Hours: Full-Time, 40 per...

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 7AM to 4:00 PM -

HD Biosciences, Inc. (San Diego), a WuXi AppTec Company, is expanding its in vivo Pharmacology Division. We’re seeking a highly motivated Research Associate II to join the team.

As the Business Development Manager, you will spearhead activities to identify and nurture client business opportunities, leading to the expansion of the client base and revenue growth for OXGENE and WuXi Advanced Therapies.

The Business Development Manager will cultivate growth of WuXi AppTec’s Medical Device Business. The role calls for dedicated and passionate candidates with strong communication and analytical skills, as the position will be central to developing sales initiatives, garnering support directly from clients through traditional sales channels, as well as working with internal stakeholders within multiple business & departmental functions to maintain a foundation for effective business collaboration and enhanced customer experience. Strategic planning, sales, sales-support processes, marketing & promotions will be routinely engaged in this role.

Responsible for providing direct oversight and leadership in the manufacture of Master and Working Cell Banks and performing activities within production facilities to support manufacture of Cell & Gene Therapy products, and final product fills according to current Good Manufacturing Practices (cGMPs).   PLEASE NOTE:  This is a night shift role.  Schedule is Monday - Friday and hours from 6:00pm - 2:30am

This individual will be responsible for performing the technical aspects of assigned tests in compliance with GLP, USDA and AAALAC guidelines.   Position Details: - Sunday to Thursday 7 AM to 3:30 PM (Training on Monday to Friday) - Anticipated Compensation: $19 per hour - Full-time position offering competitive benefits including Health, Vision, and Dental Insurance, 401K matching, and paid time off

HD Biosciences, a WuXi AppTec company is searching for a Director- In Vivo Pharmacology to manage team and project operations. The candidate must provide leadership, scientific, and operational support for a diversified research staff. This role requires experience and an established track record in working with multi-functional teams outside their reporting structure and presenting research strategies and results. Along with scientific strength, the successful candidate must have a proven track record of instilling teamwork and operational excellence while successfully executing against objectives. This key position will report directly to the head of In Vivo Pharmacology Department.

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.

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 scientist to join our fast-growing bioanalysis team. The position will independently design, execute, trouble shoot and deliver the projects with LCMS, including small molecules and biologics.

Manages the QC Flow Cytometry operations and staff.  Demonstrates mastery of flow cytometry theory and practice on multiple platforms.  Experienced Manager that demonstrates leadership in a fast-paced industry setting and operates with minimal oversight and has a clear understanding of business and GMP regulatory demands.   Exhibits rigorous scientific and supervisory skills, a strong practical knowledge of...

The Associate Director, HR Business Partner will provide a broad range of Human Resources expertise to support the achievement of business objectives of WuXi AppTec’s Medical Device Testing business and WuXi AppTec’s U.S. Operations and Finance units. Acting as a partner to Senior Management, the incumbent will work closely with executives and other leaders to plan and execute strategic and tactical HR initiatives that are aligned with corporate and business unit goals. This position will report directly to the VP of Human Resources.

The Senior Analyst is part of the Quality Control (QC) department of STA Pharmaceuticals Switzerland. He/She is responsible for executing protocols for method validations, verifications and transfers for the QC Laboratory. The position will also perform all testing of both material and finished product in support of the larger product introduction activities e.g. testing of samples for stability registration studies, process validation or cleaning validation. Additional duties includes participation to investigations in case of deviations, cleaning validation, preliminary testing, and preparation or review of documentation

Responsible for duties associated with two or more Quality System processes, including: the administration, reporting and process creation / optimization / automation, while ensuring accordance with current good Manufacturing Practices (cGMP), current Good Laboratory Practices (cGLP) and current Good Tissue Practices (cGTP). The processes comprising the Quality Systems include: Non- conformance / Investigations, CAPA, Change Control, Customer Audits, Supplier Audits, Training, and Supplier Qualification Program. Duties include effectively interacting with Testing, Manufacturing, Project Management and Quality Assurance personnel in order to deliver...