Jobs at WuXi Chemistry

Leads project management and client coordination for life sciences research services. Responsibilities include preparing proposals and quotations, negotiating contracts, managing timelines, deliverables, work orders, change orders, and client relationships. Supports business development, analyzes business data, coordinates with R&D, legal, finance, marketing, and logistics teams, and mentors project management staff. Requires biotechnology or pharmaceutical industry knowledge, preclinical research and CRO experience, project management and business development experience, strong communication skills, Microsoft Office proficiency, and willingness to travel.

Manages client relationships and strategic oversight for complex CMC programs. Serves as the bridge between clients and internal technical teams, aligning priorities, timelines, risks, and commitments. Builds trust across R&D, Quality, Regulatory, Procurement, and manufacturing stakeholders while supporting proposals, governance meetings, account growth, and senior client discussions. Requires strong CMC industry knowledge, exceptional communication, Mandarin fluency, and experience in pharmaceutical, CRO, or CDMO environments.

Leads CMC projects across API and drug product development and manufacturing, managing initiation, planning, timelines, budgets, risks, deliverables, client communications, and cross-functional teams. Supports technical problem-solving, proposals, change orders, business development, customer visits, conferences, and project reporting. Requires pharmaceutical or CRO/CMO experience, CMC and GMP knowledge, strong project management skills, English and Mandarin proficiency, and approximately 25% travel.

Supports environmental, health, and safety compliance and risk management at an onsite pharmaceutical and bioscience campus. Responsibilities include developing EHS programs and SOPs, leading training and emergency preparedness, conducting audits and inspections, managing hazardous waste, supporting industrial hygiene assessments, investigating incidents, tracking metrics, and advising laboratories on compliance. The role requires collaboration across laboratory environments, domestic travel up to 10%, and work with biohazards, chemicals, PPE, and variable conditions.

Drives regional sales growth for WuXi Biology by prospecting, developing customer relationships, qualifying opportunities, negotiating proposals, and closing new business. Partners with scientific and internal teams to deliver client solutions, achieve sales and profitability targets, manage customer relationships, and expand accounts. Represents the organization at conferences and facilitates customer travel to China. The remote role preferably supports East Coast coverage and requires significant client and conference travel.

Scientific Director serving as an immunology and autoimmune disease subject matter expert for client-facing business development. Provides scientific consultation, translates client needs into proposals, supports presentations and RFPs, trains business development teams, collaborates with global technology teams, and represents the company at conferences. Requires deep in vitro and in vivo research expertise, drug discovery experience, and strong communication skills.

Supports environmental, health, and safety compliance and risk management at a laboratory and manufacturing site. Responsibilities include environmental reporting, hazardous waste management, incident investigations, CAPA management, inspections, ergonomic and industrial hygiene assessments, emergency response planning, employee training, KPI tracking, and EHS software administration. The role also supports regulatory programs, process improvements, ESG waste reporting, and site safety strategy.

Leads U.S. accounting operations across multiple entities, overseeing month-end close, financial reporting, internal controls, cash management, cost accounting, fixed assets, AP, audits, and tax support. Manages GL and AP teams while partnering on SAP S/4HANA transformation, manufacturing finance, budgeting, forecasting, and process standardization. Ensures compliance with U.S. GAAP and IFRS and supports operational integration, policy deployment, and staff development.

Lead the digitalization roadmap for a pharmaceutical manufacturing site, managing ERP, LIMS, MES, and WMS implementations, integrations, upgrades, and maintenance. Coordinate IT, manufacturing, quality, supply chain, vendors, and global teams while ensuring FDA/EMA, GMP/GxP, ALCOA+, and data integrity compliance. Manage project budgets, timelines, risks, governance, and milestones, reporting progress to site leadership and steering committees.

Director-level in vivo oncology subject matter expert supporting business development and US client engagement. Provides scientific consultation on oncology services, translates client needs into proposals, presents complex technical capabilities, trains BD teams, collaborates with China-based technology teams, and represents the company at conferences. Requires deep expertise in tumor biology, oncology pharmacology models, and preclinical drug development, with occasional travel to China.

Conduct cell-based and biochemical assays, support high-throughput screening in 96- and 384-well formats, perform mammalian cell culture and compound handling, and contribute to assay development for SAR screening. The role requires strong molecular and cell biology expertise, accurate execution of complex scientific procedures, effective communication with colleagues and clients, and the ability to work safely in laboratory environments involving chemicals, biohazards, animals, and PPE.

Leads European business development for WuXi AppTec discovery services, owning regional strategy, strategic accounts, pipeline growth, VC and incubator partnerships, commercial negotiations, and client transitions. Partners with technical, marketing, project management, and operations teams to drive revenue and client satisfaction. Requires deep drug discovery expertise, senior-level business development experience, strategic account management, and approximately 30% domestic and international travel.

Develops and executes marketing strategy across planning, campaigns, tradeshows, events, digital channels, and CRM. Manages event logistics, lead collection, campaign tracking, CRM workflows, segmentation, dashboards, and performance reporting. Collaborates with marketing, sales, scientific, content, and business teams to improve lead generation, customer engagement, brand awareness, and lifecycle management.

Perform cell-based assays, culture primary cells and cell lines, develop and validate assay formats, document experiments, analyze data, and contribute to reports and presentations. The role requires hands-on cell culture and molecular biology experience, accurate documentation, teamwork, and English and German proficiency. Experience with 3D cell culture and organoids is preferred.

Drives sales growth for toxicology and DMPK laboratory testing services across discovery, development, and clinical stages. Builds relationships with Pharma and Biotech decision-makers, sources and closes IND and NDA service deals, manages customer accounts, identifies regional opportunities, supports product launches, and tracks pipeline activity and KPIs in Salesforce. Requires strong technical sales, presentation, analytical, and relationship-building skills, with travel up to 50%.

Directs pharmaceutical and CRO/CMO project management activities from proposal through completion. Leads project managers, coordinates technical and business development teams, establishes timelines and budgets, monitors delivery, manages client communications, resolves issues, and reports progress. Supports proposals, client visits, conferences, and business development. The role requires strong cross-functional leadership, pharmaceutical development knowledge, project management expertise, and fluency in English and Mandarin.

Principal Pathologist responsible for pathology activities in nonclinical toxicology, safety, biocompatibility, and medical device studies. Duties include macroscopic and microscopic examinations, pathological data evaluation, comprehensive reporting, peer review, principal investigator responsibilities, sponsor communication, study consultation, junior pathologist training, and compliance with GLP, protocols, and SOPs.

Leads CMC drug development projects from proposal through completion, establishing timelines, deliverables, resources, budgets, and risk controls. Acts as the primary liaison among clients, technical teams, and business development, coordinating meetings, communications, action items, proposals, quotations, and change orders. Evaluates project outcomes and recommends improvements. Supports client visits, conferences, and trade shows while coordinating cross-functional CMC business units. Requires bilingual English and Mandarin proficiency and up to 10% travel.

Leads complex DMPK and non-GLP bioanalytical method development, qualification, sample analysis, reporting, and study coordination. Supervises and mentors scientists, serves as study director or project coordinator, reviews technical work, develops SOPs, communicates with sponsors, and supports pharmaceutical bioanalysis involving small and large molecules across biological matrices.

Develops and manages business opportunities for oligonucleotide and peptide contract development and manufacturing services. Responsibilities include prospecting, lead qualification, client presentations, conference and tradeshow participation, campaign follow-up, account management, industry trend monitoring, networking, and CRM documentation. The role supports clinical-to-commercial customer acquisition and revenue growth for WuXi TIDES and STA Pharmaceutical.