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WuXi AppTec

Global contract research, development, manufacturing organization

Associate Director - New Product Introduction

Bioprocess & BiomanufacturingConfirmed live in the last 24 hours
Full-timeCouvet, Val-de-Travers, SwitzerlandNo salary listedIn-person

About the Job

Requirements

  • A bachelor's degree or above in Pharmaceutical Sciences, Chemical Engineering, Chemistry, or a related scientific or engineering discipline.
  • 10–15+ years of pharmaceutical industry experience in Technical Operations, R&D, MS&T, or NPI management.
  • At least 3 years of leadership experience focused on Drug Product processes, technology transfer, and scale-up.
  • Deep understanding of late-phase and commercial drug product manufacturing requirements.
  • Working knowledge of global regulatory requirements, including FDA and EMA regulations, cGMPs, ICH guidelines, and best practices such as SUPAC.
  • Exceptional communication, stakeholder management, and matrix leadership skills.
  • Organizational and project management skills.
  • Fluency in English.
  • Experience with Oral Solid Dosage (OSD).

Responsibilities

  • Lead end-to-end technology transfer from internal development sites, client sites, or third-party facilities into the Couvet site.
  • Select, evaluate, and scale process technology, tooling, and methods.
  • Develop and optimize critical process parameters (CPPs) and critical quality attributes (CQAs).
  • Troubleshoot production batches, support complex deviations, and provide technical guidance to ensure cGMP compliance and high safety standards.
  • Ensure on-time delivery of technical, registration, clinical, stability, PPQ, and commercial launch batches.
  • Serve as the primary site contact for clients regarding NPI, building relationships through proactive communication and risk mitigation.
  • Understand client needs and align them with site capabilities to deliver robust solutions.
  • Guide, mentor, and develop the NPI team, fostering trust and personal accountability.
  • Align with site leadership to set strategic priorities, drive continuous improvement in NPI business processes, and establish and monitor team KPIs.
  • Clarify roles and responsibilities across matrixed project teams.
  • Collaborate with Technical Operations and Production teams to support process validation (PPQ) strategy and execution.
  • Support Continued Process Verification (CPV) and commercial launch readiness.
  • Act as a Subject Matter Expert (SME) during Pre-Approval Inspections (PAI) to ensure regulatory readiness.

Desired Qualifications

  • Experience with injectables.
  • PMP certification.

About the Company

WuXi AppTec

Global contract research, development, manufacturing organization

WuXi AppTec provides an open-access, global platform that offers contract research, development, and manufacturing services (CRDMO) for the pharmaceutical, biotechnology, and medical device industries. Its services cover the full product lifecycle—from discovery and preclinical work to clinical and commercial manufacturing—delivered through a wide range of lab, testing, process development, and manufacturing capabilities that clients can access as needed. The company distinguishes itself by combining broad geographic reach with a comprehensive, end-to-end service portfolio and strategic acquisitions to support projects worldwide. Its goal is to help innovators bring new medicines and healthcare products to market faster and with high quality.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Huangpu, China
Founded
2000

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