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Client Lead, ADC Conjugation Facility

Job in Gaithersburg, Montgomery County, Maryland, 20883, USA
Listing for: AstraZeneca
Full Time, Part Time position
Listed on 2026-02-23
Job specializations:
  • Engineering
    Operations Manager
  • Management
    Operations Manager
Salary/Wage Range or Industry Benchmark: 193304 - 289957 USD Yearly USD 193304.00 289957.00 YEAR
Job Description & How to Apply Below

Overview

Client Lead, ADC Conjugation Facility

Location:

Virginia, US
Hybrid working model, 3 days per week in the office location

Introduction to role:

Are you ready to build a flagship ADC conjugation facility that accelerates life-changing medicines to patients? A rare opportunity exists to lead the launch of a new facility on our Virginia campus. This campus will be built to support a rapidly growing pipeline in oncology, weight management, and metabolic disease. You will set the direction, shape how the facility operates, and ensure it delivers reliably and safely from day one.

As the Client Lead, you will define user requirements, align global partners, and operationalize the facility through start-up, product launch, regulatory approvals and into steady-state supply. Collaborate closely with a parallel program in Singapore and campus-wide teams to establish the right infrastructure and ways of working. You will be the leader who turns a blueprint into first batches and a sustainable, scalable operation—and position yourself to transition into the Site Lead role once the facility is running!

Responsibilities

Accountabilities:

  • Program Leadership: Define the facility’s user requirements and long-term vision; ensure delivery of a site that meets business needs for ADC conjugation and supports the broader portfolio.
  • Facility Readiness and Start-up: Lead the operationalization of the Virginia conjugation facility, including commissioning, qualification, and readiness for new product introduction and regulatory approvals.
  • Global Alignment: Coordinate closely with related global work streams, including the Singapore ADC program and campus initiatives, to ensure integrated design, execution and knowledge sharing.
  • Safety and Compliance: Establish and reinforce a strong safety culture; ensure compliance with all relevant safety, environmental and regulatory requirements from design through routine operations.
  • Manufacturing Execution: Oversee production planning, scheduling and execution to meet demand, achieve right-first-time performance and uphold rigorous quality standards.
  • Team Development: Recruit, mentor and inspire a high-performing, diverse team; build capabilities that support safe, efficient and compliant conjugation operations.
  • Process Optimization: Drive continuous improvement using lean principles and advanced bioprocessing techniques to boost productivity, reduce cost and enhance reliability.
  • Quality and Inspection Readiness: Partner with Quality Assurance and Quality Control to implement robust quality controls and maintain inspection readiness throughout start-up and beyond.
  • Stakeholder Engagement: Build trusted relationships with site functions, global partners, senior leadership and external partners to enable clear decisions and timely delivery.
  • Budget and Resources: Support development of program budgets and resource plans; prioritize investments to achieve milestones and long-term value.
  • Risk Management: Identify, assess and mitigate technical, schedule and operational risks; implement contingency plans to protect program timelines and supply commitments.
Qualifications

Essential Skills/

Experience:

  • Proven expertise in pharmaceutical manufacturing, with good understanding of the specific requirements of ADC conjugation.
  • Demonstrated experience defining user requirements and operationalizing new GMP facilities from design through start-up and new product introduction would be advantageous.
  • Track record overseeing manufacturing execution, including production planning, scheduling and delivery to quality standards.
  • Strong knowledge of safety, environmental and regulatory requirements in a GMP setting; proven ability to promote a strong safety culture.
  • Experience driving continuous improvement using lean manufacturing principles and advanced bioprocessing techniques.
  • Effective collaboration with site functions such as Engineering, MSAT, Supply Chain, HR, Finance and Quality, and with global functions including Capital Engineering, Global Tech Ops, PT&D, Quality, Finance, IT and Global Supply Chain.
  • Experience implementing robust quality control measures and working in close partnership with Quality…
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