Associate Director, Technical Operations - Molecule Drug Substance
Job in
Elkton, Rockingham County, Virginia, 22827, USA
Listed on 2026-10-08
Listing for:
Merck Sharp & Dohme (MSD)
Full Time
position Listed on 2026-10-08
Job specializations:
-
Manufacturing / Production
Validation Engineer, Quality Engineering, Chemical Manufacturing
Job Description & How to Apply Below
Location: Elkton
Job Description We have an exciting opportunity for an Associate Director, Technical Operations – Drug Substance at our Elkton Site in Virginia, USA.At our company, we aspire to be the premier research-intensive biopharmaceutical company, using the power of leading-edge science to save and improve lives around the world. We are at the forefront of research to deliver innovative health solutions that advance the prevention and treatment of diseases in people and animals.
Join a purpose-built, agile small molecule manufacturing site where your work will help bring important medicines to patients in the U.S. This facility is designed to move quickly and reliably, receiving technology transfers from commercialization sites and fast-following into production with a focus on quality, safety, and operational excellence. At our site, you’ll be part of a team committed to creating a safe, environmentally responsible, and compliant workplace where people can do their best work.
We are building deep small molecule expertise in the U.S., and we want team members who are excited to grow their skills, help improve how we operate, and contribute to a site positioned for future growth. The successful candidate will provide technical leadership and operational support for the startup, technology transfer, validation, and ongoing commercial manufacture of active pharmaceutical ingredients (APIs).This
role is responsible for leading technical activities across assigned processes and projects, supporting the capital project and facility startup phase through to commercialization and lifecycle management. The Associate Director will ensure safe, compliant, and reliable process performance, while driving continuous improvement and technical excellence.
Key Responsibilities Technical Leadership Recognized subject matter expert in Drug Substance process support, and commercial manufacturing
Provide technical oversight and hands-on leadership for API manufacturing processes, including:
Chemical synthesis
Purification
Crystallization and drying operations
Support the Capital Project Team, contributing to design, commissioning, qualification, and startup readiness
Lead process scale-up, technology transfer, and validation (pre-PPQ, PPQ) activities for assigned processes
Drive improvements in process performance, yield, robustness, and impurity control
Provide technical guidance on:
Process chemistry
Reaction performance
Critical process parameters and control strategies
Analyze technical data and support decision-making for process performance and improvements
Identify and escalate risks, proposing practical, science-based solutions
Technology Transfer Lead and execute technology transfer activities for assigned processes across internal sites and external partners
Support development and execution of tech transfer plans aligned with project timelines
Provide technical support for:
Raw material evaluation
Process fit and manufacturability
Scale-up readiness [Ensure accurate process documentation, knowledge transfer, and batch record readiness
Support process validation and continued process verification
Operational Excellence Partner with Manufacturing to ensure safe, efficient, and reliable plant performance
Provide direct technical support to:
Campaign preparation, execution, and follow-up Process troubleshooting during manufacturing
Lead and support deviation investigations, OOS, and CAPA, applying structured root cause analysis
Monitor process performance and cycle times, identifying improvement opportunities
Drive continuous improvement initiatives for yield, cycle time, and cost Support process optimization and debottlenecking activities
Regulatory & Compliance Ensure assigned processes operate in compliance with cGMP and…
Position Requirements
10+ Years
work experience
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