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Process Engineer, Technical Operations - Molecule Drug Substance

Job in Elkton, Rockingham County, Virginia, 22827, USA
Listing for: Merck
Full Time position
Listed on 2026-07-14
Job specializations:
  • Manufacturing / Production
    Validation Engineer, Quality Engineering
Salary/Wage Range or Industry Benchmark: 87300 - 137400 USD Yearly USD 87300.00 137400.00 YEAR
Job Description & How to Apply Below
Position: Process Engineer, Technical Operations - Small Molecule Drug Substance
Location: Elkton

Process Engineer, Technical Operations – Drug Substance

We have an exciting opportunity for a Process Engineer, Technical Operations – Drug Substance to join our growing team.

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 support for the facility design, commissioning, qualification through technology transfer, validation and ongoing commercial manufacture of active pharmaceutical ingredients (APIs). In this role, you will work as part of a cross‑functional team, initially supporting the capital project and transitioning to technology transfer and commercial manufacturing
, while building deep technical expertise and contributing to operational excellence.

Technical & Process Support
  • Support the Capital Project Team, contributing to design, commissioning, qualification, and startup readiness
  • Provide technical support for API manufacturing processes, including:
    • Chemical synthesis
    • Purification and isolation
    • Crystallization and drying operations
  • Take ownership of assigned process equipment and manufacturing processes
  • Support process scale‑up, technology transfer, and validation activities (e.g., pre‑PPQ, PPQ)
  • Analyze process data to support performance monitoring, troubleshooting, and improvement
  • Provide on‑the‑floor technical support during manufacturing campaigns
Technology Transfer & Commercialization
  • Support execution of technology transfers for new products and processes into the facility
  • Partner with global R&D and receiving sites to ensure effective process knowledge transfer
  • Contribute to process fit assessments, scale‑up readiness, and manufacturability evaluations
  • Support development and review of batch documentation and process instructions
  • Assist in integration of new technologies into manufacturing operations
Process Optimization & Operational Excellence
  • Partner with Manufacturing to support safe, efficient, and reliable plant performance
  • Identify and implement improvements in process robustness, product quality, and plant performance
  • Support activities related to operational excellence and cost reduction
  • Contribute to cleaning and turnaround optimization activities
  • Assist in deviation investigations, root‑cause analysis, and implementation of CAPAs
  • Monitor process performance, yields, and cycle times to identify improvement opportunities
  • Drive or participate in continuous improvement initiatives focused on:
    • Yield and throughput
    • Cycle time reduction
    • Cost and efficiency improvements
Compliance & Documentation
  • Ensure all activities are conducted in compliance with cGMP, safety, and environmental standards
  • Support campaign preparation, execution, and post‑campaign review activities
  • Support batch record generation, review, and ongoing optimization
  • Assist in regulatory and inspection readiness activities
  • Ensure accurate documentation of process knowledge, investigations, and improvements
Cross‑functional Collaboration
  • Work closely with Manufacturing, Quality, Engineering, Supply Chain, and R&D teams
  • Provide technical input into projects, process changes, and ongoing operations
  • Participate in cross‑functional teams supporting product introduction and lifecycle manage
Qualifications
  • Degree in Chemical…
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