Process Engineer, Technical Operations - Molecule Drug Substance
Job in
Virginia, St. Louis County, Minnesota, 55792, USA
Listed on 2026-07-14
Listing for:
MSD Malaysia
Full Time
position Listed on 2026-07-14
Job specializations:
-
Engineering
Process Engineer, Validation Engineer, Quality Engineering
Job Description & How to Apply Below
## Process Engineer, Technical Operations
- Small Molecule Drug Substance Apply remote type:
Not Applicable locations:
USA
- Virginia
- Elktontime type:
Full time posted on:
Posted Todaytime left to apply:
End Date:
July 25, 2026 (14 days left to apply) job requisition :
R405916
** Job Description
** 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.#
** Key Responsibilities**##
** 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…
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