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# TS/MS Scientist - Dry EM

- **Company:** Validation & Engineering Group, Inc.
- **Location:** United States
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** SAP ERP, Trackwise, Data Management
- **Published:** October 13, 2026
- **Apply:** https://www.thejobnetwork.com/job/ae5a9ceb-93f2-4004-ad8f-524cedde1c65/tsms-scientist-dry-em

## About the Role

* Bachelor's degree (minimum) in scientific disciplines of Chemistry, Pharmacy, or Engineering
 * 5+ years of demonstrated hands-on working experience and proficiency with spray dry, solid dosage manufacturing and packaging
 * Working knowledge of regulatory expectations (cGMPs and applicable global regulatory guidance)
 * Strong understanding of regulatory requirements and their application in a manufacturing environment
 * Proficient in data management practices across manufacturing and packaging operations
 * Proven ability to effectively communicate and influence across diverse technical and business teams
 * Demonstrated project management expertise with a track record of coordinating and executing multifaceted projects
 * Demonstrates adaptability, a collaborative mindset, and a positive attitude toward change
 * Available to support 24/7 operations and issue resolutions across multiple time zones as needed
 * Fluent in English and Spanish, with the ability to communicate effectively across diverse teams and stakeholders
 * Experience supporting External Manufacturing Organizations (CMOs)
 * Spray Dry Dispersion (SDD) experience
 * Oral Solid Dosage manufacturing experience
 * Technology Transfer experience
 * GMP regulatory inspection support experience
 * TrackWise experience
 * SAP experience
 * Statistical analysis experience
 * FDA regulated manufacturing experience

## Description

* Provide technical oversight for spray dry, solid dosage manufacturing and packaging processes, leveraging a strong technical foundation and previous experience supporting these processes.
 * Participate in resolution of technical issues, including those related to control strategy and manufacturing.
 * Possess excellent technical writing capabilities, including authoring of deviations and change controls.
 * Participating in root cause investigations to support Corrective Actions and Preventive Actions (CAPA) closure Activities within the expected timeline.
 * Employ excellent communication skills to manage internal and external relationships with external partners, site management, and cross-functional teams.
 * Build and maintain relationships with development and central technical organizations.
 * Ensure that manufacturing processes are compliant, capable, in control, and maintained in a validated or qualified state.
 * Understand, justify, and document the state of process validation with data that evaluates the capability of the manufacturing process to meet its stated purpose.
 * Maintain processes in a state of compliance with US and global regulations, including cGMPs and applicable global regulatory manufacturing guidance.
 * Support ongoing manufacturing at External Partners through process monitoring, issue response, and process improvements where necessary.
 * Support technical transfer and validation activities to external partners manufacturing and packaging sites by review technical transfer documentation, participate in process qualifications activities and support validation campaigns.
 * Work cross-functionally within the site and other functions to deliver on technical objectives. * Some flexibility may be required to support 24/7 operations and issue resolutions with external partners across different time zones.