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# Senior Compliance Specialist & Technical Writer

- **Company:** Eurofins USA
- **Location:** West Point, PA, United States
- **Experience:** Expert
- **Contract:** Permanent contract
- **Skills:** Data Integrity, Laboratory Information Management Systems, Data Streaming, GXP
- **Published:** November 5, 2026
- **Apply:** https://www.thejobnetwork.com/job/82c85428-70eb-4029-9408-302d96f37797/senior-compliance-specialist-technical-writer

## About the Role

* Expertise in technical writing, including reports and controlled procedures.
 * Experience conducting, auditing, and supporting GxP laboratory documentation, protocols, and testing.
 * Experience leading process-improvement efforts in laboratory, quality, and/or compliance settings.
 * Experience training staff in procedures, assays, and laboratory systems.
 * Experience operating in a GxP laboratory environment.
 * Strong critical-thinking, troubleshooting, verbal-communication, and written-communication skills.
 * Ability to follow procedures and thoroughly document laboratory work.
 * Ability to work independently with limited supervision and meet project timelines.
 * Strong attention to detail and the ability to manage multiple priorities.
 * Adherence to applicable safety procedures in a BSL-2 laboratory.

Preferred Experience & Skills

 * Experience in a GxP bioanalytical or clinical testing laboratory.
 * Experience with Laboratory Information Management Systems, electronic laboratory notebooks, and other scientific applications.

## Description

* Lead technical-writing activities for the Compliance team, including procedures, process flows, regulatory and audit responses, and reports associated with trending, deviations, investigations, and validation.
 * Lead quality-process improvements that strengthen GxP testing operations, systems, procedures, and documentation practices.
 * Conduct detailed laboratory data and in-lab process reviews to support the integrity, accuracy, completeness, and quality of GxP data.
 * Collaborate with Quality Assurance to maintain alignment with company policies and applicable federal regulations and support ongoing inspection readiness.
 * Participate in regulatory inspections and internal Quality Assurance audits, including related preparation and follow-up activities.
 * Monitor laboratory operations and quality metrics, identify trends, and drive related processes and procedural improvements.
 * Evaluate system data integrity and end-to-end data flows, identify opportunities for enhancement and/or modernization, and participate in validation of computer and laboratory systems.
 * Develop and/or update procedures supporting documentation reviews and process reviews.
 * Lead training and coach department staff on adherence to SOPs, documentation requirements, procedures, assays, and laboratory systems.
 * Participate in and/or lead internal initiatives that strengthen quality operations and support the setup of the new facility and laboratories.