Senior Compliance Specialist & Technical Writer

• 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.

• 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.

Position is full-time, Mon-Fri 8am-5pm. Candidates currently living within a commutable distance of West Point, PA are encouraged to apply.

• Excellent full time benefits including comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays

Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.