Senior Quality Specialist: Lab Compliance Chemistry

Short Summary

Senior Quality Specialist: Lab Compliance Chemistry with Eurofins. Applies GMP/GLP in all areas of responsibility, as appropriate Monitor laboratory compliance with respect to expired reagents, reagent labeling, lab cleanliness, training records, PPE adherence, and other cGXP items, as needed to help minimize laboratory audit findings. Perform/Support Internal audits, as well as help, implement the resolution of…

Key Details

• Position / opportunity: Senior Quality Specialist: Lab Compliance Chemistry
• Organization: Eurofins
• Country / coverage: United States
• Location: Lancaster, PA, United States
• Work arrangement: On-site
• Opportunity type: Jobs
• Sector: Health
• Compensation: Not specified
• Duration: Not specified
• Start date: 2026-08-21
• Application deadline: Not specified

Description

Applies GMP/GLP in all areas of responsibility, as appropriate Monitor laboratory compliance with respect to expired reagents, reagent labeling, lab cleanliness, training records, PPE adherence, and other cGXP items, as needed to help minimize laboratory audit findings. Perform/Support Internal audits, as well as help, implement the resolution of internal/external audit findings Review Instrument qualifications to ensure that work is performed as per the procedure Review and verify invalid data and system suitability failures Review and close Exceptions under Non-Routine Events, System Suitability Failure, and Deviations Approve Analytical Method/Protocol/SMIS/Client Parameter per QA procedure Track and Analyze quality metrics (exception rate, rejection rate etc) and train laboratory personnel, as needed, to help reduce/eliminate rework Support other QA compliance-related activities, as needed Diagnose problems, solve simple problems, and suggest solutions to complex problems in the professional area Keep oneself and peers abreast of current developments and trends in the professional area by reading and understanding internal procedures, attending training sessions, by writing/revising SOPs (as required), and by assisting Group Leader/Principal Specialists in training new employees Exercise discretion and independent judgment with respect to matters of significance directly related to the management or general business operations through the data review process May serve as technical advisor for analysts with regard to QA/QC of data Communicate with internal clients to discuss any findings and notify them of any necessary rework or compliance/regulatory concerns Basic Minimum Qualifications: Bachelor's degree in Chemistry or related science field Minimum of three years of pharmaceutical laboratory experience with knowledge of regulatory requirements Authorization to work in the United States indefinitely without restriction or sponsorship Preferred Qualifications: E xperience in performing Pharmaceutical analytical testing Computer skills including word processing, spreadsheets, PowerPoint and database is a plus Experience with cGMP and/or FDA regulated environments is a plus Technical writing and review Tracking action items and driving to completion Ability to identify trends in recurring events Batch record review, pharmaceutical testing and room clearance activities Work with the laboratory and support groups to improve quality metrics, and enable CAPA implementation Internal audits support Review/write QAU procedures. Position is full-time, Monday-Friday, 8:00 a.m.-5:00 p.m. with additional hours, as needed. Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply. We offer excellent full-time benefits including : Comprehensive medical coverage, Life and disability insurance, 401(k) with company match, Paid holidays and vacation, Dental and vision options. Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer. Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

Responsibilities

• Applies GMP/GLP in all areas of responsibility, as appropriate Monitor laboratory compliance with respect to expired reagents, reagent labeling, lab cleanliness, training records, PPE adherence, and other cGXP items, as needed to help minimize laboratory…
• Perform/Support Internal audits, as well as help, implement the resolution of internal/external audit findings Review Instrument qualifications to ensure that work is performed as per the procedure Review and verify invalid data and system suitability…
• Position is full-time, Monday-Friday, 8:00 a.m.-5:00 p.m.
• Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply.
• We offer excellent full-time benefits including : Comprehensive medical coverage, Life and disability insurance, 401(k) with company match, Paid holidays and vacation, Dental and vision options.
• Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

Requirements / Eligibility

• to ensure that work is performed as per the procedure Review and verify invalid data and system suitability failures Review and close Exceptions under Non-Routine Events, System Suitability Failure, and Deviations Approve Analytical…
• Position is full-time, Monday-Friday, 8:00 a.m.-5:00 p.m.
• Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply.
• We offer excellent full-time benefits including : Comprehensive medical coverage, Life and disability insurance, 401(k) with company match, Paid holidays and vacation, Dental and vision options.
• Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

How To Apply

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