Compliance Specialist - Pharmaceuticals

Eurofins; West Point (PA); On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

Medical coverage

Dental & Vision

Life Insurance

Disability Insurance

401(k) with match

Paid vacation & holidays

Bonus eligibility

Job summary

Eurofins PSS in the United States seeks a Compliance Specialist to support Regulatory Bioanalytical and Laboratory Operations through audits of records, data systems, and processes. You will ensure compliance with regulatory requirements, quality standards, and data integrity while maintaining audit documentation and preparing records for inspections.

This full-time role emphasizes trend analysis, corrective actions, and cross-functional collaboration to improve quality systems.

Qualifications

• Bachelor's degree in a scientific, engineering, quality, regulatory, or related discipline.
• Experience in quality assurance, compliance, auditing, laboratory operations, or regulated environments.
• Knowledge of regulated laboratory environments and data integrity principles.
• Strong documentation review and record management skills.
• Experience preparing reports, compliance metrics, and audit findings.
• Must be eligible to work in the United States indefinitely without restriction or sponsorship.
• Experience in bioanalytical, pharmaceutical, biotechnology, or regulated research environments.
• Familiarity with regulatory inspection readiness activities.
• Working knowledge of GxP principles, quality systems, and accreditation requirements.
• Experience supporting internal audits and compliance reviews.

Responsibilities

• Audit scientist and engineer records for completeness, accuracy, and appropriateness.
• Audit bioanalytical data records, laboratory systems, and related documentation.
• Prepare audit-ready records and documentation packages for reviews.
• Monitor compliance trends and identify emerging risks.
• Support regulatory inspections and prepare documentation and responses.
• Track audit completion against schedules and procedures.

Skills

Quality assurance

Auditing

Regulatory compliance

Data integrity

Documentation

Communication

Education

Bachelor's degree in science/regulatory

Job description

The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, we put a focus on your professional growth. We provide our employees the ability to break into the biopharmaceutical industry and grow from the bottom up. We have the supportive teams and tools available to invest in you while also affording you work-life balance and a competitive benefits package.

Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and in the support of clinical studies.

Job Description

Position Summary:

The Compliance Specialist will support Regulatory Bioanalytical and Laboratory Operations by conducting quality and compliance audits of scientist and engineer records, bioanalytical data systems, and departmental processes. This role ensures adherence to regulatory requirements, quality standards, data integrity expectations, and accreditation requirements while driving continuous improvement across departmental operations. The specialist will maintain audit documentation, prepare audit-ready records, generate compliance trend reports, and support internal and external inspections.

Key Responsibilities:

Quality & Compliance Auditing

• Conduct audits of scientist and engineer records to ensure completeness, accuracy, and appropriateness.
• Perform cross-checks against source documentation and analyze selected data elements for compliance and integrity.
• Audit bioanalytical data records, laboratory systems, and associated documentation.
• Assess adherence to quality standards, regulations, policies, procedures, and accreditation requirements.
• Maintain detailed audit records and documentation supporting audit findings.

Regulatory & Inspection Readiness

• Prepare and organize audit-ready records and documentation packages for management reviews, project reviews, and internal audits.
• Support regulatory and accreditation surveys by preparing documentation, facilitating responses, and coordinating follow-up actions.
• Assist in maintaining inspection readiness across the department.
• Monitor compliance trends and identify emerging risks.

Process Improvement & Reporting

• Develop audit summaries and trending reports to communicate compliance performance.
• Analyze findings and identify opportunities to improve quality, efficiency, and data integrity.
• Prepare recommendations for corrective and preventive actions.
• Track audit completion against established schedules and procedures.
• Support continuous improvement initiatives related to quality systems and record management.

Departmental Compliance Support

• Training compliance
• Timekeeping accuracy
• Policy and procedure management
• Laboratory development plans and assessments
• Regulatory record maintenance
• Ensure compliance documentation remains current, complete, and inspection ready

Qualifications

Basic Minimum Qualifications:

• Bachelor's degree in a scientific, engineering, quality, regulatory, or related discipline.
• Experience in quality assurance, compliance, auditing, laboratory operations, or regulated environments.
• Knowledge of regulated laboratory environments and data integrity principles.
• Strong documentation review and record management skills.
• Experience preparing reports, compliance metrics, and audit findings.
• Excellent attention to detail and organizational skills.
• Strong written and verbal communication skills.
• Must be eligible to work in the United States indefinitely without restriction or sponsorship.

Preferred Qualifications:

• Experience in bioanalytical, pharmaceutical, biotechnology, or regulated research environments.
• Familiarity with regulatory inspection readiness activities.
• Working knowledge of GxP principles, quality systems, and accreditation requirements.
• Experience supporting internal audits and compliance reviews.

Additional Information

This role is a full-time, permanent positionMonday-Friday1st Shift. Candidates currently located within commutable distance to West Point, PAare encouraged to apply.

Excellent full-time benefits include:

• Comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays
• Eligibility for yearly goal-based bonus & merit-based increases

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