Data Integrity Compliance Lead

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Cold Room/Freezers -22degreesF/-6degrees C, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Warehouse

Job Description

Data Integrity Compliance Lead

Division / Site Specific Information

Location: Ridgefield, New Jersey – Sterile Fill-Finish & Packaging Site

Our state-of-the-art sterile fill-finish and packaging facility in Ridgefield, NJ, is dedicated to meeting the growing needs of biotech and pharmaceutical drug developers. With expanded capabilities in pre-filled syringe and liquid vial manufacturing, the site increases U.S. capacity to manufacture the medicines patients rely on every day.

As part of Thermo Fisher Scientific’s global network, Ridgefield complements our world-class contract development and manufacturing services and strengthens our sterile fill-finish footprint—now spanning seven sites worldwide, including three in the U.S. (Greenville, NC; Plainville, MA; and Ridgefield, NJ). Strategically located along the East Coast to streamline logistics and attract top talent, the 360,000 sq. ft. Ridgefield site plays a vital role in the global pharmaceutical supply chain, with products distributed to more than 67 countries across all continents.

Discover Impactful Work:

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day—enabling our customers to make the world healthier, cleaner and safer. As the Data Integrity Compliance Lead, you will serve as the site subject matter expert (SME) for data integrity, ensuring compliance with global regulatory requirements and Thermo Fisher Scientific standards. You will drive a culture of integrity and quality by leading governance, risk management, and continuous improvement initiatives that safeguard the reliability, accuracy, and completeness of data across the entire lifecycle.Your leadership will directly support the safe and compliant manufacture of life-saving medicines relied upon by patients worldwide.

A Day in the Life:

• Develop and implement site-based data integrity procedures aligned with industry regulations and Thermo Fisher global policies.

• Define and monitor controls for ALCOA(+) principles: Attributable, Legible, Contemporaneous, Original, Accurate, plus Complete, Consistent, Enduring, and Available.

• Lead training and awareness programs to educate colleagues on data integrity best practices and compliance standards.

• Coach teams on Good Documentation Practices (GDP) for both paper and electronic records.

• Serve as site SME during regulatory inspections and internal/external audits.

• Prepare evidence packages, responses, and follow-up actions.

• Establish and chair Data Integrity Governance Team meetings.

• Collaborate cross-functionally to ensure data integrity throughout the data lifecycle.

• Conduct risk assessments to identify data integrity gaps across systems (e.g., LIMS, ERP, QMS, eBatch Records, Chromatography Data Systems (CDS)/Empower, validation tools) and manual processes.

• Provide technical guidance on computerized system validation (CSV), data integrity by design, and configuration management.

• Drive lifecycle management: data creation, review/approval, storage/retention, archival, retrieval, and disposal.

• Define and monitor KPIs and metrics related to data integrity performance; report trends and improvement plans to site leadership.

• Lead investigations and remediation efforts related to data integrity events.

• Support incident management for data discrepancies, data loss, and cybersecurity events impacting data reliability.

• Coordinate cross-functional remediation and continuous improvement initiatives.

• Maintain current knowledge of evolving regulatory requirements (FDA, EMA, MHRA, ICH, WHO) and ensure alignment with corporate governance and change control processes.

• Contribute to global policy updates as applicable.

• May serve as the site’s AI Champion within the Thermo Fisher Quality AI community.

• Drive awareness and adoption of AI-enabled tools and ensure site alignment with Thermo Fisher AI standards.

Keys to Success:

Education

• Bachelor’s degree in a scienti