Compliance Data Specialist - GMP Investigations at Eurofins

Rensselaer, New York, United States -

Full Time

Start Date

Immediate

Expiry Date

05 Jan, 26

Salary

26.25

Posted On

07 Oct, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Data Analysis, Power BI, Excel, Communication Skills, Detail-Oriented, GMP Investigations, Regulatory Compliance, Quality Assurance, LIMS, QMS, Veeva, SQL, Python, R, VBA, Biologics Manufacturing

Industry

Medical and Diagnostic Laboratories

Description

Company Description The work we do at Eurofins matters, and so do our employees. At Eurofins, 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. If you’re looking for a rewarding career, apply with us today! Job Description Lead the collection, manipulation, and analysis of compliance-related data to support GMP investigations and continuous improvement initiatives. Assist with internal audits Develop and maintain Power BI dashboards and visualizations to communicate compliance trends, metrics, and investigation outcomes to stakeholders. Collaborate with cross-functional teams to identify root causes of non-conformances and recommend corrective and preventive actions (CAPAs). Support the preparation of investigation reports for medium to high-severity events, ensuring clarity, accuracy, and alignment with regulatory expectations. Monitor production and quality systems to gather data that informs investigation findings and compliance trends. Assist in the review and revision of controlled documents (e.g., SOPs, batch records, logbooks) to ensure alignment with cGMP standards. Participate in cross-functional meetings to present findings and drive resolution of compliance issues. Contribute to the development of quality metrics and KPIs that align with site and client goals. Qualifications Minimum Qualifications Bachelor’s degree in Life Sciences, Chemistry, Biology, or a related technical field. Authorization to work in the US indefinitely, unrestricted and without sponsorship. 2+ years of experience with data analysis tools, particularly Power BI, Excel, and other visualization platforms. Excellent written and verbal communication skills, with the ability to present complex data clearly. Detail-oriented, self-motivated, and able to work independently in a client-facing environment. Preferred Qualifications Familiarity with GMP investigations and regulatory compliance. Experience supporting QA/Compliance functions in a pharmaceutical setting. Experience with systems, such as LIMS, QMS, or Veeva Experience with coding languages, such as SQL, Python, R, VBA Prior involvement in investigation authoring or review. Understanding of biologics manufacturing operations and quality systems. Candidates located within a commutable distance of Rensselaer, NY are encouraged to apply. Additional Information Position is full-time, Monday-Friday, 8:00am-5:00pm. Base compensation is $21.50 - $26.25 per hour based on degree and relevant experience. #LI-EB1 Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Responsibilities

Lead the collection, manipulation, and analysis of compliance-related data to support GMP investigations and continuous improvement initiatives. Collaborate with cross-functional teams to identify root causes of non-conformances and recommend corrective and preventive actions (CAPAs).