Eurofins Laboratory Data Compliance Specialist - GMP Investigations \\\| SmartRecruiters Google Chrome Microsoft Edge Apple Safari Mozilla Firefox . Laboratory Data Compliance Specialist - GMP Investigations Full-time Compensation: USD 21.5 \- USD 26.25 \- hourly 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 youre looking for a rewarding career, apply with us today! Job Description Compliance & Investigation Support Lead data collection and analysis for GMP investigations and continuous improvement. Prepare clear, accurate reports for medium to high-severity events. Monitor production and quality systems to inform findings and trends. Data Visualization & Reporting Build and maintain Power BI dashboards to communicate compliance metrics and outcomes. Develop quality KPIs aligned with site and client goals. Audit & Documentation Assist with internal audits. Review and revise controlled documents (SOPs, batch records, logbooks) for cGMP alignment. Cross-Functional Collaboration Participate in meetings to present findings and resolve compliance issues. Work with teams to identify root causes and recommend CAPAs. Qualifications Minimum Qualifications Bachelors degree in Life Sciences, Chemistry, Biology, or related field Authorized to work in the U.S. indefinitely without restrictions or sponsorship 2+ years of experience with data tools - building Power BI dashboards, Excel, visualization platforms) Strong written and verbal communication skills Detail-oriented, self-motivated, and able to work independently in a client-facing role Preferred Qualifications Familiarity with GMP investigations and regulatory compliance Experience in QA/Compliance within a pharmaceutical setting Proficiency with systems like LIMS, QMS, or Veeva Coding experience (SQL, Python, R, VBA) Prior involvement in investigation authoring or review Understanding of biologics manufacturing and quality systems 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. Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer. I'm interested I'm interestedCookies Settings I'm interested Refer a friend share this job Share on LinkedIn Share on Facebook Share on Twitter Share via email Share on Xing Share on WeChat Share to WeChat × Copy the link and open WeChat to share. Copy to clipboard Open WeChat Share to WeChat × Use Scan QR Code in WeChat and click ··· to share. Laboratory Data Compliance Specialist - GMP Investigations Rensselaer, NY, USA Full-time I'm interested I'm interested

The role requires a Bachelor's degree in Life Sciences, Chemistry, Biology, or a related field. Candidates must be authorized to work in the U.S. indefinitely without restrictions or sponsorship. A minimum of two years of experience with data tools, including building Power BI dashboards, using Excel, and other visualization platforms, is necessary. Strong written and verbal communication skills are essential, along with being detail-oriented, self-motivated, and capable of working independently in a client-facing capacity. Familiarity with GMP investigations and regulatory compliance, experience in QA/Compliance within a pharmaceutical setting, and proficiency with systems like LIMS, QMS, or Veeva are preferred qualifications. Coding experience in SQL, Python, R, or VBA, prior involvement in investigation authoring or review, and an understanding of biologics manufacturing and quality systems are also considered beneficial.