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 laboratories work with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.

The Eurofins network of companies is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. It is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. It also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.

In over 30 years, Eurofins has grown from one laboratory in Nantes, France to 58,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 54 countries. Eurofins companies offer a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.

• Maintenance of tracker for all ongoing work (method establishment and ongoing routine/stability testing; large and small molecule)
• Help ensuring that the tracker toolkit provides Departments with forecasting information for stability and establishment work
• Generation of the invoice data package which helps track spend/utilization month by month per product. Utilization should be detailed enough to reflect the cost per project (for client) and costs associated with various stages of a project (ELLI).
• Contribute to the re-evaluation and improvement of key performance indicators (KPIs) and metrics around both quality, performance and cost-efficiency. 
• Maintain and help re-evaluating the tools/trackers to assist in capturing the data and extracting the identified KPIs.
• creation of report for the client to summarize all metrics and break them out to provide meaningful insight into each category/project.
• Contribute in the development of tool to estimate utilization and cost for life cycle of a project.
• creation of other visual KPI presentation and monitoring techniques that support FTE resources monitoring, depending on FTE program characteristic or client requests
• Demonstrates ability to work on multiple projects at one time
• Communicates effectively with client staff members
• Conducts all activities in a safe and efficient manner
• Performs other duties as assigned

• BSc in Chemistry, Biochemistry, Analytical Sciences, or any other applied science.
• Experience in an FDA regulated Biotech/Pharmaceutical industry
• Experience in working in an FTE team or good understanding of FTE team required
• Technical expertise in (Bio)Pharmaceutical Product testing preferred
• Understanding and practitioner of Lean and/or Six Sigma principles and Project Management Methodology
• Skilled level in process improvement tools and methodologies
• Computer skills (expertise with MS Project, Excel, and other Windows related applications)
• Independent work skills, strong work ethic and organization skills
• Authorization to work in the United States indefinitely without restriction or sponsorship

Position is Full-time, Monday-Friday, 8:00 a.m.-5:00 p.m., with overtime as needed.  Candidates currently living within a commutable distance of Lancaster, Pennsylvania are encouraged to apply.

Excellent full-time benefits including:

• Comprehensive medical coverage, dental, and vision options
• Life and disability insurance
• 401(k) with company match
• Paid vacation and holidays

Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.