Job Description:

Company Description



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 Organization 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 Organizations. It also has a rapidly developing presence in highly specialized 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 decentralized 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.


In 2021, Eurofins generated total revenues of EUR 6.72 billion, and has been among the best performing stocks in Europe over the past 20 years.





Job Description




Position Overview:



Eurofins Clinical Enterprise are seeking an experienced and dedicated Clinical Laboratory Manager to oversee the operations of our clinical laboratory, with additional responsibilities in Quality Assurance (QA) and inventory management for a new lab in Louisville, Kentucky. The ideal candidate will possess strong leadership skills, extensive knowledge of laboratory procedures and regulations, and a commitment to maintaining the highest standards of quality and accuracy.



Key Responsibilities:



1. Laboratory Management:


- Oversee the day-to-day operations of the clinical laboratory, ensuring efficient workflow, timely completion of tests, and adherence to protocols and regulations.


- Supervise laboratory staff, including hiring, training, scheduling, and performance evaluation.


- Develop and implement laboratory policies and procedures to ensure compliance with regulatory requirements and industry best practices.


- Maintain laboratory equipment, troubleshoot technical issues, and coordinate repairs and maintenance as needed.


- Manage laboratory supplies and reagents, ensuring adequate inventory levels and timely procurement.


2. Quality Assurance (QA):


- Develop and implement quality control measures to ensure the accuracy and reliability of laboratory test results.


- Conduct regular quality assurance audits and assessments to identify areas for improvement and implement corrective actions.


- Monitor proficiency testing programs and ensure compliance with regulatory standards and accreditation requirements.


- Investigate and resolve quality-related issues, including non-conformances, deviations, and customer complaints.


3. Inventory Management:


- Oversee inventory management processes, including ordering, receiving, storage, and distribution of laboratory supplies and reagents.


- Maintain inventory control systems to track usage, minimize waste, and prevent stockouts.


- Conduct periodic inventory audits to reconcile stock levels and identify discrepancies.


4. Regulatory Compliance:


- Ensure compliance with all relevant regulatory requirements, including CLIA, CAP, FDA, and OSHA regulations.


- Keep abreast of changes in regulations and industry standards and implement necessary updates to laboratory practices and procedures.


- Prepare for and participate in regulatory inspections and audits, addressing any findings or deficiencies in a timely manner.



Qualifications



- Bachelor's degree in Medical Laboratory Science, Biology, Chemistry, or related field; Master's degree preferred.


- Certification as a molecular biology technologist MB(ASCP) not 100% needed


- Minimum of 6 years of experience working in a clinical laboratory setting performing high complexity testing in molecular techniques with at least 2 years in a supervisory or managerial role.


- Strong knowledge of laboratory operations, including testing methodologies, instrumentation, and quality control principles.


- Familiarity with regulatory requirements and accreditation standards for clinical laboratories (CLIA, CAP, etc.).


- Excellent leadership, communication, and interpersonal skills, with the ability to motivate and inspire a team.


- Proficiency in inventory management systems and Microsoft Office Suite (Word, Excel, Outlook).


- Attention to detail, critical thinking skills, and ability to multitask in a fast-paced environment.





Additional Information



Position is full-time Monday-Friday 9:00am-5:30pm, with overtime as needed. Candidates currently living within a commutable distance of Louisville, KT 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

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What Happens Next


Our people are the backbone of what we do, so it's incredibly important we find the right individuals to join us. As a potential new recruit you'll be invited to meet the team in the form of an assessment centre or a staged interview process dependent on the role and it's requirements, this will give you the opportunity to see what working for Eurofins is really like and enable us to get you know your key skills and strengths.



Your data


As part of any recruitment process, the company collects and processes personal data relating to job applicants. The company is committed to being transparent about how it collects and uses that data and to meeting its data protection obligations.



Closing Date



We reserve the right to close or extend this position depending on application numbers. Therefore we would urge candidates to submit an application as early as possible.


Due to the high volume of applications we receive please be aware that if you do not receive a response within 4 weeks of the vacancy expiry date unfortunately, on this occasion your application has been unsuccessful.



Eurofins is aM/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.




Eurofins is aM/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

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