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 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.

In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to over 47,000 staff across a network of more than 900 independent companies in over 50 countries and operating more than 800 laboratories. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products, as well as providing innovative clinical diagnostic testing services, as one of the leading global emerging players in specialised clinical diagnostics testing.

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

Our Supervisors play a critical role in ensuring seamless laboratory operations and exceptional client service. This role is responsible for overseeing technical activities, training employees, and maintaining compliance with regulatory standards. As a Supervisor, you will have the following responsibilites: 

 

Technical Responsibilities

Train or schedule training for all employeesEnsures superlative customer service to clientsCollects samples and documents results Receiving, handling, and disposing of samplesPerforms testing on pharmaceutical utilities (e.g. air, gas, and water)Accurately records sampling/testing activities and reports any quality anomaliesCalibrates or verifies calibration of instruments/devices before use.May assist in validation of methodsUses sterile technique to gown into clean room environmentMaintains laboratory supplies and performs laboratory housekeeping as assignedParticipates in required training activitiesComplies with all pertinent regulatory agency requirementsCommunicating findings and recommendations at group meetingsParticipating in and/or leading cross-functional teams to support optimal client servicesIndependently investigating team quality deviations and preventing reoccurrences in support of QC operationsDocumenting all trainingTraining new employees on some GMP related responsibility relevant to the supervised functional areas where appropriateMay support reviewing, editing, and revising controlled documents (batch records, logbooks, SOPs, etc.) in accordance with cGMP standards to ensure compliance with written procedures

Leadership Responsibilities:  

Leading direct reports, group leaders and their teams, and serving clients in technical settings, such as laboratories or manufacturing facilitiesDisseminate administrative communicationsDemonstrate and promote the company visionMeet all quality and productivity metrics, and demonstrate strong teamwork and collaborationCoordinate scheduling and allocation of responsibilities, and new hire on-boarding processCoordinates training program

Qualifications

The Ideal Candidate will Have: 

Ability to work independently and as part of a team in a client-facing environment.Self-motivated, adaptable, and a positive attitudeExcellent communication (oral and written) and attention to detailProactively plan and multitask to maximize productivityDevelopment of teambuilding strategies and initiatives

Minimum Qualificaitons: 

Bachelor’s degree in Life Sciences, or other science-related degree concentration, or equivalent directly-related experience3-5 years of  previous leadership experienceExperience working in a fast-paced GMP environment Authorization to work in the United States indefinitely without restriction or sponsorship

What to Expect in the Hiring Process: 

10-15 minute phone interview with the Recruiter60 minute virtual meeting with the Hiring Team30 minute virtual meeting with the Site Diretor

Additional Information

The position is a full-time, 1st shift role.  Hours will be Mon-Fri from 8 am-4:30 pm. Candidates living within a commutable distance of Rensselaer, NY are encouraged to apply. The position includes excellent full-time benefits; including comprehensive medical coverage, dental, and vision options.

Excellent full-time benefits including comprehensive medical coverage, dental, and vision optionsLife and disability insurance401(k) with company matchPaid vacation and holidaysBase compensation is $35-41 per hour based on experience

Eurofins Lancaster Laboratories Professional Scientific Services® (PSS) is a global, award-winning insourcing solution that places our people at our clients’ sites dedicated to running and managing laboratory services while eliminating headcount, co-employment, and project-management worries.

We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR, and a great place to work best practices, to recruit, hire, train, and manage highly qualified scientists to perform laboratory services using our client’s quality systems and equipment.

To learn more about Eurofins Lancaster Laboratories, please explore our website www.eurofinsus.com.

 

Eurofins USA PSS Insourcing Solutions is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.