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 DescriptionWater SystemsGMP review of microbiological testing of the facility and/or laboratory water purification system samples. Tests included are LAL and Bioburden.GMP review of analytical testing of the facility and/or laboratory water purification system samples. Tests included are TOC, Conductivity, EU WFI Chemical Testing.GMP review of Qualification and Media Release testing.GMP review of facility cleaning data and in-processing testing, including but not limited to endotoxin, bioburden, BI, HPLC, Protien Concentration, pH and Osmolality.Initiation and follow-up of exceeded alert and action limits per procedures.Participate in preparation of quarterly trending reports​Raw MaterialsGMP review of general appearance/identifications and FTIRGMP review of house gas/air sampling and testingInitiation and follow-up of OOS and action limits per procedureElectronic and physical receipt, log-in and distribution of samples and testings materials coming into QC.Discarding / completing sample custody chainPreparation and shipping of sample/materialsAliquoting of bulk samples, assay standards, assay controls and custom assay reagentsLaboratory SupportAssist in updating and writing SOP'sRoutine calibration and maintenance of laboratory equipment which includes pipettes, balances, plate readers and pH metersCleaning of incubators, laminar flow hoods and biosafety cabinetsCleaning of refrigerators and cold roomsDefrosting of freezersDisinfectant preparationMaintenance of solvent wash bottlesCleaning of water bathsGMP lab sweepsEquipment out-of-tolerance (OOT) and refrigerator, freezer, incubator and pipette investigationsWeekly distributed control system (DCS) documentation review and maintenanceParticipate as required in any investigations associated with their deliverables supporting this task order

QualificationsB.S. degree with 1 year of Quality Control experience in the Pharmaceutical industryExperience in a Quality Control Lab is preferredWork experience in a cGMP environment is requiredExperience with Microsoft Word and Excel is requiredStrong computer, scientific, and organizational skillsExcellent communication (oral and written) and attention to detailAbility to work independently and as part of a team, self-motivated, adaptability, and a positive attitudeAbility to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policiesAuthorization to work in the United States indefinitely without restriction or sponsorship

Additional Information

What to Expect in the Hiring Process: 

10-15 Minute Phone Interview with Region Recruiter45-60 Minute Virtual Interview with Manager and/or Group Leader

Additional Details: 

The position is permanent, on-site and full-time, Monday-Friday from 7 am-3 pm. Candidates living within a commutable distance of King of Prussia, PA, and the surrounding areas are encouraged to apply. 

Excellent full-time benefits include:

comprehensive medical coverage, dental, and vision optionsLife and disability insurance401(k) with company matchPaid vacation and holiday

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 clients’ 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 Disabled and Veteran Equal Employment Opportunity employer.