Company Description

The work we do at Eurofins Professional Scientific Services matters, and so do our employees. At Eurofins PSS, 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 you’re looking for a rewarding career, a place to call home, apply with us today!

Job Description

POSITION SUMMARY:

The Pathogen Safety Scientist will be responsible for performing multiple tasks within the Process Development group in support of biologics manufacturing process. The Scientist will perform a variety of responsibilities in both a team and individual setting. This position is a remote  position.

POSITION RESPONSIBILITIES:

Design and conduct virus validation studies and develop dedicated as well as contributing virus elimination steps in manufacturing processesDevelop experimental study designs in consultation with Client employeesGuide study personnel in the conduct of virus validation studiesPreparation of (GLP) study documentation (protocols, reports)Plan and conduct experimental work including data analysis and communication of results to Client project team in the form of a report or presentationControl and maintain biological systems (cell culture work, virus, and cell strain maintenance)Perform viral titrations to determine viral titers under L2/S2 (and L3/S3) conditions.Perform various analytical methods (protein determinations, pH measurements, etc.)Operation of complex instruments and processing/preparation of raw dataCollect, prepare, and distribute samples/data in coordination with other departmentsParticipation in local and global projectsCreate and maintain records within internal documentation systemsCreate and revise technical documents, including operating procedures, test, or process protocols, and reportsAssist in the procurement of new equipment and systemsMaintain laboratory equipment according to specific quality standards (e.g., GLP)Coordinate availability of materials, solutions, and reagentsStorage, retrieval of original documentation in a warehouseMaintaining stock lists / databaseScanning of documents in SaperionInventory check, destruction, and documentationCarrying out and documenting GLP tests in the laboratory e.g. spike tests, virus titrations, etc. according to the current test plans / SOPsMaintenance of laboratory systems e.g., cell banks, virus stacks, reagents, equipmentTimely completion of test documents (test plans, GLP final reports) and other GLP relevant documents e.g., analytical test protocols, buffer preparation protocolsSupporting the study director in the drafting of study documents, if necessaryPreparation, review, and training of SOPs for the laboratory area

Qualifications

BASIC MINIMUM QUALIFICATIONS:

BS degree in biological or related sciencesScience backgroundFamiliarity with USP, EU guidelinesEffective oral and written communicationsStrong problem-solving skillsAbility to support outside standard hours

PREFERRED QUALIFICATIONS:

At least 3 years of experience in sciencePathogen safety experienceBackground with regulatory landscapeAbility to network

Additional Information

Position is Full Time, Monday – Friday First Shift with occasional support globally outside standard hours. Although a remote position, candidates currently living within a commutable distance of Bradley, IL are encouraged to apply.

What we offer:

Excellent full time benefits including comprehensive medical coverage, dental, and vision optionsLife and disability insurance401(k) with company matchPaid vacation and holidaysYearly goal-based bonus & eligibility for merit-based increases

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