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.
Join us in shaping a safer, healthier, and more sustainable world. Explore opportunities with Eurofins and be part of a global team driving scientific excellence. Apply today and make a meaningful impact!
Job DescriptionLaboratory Responsibilities:
Performs all duties relevant to the Quality Control Raw Materials Sampling Analyst position as required.Collecting solid and/or liquid samples from raw materials used in the manufacturing processHandles, documents, and manages samples according to procedures and GMP requirementsPerform quality analysis on containersCalibrates or verifies calibration of instruments/devices before use.Uses sterile technique to gown into a clean room environmentMaintains laboratory supplies and performs laboratory housekeeping as assignedParticipates in required training activitiesDocumenting all trainingTraining new employees on some GMP-related responsibilities relevant to the supervised functional areas, where appropriateComplies 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 operationsMaintains laboratory supplies, media, and reagents inventoryUses Laboratory Information Management System (LIMS) for samples.Schedules tasks above on a weekly, monthly, and quarterly basisA strong work ethic and ability to meet physical demands, but not limited to, routinely lifting objects of 25 lbs. or more, walking and standing for extended periods of time, pushing or pulling carts and drums, and bending down or reaching for supplies.Leadership Responsibilities:
Supports and monitors the performance of the team of employeesMay participate in new hire interviewsSupports the onboarding process of new employeesParticipates in the training of other employees.Performs peer review of data.Assists in coordinating equipment maintenance and calibration.Disseminate administrative communicationsDemonstrate and promote the company visionMeet all quality and productivity metrics, and demonstrate strong teamwork and collaborationCoordinate scheduling and allocation of responsibilities, and the new hire onboarding processCoordinates training programPosition requires significant time spent in biopharmaceutical manufacturing ISO 8+ level cleanrooms with the following restrictions:
No cosmetic products (such as makeup, false lashes, spray tans, etc) are permitted and must be removed prior to entryNails must be kept short, trimmed, and unadorned (no nail polish, adornments, etc)No jewelry may be worn, (exceptions are medical alert related and one smooth ring band)Hair must be able to be neatly tied back and contained in a hairnet and all facial hair must be neatly trimmed and able to be secured in a beard cover.QualificationsPreferred Qualifications:
Laboratory experience1+ years of cGMP experienceStrong computer, scientific, and organizational skillsExcellent communication (oral and written) and attention to detailAbility to work independently and as part of a team, self-motivation, adaptability, and a positive attitude in a client-facing environmentAbility to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policiesExcellent communication (oral and written) and attention to detailProactively plan and multitask to maximize productivityExperience with LIMS preferredMinimum Qualifications:
Bachelor’s degree in Life Sciences, or other science related degree concentration, or equivalent directly related experience1+ years previous leadership experienceAuthorization to work in the United States indefinitely without restriction or sponsorshipAdditional InformationWhat to Expect in the Hiring Process:
10-15 Minute Phone Interview with Region Recruiter45-60 Minute Virtual Interview with Manager and/or Group Leader30 Minute Virtual Interview with Site DirectorAdditional Details:
This is a full-time, onsite position based on a first-shift schedule (Monday through Friday, 6:00am to 2:30pm), with overtime required as needed. Candidates located within a commutable distance to Rensselaer, New York, are strongly encouraged to apply.
Excellent full-time benefits include:
Comprehensive medical coverage, dental, and vision optionsLife and disability insurance401(k) with company matchPaid vacation and holidaysHourly rate is between $28-$33, depending on education and experienceEurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.