Quality Assurance Technician

Company DescriptionEurofins 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 Organisation 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 Organisations. It also has a rapidly developing presence in highly specialised 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 decentralised 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 DescriptionCollecting details from cross-functional departments to author change controls for components and raw materialsEntering change controls into electronic system (QTS) and routing to departments for assessmentsTracking and project managing the assessment completionRouting the change control for approvalsTracking and project managing approvalsTracking task completion associated with approved change control and working with owners to ensure tasks are completed by assigned due datesEntering new enrollment tasks into electronic system (QTS) and assigning task ownersExtending enrollment due dates when neededAdhere to site SOPs and cGMPs for production activities in the manufacturing facilitiesAdhere to site safety standards, participate in routine safety training events, and enforce safety and biosafety requirements as they relate to the Clinical Manufacturing departmentQualificationsHigh School Diploma or Bachelor's degree in a scientific or engineering discipline or similar, with a minimum of 1-2 years GMP experienceKnowledge of pharmaceutical supply chain or QA experience preferredStrong computer skills; specifically Excel and SAPOrganization/project management skillsAble to work both independently and as a member of a cross-functional project team in a fast-paced environmentAuthorization to work in the United States indefinitely without restriction or sponsorshipValid driver's license and personal transportationAdditional Informationployment and project-management worries.

Position is Monday- Friday 8:00 am- 5:00 pm. Overtime as needed. Candidates currently living within a commutable distance of Durham, NC are encouraged to apply. Excellent full-time benefits including comprehensive medical coverage, dental, and vision optionsLife and disability insuranceEurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.401(k) with company matchPaid vacation and holidays#LI-EB1Authorization to work in the United States indefinitely without restriction or sponsorshipEurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.