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 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 Description
Collecting details from cross-functional departments to author change controls for components and raw materials
Entering change controls into electronic system (QTS) and routing to departments for assessments
Tracking and project managing the assessment completion
Routing the change control for approvals
Tracking and project managing approvals
Tracking task completion associated with approved change control and working with owners to ensure tasks are completed by assigned due dates
Entering new enrollment tasks into electronic system (QTS) and assigning task owners
Extending enrollment due dates when needed
Adhere to site SOPs and cGMPs for production activities in the manufacturing facilities
Adhere to site safety standards, participate in routine safety training events, and enforce safety and biosafety requirements as they relate to the Clinical Manufacturing department
Qualifications
Associatesdegree with 1-2 years, or Bachelor of Science with 0-1, or High School Diploma with 8 years of relevant experience.
Minimum of 1-2 years GMP experience
Knowledge of pharmaceutical supply chain or QA experience preferred
Strong computer skills; specifically Excel and SAP
Organization/project management skills
Able to work both independently and as a member of a cross-functional project team in a fast-paced environment
Authorization to work in the United States indefinitely without restriction or sponsorship
Valid driver's license and personal transportation
Additional Information
Position is full-time, Monday-Friday, from 8:00 AM - 5:00 PM.
overtime as needed
Candidates currently living within a commutable distance of Durham, NCare encouraged to apply.
Excellent full-time benefits including comprehensive medical coverage, dental, and vision options
Life and disability insurance
401(k) with company match
Paid vacation and holidays
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Authorization to work in the United States indefinitely without restriction or sponsorship
Eurofins is aM/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.