The work we do at Eurofins matters, and so do our employees. At Eurofins, 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!
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 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
Bachelor's degree in a scientific or engineering discipline or similar, with aminimum of 1 year GMP experience
Lab experience is beneficial, but not required.
Experience with changing lab processes, SOP's, procedures, etc.
Knowledge of pharmaceutical supply chain or QA experience preferred
Strong computer skills; specificallyExcelandSAP
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
This is anon-lab based-role- all duties will take place in an office environment.
Position is full-time, Monday - Friday 8:00am - 5:00pm. Candidates currently living within a commutable distance ofSanford, 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 holiday
Eurofins is aM/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.