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Form of workEurofins 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.
- 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
The purpose of this role is to author technical documents in an effort to change current processes for drug development.
Group Leader Essential Duties and Responsibilities:
- Applies GMP/GLP in all areas of responsibility, as appropriate
- Demonstrates and promotes the company's vision
- Regular attendance and punctuality
- Ensure that the quality policy program is understood, implemented, and maintained at all levels of the organization; identify, prevent, or correct any departures from the quality system
- Perform work for both routine and non-routine work as specified by separate and applicable technical job descriptions for individual
- Develop and implement operational improvements
- Supervise others in performing client's service requirements
- Coach, train, and develop others within the group with respect to their personal development and effective implementation of operational improvements
- Coordinate workflow and perform daily monitoring to meet TAT
- Conduct semiannual performance reviews, interview applicants, keep training records up to date for assigned employees, perform succession planning in preparation for growth
- Confront and address problems, concerns, and performance issues
- Coach and develop individuals and teams to maximize performance
- Foster motivation and morale
- Monitor and approve employees' time worked through time-entry system
- Support and promote company policies and procedures
- Expand self-awareness and develop leadership skills as defined; attend applicable leadership training based on identified needs
- Perform and/or assign other duties as requested to ensure the smooth operations of department
- min 1 year leadership experience
- Bachelor's degree in a scientific or engineering discipline or similar, with a minimum 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; specifically Excel and SAP
- Able to work both independently and as a member of a cross-functional 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
- Position is full-time, Monday- Friday 8:00 AM- 5:00 PM overtime as needed
- Candidates currently living within a commutable distance of Sanford, NC are 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
- #LI-EB1
- Authorization to work in the United States indefinitely without restriction or sponsorship
Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
