Job Information
Eurofins Manager Specimen Management in Breda, Netherlands
Eurofins Central Laboratory is a dynamic, global organization fully committed to providing global central laboratory services to support all phases of clinical trials. At Eurofins Central Laboratory we go further than expected. Because we are purely a central laboratory, there are no distractions that allow us to stay focused on the best science, technology and people.
We are part of one of the world's leading laboratory organizations Eurofins Scientific, which is why we provide end-to-end testing solutions that are unsurpassed in the industry. Eurofins Central Laboratory sets new standards with GLP capabilities embedded in our Central Laboratory. We support our customers with laboratory facilities in the US, Europe, Singapore and China and a back office in India.
The Manager Specimen Management has the overall responsibility of the department Specimen Management as far as it concerns the tasks described below.
Manages and is accountable for departmental operations. Supervises and coordinates the activities of personnel to efficiently handle the day to day workload.
Hires, transfers, promotes, disciplines, and terminates employees according to existing policies.
Monitors the overall performance of employees. Prepares and delivers annual and interim performance evaluations.
Prepares departmental budget in conjunction with operations management, researches and makes recommendations for new capital equipment.
Monitors budget performance, prepares variance analysis and takes corrective action to ensure acceptable budget performance.
Oversees staff in the development and evaluation of new products and procedures to increase efficiency and reduce costs.
Responsible for the execution of the quality system of the departments.
Provides leadership for the establishment, monitoring, and analysis of departmental QA process (Jira).
Participates in operational meetings and conducts regularly scheduled departmental meetings.
Reviews, interprets and monitors compliance with pertinent regulations/standards. Interacts with Client audits and regulatory agencies as needed. Reviews departmental policies and procedures manuals to maintain regulatory compliance.
Works with other Business Process Owners to ensure that area specific departments of responsibility are harmonized with the other ECL sites.
Maintains an awareness of emerging technology in the field of specialty. Provides continuing education and training opportunities to staff, other ECL personnel, and external customers (when appropriate).
Experience
• Minimum of 10 years in a Central Laboratory Environment
Education
• Bachelor or Master in Healthcare or Pharmaceutical science, or technical discipline.
Skills
• Strong leadership abilities
• Strong coaching and mentoring skills
• Strong attention to detail
• Excellent communicator
• Ability to multi task
• Fluent in English
Do you meet the above profile and are you interested in an international working environment? We are looking forward to receive your CV and motivation letter.
