Clinical Laboratory Manager (m/f)
Our client is a multinational company providing wide range of services and solutions for its clients. Currently we are looking to recruit an experienced Clinical Laboratory Manager. This is an exciting opportunity for an independent, creative, service-oriented individual to help build PCR sequencing laboratory services. The candidate will be responsible for daily supervision of a high throughput clinical laboratory including oversight of laboratory technologists, technical trouble-shooting validation and testing processes, reviewing lab results, developing and writing operational procedures, monitoring laboratory key performance indicators, quality metrics and the QC program, timely reporting of quality event reporting to the laboratory director and to quality management, and provide regulatory, due diligence and internal auditing support. Must have experience and be able to apply regulations to clinical diagnostic operations.
Duties and Responsibilities:
- Manage the daily operations of assigned laboratory personnel to ensure that specimens are properly shipped and received, tests are performed accurately and efficiently, and results are reported in a timely manner.
- Perform pre-analytical, analytical and post analytical test process and evaluate results produced relative to the diagnostic assessment.
- Evaluate data for accuracy and verify any questionable finding with proper documentation, thorough investigation, and appropriate follow-through.
- Assist with designing processes and procedures to ensure efficient turn-around time and accuracy of results.
- Prepare and manage laboratory budget.
- Coach and mentor staff on technical expertise and assist in evaluation of employee competencies.
- Engage in continuous process and service improvement. Make and implement recommendations to improve operational efficiency and implement new services for areas of responsibility.
- Requires strict adherence to quality control guidelines to ensure integrity of laboratory specimens and accuracy of results.
- Ensure all work is in accordance with state and Federal regulations, organizational policy, and accreditation/compliance requirements.
- Assist in maintaining CAP and other accreditation and regulatory agency standards and regulations.
- Performing bench work and other duties as required including shift work.
- Bachelor's degree in biology or related scientific discipline and a minimum of 10 years of clinical molecular experience
- Previous Supervisory/Management experience in a clinical laboratory setting.
- Quality Assurance and Quality Control applications in clinical diagnostics.
- Must be detail oriented, organized, with excellent verbal and written communication skills.
- Ability to troubleshoot technical applications and work independently under pressure of deadlines and a fast paced, high throughput team environment.
- Practical knowledge of routine laboratory equipment and procedures.
- Experience with LIMS and laboratory automation highly desired.
- Clinical and research lab environment; exposure to blood borne pathogens; must wear protective lab gear including lab coat, gloves and completely closed footwear.
- Employee may be requested to work shifts other than daylight depending on the needs of the laboratory. Weekend rotation may be required.
- Travel is not required.
- Ensure safety, security, and the environment in all aspect of the daily activities, and any potential safety hazards are addressed and corrected immediately.
- International environment.
- Incentive financial package.
- Job location: Great Britain.
- Job duration: definite time.
We are expecting candidate’s applications and certificates in English via email: Helena@riv.si or via Application link below.