Clinical Laboratory Scientist
Pharma
Job description
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 Organization 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 Organizations. It also has a rapidly developing presence in highly specialized 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 decentralized 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. The clinical laboratory shall employ a sufficient number of properly qualified technical personnel, including a sufficient number of technicians and technologists (10 NYCRR Subpart 58-1.5, MA 105 CMR 180.180) to meet the workload demands of the laboratory. Clinical laboratory scientists shall be present in sufficient number to adequately supervise the work of technicians and trainees. Clinical Laboratory Scientist  means a clinical laboratory practitioner who, in accordance with approved protocols of Boston Heart Diagnostics, performs clinical laboratory procedures and examinations and any other tests or procedures conducted by a clinical laboratory which require the exercise of independent judgment and responsibility (as determined by the department), with minimal supervision by the director or supervisor, in only those specialties or subspecialties in which they are qualified by education, training and experience. With respect to specialties in which the medical technologist is not qualified by education, training or experience, the individual shall function only under direct supervision and perform only tests which require limited technical skill and responsibility. Level I – Minimum Follow the laboratory's procedures for specimen handling and processing, and maintaining records of test examinations. Perform ancillary tasks to ensure a smooth operation, including but not limited to preparation and qualification of reagents and materials required for test processes, as well as label, retrieve, re-file, and properly store specimens for testing/repeat testing/long term storage. Take an active role in cleaning, organizing, and restocking duties. Operate, calibrate and maintain all laboratory equipment and instruments according to standard operating procedures to ensure quality results. Maintain records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens. Adhere to the laboratory's quality control policies, document all quality control activities, instrument and procedural calibrations and maintenance performed. Follow the laboratory's established policies and procedures whenever test systems are not within the laboratory's established acceptable levels of performance. Identify problems that may adversely affect test performance or reporting of test results and either immediately correct the problems or notify the supervisor, manager, director or designee. Adhere to established processing timelines. Ensures follow-up and demonstrates an understanding of actions taken to resolve problems. Demonstrate strong teamwork skills by effectively communicating, knowledge sharing and adequately prioritizing tasks to efficiently complete daily activities. Maintain adequate inventory of supplies, reagents and material – notify supervisor, manager or director immediately when faced with shortage of supplies. Document all corrective actions taken when test systems deviate from the laboratory's established performance specifications. Participate on special projects or assignments as requested by management. Trains other technicians on key aspects of the laboratory assay(s), proficient with the performance of competency assessments. Plays an active role in process improvement projects with potential for significant improvement in quality, efficiency, and/or reduction in cost of testing. Possess critical thinking skills and is able to actively troubleshoot when even the slightest deviations are observed. Level II – Fully meets the responsibilities of Level I plus the following: General knowledge of Standard Operating Procedure writing, assay theory, and instrumentation.   Orient, mentor and teach clinical laboratory methods, procedures, and techniques to new Associates.   Demonstrate effective teamwork skills by knowledge sharing.   Take on formally assigned additional duties, such as training, as a part of routine job performance.   Participate in special project teams as requested by supervisory staff. Level III – Fully meets the responsibilities of Level II plus the following: Obtain advanced knowledge of Viracor Eurofins standard operating procedures, assays, and instrumentation.   Participate in troubleshooting activities in conjunction with Technical Supervisor.   Volunteer to serve on various committees and panels to the benefit of the laboratory or company in general (e.g., Safety Committee).   Performs train the trainer and Qualified Personnel responsibilities as assigned. New York definition of Medical Technologists: Bachelor’s degree in Medical Technology or Bachelor’s degree in chemical, physical or biological science plus 1 year experience in specialty. Level  I – Minimum (1) Successful completion in an accredited college or university of a full course of study which meets all academic requirements for a bachelor's degree in medical laboratory science; the degree program shall have included a one year structured clinical laboratory experience in either (a) the general areas of a clinical laboratory, or (b) in a specialty area; or (2) Successful completion of three academic years of study (a minimum of 90 semester hours or equivalent) in an accredited college or university which met the specific requirements for entrance into a school of medical laboratory science and the successful completion of a course of training of at least 12 months in a school of medical technology approved by the Council on Medical Education of the American Medical Association; or (3) Successful completion in an accredited college or university of a course of study which meets all academic requirements for a bachelor’s degree in one of the chemical, physical or biological sciences and, in addition, at least one year of full-time laboratory experience and/or training subsequent to graduation covering the specialty(ies) or subspecialty(ies) in which the individual performs tests; or (4) Successful co
Stand out for this role
NoxPharm tailors your CV to this exact job description — matching the keywords recruiters and ATS systems screen for. Built for pharma & life sciences.
Tailor my CV now — free to trySimilar Pharma jobs
Contract Specialist - FSP Dedicated - Belgium & Netherlands
Thermo Fisher Scientific — 2 Locations
Field Applications Engineer (Semiconductor)
Thermo Fisher Scientific — Remote, Oregon, USA
Country Approval Specialist - FSP- Israel
Thermo Fisher Scientific — Remote, Israel
Field Service Engineer (인재풀)
Thermo Fisher Scientific — Giheung, Korea, Republic of
Operation Manager
Thermo Fisher Scientific — Shanghai, China
Clinical Research Nurse
Thermo Fisher Scientific — Lodzi, Poland