Laboratory Specimen Processor – Monday-Friday 7:00am-12:00pm – 744000019959035-2643

Eurofins Viracor, LLC

This job was posted by https://www.kansasworks.com : For more
information, please see: https://www.kansasworks.com/jobs/13075994

Company 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 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 is the global leader in food, environment, pharmaceutical and
cosmetic product testing and in agroscience Contract Research
Organisation services. Eurofins 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. The Group also has a
rapidly developing presence in highly specialised and molecular clinical
diagnostic testing and in-vitro diagnostic products.

In over just 30 years, Eurofins has grown from one laboratory in
Nantes, France to 55,000 staff across a decentralised and
entrepreneurial network of 900 laboratories in over 50 countries.
Eurofins offers a portfolio of over 200,000 analytical methods to
evaluate the safety, identity, composition, authenticity, origin,
traceability and purity of biological substances and products.

Job Description

Basic Function and Scope of Responsibility:

The Laboratory Specimen Processor is primarily responsible for
performing duties related to accessioning and data entry with a high
degree of proficiency.

Essential Job Duties:

Level I – Minimum

– Demonstrate data entry proficiency with the Laboratory Information
Management System (LIMS) and/or other specimen tracking system.
– Examine samples for accuracy and other requirements (sample type,
stability, volume, etc.)
– Label samples for delivery to proper area(s)
– Use and maintain applicable sample storage materials (i.e. dry ice)
– Make appropriate internal or external contact to resolve patient
demographic issues or discrepancies.
– Complete correction requests as needed.
– Adhere to all Data Management policies and protocols.
– Maintain quality control and quality assurance records as required.
– Adhere to all quality and safety standards, as well as ensuring
compliance with all applicable regulatory agencies.
– Work closely and communicate with other lab associates to complete
daily activities efficiently.
– Maintain other Clinical Laboratory databases as needed or assigned.
– Provide administrative support for Clinical Laboratory projects as
needed.
– Represent department and the organization favorably and in
accordance with established Company standards and associate
attributes at all times.
– Other duties as assigned by management.

Level II – Fully meets the qualifications of Level I plus the following:

– Manage issues and projects; resolve escalated issues as appropriate.
– Demonstrate superior understanding of Laboratory operations.

Level III – Fully meets the qualifications of Level I and II plus the
following:

– Demonstrate leadership skills through the supervision, coaching and
mentoring of others as required.
– Ensure department adheres to policies and procedures.

Qualifications

Essential Knowledge, Skills, and Abilities:

Level I – Minimum

– High School diploma or equivalent required
– Specimen processing in a Clinical Laboratory setting or equivalent
experience preferred.
– Must be comfortable with raw specimen handling.
– Applicants will be tested during the i terview stages to determine
their proficiency in typing, with a minimum requirement of 30 words
per minute.
– Ability to read, interpret, and comply with documents such as
internal SOPs, operating and maintenance instructions, and company
policies.
– Position may require evening and weekend hours.
– Goal oriented, with excellent time management and organizational
skills
– Excellent interpersonal skills, with ability to interact effectively
and work efficiently with people at all levels in an organization.
– Excellent verbal & written communication skills
– Keenly attentive to detail
– Ability to keep sensitive information confidential.
– High level of proficiency with PC based software programs; strong
database skills; 1 year of data entry experience preferred with
strong typing skills.

Level II – Fully meets the qualifications of Level I plus the following:

– Advanced problem-solving skills.
– Demonstrated leadership abilities.

Level III – Fully meets the qualifications of Level I and II plu

Show Full Vacancy