Microbiology Supervisor
Company: Eurofins
Location: Littleton
Posted on: April 25, 2025
Job Description:
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
The Microbiology Supervisor (MS) will work under the general
direction and guidance of the Department Manager and Laboratory
Operations Management. The MS will perform job duties in accordance
with GMPs, policies and procedures, and testing requirements. The
MS will be responsible for training/advising of technologists and
support staff and providing specialized expertise in assigned
technical areas. The MS will handle laboratory proficiency
testing/reporting and evaluate/recommend new testing procedures.
The incumbent will apply technical skills and knowledge as it
relates to laboratory results and accreditation, handling technical
support issues for the department. Also responsible for critical
review of patient results and reporting.
ESSENSITAL JOB DUTIES
- Supervise the day-to-day operation of the department to insure
smooth flow of samples and testing.
- Oversees the scheduling of staff to ensure production schedules
are met.
- Counsels staff with regard to problems encountered in daily
operations.
- Works with Quality Assurance to resolve client complaints by
investigating problems, developing solutions and making
recommendations to management.
- Identifies process improvements to better meet client
expectations and company objectives.
- Recommends new equipment for the department.
- Oversees the monitoring of inventory/ordering by establishing
and maintain par levels and re-stocking points for supplies and
reagents
- Performs duties in compliance with all applicable regulatory
and accrediting agencies.
- Supports Eurofins DPT's business philosophy, leadership values
and ethics.
- Assures technologists are adequately trained. Provides training
and technical advice to technologists and other support staff.
Promotes uniformity in the implementation of policies and
procedures.
- Performs technologist job duties as needed to support
appropriate staffing levels.
- Assures that reviews of test results are timely and accurate
and have involvement with reporting patient results.
- Compiles statistics.
- Tracking and trending of department data.
- Counsels laboratory staff with regard to problems encountered
in daily operations.
- Oversees the checking and transfer of data as necessary and
takes steps to correct possibly inaccurate data prior to continued
processing or release. Qualifications
- Supervisory/Managerial Experience
- Bachelor's Degree in a chemical, biological science or a
clinical laboratory science/medical technology program by an
accrediting institution. Knowledge of regulatory requirements in
both the CAP/CLIA setting as well as knowledge of FDA, and industry
standards
- Must be able to interpret and apply government and industry
regulations
- Excellent and effective written and oral communication skills,
including presentation skills and interpersonal skills
- Exceptional cross-functional team leadership skills and ability
to work in close collaboration with others
- Strong organizational and planning skills as well as strong
attention to detail
- Ability to work independently with limited supervision, adapt
to change and manage multiple tasks
- Ability to analyze, define and effectively convey difficult and
complex issues in a way that accurately communicates the issues to
leadership
- Ability to problem-solve and make decisions on complex issues,
often in a cross-functional team setting
- Technical knowledge of applicable regulations
- Minimum of 4 years CLIA experience from a CLIA certified
establishment
- Microbiology background (preferred)
- Cleanroom/Aseptic Processing/Filling experience
(preferred)
- Effecting operations of a clinical reference laboratory
- Analytical thinking and communication skills PHYSICAL
REQUIREMENTS
- Physical dexterity sufficient to use hands, arms, and shoulders
repetitively to operate a keyboard and other office equipment, use
a telephone, access file cabinets and other items stored at various
levels, including overhead
- Ability to speak and hear well enough to communicate clearly
and understandably with sufficient volume to ensure an accurate
exchange of information in normal conversational distance, over the
telephone, and in a group setting
- Ability to continuously operate a personal computer for
extended periods of time (4 or more hours)
- Mental acuity sufficient to collect and interpret data,
evaluate, reason, define problems, establish facts, draw valid
conclusions, make valid judgments and decisions The essential
physical and mental requirements described here are representative
of those that must be met by an employee to successfully perform
the essential functions of the job. Reasonable accommodations may
be made to enable individuals with disabilities to perform the
essential functions.
Additional Information
Compensation:
- Salary: $65k-$85k Schedule:
- Regular: Monday-Friday 1:00pm-9:30pm
- Training: Monday-Friday 8:00am-4:30pm What we offer:
- 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
Eurofins USA Clinical Diagnostics is a Disabled and Veteran Equal
Employment Opportunity employer.
PandoLogic. Keywords: Microbiology Section Head, Location:
CENTENNIAL, CO - 80120 , PL: 597440188
Keywords: Eurofins, Boulder , Microbiology Supervisor, Other , Littleton, Colorado
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