Laboratory Operations Manager - Monday-Friday 8:00am-5:00pm at Eurofins Viracor, LLC in Lenexa, Kansas

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




Basic Function and Scope of Responsibility:



The Laboratory Operations Manager is primarily responsible for successful day to day operations of the Clinical Laboratory.



Essential Job Duties:

• Manage "key indicators" of clinical lab as identified by Director, Clinical Lab Operations


• Work closely and effectively with the Director of Clinical Lab Operations, Director of Clinical Laboratory, or Quality Team to ensure all test systems are properly operating and that Eurofins Viracor's test results are most accurate, robust and clinically meaningful results available


• Develop effective working relationship with Regulatory Affairs to assure that clinical lab is implementing Eurofins Viracor's established guidelines for GLP compliance, CLIA certification, CAP certification and state licensing


• Employ sufficient number of properly qualified lab personnel to meet growing test volumes at Viracor Eurofins


• Lead continuous improvement initiatives that focus on processes, work flow and throughput so clinical lab can efficiently and effectively handle growth while maintaining high quality standards


• Work closely with Clinical Lab Director to facilitate quality control, quality assurance and technical competency programs


• Manage clinical lab budget and clinical lab vendor contracts


• Conduct lab team meetings which focus on associate training, associate development and continuous improvement in processes


• Manage and direct activities of direct reports through effective hiring, onboarding, training, and supervision of work activities of team members


• Conduct regularly scheduled one-on-one meetings with direct reports focused on performance goals, progress, and career growth and development


• Assess team members by conducting effective performance reviews, and coach associates through necessary performance improvements as needed


• Conduct regular team meetings and/or provide regular communication to team members


• Represent department and the organization favorably and in accordance with established Company standards and associate attributes


• Other duties as assigned by management

Qualifications




Essential Knowledge, Skills and Abilities:

• Must have extensive PCR experience and a high knowledge base for sequencing and NGS


• Bachelor's Degree (BS or BA) in biological, physical, chemical or clinical laboratory science, plus six years of clinical laboratory experience required; OR Master's (MA or MS) degree in biological, physical, chemical or clinical laboratory science, plus four years of clinical laboratory experience; OR PhD in similar fields plus two year clinical laboratory experience.


• Minimum of one year of supervisory experience in a laboratory setting required; 2+ years preferred.


• Demonstrated large project management skills


• In-depth knowledge of legal and regulatory requirements


• Ability to make independent decisions regarding matters of significance


• Demonstrated leadership and critical thinking abilities


• Excellent verbal & written communication skills


• 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


• Keenly attentive to detail


• Ability to keep sensitive information confidential


• High level of proficiency with PC based software programs

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 stand for extended periods of time as necessary in the laboratory (4 or more hours)


• Ability to lift and move items weighing up to 15 pounds


• Physical dexterity sufficient to move body frequently around laboratory equipment and instrumentation


• 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



Eurofins Viracor LLC is an equal opportunity employer and encourages individuals from all backgrounds to apply. By submitting your application, you acknowledge and agree to the following conditions:

Drug Screen: Successful candidates will be required to pass a standard drug screen as part of the pre-employment process.

Background Check: A thorough background check will be conducted for all potential employees. This may include, but is not limited to, criminal history, education verification, and employment history.

Visa Sponsorship: Eurofins Viracor LLC does not sponsor employment visas. All candidates must have the legal right to work in Lenexa, KS without requiring sponsorship. Unless approved by HR and supporting parties.

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 is aM/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

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