Laboratory Supervisor (3rd Shift)

Company Description

Eurofins Scientific is an international life sciences company, which provides a unique range of analytical testing services to clients across multiple industries. The Group believes it is the world leader in food, environment, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, CDMO, advanced material sciences and for supporting clinical studies. In addition, Eurofins is one of the leading global emerging players in specialty clinical diagnostic testing.

In 2018, Eurofins generated 4.2 billion Euro proforma turnover in 800 laboratories across 47 countries, employing about 45.000 staff.

Eurofins stands for a conception of clinical diagnostics entirely focused on excellence, innovation and technological investment. Eurofins clinical diagnostics offers testing services in all medical specialties. 

As a central element in healthcare, clinical diagnostics contributes to every stage of patient care: predisposition, prevention, diagnostics, treatment monitoring and prognosis. 

With hundreds of thousands of clinical diagnostics tests performed every day, the laboratories of the clinical diagnostics division strive to ensure that every patient, wherever he or she lives, has access to the most specialized and most innovative techniques for diagnosis, monitoring and therapeutic adjustment. Our logistics expertise and our daily sample collection and delivery network, guarantee perfect continuity in the provision of care while ensuring the same standard of quality and access to innovation across all the regions we serve.

Job Description

Laboratory Supervisor responsibilities include, but are not limited to, the following:

• Supervise the day-to-day operation of the department to ensure 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 recommendation 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 maintaining par levels and restocking points for supplies and reagents
• Serves as a liaison for the department to outside vendors
• Performs duties in compliance with all applicable regulatory and accrediting agencies
• Supports Eurofins DPT’s business philosophy, leadership values and ethics
• Conducts timely investigations in coordination with Quality Assurance Related to site quality events, including but not limited to customer complaints, inquiries, non-conformances, corrective actions, and audit findings.
• Performs duties in compliance with all applicable regulatory and accrediting agencies and cGMP expectations, including, but not limited to: Facility and equipment maintenance, validation review and approval, training (internal, continuing education, proficiency testing, annual GMP, etc.)
• Meets basic expectations of DPT’s quality management system, including but not limited to good workmanship, adherence to standard operational procedures, training, good documentation practices, accurate recordkeeping so the company may meet its stated quality policy and objectives.

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.

Qualifications

Minimum Educational Requirements: 

• Bachelor’s degree in Chemical, Physical, or Biological Science or Medical Technology required.

Basic Minimum Qualifications :

• Meet the minimum, applicable work experience to work in a CMS CLIA designated highcomplexity laboratory per 42 CFR Part §493.1461.
• For Denver ID, Denver Micro, Denver IG, Los Angeles ID, Los Angeles HLA, & Philadelphia labs:
  • Meet the minimum, applicable work experience requirements to fulfill NYSDOH SubPart 58.1 SubSection 58-1.4.
• Considerable knowledge of the methods, materials, and techniques used in laboratory testing
• Considerable knowledge of the use of laboratory apparatus and equipment
• Ability to organize, communicate, teach, and work with others in an effective manner
• Ability to manage and schedule the w