Clinical Laboratory Quality Coordinator

Labcorp is seeking a Laboratory Quality Coordinator to join our Quality team in Westborough, MA. The Quality Assurance team provides vital support to the laboratories, senior management as well as our clients, and other Labcorp sites.   This position is a great opportunity for laboratory professionals that have an eye for detail and a passion for quality assurance.

Work Schedule: Monday - Friday 8:30 am - 5:00pm

Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan.  Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here. 

Job Responsibilities

• Support projects and activities related to quality assurance, control, improvement and training
• Prepare and support the laboratory for regulatory inspections
• Maintain all necessary documents and materials required for inspections
• Provide backup inspection support to laboratory during inspections
• Keep up with all required proficiency testing and examinations
• Coordinate and track external and internal proficiency testing
• Perform internal audits and prepare audit reports
• Prepare reoccurring quality reports for laboratory operations
• Stay current with all regulatory agency and proficiency test requirements
• Provide proper initiation and use of Master Control forms for audit purposes
• Participate in monthly Quality Meeting and compose minutes
• Perform administrative and clerical duties as needed

Requirements:

• Associate’s degree in a Chemical or Biological science, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requirements – Bachelor’s degree is a plus
• Previous experience as a Medical Technologist/Technician or in a quality-related position.
• Prior experience in a clinical laboratory is highly preferred
• General knowledge of laboratory regulations (CAP/CLIA/ISO) and licensing requirements
• Basic understanding of audit related requirements and procedures
• Working knowledge of quality assurance best practices and procedures
• Excellent analytical, critical thinking and problem solving skills
• Strong communication skills; both written and verbal
• High level of attention to detail with strong organizational skills
• Ability to work independently and within a team environment
• Strong computer skills with proficiency with MS Office programs

If you're looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference, apply today!

Labcorp is proud to be an Equal Opportunity Employer:

As an EOE/AA employer, Labcorp strives for diversity and inclusion in the workforce and does not tolerate harassment or discrimination of any kind. We make employment decisions based on the needs of our business and the qualifications of the individual and do not discriminate based upon race, religion, color, national origin, gender (including pregnancy or other medical conditions/needs), family or parental status, marital, civil union or domestic partnership status, sexual orientation, gender identity, gender expression, personal appearance, age, veteran status, disability, genetic information, or any other legally protected characteristic. Additionally, all qualified applicants with arrest or conviction records will be considered for employment in accordance with applicable law.

We encourage all to apply

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