Validation Scientist (Drug Monitoring) - Quest Diagnostics

Overview:This position manages analytical projects in R & D, supervises projects from the assay design, validation and implementation. This position also manages special projects in R & D, and operates as a technical consultant in maintaining current testing reliability including diagnosing test failures and implementing corrective action. The incumbent assists in the development and maintenance of the R & D Department.  Responsibilities:

• Coordinates and provides bench level supervision of projects for R & D using HPLC, GC, GC/MS, LC-MS/MS, AA and ICP/MS techniques as directed by the Technical Director.  
• Coordinates the implementation of new procedures within the department and with other support departments.  
• Performs statistical analysis and validation of new methods. Provides written summaries of work to be used for method documentation.  
• Trains staff in new methods both in technical and instrumental aspects.  
• Manages special projects with the duties of coordination of resources and personnel.  
• Serves as a resource for HPLC, GC, GC/MS and LC-MS/MS related questions.  
• Writes technical proposals soliciting drug analysis services and contributes as requested to the business proposals for these solicitations.  
• Maintains present testing reliability including diagnosing test failures (instrumental and chemical) and implementing corrective action. 
• Provides technical understanding of analytical techniques with particular emphasis on instrumental methods of analysis.  
• Responsible for informing the appropriate supervisor of all problems associated with the proper performance of test procedures.  
• Maintains accurate records of all corrective and preventive maintenance to satisfy to licensing requirement.  
• Actively supports and complies with laboratory policies and procedures.  
• Other duties as assigned. This is not an exhaustive list of all duties and responsibilities, but rather a general description of work performed by the position. 

Qualifications:QUALIFICATIONS

Required Work Experience:  

• Six (6) years of R & D experience with extensive experience in following analytical techniques, HPLC, Gas Chromatography, GC/MS, LC-MS/MS, AA and ICP/MS required.

Preferred Work Experience:  

N/A 

Physical and Mental Requirements:  

Ability to sit and/or stand for long periods. 

Knowledge:  

N/A 

Skills:  

• Ability to see projects to completion.  
• Ability to manage time and details.  
• Good verbal and written skills required.  
• Interpersonal skills necessary to deal courteously and effectively with supervisors, co-workers and clients. 

EDUCATION
Bachelor’s Degree(Required)
Master’s Degree

LICENSECERTIFICATIONS

EEO:

Quest Diagnostics is an equal employment opportunity employer. Our policy is to recruit, hire and promote qualified individuals without regard to race, color, religion, sex, age, national origin, disability, veteran status, sexual orientation, gender identity, or any other status protected by state or local law. Quest Diagnostics observes minimum age requirements established by federal, state and/or local laws, and will ask an applicant for verification when deemed necessary.