Scientist (LCMS)

Quest Diagnostics; Lewisville (TX); On-site; USD 90,000 - 120,000; Full time

Job summary

Quest Diagnostics is seeking an experienced R&D supervisor to manage analytical projects from assay design through validation and implementation. You will supervise bench work, diagnose test issues, and drive corrective actions while supporting the R&D department’s development and maintenance efforts.

The role requires strong expertise in HPLC, GC, GC/MS, LC-MS/MS and ICP/MS, plus the ability to train staff and coordinate across departments.

Qualifications

• Six years of R&D experience with extensive experience in HPLC, GC, GC/MS, LC-MS/MS and ICP/MS required or relevant advanced degree.
• Bachelor’s Degree in appropriate clinical or applied science required.
• Master’s Degree or PhD preferred.

Responsibilities

• Coordinates and provides bench level supervision of projects for R&D using HPLC, GC, GC/MS, LC-MS/MS and ICP/MS as directed by Technical Director.
• Coordinates implementation of new procedures within the department and with other support departments.
• Performs statistical analysis and validation of new methods; provides written summaries for method documentation.
• Trains staff in new methods both in technical and instrumental aspects.
• Manages special projects with coordination of resources and personnel.
• Serves as a resource for HPLC, GC, GC/MS and LC-MS/MS questions.
• Writes technical proposals soliciting drug analysis services and contributes to business proposals.
• Maintains testing reliability including diagnosing test failures and implementing corrective action.
• Provides technical understanding of analytical techniques with emphasis on instrumental methods.
• Informs supervisor of problems with test procedures.
• Maintains records of corrective and preventive maintenance to satisfy licensing requirements.
• Supports and complies with laboratory policies and procedures.

Skills

Project supervision

Time management

Verbal & written communication

Interpersonal skills

Education

Bachelor’s Degree in clinical or applied science

Master’s Degree in clinical or applied science

PhD in clinical or applied science

Tools

HPLC

Gas Chromatography

GC/MS

LC-MS/MS

ICP/MS

Job description

Job Description

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.

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, 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

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, and ICP/MS required or relevant advanced degree as a requirement.

Physical And Mental Requirements

Ability to sit and/or stand for long periods.

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 B. S. in appropriate clinical or applied science (Required)
• Master’s Degree M. S. in appropriate clinical or applied science (Preferred)
• PhD in appropriate clinical or applied science (Preferred)

About The Team

Quest Diagnostics honors our service members and encourages veterans to apply.

While we appreciate and value our staffing partners, we do not accept unsolicited resumes from agencies. Quest will not be responsible for paying agency fees for any individual as to whom an agency has sent an unsolicited resume.

Equal Opportunity Employer: Race/Color/Sex/Sexual Orientation/Gender Identity/Religion/National Origin/Disability/Vets or any other legally protected status.