Scientist - Sr

Quest Diagnostics; Lewisville (TX); On-site; USD 85,000 - 110,000; Full time

Job summary

Quest Diagnostics in Texas is seeking a qualified professional to manage analytical projects in R&D, supervising assay design, validation and implementation. The role also handles special projects and acts as a technical consultant to maintain testing reliability, diagnose failures and implement corrective action.

You will assist in developing and maintaining the R&D department, train staff on new methods, coordinate resources, and ensure documentation meets licensing requirements.

Qualifications

• 2–5 years of R&D experience with a Bachelor's degree in an appropriate clinical or applied science field of study, or 1–2 years of experience with a Master's or a PhD with extensive experience in the listed analytical techniques.
• Experience supervising bench-level projects and coordinating resources across R&D teams.
• Strong analytical and problem-solving abilities with attention to detail.

Responsibilities

• Coordinates and provides bench level supervision of projects for R&D using HPLC, GC, GC/MS, LC-MS/MS, and ICP/MS techniques.
• Coordinates the implementation of new procedures within the department and with other support departments.
• Performs statistical analysis and validation of new methods; writes summaries for method documentation.
• Trains staff in new methods and instrumental aspects.
• Manages special projects and coordinates resources and personnel.
• Acts as a resource for HPLC, GC, GC/MS and LC-MS/MS related questions.
• Maintains testing reliability; diagnosing test failures and implementing corrective action.
• Maintains records of maintenance to satisfy licensing requirements.

Skills

Project management

Time management

Verbal and written communication

Interpersonal skills

Education

Bachelor's degree in clinical or applied science

Master's or PhD in clinical or applied science (preferred)

Clinical Chemistry licenses (preferred)

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.

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.

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

• 2-5 years of R&D experience with a Bachelor's degree in an appropriate appropriate clinical or applied science field of study, or 1-2 years of experience with a Master's or a 0 years of experience with a PhD 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 in an appropriate clinical or applied science field of study (Required)
• Master's or PhD in an appropriate clinical or applied science field of study (Preferred)
• Clinical Chemistry licenses, ABCC, NRCC, ASCP, etc. (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.