Pay Range: $85,000.00 - $110,000.00 / year
Salary offers are based on a wide range of factors including relevant skills, training, experience, education, and, where applicable, certifications obtained. Market and organizational factors are also considered. Successful candidates may be eligible to receive annual performance bonus compensation.
Benefits Information:
We are proud to offer best-in-class benefits and programs to support employees and their families in living healthy, happy lives. Our pay and benefit plans have been designed to promote employee health in all respects – physical, financial, and developmental. Depending on whether it is a part-time or full-time position, some of the benefits offered may include:
· Day 1 Medical, supplemental health, dental & vision for FT employees who work 30+ hours
· Best-in-class well-being programs
· Annual, no-cost health assessment program Blueprint for Wellness®
· healthyMINDS mental health program
· Vacation and Health/Flex Time
· 6 Holidays plus 1 "MyDay" off
· FinFit financial coaching and services
· 401(k) pre-tax and/or Roth IRA with company match up to 5% after 12 months of service
· Employee stock purchase plan
· Life and disability insurance, plus buy-up option
· Flexible Spending Accounts
· Annual incentive plans
· Matching gifts program
· Education assistance through MyQuest for Education
· Career advancement opportunities
· and so much more!
To advance technology necessary to develop state-of-the-art assays. To plan, organize, and implement basic experiments to achieve this goal. Train and provide scientific direction to scientific personnel of various levels as needed. Also provide scientific design and statistical analysis.
- Under the direction of the Scientific Director, Lead Scientist or R&D Manager, initiate experimental design for assay development.
- Conduct assay system development, optimization and validation.
- Prepare technical SOP's as required for Medical or Scientific Director (licensed) review and approval.
- Prepare assay validation reports and other assay-related documentation as defined by the licensed Scientific Director and Medical Director.
- Work closely with informatics personnel to develop computer programs and databases as required for assay execution, automation and data management.
- Keep Scientific Director and/or R&D manager informed about status of on going projects.
- Prepare written and oral presentations of scientific updates for presentation at R&D meetings and conferences.
- Maintain awareness of current and developing technologies.
- Interact with Academic Associates and other outside sources of emerging technologies, science and materials.
- Add input to annual review for research personnel supervised while working on special projects.
- Complies with industry regulatory and quality standards for the R&D Assay Design Control processes.
- Assists licensed supervisor with troubleshooting, including reviewing procedural execution for possible cause of out of control results. Carries out simple troubleshooting procedures and performs R&D problem solving experiments as instructed.
Required Work Experience:
- 5-7 years experience in following analytical techniques, HPLC, LC-MS/MS required in a research and development laboratory for candidates with a BS/BA degree;
- 2-5 years experience for candidates holding an MS/MA degree;
- 0-2 years experience for candidates holding a Ph. D. degree.
Physical and Mental Requirements:
Ability to sit or stand for long periods of time
Skills:
- Proven ability to accomplish technical tasks both independently and as a member of a research team.
- Written and Verbal Communication Skills
Education
- Bachelor’s Degree BS/BA in Biology, Biochemistry, Chemistry or related field required. (Required)
- Master’s Degree (Preferred)
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.
Skills Required
- Bachelor's Degree (BS/BA) in Biology, Biochemistry, Chemistry or related field
- 5-7 years experience with HPLC and LC-MS/MS in an R&D laboratory (for BS degree)
- 2-5 years experience with HPLC and LC-MS/MS in an R&D laboratory (for MS degree)
- 0-2 years experience with HPLC and LC-MS/MS in an R&D laboratory (for PhD degree)
- Experience preparing SOPs, assay validation reports, and assay-related documentation
- Experience collaborating with informatics to develop programs and databases for assay execution and data management
- Proven ability to perform technical tasks independently and as part of a research team
- Strong written and verbal communication skills
- Master's Degree (preferred)
What We Do
Quest Diagnostics (NYSE: DGX) empowers people to take action to improve health outcomes. Derived from the world's largest database of clinical lab results, our diagnostic insights reveal new avenues to identify and treat disease, inspire healthy behaviors and improve health care management. Quest annually serves one in three adult Americans and half the physicians and hospitals in the United States, and our 47,000 employees understand that, in the right hands and with the right context, our diagnostic insights can inspire actions that transform lives. The company offers physicians the broadest test menu (3,000+ tests), is a pioneer in developing innovative new tests, is the leader in cancer diagnostics, provides anatomic pathology (AP) services, & interpretive consultation through its medical & scientific staff of about 900 M.D.s & Ph.D.s. The company reported 2020 revenues of $9.44 billion. Quest Diagnostics offers the most extensive clinical testing network in the U.S., with laboratories in most major metropolitan areas, & in Mexico, the UK & India. The company also operates four esoteric laboratories, 40 outpatient AP laboratories, & 160 smaller, rapid-response laboratories. Patients may have specimens collected in any of the company’s approximately 2,250 patient service centers. On a typical workday, testing is performed for about 550,000 patients. Quest Diagnostics empowers healthcare organizations & clinicians with state-of-the-art connectivity solutions. The company is the leading provider of pre-employment drugs-of-abuse screening for employers & risk assessment services for the life insurance industry. It is the world’s 2nd largest provider of clinical trials testing for new pharmaceuticals. More information is available at www.questdiagnostics.com. Language Assistance / Non-Discrimination Notice Asistencia de Idiomas / Aviso de no Discriminación 語言協助 / 不歧視通知 www.QuestDiagnostics.com/home/nondiscrimination






