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Labcorp

Scientist (LCMS)

Posted 9 Days Ago
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In-Office
Singapore, SGP
Mid level
In-Office
Singapore, SGP
Mid level
Conducts quantitative LC-MS analysis of clinical samples, including method development, validation, testing, data review, troubleshooting, and quality control. Maintains laboratory records, SOPs, protocols, and reports while supporting regulatory compliance and corrective actions. Leads project activities, mentors technical staff, evaluates equipment, participates in client interactions, and contributes to process improvements. Requires a relevant bachelor’s degree and at least three years of quantitative chemical analysis experience, preferably involving LC-MS and sample extraction techniques.
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Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes. Through our unparalleled science, data, technology and laboratory network, we advance diagnostics, accelerate innovation and help address some of the world’s most important health challenges. As we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. With our global scale and deep expertise, you’ll have the opportunity to do meaningful work, grow your career and make a real impact on people’s health around the world. Together, we’re improving health and improving lives.


Scientist

Labcorp is seeking a LCMS Scientist to join our team in Singapore

Job Responsibilities:

  • Organizes, conducts and evaluates analytical results and testing.
  • Maintains study documentation and laboratory records.
  • Independently sets-up, maintains, operates and performs routine and non-routine maintenance on general equipment, including problem identification and resolution.
  • Performs quality control review of data.
  • Informs Study Director, Principal Investigator and/or management of any problems and/or deviations that may affect integrity of the data; participates in corrective action of problems.
  • Promotes a cohesive team environment.
  • With supervisory assistance, assures technical staff compliance to SOPs and other regulatory agency guidelines.
  • Assists in setting up and performing method development and validation of various analytes in a variety of matrices.
  • Performs complex analyses using unfamiliar or new methods, asking for scientific guidance as needed.
  • Makes suggestions for modifications in test methods or procedures.
  • Provides input and participates in project meetings, plans, monitors and guides project work.
  • With supervisory assistance, serves as a lead chemist on projects, overseeing a small group of technical staff.
  • Trains, mentors, and assists less experienced staff.
  • Maintains a clean and safe laboratory work environment.
  • Participates in new equipment and instrument assessment and qualification, as appropriate.
  • Participates in client visits as needed, assists in communicating technical information.
  • Participates in process improvement initiatives.
  • Assists in evaluation of data for incorporation into written reports.
  • Effectively plans and utilizes personnel and resources for timely completion of assigned projects.
  • Assists in writing reports and protocols.
  • Writes SOPs and methods.
  • Performs other related duties as assigned.

Minimum Qualifications:

  • Bachelor's degree in pharmacy, pharmaceutical analysis, chemistry, analytical chemistry or any other relevant specialization.
  • 3 or more years of experience in quantitative chemical analysis.

Preferred Qualifications:

  • 3 years or more experience with quantitative analysis of clinical samples using LC-MS.
  • 3 years or more hands-on experience with sample extraction using PPT, LLE, SPE.
  • 3 years or more experience in analytical equipment and troubleshooting.

Additional Job Standards:

  • Able to work in a team-centric setting.
  • Familiar with the use of standard laboratory equipment.
  • Effective communication (verbal and written), presentation and interpersonal skills.
  • Ability to perform advanced computer skills (e.g., Word, Excel).
  • Mon-Fri 9am-6pm (OT is dependent on workload and business demands).

At Labcorp we have a passion for helping people live happy and healthy lives. Every day we provide vital information that helps our clients and patients understand their health. If you are passionate about helping people and have a drive for service, then Labcorp could be a great next career step!


Labcorp is proud to be an Equal Opportunity Employer:

Labcorp strives for inclusion and belonging 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 and merit of the individual. Qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex (including pregnancy, childbirth, or related medical conditions), 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

If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility. For more information about how we collect and store your personal data, please see our Privacy Statement.


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