LC-MS Scientist: Method Development & Lead Chemist

Labcorp; Singapore; On-site; SGD 70,000 - 110,000; Full time

Job summary

Labcorp Singapore is seeking an LCMS Scientist to join our team in Singapore. You will conduct analytical results, develop methods, and ensure data integrity while adhering to SOPs and regulatory guidelines.

The role requires a Bachelor's in chemistry or pharmaceutical science and 3+ years in quantitative LC-MS analysis, with hands-on sample prep and equipment troubleshooting. Collaboration with Study Director and clients is expected, with standard 9am-6pm hours.

Qualifications

• Bachelor's degree in a relevant field and 3+ years of experience in quantitative chemical analysis.
• 3+ years of experience with quantitative analysis of clinical samples using LC-MS.
• 3+ years hands-on experience with sample extraction using PPT, LLE, SPE.
• 3+ years experience with analytical equipment and troubleshooting.

Responsibilities

• Organizes, conducts and evaluates analytical results and testing.
• Maintains study documentation and laboratory records.
• Sets up, maintains, operates and performs maintenance on general equipment; identifies problems.
• Performs quality control review of data; informs management of deviations.
• Promotes a cohesive team environment; leads a small group of technical staff with supervision.
• Trains, mentors and assists less experienced staff.
• Maintains a clean and safe laboratory work environment.
• Participates in method development and validation of analytes; supports client communications.
• Writes SOPs and methods; assists in writing reports and protocols.
• Performs other related duties as assigned.

Education

Bachelor's degree in pharmacy, pharmaceutical analysis, chemistry, analytical chemistry or any other relevant specialization

Tools

LC-MS

PPT

LLE

SPE

Job description

Labcorp Singapore is seeking an LCMS Scientist to join our team in Singapore. You will conduct analytical results, develop methods, and ensure data integrity while adhering to SOPs and regulatory guidelines.

The role requires a Bachelor's in chemistry or pharmaceutical science and 3+ years in quantitative LC-MS analysis, with hands-on sample prep and equipment troubleshooting. Collaboration with Study Director and clients is expected, with standard 9am-6pm hours.