Mô tả công việc

• Perform physical and chemical analysis of raw materials, in-process, and finished pharmaceutical products, including products on stability, according to written methods, material specification, and company policies as identified in standard operating procedures (SOPs). Comply with cGMps, SOPs, and STPs to avoid out-of-specification situation.
• Perform process validation/method transfers and cleaning validation/verification testing on various drugs. Assist other scientists with analytical, instrument and software related problems as required.
• Document steps followed during analysis execution, calculate and report results.
• Review laboratory analysis data for completeness, specification compliance, and compliance with company policies.
• Report any abnormal findings, and assist in troubleshooting of analytical methods.
• As assigned, perform in-depth review of analytical records/reports to assure that calculations and other data are technically correct and compliant to relevant specifications.
• Handling non-routine special projects requiring activities such as out-of-specification investigations and out-of-alert limit investigations in the laboratory.
• Assist with hands-on training of newly hired Technicians.
• Perform other laboratory duties as assigned.

Yêu cầu công việc

• Bachelor’s degree in Chemistry/ Pharmacy (preferred) or related science field.
• Understands cGMP concepts and general practices.
• Minimum 2 years of experience working in a pharmaceutical factory (tablets, capsules, and sachets are preferred).
• Proficient with software applications applicable to the job.
• Equipment experience with HPLC, UV/Vis, FT-IR…
• English fluency.
• Change management, adaptability, ability to work under pressure.
• Excellent organizational and time-management abilities.

Schedule: T2 - T6 office hours

Working location: District 1