Laboratory Supervisor

Dexa Group; Jakarta Utara; On-site; IDR 500.333.000 - 750.501.000; Full time

Job summary

A leading pharmaceutical company is seeking a Laboratory Manager for its Oil Analysis Laboratory located in South Jakarta. The successful candidate will supervise the QMS Laboratory, ensure compliance with ISO 17025, and manage laboratory inventory. They should possess a Bachelor's degree in Chemistry, Biology, or related fields, along with a minimum of 3 years of experience in laboratory testing or calibration analysis. Strong communication skills and fluency in English are necessary for this role.

Qualifications

• Minimum 3 years experience in chemical and Microbiology laboratory testing.
• Experience as a QC Officer in the Pharmaceutical industry preferred.
• Familiarity with GLP and regulatory compliance.

Responsibilities

• Ensure supervision of QMS Laboratory and utility activities.
• Maintain laboratory management system as per ISO 17025.
• Develop methods of testing and study.

Skills

Laboratory management

ISO 17025 implementation

Pharmaceutical analysis

Microbiology testing

Good communication

Fluent in English

Education

Bachelor’s degree in Chemistry, Biology, Pharmacy or related field

Tools

ICP-OES

GC

Job description

Ensure supervision of QMS Laboratory and utility activity to meet service time satisfaction.

Supervise the implementation and maintain laboratory management system as per ISO 17025, Calibration program of all Lab Instruments, Verification/Validation of method of analysis.

Develop method of testing and study.

Ensure availability and inventory management of Lab.

Verify result of analysis of Lab staff.

Regular Report to Operations Manager.

Requirements

• Min Bachelor’s degree in Chemistry, Biology, Pharmacy, Chemical Engineering, or related field
• Experience in handling laboratory test or calibration analysis minimal 3 years in chemical and Microbiology.
• Preferably having experience as QC Officer in Pharmaceutical industry or Feed/Food Analysis.
• Has implemented/trained/understand about ISO17025 and or familiar with GLP
• Used to analyzing “Pharmaceutical Analysis” as per Compendial (USP, BP, FI)
• Experience in of ICP-OES, GC and microbiology test
• Good communication and fluent in English (both oral & written)
• Willing to be assigned in Fatmawati (South Jakarta) and Cikarang

Laboratory Manager – Oil Analysis Laboratory

South Jakarta, Jakarta, ID

Quality Assurance Staff

PT. Daewoong Pharmaceutical Indonesia