Job Description

Description

• For Analytical: Perform chemistry, biochemistry analysis of in-process samples, bulk drug substance (BDS), non-routine samples.
• For Raw Material: Perform analysis of water and cleaning samples as well as incoming raw material samples.
• Ensure tests assigned are performed in a timely manner in compliance to Standard Operating procedures
• Perform equipment calibration and maintenance.
• Perform review/approval of QC records/ logbooks.
• Perform trending of lab results.
• Initiate and participate in Out Of Specification (OOS), Invalid test and Lab Deviation Investigation Write-Up and assist in timely closure of laboratory invalid results, lab investigation and CAPA.
• Write/revise SOPs, forms, training qualifications (TQ) and risk assessments (RA).
• Provide technical support to QC Personnel in laboratory related troubleshooting e.g. lab equipment failure, method
• Participate in method validation/ transfer or equipment qualification when necessary.
• Ensure proper, safe handling and disposal of waste; ensuring a safe working environment.
• Carry out 5S and ensures good housekeeping of Analytical Lab area.
• Support and participates in Operation Excellence initiatives (such as GEMBA and GMP walk).
• Participate in projects towards improving safety performance and continuous improvement initiatives.
• Assist Supervisor to support internal and external compliance audits.
• Adherence to site\'s EHS requirements.
• Commit to a fair and respectful relationship with other employees and behaviors in accordance to Takeda\'s Code of Conduct.
• Perform master data creation, validation and any tasks associated with GLIMS/MODA implementation.
• For Analytical: Perform chemistry, biochemistry analysis of in-process samples, bulk drug substance (BDS), non-routine samples.
• For Raw Material: Perform analysis of water and cleaning samples as well as incoming raw material samples.
• Ensure tests assigned are performed in a timely manner in compliance to Standard Operating procedures
• Perform equipment calibration and maintenance.
• Perform review/approval of QC records/ logbooks.
• Perform trending of lab results.
• Initiate and participate in Out Of Specification (OOS), Invalid test and Lab Deviation Investigation Write-Up and assist in timely closure of laboratory invalid results, lab investigation and CAPA.
• Write/revise SOPs, forms, training qualifications (TQ) and risk assessments (RA).

Requirements

• Min Diploma / Degree in Chemistry
• Min 2 years of chemist experience
• Proficient in HPLC
• Able to start work immediately

Interested candidates, please forward your resume to kevynhuang@recruitexpress.com.sg

Consultant: Huang Jingsheng Kevyn (R1333338)

Recruit Express Pte Ltd (99C4599)

Recruiter Ref code: #HKH

Industry

Healthcare / Pharmaceutical / Life Science / Medical Device

Specialization

Chemist / Research Scientist
Healthcare - Pharmaceutical / Life Science / Medical Device / Clinical Research / Regulatory Affairs

Location

Central, North, East, West

Employment Type

Contract / Temp

Salary

Negotiable

If you meet the requirements of this role, please email a detailed resume in Word document to Kevyn Huang Jingsheng.
CEI Registration No.: R1333338
Email: kevynhuang@recruitexpress.com.sg
Tel: 67363280
*All information will be treated with strictest confidence. We regret that only short-listed applicants will be notified.

Recruit Express