QC Chemist (1-year Contract/Pharma/Tuas)

Manpower Staffing Services; Singapore; On-site; SGD 40,000 - 60,000; Full time

Job summary

A staffing services firm in Singapore is seeking an analytical technician to perform and document testing in compliance with protocols and regulations. The ideal candidate will have a diploma in Chemical or Biotechnology, a minimum of 2 years of experience in the pharmaceutical industry, and effective problem-solving skills. This role involves conducting equipment verification, supporting lab investigations, and participating in continuous improvement efforts within the quality control laboratory.

Qualifications

• Minimum 2 years of relevant experience, preferably in Pharmaceutical/Biotechnology.
• Possess a can-do/pride-to-succeed attitude.
• Embrace the use of digital technology.

Responsibilities

• Perform analytical testing and document results according to protocols.
• Conduct equipment verification and calibration as per procedures.
• Support laboratory investigations and troubleshoot equipment issues.

Skills

Effective problem-solving skills

Demonstrated ability to perform in a team

Knowledge of cGMPs and ALCOA principles

Education

Diploma in Chemical/ Biotechnology or related field

Job description

Perform, review, and document analytical testing and results accurately in accordance with test methods, site SOPs, and relevant protocols, adhering to ALCOA principles and Data Integrity (DI) requirements.

Perform, review, and document equipment verification and calibration according to procedures.

Highlight any abnormalities detected during testing/review and raise laboratory investigations as required.

Support laboratory investigations and perform equipment troubleshooting where required.

Participate in 5S team initiatives and practice good housekeeping, ensuring all safety procedures are followed.

Author SOPs, analytical method transfer protocols and reports, and other GMP documentation (e.g., trend reports).

Set up and maintain QC processes (e.g., reference standards and retention sample management), and perform investigations as required for associated deviations.

Conduct training for fellow colleagues from QC and other departments (e.g., Production).

Uphold Company’s code of conduct and values.

Collaborate with cross-functional teams to drive flawless execution.

Play an active and impactful role in Tier processes by updating performance against metrics, highlighting issues, and supporting development and implementation of solutions.

Contribute to continuous improvement activities in QC laboratory or cross-functional teams as nominated.

Requirements

• Minimum Diploma in Chemical/ Biotechnology or related field
• Minimum 2 years of relevant experience desirably in Pharmaceutical/Biotechnology industry
• Effective problem-solving skills.
• Demonstrated ability to perform in a team.
• Knowledge of cGMPs and ALCOA principles.
• Possess a can-do/pride-to-succeed attitude.
• Embrace the use of digital technology to scale and speed up every form of interaction and action.