Total 7 research associate job vacancies in Quality Assurance / Control category in D12 Balestier, Serangoon, Toa Payoh

Responsibilities:

• Performs the set-up, calibration, testing and troubleshooting of circuits, components, instruments and mechanical assemblies
• Determines and may develop test specifications, methods and procedures from blueprints, drawings and diagrams.
• Tests and troubleshoots assemblies and/or final systems. May complete rework on assemblies and/or systems as a result of testing.
• Prepares technical reports summarizing findings and recommending solutions to technical problems.
• May assist in the selection and set-up of specialized test equipment.

Requirements:

• Diploma or Bachelor Degree in Engineering.
• Ability to read technical drawings/procedures and use a variety of precision testing and measuring instruments.
• Previous hands-on experience with semiconductor equipment
• Experience with optics alignment will be adventagous
• Strong troubleshooting and analytical skills to resolve technical problems, set up experiments, and perform data analysis.
• Excellent communication, teamwork, and people skills are required.
• Comfortable working in shifts and cleanroom environment

Responsibilities:

• Performs the set-up, calibration, testing and troubleshooting of circuits, components, instruments and mechanical assemblies
• Determines and may develop test specifications, methods and procedures from blueprints, drawings and diagrams.
• Tests and troubleshoots assemblies and/or final systems. May complete rework on assemblies and/or systems as a result of testing.
• Prepares technical reports summarizing findings and recommending solutions to technical problems.
• May assist in the selection and set-up of specialized test equipment.

Requirements:

• Diploma or Bachelor Degree in Engineering.
• Ability to read technical drawings/procedures and use a variety of precision testing and measuring instruments.
• Previous hands-on experience with semiconductor equipment
• Experience with optics alignment will be adventagous
• Strong troubleshooting and analytical skills to resolve technical problems, set up experiments, and perform data analysis.
• Excellent communication, teamwork, and people skills are required.
• Comfortable working in shifts and cleanroom environment

Responsibilities:

• Performs the set-up, calibration, testing and troubleshooting of circuits, components, instruments and mechanical assemblies
• Determines and may develop test specifications, methods and procedures from blueprints, drawings and diagrams.
• Tests and troubleshoots assemblies and/or final systems. May complete rework on assemblies and/or systems as a result of testing.
• Prepares technical reports summarizing findings and recommending solutions to technical problems.
• May assist in the selection and set-up of specialized test equipment.

Requirements:

• Diploma or Bachelor Degree in Engineering.
• Ability to read technical drawings/procedures and use a variety of precision testing and measuring instruments.
• Previous hands-on experience with semiconductor equipment
• Experience with optics alignment will be adventagous
• Strong troubleshooting and analytical skills to resolve technical problems, set up experiments, and perform data analysis.
• Excellent communication, teamwork, and people skills are required.
• Comfortable working in shifts and cleanroom environment

Responsibilities:

• Performs the set-up, calibration, testing and troubleshooting of circuits, components, instruments and mechanical assemblies
• Determines and may develop test specifications, methods and procedures from blueprints, drawings and diagrams.
• Tests and troubleshoots assemblies and/or final systems. May complete rework on assemblies and/or systems as a result of testing.
• Prepares technical reports summarizing findings and recommending solutions to technical problems.
• May assist in the selection and set-up of specialized test equipment.

Requirements:

• Diploma or Bachelor Degree in Engineering.
• Ability to read technical drawings/procedures and use a variety of precision testing and measuring instruments.
• Previous hands-on experience with semiconductor equipment
• Experience with optics alignment will be adventagous
• Strong troubleshooting and analytical skills to resolve technical problems, set up experiments, and perform data analysis.
• Excellent communication, teamwork, and people skills are required.
• Comfortable working in shifts and cleanroom environment

QA Associate

The QA Associate coordinates and conducts activities of the Quality Assurance Department to provide overall site function support included manufacturing floor support and ensure quality oversight throughout the facility's operational hours for all ongoing GMP activities.

Your responsibilities include, but are not limited to:

• Participate in setting up and maintaining of Quality Assurance documentation.
• Responsible for briefing relevant Facilities/Engineering/Supply Chain and Quality Control personnel on cGMP and hygiene procedures required for entering the dispensing and production areas.
• Writing, reviewing and/or approving QA-controlled documentation (such as SOPs, batch records, and work instructions).
• Writing and issuing SOPs for site qualification and validation projects as needed, example technology transfer project.
• Preparing manufacturing final batch release documentation, reviewing and approving related final batch records and ensure timely closure of manufactured batches.
• Reviewing and approving routine facilities/utilities/equipment, computerized systems scheduled maintenance/calibration records to ensure cGMP compliance.
• Reviewing and approving environmental monitoring data and analyse the trending for any potential impact.
• Reviewing and approving validation deliverables related to facilities/utilities/equipment, computerized systems (automation), and laboratory equipment/systems to ensure compliance with company procedures, regulatory requirements, cGMP expectations, and project schedules.
• Participate and provide QA input for Risk Assessment to ensure the compliance to cGMP requirements.
• Participate and provide QA input for User Requirements Specification to ensure compliance to cGMP requirements.
• Participate and provide QA input for Facilities/Engineering Qualifications, Processes Validation, and Computerized System Validations to comply with cGMP requirements.
• Participate and support in deviation root-cause investigation, reviewing/approving deviation closure with solid CAPA implementation.

EXPERIENCE REQUIREMENTS

1. Bachelor’s Degree.
2. More than 3 years of experience in a Bio-Life science environment. GMP experience is advantageous.
3. Working understanding of GLP-Lab/GMP Operations, QC, QA, Process Development, Supply Chain, and related functions such as Facilities/Engineering.
4. Strong knowledge and understanding of Quality System functions, manufacturing/packaging processes, validation, engineering drawings, and basic statistical processes.
5. Involvement in setting up a New Site and/or Project Management is an added advantage.
6. Motivated self-starter, capable of influencing change in an ambiguous environment.
7. Matured, able to work in fast phase and high-pressure environment.
8. Good technical writing, communication, and presentation skills.

Key Highlights:

• Starting salary from $3,500 + Allowance + Performance Bonus

• New headcounts as part of business expansion plans

• Career advancement opportunities

Job Scope:

• Conduct full range of audit for listed companies and SMEs, both in Singapore and overseas, from planning to completion, monitoring the engagement progress against budget and timeline

• Develop good problem-solving skills and provide sound recommendation of management actions based on industry research, insightful analysis and investigation

• Promote positive team work - coach junior employees, share learnings, understand how own work impacts others

• Attend client meetings, contribute by supporting senior team members

• Other ad-hoc duties as assigned by Supervisor

Job Requirement:

• Degree or professional accounting qualifications recognised by ISCA

• Minimum 1-2 years’ relevant experience with large/mid-tier international accounting firms

• Proactive, committed and able to work under pressure

• Possess initiative and the ability to work independently

• Team player

For interested applicants, kindly send a copy of your resume to [email protected] or simply click the button to APPLY NOW! We regret that only shortlisted applicants will be notified.

EA Licence No.: 16C8261 | EA Personnel: Tan Jessie | EA Personnel Reg. No: R1879285

QA Associate

The QA Associate coordinates and conducts activities of the Quality Assurance Department to provide overall site function support included manufacturing floor support and ensure quality oversight throughout the facility's operational hours for all ongoing GMP activities.

Your responsibilities include, but are not limited to:

• Participate in setting up and maintaining of Quality Assurance documentation.
• Responsible for briefing relevant Facilities/Engineering/Supply Chain and Quality Control personnel on cGMP and hygiene procedures required for entering the dispensing and production areas.
• Writing, reviewing and/or approving QA-controlled documentation (such as SOPs, batch records, and work instructions).
• Writing and issuing SOPs for site qualification and validation projects as needed, example technology transfer project.
• Preparing manufacturing final batch release documentation, reviewing and approving related final batch records and ensure timely closure of manufactured batches.
• Reviewing and approving routine facilities/utilities/equipment, computerized systems scheduled maintenance/calibration records to ensure cGMP compliance.
• Reviewing and approving environmental monitoring data and analyse the trending for any potential impact.
• Reviewing and approving validation deliverables related to facilities/utilities/equipment, computerized systems (automation), and laboratory equipment/systems to ensure compliance with company procedures, regulatory requirements, cGMP expectations, and project schedules.
• Participate and provide QA input for Risk Assessment to ensure the compliance to cGMP requirements.
• Participate and provide QA input for User Requirements Specification to ensure compliance to cGMP requirements.
• Participate and provide QA input for Facilities/Engineering Qualifications, Processes Validation, and Computerized System Validations to comply with cGMP requirements.
• Participate and support in deviation root-cause investigation, reviewing/approving deviation closure with solid CAPA implementation.

EXPERIENCE REQUIREMENTS

1. Bachelor’s Degree.
2. More than 3 years of experience in a Bio-Life science environment. GMP experience is advantageous.
3. Working understanding of GLP-Lab/GMP Operations, QC, QA, Process Development, Supply Chain, and related functions such as Facilities/Engineering.
4. Strong knowledge and understanding of Quality System functions, manufacturing/packaging processes, validation, engineering drawings, and basic statistical processes.
5. Involvement in setting up a New Site and/or Project Management is an added advantage.
6. Motivated self-starter, capable of influencing change in an ambiguous environment.
7. Matured, able to work in fast phase and high-pressure environment.
8. Good technical writing, communication, and presentation skills.
9. Able to speak, read, and write Chinese.