Chemist I (12 hours shift)

LabRulez; Singapore; On-site; SGD 42,000 - 60,000; Full time

Job summary

Thermo Fisher Scientific is seeking a Chemist I (12 hours shift) to join its Quality Control team. You will perform QC testing of raw materials, intermediates and finished products, document results, and contribute to investigations in a GMP environment.

Responsibilities include equipment calibration, method transfer support, document maintenance, and cross-site communication. The role emphasizes accuracy, teamwork, and continuous quality improvement.

Qualifications

• Be part of our Quality Control team in a GMP environment.
• Perform testing and analysis using analytical techniques.
• Document results and participate in investigations.

Responsibilities

• To perform QC testing of raw materials, incoming goods, intermediates, and/or finished products under cGMP conditions for QC release or as part of stability studies.
• To perform and coordinate monitoring, calibration, and maintenance of laboratory equipment.
• To lead the preparation of technical documentations such as protocols, position papers and risks assessments.
• To perform write up for laboratory investigations, deviation and on time closure in line with Quality Management system procedures. (if required)
• To support method transfer/verification/validation for new product introduction.
• To perform periodic reviews for laboratory documents.
• To manage QC chemicals and consumables inventory stock check.
• To maintain the accuracy, completeness, and compliance of laboratory data.
• To maintain own training records.
• To communicate effectively with others on site and internationally and to participate with them in problem solving activities.
• To ensure cGMP is applied and adhered to in their area of work.
• To support shift work (if necessary).
• Participate/contribute in Practical Process Improvement initiatives (PPI) or continuous improvement in the lab.
• Support and encourage a "Quality Culture" and company 4i values throughout QC.
• Ensure cGMP is applied in their area of work and comply with cGMP in all areas of the business.
• Undertake ad-hoc activities that may be required by the business.

Skills

Independence

Communication

Attention to detail

Organization

Analytical skills

Education

Bachelor's degree in Chemistry

Job description

Analytical chemist, Quality Control (QC)

As the world leader in serving science, our work is more than something that fills our days - what we do has great purpose. Our industry-leading scale means unparalleled commercial reach, unique customer access and a global footprint. Our broad customer base, from research to clinical to commercial production means you can have a broad and meaningful impact here at Thermo Fisher Scientific. All while working in an environment where you will be supported, valued and rewarded for your performance.

Chemist I (12 hours shift)

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Laboratory Setting, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.), Will work with hazardous/toxic materials

Job Description

DESCRIPTION:

Be part of our Quality Control team at Thermo Fisher Scientific, where you'll perform testing and analysis to support the development of innovative therapeutic products. You'll conduct quality control testing of raw materials, in-process samples, and finished products using various analytical techniques. You'll document and analyze test results, participate in investigations, and contribute to continuous improvement initiatives. This role offers opportunities for professional growth while working with skilled colleagues who share our commitment to excellence and innovation.

Responsibilities

• To perform QC testing of raw materials, incoming goods, intermediates, and/or finished products under cGMP conditions for QC release or as part of stability studies.
• To perform and coordinate monitoring, calibration, and maintenance of laboratory equipment.
• To lead the preparation of technical documentations such as protocols, position papers and risks assessments.
• To perform write up for laboratory investigations, deviation and on time closure in line with Quality Management system procedures. (if required)
• To support method transfer/verification/validation for new product introduction.
• To perform periodic reviews for laboratory documents.
• To manage QC chemicals and consumables inventory stock check.
• To maintain the accuracy, completeness, and compliance of laboratory data.
• To maintain own training records.
• To communicate effectively with others on site and internationally and to participate with them in problem solving activities.
• To ensure cGMP is applied and adhered to in their area of work.
• To support shift work (if necessary).
• Participate/contribute in Practical Process Improvement initiatives (PPI) or continuous improvement in the lab.
• Support and encourage a "Quality Culture" and company 4i values throughout QC.
• Ensure cGMP is applied in their area of work and comply with cGMP in all areas of the business.
• Undertake ad-hoc activities that may be required by the business.

Knowledge, Skills, Abilities:

• Ability to work independently and adhere to critical timelines.
• Effective communication skills at all internal and external levels.
• Excellent attention to detail.
• Excellent organizational skills.
• Strong in analytical skill and problem-solving skills.

Preferred Experience and Skills:

• Degree in Chemistry or strongly related scientific discipline.
• At least 2-3 years relevant industrial experience.
• Ability to apply GMP regulations and other international guidelines to all aspects of the position.
• Ability to work independently and adhere to critical timelines.