Chemist I (12 hours rotating shift)

ThermoFisher Scientific; Singapore; On-site; SGD 50,000 - 70,000; Full time

Job summary

A leading scientific company in Singapore is seeking a Quality Control Specialist to perform QC testing, maintain compliance with GMP regulations, and support technical documentation preparation. The ideal candidate has a degree in Chemistry, at least 2 years of pharmaceutical experience, and strong analytical skills. This role offers opportunities for continuous improvement and requires the ability to work in a fast-paced environment.

Qualifications

• At least 2 years of pharmaceutical industrial experience.
• Proficiency in implementing GMP regulations.
• Hands-on experience with analytical techniques.

Responsibilities

• Perform QC testing of raw materials and finished products.
• Support equipment qualification and maintenance.
• Lead preparation of technical documentation.

Skills

Ability to work independently

Effective communication skills

Attention to detail

Organisational skills

Analytical thinking

Education

Degree in Chemistry

Tools

HPLC

GC

Job description

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

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 support equipment qualification (if required).

• 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 (e.g., SOPs, test methods) to ensure current, accurate and reflective of actual practices.

• To manage QC chemicals and consumables inventory stock check.

• To maintain the accuracy, completeness, and compliance of laboratory data.

• To participate in continuous improvement activities.

• To maintain own training records.

• To communicate effectively with cross-functional team and participate in problem solving activities.

• To guarantee the application and adherence to cGMP in their field.

• Be flexible to support shift work patterns (e.g., staggered shifts, weekend work) as required by business needs to ensure uninterrupted laboratory operations.

• 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 align with cGMP in all areas of the business.

• To work with HSE, cGMP and 5S in mind at all times.

• Undertake ad-hoc activities that may be required by the business.

Knowledge and Skills

• Ability to work independently with minimal supervision and adhere to critical timelines in a fast-paced environment.

• Effective verbal and written communication skills, with the ability to interact at all internal and external levels, including during regulatory audits.

• Excellent attention to detail with a rigorous approach to data recording and analysis.

• Excellent organisational and time-management skills, with the ability to prioritize multiple tasks effectively.

• Strong analytical thinking and systematic problem-solving skills.

Education and Work Experience

• Degree in Chemistry

• At least 2 years Pharmaceutical industrial experience.

• Proficiency in implementing GMP regulations and adhering to various international standards throughout all facets of the role.

• Demonstrated ability to apply GMP regulations (FDA, EMA, etc.) and other international guidelines to all aspects of the work.

• Hands-on experience with analytical techniques such as HPLC, GC and dissolution

• Proven experience in writing technical documentation and conducting laboratory investigations.

Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.