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Chemist I (12 hours rotating shift) Job Opening In Singapore, Singapore – Now Hiring Thermo Fisher Scientific


Job description

  • 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 (, 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 (, 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.
  • Required Skill Profession

    Physical Scientists


    • Job Details

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