Scientist (Anatomic Pathology)

at  Q Solutions

Singapore, Southeast, Singapore -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate09 Nov, 2024Not Specified10 Aug, 20241 year(s) or aboveGood communication skillsNoNo
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Description:

Job Overview
Responsible for performing a variety of technical procedures and experimental execution in support of sample analysis and validation. Responsible for root cause analysis, troubleshooting, and supporting process improvements.

Essential Functions

  • Responsible for performing and documenting analytical procedures in accordance with company procedures and regulatory guidelines.
  • Assists in troubleshooting and process improvements to increase data quality, lower costs, or reduce turnaround times to include, updating standard procedures, assisting with troubleshooting.
  • Acts as a technical resource for laboratory staff and support the team in the absence of the line manager.
  • Performs routine data analysis to determine if an analytical procedure is proceeding according to expectations and that the results are within acceptable tolerances.
  • Identifies and documents potential performance errors or otherwise unusual results and escalates to senior lab personnel.
  • Prepares data analysis results for upload to LIMS system under the guidance of senior level staff.
  • Contributes to CAPA investigations, deviations, and resolution.
  • Responsible for clear, accurate, and timely communications with cross functional stakeholders.
  • Assists in maintaining laboratory equipment and may offer suggestions for new equipment.
  • Assists in good housekeeping of the lab environment, consistent with 6S standards.
  • Assists in maintaining adequate inventory.
  • Responsible for preparation of buffers and solutions for analysis, as required.
  • Performs and documents calibration and maintenance of laboratory equipment as assigned.
  • Performs and documents hands on training for other lab personnel in areas of proven competency as assigned.
  • Participates in continuing education through self-study, attending training sessions and lectures and meetings.
  • May lead a laboratory or cross functional projects and assist with implementation of changes.
  • May be responsible for contributing to the design and development execution of routine methods/assays under moderate supervision.
  • Supports safety, quality, and 6S requirements and initiatives.
  • Complies with company’s procedures and applicable regulatory requirements.

Qualifications

  • Bachelor’s Degree Bachelors Degree Or equivalent combination of education and experience (Some CAP/CLIA lab locations may require a BSc in in a chemical, physical, biological or clinical laboratory science,

medical laboratory technology or cytotechnology.) Req

  • Typically requires >2 of experience. Req
  • Minimum 1 year of experience in a regulated laboratory environment preferred. Pref
  • Sound knowledge of principles, theories, and concepts in job area.
  • Working knowledge of any applicable regulatory standards within area of responsibility.
  • Proficiency with relevant laboratory techniques.
  • Knowledge of laboratory safety and infection control procedures and practices including standard precautions and hazardous chemical handling ,
  • Strong technical knowledge of complex testing procedures and science supporting the analysis.
  • Proficiency with complex laboratory calculations regarding batches and specimens.
  • Ability to troubleshoot laboratory equipment and resolve process issues.
  • Good computer skills including proficiency with Microsoft Excel, PowerPoint and Word.
  • Effective organizational and interpersonal skills.
  • Effective communication and presentation skills.
  • Capable of handling multiple tasks simultaneously.
  • Strong attention to detail and accuracy.
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients.

Q² Solutions, IQVIA’s laboratory business, creates connected intelligence by combining our expertise, technology and analytics - this fuels unparalleled research & development solutions. We uphold a deep commitment to patients, sites, customers, and each other. https://www.q2labsolutions.com/career

Responsibilities:

  • Responsible for performing and documenting analytical procedures in accordance with company procedures and regulatory guidelines.
  • Assists in troubleshooting and process improvements to increase data quality, lower costs, or reduce turnaround times to include, updating standard procedures, assisting with troubleshooting.
  • Acts as a technical resource for laboratory staff and support the team in the absence of the line manager.
  • Performs routine data analysis to determine if an analytical procedure is proceeding according to expectations and that the results are within acceptable tolerances.
  • Identifies and documents potential performance errors or otherwise unusual results and escalates to senior lab personnel.
  • Prepares data analysis results for upload to LIMS system under the guidance of senior level staff.
  • Contributes to CAPA investigations, deviations, and resolution.
  • Responsible for clear, accurate, and timely communications with cross functional stakeholders.
  • Assists in maintaining laboratory equipment and may offer suggestions for new equipment.
  • Assists in good housekeeping of the lab environment, consistent with 6S standards.
  • Assists in maintaining adequate inventory.
  • Responsible for preparation of buffers and solutions for analysis, as required.
  • Performs and documents calibration and maintenance of laboratory equipment as assigned.
  • Performs and documents hands on training for other lab personnel in areas of proven competency as assigned.
  • Participates in continuing education through self-study, attending training sessions and lectures and meetings.
  • May lead a laboratory or cross functional projects and assist with implementation of changes.
  • May be responsible for contributing to the design and development execution of routine methods/assays under moderate supervision.
  • Supports safety, quality, and 6S requirements and initiatives.
  • Complies with company’s procedures and applicable regulatory requirements


REQUIREMENT SUMMARY

Min:1.0Max:6.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

BSc

Chemical

Proficient

1

Singapore, Singapore