Senior QC Technician

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profile Job Location:

Brisbane - Australia

profile Monthly Salary: Not Disclosed
Posted on: 02-11-2025
Vacancies: 1 Vacancy

Job Summary

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Laboratory Setting

Job Description

At Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life To enable our customers to make the world healthier cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond by developing solutions for some of the worlds toughest challenges like protecting the environment making sure our food is safe or helping find cures for cancer.

Discover Impactful Work:

As a member of the Thermo Fisher Scientific team you will engage in important tasks. Surrounded by collaborative colleagues youll have the support and opportunities that only a global leader can give you. Our respected growing organisation has an outstanding strategy for the near term and beyond. Join our dynamic team and assist us in making substantial impacts worldwide.

Location/Division Specific Information:

The TFS site in Brisbane is involved in the development and production of biopharmaceutical items for use in clinical trials and commercial applications.

This candidate will join our outstanding Quality Control Physio-Chemistry and Raw Materials Team who is responsible for testing review and release of materials and products.

Key responsibilities:

  • Perform analytical testing against predefined specifications and procedures using wet chemistry analysis and scientific equipment (pH Conductivity Osmolality Total Organic Carbon Analysis LOD titrations Karl Fischer FTIR and RAMAN spectroscopy)
  • Analysis assessment and efficiently detailing of documentation for customer needs.
  • Sampling of raw material according to the guidelines and in a controlled environment.
  • Peer review and approval of analysis for completeness and correctness.
  • Identify and report non-conformances and out of specification/unexpected results directly to Team Leader Supervisor and Manager.
  • Display solid understanding of Quality Control practices and principles applied to all site manufacturing services.
  • Working in a highly dynamic frequently changing environment with a wide variety of people and perspectives.
  • Participate in PPI activities and contribute ideas to improve workflows and reduce inefficiencies.

Keys to Success:

Qualifications & Experience

  • Tertiary Academic level in a relevant field (Biotechnology Biochemistry Microbiology Chemistry Pharmacology or equivalent).
  • Specific knowledge of Bio-pharmaceutical/Pharmaceutical processes guidelines and principals of preferred.
  • Knowledgeable in cGMP practices preferred.
  • Experience in the pharmaceutical and/or pharmaceutical industry aligned to Analytical and Quality Control fields preferred.
  • Background in analytical theory and technical proficiency with laboratory analysis desirable.
  • Knowledge of Aseptic techniques principles would be advantageous.
  • Ability to communicate in multiple modalities (e.g. electronic written verbal etc.)
  • Capacity to balance multiple projects concurrently and show proactivity in finishing tasks in line with company objectives.
  • Strong team working and collaborative skills.
  • Good knowledge of Microsoft applications (e.g. Excel Word Outlook PowerPoint) and familiarity with Smartsheets is a plus.

Skills & Abilities

  • Quality Orientation: Ability to interpret and apply cGMP principles strong attention to detail and accurate completion of test records. Strives for right first time in every task undertaken.
  • Adaptability: Ability to adapt to daily business requirements and multitask.
  • Collaborating: Demonstrates proficiency in collaborating with all departments and colleagues from a diverse group of backgrounds.
  • Initiating Action: Displays a dedication to pushing boundaries to improve PPI.

Other Job Requirements:

  • Adhere to EHS policies and procedures and ensure a safe and healthy workplace environment.
  • Ensure hazardous conditions hazardous actions incidents and near-miss incidents are reported.
  • Not knowingly pollute the environment.


Required Experience:

Senior IC

Work ScheduleStandard (Mon-Fri)Environmental ConditionsLaboratory SettingJob DescriptionAt Thermo Fisher Scientific youll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life To enable our customers to make the world healthier ...
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Key Skills

  • Laboratory Experience
  • Aseptic Technique
  • ELISA
  • FDA Regulations
  • PCR
  • High-Performance Liquid Chromatography
  • Microbiology
  • Quality Control
  • GLP
  • cGMP
  • Laboratory Information Management Systems
  • QA/QC

About Company

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Electron microscopes reveal hidden wonders that are smaller than the human eye can see. They fire electrons and create images, magnifying micrometer and nanometer structures by up to ten million times, providing a spectacular level of detail, even allowing researchers to view single a ... View more

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