JOB DETAILS

Quality Assurance Officer

CompanyThermo Fisher Scientific
LocationCity of Brisbane
Work ModeOn Site
PostedMarch 31, 2026
About The Company
About Thermo Fisher Scientific Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD. For more information, please visit www.thermofisher.com.
About the Role

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, Office

Job Description

As part of the Thermo Fisher Scientific team, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable our customers to make the world healthier, cleaner and safer. We provide our global teams with the resources needed to achieve individual career goals while helping to take science a step beyond by developing solutions for some of the world’s toughest challenges, like protecting the environment, making sure our food is safe or helping find cures for cancer.

DESCRIPTION:
At Thermo Fisher Scientific, you'll join a quality assurance team focused on ensuring consistent execution of quality standards and regulatory compliance. You'll play a vital role in enabling our customers to make breakthrough discoveries and innovations that make the world healthier, cleaner and safer. You'll ensure product quality, drive continuous improvement initiatives, and collaborate with cross-functional teams to maintain the highest standards of quality and compliance in a GMP environment.

REQUIREMENTS:

  • Bachelor's Degree required, 2-3 years experience in pharmaceutical, medical device or regulated industry preferred
  • Preferred Fields of Study: Chemistry, Biology, Biotechnology, Engineering, or related scientific/technical field
  • Additional certifications in Quality Systems or GMP preferred
  • Strong knowledge of cGMP, ISO standards (13485/9001), and international regulatory requirements
  • Experience with quality systems and documentation including batch records, SOPs, deviations, CAPA
  • Proficiency in quality management software systems (TrackWise, SAP, etc.)
  • Demonstrated ability to perform detailed documentation review and quality assessments
  • Strong analytical and problem-solving skills for quality investigations and root cause analysis
  • Excellent written and verbal communication skills
  • Ability to work independently and collaborate effectively with cross-functional teams
  • Experience conducting internal quality audits and supporting external regulatory audits
  • Proficient computer skills including Microsoft Office applications
  • Strong attention to detail and commitment to accuracy
  • Ability to prioritize and adapt in a changing environment
  • Experience with continuous improvement methodologies (Lean, Six Sigma) preferred
  • May require up to 10% travel
  • Must be able to work in controlled environments wearing required PPE

Key Skills
GMPcGMPISO StandardsRegulatory RequirementsQuality SystemsBatch RecordsSOPsDeviationsCAPATrackWiseSAPDocumentation ReviewQuality AssessmentsRoot Cause AnalysisInternal AuditsLean
Categories
Science & ResearchManufacturingHealthcareAdministrative
Job Information
📋Core Responsibilities
This role focuses on ensuring consistent execution of quality standards and regulatory compliance within a GMP environment, playing a vital role in maintaining product quality and driving continuous improvement initiatives.
📋Job Type
full time
📊Experience Level
2-5
💼Company Size
99695
📊Visa Sponsorship
No
💼Language
English
🏢Working Hours
40 hours
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