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Thermo Fisher Scientific

Makes lab instruments, reagents and supplies

Quality Assurance Officer

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeBrisbane QLD, AustraliaNo salary listed

About the Job

Requirements

  • Tertiary academic-level qualification in a relevant discipline: Biotechnology, Biochemistry, Microbiology, Chemistry, Pharmacology, or equivalent.
  • At least 3 years of experience in a GMP-regulated environment.
  • Knowledge of pharmaceutical cGMP quality systems and international cGMP regulations and guidelines.
  • Strong communication skills.
  • Strong written, verbal, and presentation skills.
  • Adhere to EHS policies and procedures and ensure a safe and healthy workplace environment.
  • Report hazardous conditions, hazardous actions, incidents, and near-miss incidents.

Responsibilities

  • Perform real-time batch record reviews, including reviewing protocols during manufacturing and postproduction to ensure product quality.
  • Perform routine audits of logbooks used in operations and QC areas for completeness and cGMP compliance.
  • Perform final QA review and approval of batch-related documentation.
  • Actively participate in deviation investigations.
  • Review and approve Process Validation documents, including microbial mapping validation protocols, resin re-use protocols, and cleaning validation protocols.
  • Approve quality records, including deviations, out-of-specifications, CAPAs, and audit findings.
  • Review and approve QA-controlled documents within the Quality Management System.
  • Support compliance with system timeframes for raising, processing, or performing associated tasks, including Change Control actions, DR investigations, and CAPA processing.
  • Issue protocols to other departments as required.
  • Perform quality functions, including rejects, vial thaw, and drug-substance shipping, as required.
  • Update SOPs and other documents to meet current regulatory and corporate standards.
  • Serve as a resource to operational areas on quality-related issues.
  • Identify continual improvement opportunities.
  • Conduct internal audits.
  • Participate in risk assessments.
  • Perform other legitimate duties requested by the QA Manager.

Desired Qualifications

  • At least 1 year of experience in Quality Assurance in a GMP-regulated environment is preferred.
  • Work from the Banyo site approximately once every two weeks (around 10–15% onsite presence) is ideally preferred.

About the Company

Thermo Fisher Scientific

Makes lab instruments, reagents and supplies

Thermo Fisher Scientific makes and sells the instruments, chemicals, consumables and lab services that drug companies, hospitals, universities and industrial labs use for research, testing and production. Its products cover work from gene sequencing and protein analysis to diagnostic tests and lab freezers, and its distribution arm ships supplies to labs worldwide. Drug developers also hire it to run clinical trials and to manufacture medicines under contract. It earns money from consumables that labs buy again and again, along with instrument sales, service contracts and outsourcing fees. The company traces its roots to Thermo Electron, founded in 1956, which merged with Fisher Scientific in 2006, and it is based in Waltham, Massachusetts.

Company size
10,001+
Company stage
IPO
Headquarters
Waltham, MA
Founded
1956

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