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Thermo Fisher Scientific

Makes lab instruments, reagents and supplies

Head of Quality Control

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

About the Job

Requirements

  • A bachelor's degree in science or a relevant scientific discipline, such as biochemistry, chemistry or biology.
  • A minimum of 8 years of QC and/or Quality-related experience in the biopharmaceutical manufacturing industry.
  • Good knowledge of current Good Manufacturing Practices (cGMP).
  • Strong working knowledge of QC laboratory operations, including sample management and flow, raw material release, in-process controls, drug substance testing, laboratory equipment and associated quality systems.
  • Demonstrated experience supporting and/or leading customer audits and regulatory inspections.
  • Demonstrated experience leading people and teams within a regulated Quality and/or QC environment.
  • Ability to work in a highly dynamic, frequently changing environment with a wide variety of people and perspectives.
  • Ability to adhere to occupational health and safety policies and procedures, ensure a safe and healthy workplace, follow Australian Heavy Vehicle National Law Chain of Responsibility obligations and environment, health and safety policies, perform only tasks for which currently competent and/or authorized, report hazards and incidents, participate in safety activities, and avoid knowingly polluting the environment.

Responsibilities

  • Set and execute the QC strategy in alignment with site and corporate Quality priorities, business demand and customer requirements.
  • Lead the QC organization through the QC management team, with clear accountability.
  • Own QC planning and performance governance, including the Annual Operating Plan, labor and capacity modeling, capital expenditure, key performance indicators and continuous improvement.
  • Contribute as a senior Quality leader to governance, including Quality Management Review, inspection readiness and contamination control.
  • Ensure timely delivery of QC testing, review and reporting activities in line with manufacturing, release, stability and customer requirements.
  • Own QC capacity and resource planning, balancing demand, capability and business priorities.
  • Monitor QC operational performance, including testing cycle times, right-first-time performance, backlog and adherence to agreed service levels.
  • Ensure effective planning and utilization of internal and external laboratory capacity.
  • Identify and address capacity, capability and delivery risks, escalating material risks through appropriate site governance.
  • Ensure effective and timely management of QC investigations, deviations, corrective and preventive actions, change controls and inspection commitments, including escalation of significant risks.
  • Ensure QC facilities, equipment, methods, systems, documentation and records comply with site procedures and applicable regulatory requirements.
  • Maintain QC inspection readiness and act as the senior QC representative during customer audits, corporate audits and regulatory inspections.
  • Own QC data integrity performance and maturity, ensuring ALCOA++ principles are embedded across paper, instrument and electronic records.
  • Partner with the Contamination Control Manager on environmental monitoring and contamination-control oversight relevant to low-bioburden drug-substance manufacturing.
  • Ensure fit-for-purpose analytical and microbiological capability for raw materials, in-process testing, drug substance, stability and facility monitoring.
  • Provide governance across the analytical method lifecycle, including development, transfer, qualification, validation and troubleshooting.
  • Own the lifecycle strategy for QC facilities, equipment and computerized systems, including investment, qualification, maintenance, obsolescence and business continuity.
  • Lead laboratory digitalization and simplification initiatives that improve compliance, capacity, review efficiency and right-first-time execution.
  • Build and sustain a capable, accountable and appropriately structured QC organization.
  • Hire, coach and develop QC leaders, ensuring effective performance management and succession planning.
  • Ensure QC personnel are trained, qualified and competent for assigned GMP, technical and safety activities.
  • Build effective relationships with global Quality, QC, analytical development and operational excellence teams to align Brisbane QC with network standards and strategy.
  • Represent Brisbane QC in global forums and initiatives, communicating site risks, priorities and resource needs.
  • Implement applicable global procedures, standards and harmonization initiatives.
  • Benchmark QC performance against network and industry practices, translating learning into improvement.
  • Maintain timely client communication on QC performance, technical issues, investigations, changes, risks and recovery plans, including significant escalation.
  • Support global commercial teams with customer proposals, technical content, pricing and scope development.

Desired Qualifications

  • A postgraduate qualification in a relevant discipline.
  • Experience within a Contract Development and Manufacturing Organisation (CDMO) environment.

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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