30 Oct
|
Biopharma Careers
|
Sydney
30 Oct
Biopharma Careers
Sydney
At Johnson & Johnson,we believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where treatments are smarter and less invasive, andsolutions are personal.Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.Learn more at jnj.com .
As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Job Function:
Quality
Job Sub Function:
Customer/Commercial Quality
Job Category:
Professional
All Job Posting Locations:
North Ryde, New South Wales, Australia
Job Description:
DePuy Synthes is recruiting for a CQ Professional, located in North Ryde, Australia.
Join our change journey at J&J;, help shape what’s next
Step into a high-impact career opportunity with real visibility
THE OPPORTUNITY
The CQ Professional supports the execution and continuous improvement of Commercial Quality (CQ) processes within the QARA International organization. This role contributes to maintaining an effective Quality Management System (QMS), and ensuring compliance with internal standards, company policies, and applicable regulatory requirements across commercial operations. Working in close partnership with regional and global stakeholders, the CQ Professional supports quality system proceses, documentation, monitoring,
and compliance activities that enable consistent, and compliant execution while protecting patient safety, product quality and business continuity.
Responsibilities
Support the documentation, maintenance, implementation and execution of Commercial Quality processes, procedures, and work instructions in alignment with global standards, requirement, and quality metrics.
Maintain accurate, complete, and compliant quality documentation and records, including SOPs, reports, controlled documents and qualification & training records.
Support the administration, coordination, and monitoring of quality system changes, including Change Controls and implementation activities, ensuring timely completion and compliance with established procedures.
Support quality risk management activities, including risk assessments, periodic reviews, and implementation of risk mitigation actions, as required.
Support the maintenance and implementation of internal quality standards, external regulations, and applicable procedures, ensuring quality system documentation remains current and compliant.
Support the administration, maintenance, continuous improvement, and user support of Quality System elements and applicable electronic Quality Management Systems (eQMS), including Qualification & Training, Document Management, Change Management, Nonconformance & CAPA Management, Escalations, Risk Management,
Supplier Management, Quality Metrics, and Quality System Management Review (QSMR) processes.
Assist with preparation and support for internal audits, external audits, supplier management, and health authority inspections, including evidence collection, coordination and follow‑up activities.
Collaborate with cross‑functional partners including Commercial, Regulatory Affairs, Supply Chain, and other QARA teams, to support compliant commercial operations and quality system requirements.
Contribute to quality metrics, trend analysis, performance reporting, and Quality System Management Review (QSMR) activities to support management oversight and continuous improvement.
Apply DePuy Synthes quality principles, compliance expectations, and Credo values in all aspects of daily activities
ABOUT YOU
REQUIRED
Typically 2-4 years of relevant experience in Quality, Regulatory Affairs, Compliance, Quality Systems, or another regulated workplace.
Foundational to working knowledgeof quality management systems, documentation practices, qualification & training processes, and compliance requirements.
Strong attention to detail with the ability to manage quality documentation accurately, consistently.
Ability to analyze data, support quality metrics and trend reporting, and contribute to continuous improvement activities.
Demonstrated organizational, communication, and problem‑solving skills, with the ability to manage multiple priorities and meet deadlines.
Ability to work effectively in a cross‑functional and collaborative environment.
Bachelor’s degree in Quality, Life Sciences, Engineering, Regulatory Affairs, or a rel
📌 CQ Professional (Sydney)
🏢 Biopharma Careers
📍 Sydney