Overview
Location: Ballina.
Department: Quality.
Job Title
Senior Quality Engineer – 12 month contract
Job Summary
We are seeking a proactive and detail-oriented
Quality Compliance Engineer
to join our Quality Assurance team for a
12 month contract
.
This role is a critical technical position responsible for ensuring that all medical device manufacturing activities meet the latest global regulatory requirements, including
ISO
and the fully implemented
EU MDR
.
Your responsibilities will include completion of end-to-end
validation lifecycle (IQ/OQ/PQ)
, performing rigorous
risk assessments (pFMEAs)
, and supporting the
change control process
to maintain product integrity.
In addition, you will be a primary
Quality Liaison
for the production floor, supporting and driving root cause investigations and ensuring that manufacturing processes are stable, compliant, and ready for regulatory inspection.
Key Responsibilities
Product and Process Validation:
Develop, review, and execute validation protocols (IQ, OQ, PQ) for manufacturing equipment and processes to ensure high-degree assurance of product requirements.
Risk Management:
Lead and maintain risk management files, including pFMEAs ensuring that all potential failure modes are identified and mitigated.
Production Quality Support:
Provide real-time QA support to the operations team to address non-conformances, perform root cause analysis, and implement effective CAPAs (Corrective and Preventive Actions).
Audit Readiness:
Support internal and external audits by maintaining accurate documentation and ensuring all plant personnel follow cGMP requirements.
Statistical Analysis:
Apply statistical techniques and tools (e.g., Minitab) to analyze process data, identify trends, and support data-driven decision-making for process improvements.
Other duties as assigned
Qualifications
Required:
Bachelor's degree in Engineering (Biomedical, Mechanical, Electrical, or related field) or Life Sciences.
5+ years of experience in quality assurance or Validation in the medical device or a similarly regulated industry.
Solid understanding of ISO *****, EU MDR, ISO ***** and relevant medical device regulations.
Strong analytical and problem-solving skills; experience with root cause analysis tools (e.g., 5 Whys, Fishbone, FMEA).
Excellent written and verbal communication skills, especially in technical writing and documentation.
Proficient in data analysis tools such as Excel, Minitab, Power BI or similar.
Preferred
Certified Quality Engineer (ASQ CQE) or similar professional certification.
Certified Internal or Lead Auditor
Knowledge of EU MDR and international medical device regulations.
Six Sigma or Lean Certification is a plus.
Competencies
Strong attention to detail and commitment to quality.
Ability to manage multiple tasks and projects in a fast-paced environment.
Collaborative mindset with ability to work effectively across departments.
Self-motivated with a continuous improvement mindset.
About Hollister Incorporated
Hollister Incorporated is an independent, employee-owned company that develops, manufactures and markets healthcare products worldwide.
The company spearheads the advancement of innovative products for ostomy care, continence care and critical care, and also creates educational support materials for patients and healthcare professionals.
Headquartered in Libertyville, Illinois, Hollister has manufacturing and distribution centers on three continents and sells in nearly 80 countries.
Hollister is a wholly owned subsidiary of The Firm of John Dickinson Schneider, Inc., and is guided both by its Mission to make life more rewarding and dignified for people who use our products and services, as well as its Vision to grow and prosper as an independent, employee-owned company, and in the process, to become better human beings.
EOE Statement
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
Job Req ID:
*****
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