Quality Engineer I (hybrid)
- Contract
- Good Manufacturing Practice (GMP)
- Ireland
This vacancy has now expired. Please see similar roles below...
Proclinical are recruiting for a Quality Engineer I to join a medical technology and devices organisation. This role is on a contract basis and is located in Galway with hybrid working available.
Please ensure that you are eligible for working in the location without any sponsorship or relocation assistance.
Responsibilities:
- Guarantee that corrective measures meet acceptable reliability standards, and that documentation is compliant with needs.
- Conduct calculations, data integrity checks, technical and record keeping tasks in compliance with company and regulatory policies and standards to meet quality and precision needs.
- You will adhere to all pertinent site wide processes and practices for safety & GMP.
- Contribute to root cause investigations and continuous improvement in daily actions, initiating suitable corrective actions and following through to execution.
- Assist the cross-functional teams in design protocols to guarantee that new products/product changes are adequately reviewed/tested to ensure compliance to all regulatory standards.
- Cooperate with engineering and manufacturing functions to assure quality standards are in place.
- Responsible for devising and executing strategies and processes for inspecting, testing and revieing the accuracy and precision of products and production equipment.
- Other duties may be assigned.
Key Skills and Requirements:
- Works well both independently as well as in a team under close supervision.
- Capable of resolving issues.
- Communication skills both verbally and in writing.
- Leadership skills and familiarity in a leadership role.
- Educated to a degree level in a relevant field with demonstrable work experience.
If you are having difficulty in applying or if you have any questions, please contact Numhom Sudsok at n.sudsok@proclinical.com.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
#QACompliance
Related jobs
US$100000 - US$120000 per annum
New Hampshire, USA
Are you passionate about quality and precision? Join our client as Director of Quality and help ensure top-tier standards every day.
Highly Competitive
Amsterdam, Nederland
Safeguarding clinical quality through precision, compliance, and unwavering attention to detail.
US$20 - US$23 per hour + Highly Competitive Salary
Philadelphia, USA
Proclinical is seeking an Inventory Control Specialist to support inventory accuracy and integrity within a facility.
Highly Competitive
Stein, Schweiz
Join a leading Swiss sterile manufacturing operation as a Sr. Quality Assurance Expert driving GMP excellence, operational partnership, and continuous quality improvement.
Highly Competitive
Philadelphia, USA
Drive the quality systems that keep GMP operations compliant, efficient, and audit‑ready.
Highly Competitive
Philadelphia, USA
Ensure GMP excellence by owning the accuracy, integrity, and compliance of critical quality documentation.
Highly Competitive
Waltham, USA
Keep quality on track and inspection‑ready by owning the systems that keep operations running smoothly.
Highly Competitive
Birmingham, USA
Be the quality gatekeeper who keeps patients safe and products flawless.
Highly Competitive
Rockville, USA
Step into a role where precision meets purpose-become a Materials Technician supporting essential pharma and respiratory operations
Highly Competitive
Liverpool, England
Are you passionate about quality and precision? Join our client in this Quality Assurance Representative and help ensure top-tier standards every day.