Similar posts
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
Highly Competitive Salary
Frankfurt am Main (60318), Germany
Leiter Methodenentwicklung (m/w/d)** | Dauerhaft | Biowissenschaften | Deutschland (Frankfurt am Main)
US$18 - US$22 per hour
Durham, USA
Are you looking to make an impact with your innovation? We are working with a well-established pharmaceutical company to recruit for a dedicated document controller.
Highly Competitive Salary
Basel, Switzerland
Proclinical is seeking a Supplier Lifecycle Management Specialist to support global vendor change notifications and ensure seamless coordination across multiple sites.
Highly Competitive
Visp, Switzerland
Step into a pivotal role at a global CMO and help shape the future of healthcare manufacturing.
Highly Competitive
Visp, Schweiz
Join a cutting-edge pharmaceutical team where your precision and passion for quality will help shape the future of life-saving medicines!
Highly Competitive
King of Prussia, USA
Proclinical is seeking a QC Environmental Monitoring Expert to support quality control operations in a GMP-regulated environment.
Highly Competitive
Jena, Germany
Proclinical sucht einen Abteilungsleiter (m/w/d) für den Bereich Qualifizierung zur Verstärkung des Teams unseres Kunden in Deutschland für eine Festanstellung.