Quality Assurance Engineer Supervisor

The purpose of the position is to Lead Design Control Quality Engineering services for New Product Introductions at this Multinational Medical Device Manufacture.

 

Based on the West Coast of Ireland I am keen to speak with Qualified Candidates who are open to relocating for this challenging role.

 

ISS Ltd Recruitment Agency is also offering a relocation package (€) for Engineers who need to move to the area.

 

A Project Leadership role you will be a key part of the Quality Engineering Team ensuring that all New Product Introductions are Manufactured in-line with current best practice – APPLY TODAY

 

Quality Design Assurance Engineer / Quality Supervisor / Manufacturing Process Engineer / Design Engineer / Design Controls / Process Validation / Medical Device / GMP / ISO 13485 / Mayo /Ireland

 

Job Title: Design Assurance Quality Engineer Supervisor

Location: Co. Mayo, Ireland

Package:

• Full Time / Perm
• € – Basic (Dependent on Experience & Open to Negotiation)
• Annual Bonus
• Health Insurance
• Parking
• Canteen
• Paid Annual Leave
• Relocation Package (€)

 

Role:

 

The primary purpose of the Design Assurance Supervisor is to lead members of the Design Assurance team and support DA initiatives as required to maintain and continuously improve the DA function.

 

Duties:

• Supervise Associates within the Design Assurance team
• Resource planning, allocation, and monitoring on projects and initiatives
• Mentor DA team on projects and ensure completion per timelines & expectations
• Lead on DA issues raised by team members and escalate for resolution if required
• Drive Continuous improvement initiatives within the DA function
• Represent Design Assurance on project teams as required
• Support the internal and external audit program
• Complete assigned Impact Assessments within the Change Control system
• Support periodic review of assigned Design Control procedures
• Support the development of the strategic direction for the DA function
• Manage training plans for the team
• Complete Gap Assessments to new standards as required

 

Experience:

 

• Third Level Qualification in Engineering / Science Discipline
• 6-10 Years Previous Experience in a Quality / Manufacturing role within the Medical Device Sector
• Experience of Design controls / New Product Commercialization Projects
• Experience of Design History Files in a Medical Device Environment
• Experience in Statistical Analysis / Process Validation

 

Skills Matrix:

 

• Statistical Data Analysis
• ISO 13485
• FDA 21 CFR Regulations
• BS EN ISO 14971

 

If you would like to be considered for this fantastic opportunity, follow the links below and send me your CV.

 

Alternatively give me a call on 00353 (0) 87 25 35 247, Just ask for Patrick.

 

Key Words: Quality Design Assurance Engineer / Quality Supervisor / Manufacturing Process Engineer / Design Engineer / Design Controls / Process Validation / Medical Device / GMP / ISO 13485 / Mayo /Ireland

 

Independent Search Solutions (ISS Ltd) is as the name suggests an Independent Recruitment Agency that aims to treat all its applicants with the up-most respect and in a professional manner. With a Company code of practice in place, you can be assured that your details will not be shown to any of ISS Ltd’s clients without your consent.