Quality Control Officer - Night Shift
In order to support
growing demand, we are looking to recruit a Quality
Control Officer to strengthen and support the ‘Night
shift’ operations and to drive improvements in the
following key area’s:-
a)
Product Quality / Consistency
b)
Training / Training records
c)
Production Output / Efficiency
d)
Identification of improvement
opportunities / resolution of problems
In order to be
considered for this role you will need to be :-
a)
Quality conscious, competent and
hard working
b)
Aware of the Injection moulding
processes and common defect modes, with the ability to
use standard measuring equipment / gauges and accurately
document results.
c)
Motivated and capable of using
your initiative for routine decision making.
d)
Reliable with a good attendance /
timekeeping record
e)
Able to work as an individual or
as part of team
f)
Able to train and communicate
information to the Production / Quality Teams as well as
feedback information to Production / Quality Management.
If you feel you
have the necessary skills, experience and personal
qualities to make a significant contribution to
maintaining and improving quality and production
performance at Europlaz, please apply in writing to the
undersigned, with a summary of how you meet the
requirements and ideally an up to date C.V.
For more information or to apply for this position
please email your c.v. to
david.bacon@europlaz.co.uk.
Quality Engineer
Quality Engineer
required for a Specialist Medical Device Supplier.
Working closely
with the Production and Quality teams you will help to
develop and control both existing and new Systems,
Product and / or Processes within the business unit,
ensuring compliance with Business Objectives, Customer
requirements and specifications, as well as the relevant
Medical Device & Quality System regulations.
Essentially you will be involved in all aspects of the
Quality Operation including:
a)
Routine
Inspection and measurement
b)
New Product /
Process Introduction
c)
Process
Validation, Statistical Analysis & Capability Studies
d)
Generation
and maintenance of Quality Records, Work Instructions &
Procedures
e)
Product
/ Process Training & Training Record
f)
Internal
Auditing
g)
Liaising with
Customers / Customer Complaint Investigations &
reporting
h)
Root cause
Analysis / Corrective & Preventive Actions
i)
Implementation of Lean principles (Identification &
elimination of Waste)
j)
Implementation of Six Sigma principles (Identification &
elimination of Variation)
Ideally
you should have:
a)
Manufacturing
Engineering background (preferably within the Medical
Device and / or the Injection Moulding Industry).
b)
A working
knowledge of
the ISO 9001:2008, 13485:2003 standards and the Medical
Device Directive, with
previous experience of working in a quality role within
the Medical Devices or Injection Moulding Industry.
c)
Good IT
Skills using Microsoft Office
d)
Excellent
numerical reasoning skills
e)
Excellent
Team working, verbal and written communication skills
f)
Experience in
Product / Process validation, Statistical analysis and
process capability studies.
g)
A
qualification and experience in Internal Auditing
h)
A working
knowledge of Kaizen, Six Sigma, Lean, Problem solving,
Continuous Improvement methodologies, tools and
techniques.
If you feel you
have the necessary skills, experience and personal
qualities to make a significant contribution to
maintaining and improving quality and production
performance at Europlaz, please apply in writing to the
undersigned, with a summary of how you meet the
requirements and ideally an up to date C.V.
For more information or to apply for this position
please email your c.v. to
david.bacon@europlaz.co.uk.