Senior Quality Control Technician (Electronics/Medical)
Summary
We are looking for an experienced Quality Control Technician from the electronics/medical industry
 
Job Detail
Location:
Crawley
Salary/Pay:
13/hr
Job Type:
Permanent
Ref No:
RU/HR
 
Description

Major responsibilities:            

 

·         Perform incoming and in-process inspection of components and sub systems.

·         To liaise with vendors on product Quality matters working with them to implement solutions.

·         Maintain discrepancy reporting system.

·         To carry out process audits of the company’s vendors and take part in any required vendor training.

·         To perform in-process audits within the Company manufacturing operation.

·         Participate in the evaluation of Engineering Designs and first of Samples.

·         To assist in the qualification of new / modified processes.

·         To assist in the development of new system test facilities for use in house and at suppliers.

·         To take part in inspection planning activities.

 

·         To undertake supplier audits

 

·         To undertake quality system audits

 

Secondary Responsibility:

 

·         Perform calibration tasks.

·         Perform final product testing.

·         Support QA Engineers in projects

·         General Q.A. duties.

 
Required Qualifications and Experience

Education / Experience:        

 

  Education requirements:                     

NVQ level 3 or greater Apprentice Served in an Electronic Engineering discipline.  HND or equivalent qualification desirable.

 

To have worked in a manufacturing environment of complex electro/ mechanical assemblies

 
Required Skills

Knowledge:                            

 

Information Technology:                       Good computer skills. Working knowledge of Microsoft office, MRP and ERP systems, Mechanical inspection software e.g. Delcam

                                         

Business Procedures:                         Conversant with the practical requirements of FDA G.M.P. and ISO9001 ISO13485 and CFR 820 in the context of a manufacturing environment. 

Technical expertise:                            To have experience and qualifications in quality control / inspection work.

 

 

Skills:                                               Effective communication skills both written and spoken.

Ability to demonstrate proven competence in the defined responsibilities listed above.

Ability to analyse components, prepare reports with well reasoned conclusions, generate and implement action plans.

                                                          Ability to maintain complete and accurate records

 
 
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