BrightOwl Loader Loading

QA Inspector Measham United Kingdom,  

DCC Vital (company)


Posted on : 03 June 2017

Project Description

Routine Activities in support of the above   
  • To follow QA procedures regarding all aspects of Good Manufacturing Practice (GMP) as defined by procedures 
  • To check, approve, or reject, and sign as appropriate, coded printed items for each batch of product for repackaging 
  • To check and approve, or reject or hold raw materials at the Goods-Inwards stage and to document findings 
  • To check and approve, if appropriate, area or machine clearances between production runs 
  • To carry out the required level of on-line Quality Assurance checks and record these accurately on the appropriate documentation 
  • To carry out checks on incoming goods (PI raw materials) including any componentry 
  • To assist the Qualified Person (QP) in the execution of their duties if asked to do so 
  • To make and retain Master Raw Materials Reference Samples when needed 
  • Liaise with Purchasing and Regulatory Affairs if an issue is identified with PI raw materials 
  • To review completed works order documentation prior to submission to the QP 
  • To bring any seen or suspected deviations from GMP to the attention of the QA Manager

   
  
Activities in support of the above  
  • To carry out the inspection and recommend the disposition of goods returned to Kent 
  • Archive PI and Generic Product Reference Samples 
  • Take part in housekeeping and self inspection audits of Units 100 and 200 
  • Assist in the preparation of samples and BPRs for the unit as appropriate               
  


Non Routine Duties and Responsibility 
To assist the warehouse and production staff in the event that help is needed, and as QA workload allows, as sanctioned by QA management 
  


Scope and Authority  
  • May suggest, but does not have the authority to change any processes described in SOPs or WIs (Standard Operating Procedures, Work Instructions) 
  • Has the authority to allow production to start production following the ratification of the defined job start-up checks 
  • Does not have the authority to authorise Production to continue on a works order if there is a GMP failure outstanding 
  • Has authority to suspend production runs if a problem is detected.  The QP is immediately to be informed and Production should not start again without the authorisation from the QP 
  • Has authority to recommend rejection, or the holding, of any material allocated for use in the PI Unit.  Final decision on rejection lies with the QP 
  • May liaise directly with the Production Staff, Production Manager, QP and Regulatory Affairs personnel  
  


Relationships   
  • Responsible to the QA Manager and Quality Operation Manager UK 
  • May liaise directly with PI Purchasing on matters relating to PI raw material 
  • May liaise with Athlone PI Regulatory on matters relating to PI raw materials 
  • Maintains information flow relating to challenges or system changes   
  • Affairs personnel. 
  • Has no authority to reprimand, discipline, suspend or dismiss any staff.  
  


Education/Background 
Educated to secondary school standard, GCSE or higher in English and Mathematics.  

  

Other Requirements
   
  • Physical good health record as some lifting work is essential 
  • Good oral/written communication skills 
  • Understand the importance of accuracy and flexibility 
  • Good numeric skills 
  • Good time keeping 
  • Computer literate 
  • Demonstrable keyboard skills 
  • Punctual, honest, reliable 
  • Polite and diplomatic 
  • Respectable appearance 
  • Neat and methodical worker 
  • Accept special assignments as necessary  
  

Locations

Measham Derbyshire DE12 7DT

Find a Job Find Candidates

Similar Jobs

More jobs from DCC Vital

Other jobs in United Kingdom

Other Jobs

Most Recent Searches

Most Famous Searches

You might also like