Manufacturing Supervisor (Multidose Filling)


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https://www.teamhorizon.ie/job-search/1177-manufacturing-supervisor-multidose-filling/operations-manufacturing/mayo/job2024-02-28 09:36:321970-01-01Team Horizon
Job TypePermanent
AreaMayo, IrelandMayoIreland
SectorOperations & Manufacturing
Start Date
AdvertiserMary King
Job Ref1003181
Job Views375
Description
 

Team Horizon is seeking a Manufacturing Supervisor (Multidose Filling) for our client based in Mayo.As the new Operations Supervisor you will be responsible for the supervision and management of all aspects of Multi Dose Compounding, Filling, within the business unit to ensure cost, compliance, safety and customer requirements are met. You will also provide support to the operations manager in achieving their operational goals and objectives.

 

 

Why you should apply:



  • This is an excellent opportunity to join a world class manufacturing operation, with an outstanding track record of reliably delivering high-quality medicines to patients around the world suffering serious illnesses.


  • There is a strong culture of continuous improvement and innovation within the company to strive for solutions that improve health outcomes and dramatically improve people’s lives.


  • Our client is developing the capability to produce all its medicines, helping to ensure continuity of supply of our medicines as they expand internationally.


 

What you will be doing:



  • Lead, motivate and mentor your team to maximise their effectiveness by clearly communicating task details and goals to your team members, allowing them to work effectively


  • Maintain capacity in line with business needs including the recruitment and management of staff.


  • Hold 1:1 performance review meetings according to company policy


  • Ensure that customer orders and requirements are met/exceeded


  • Manage new product Implementation


  • Represent the company at client and regulatory meetings and audits.


  • Ensure all activities in the department are performed in accordance with GMP, relevant SOP’s and policies.


  • Participate in management activities within the operations group to ensure timely and appropriate availability of documentation, equipment and related activities


  • Organise and lead as appropriate cross functional and departmental meetings in an effort to improve efficiencies and effectiveness


  • Attend all meetings as required or arrange an appropriate deputy

     


 

What you need to apply:



  • 3rd Level Qualification in Science or Engineering


  • Minimum of 5 years’ experience in highly regulated Pharmaceutical industry


  • Excellent scientific skills/knowledge


  • Knowledge of aseptic technology is beneficial. 


  • Proven track record in direct people management


 

 
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