Development Manager Manufacturing


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https://www.teamhorizon.ie/job-search/1362-development-manager-manufacturing/operations-manufacturing/dublin/job2024-06-20 16:13:391970-01-01Team Horizon
Job TypeContractorFixed Term
AreaDublin, IrelandRemote, IrelandDublinIreland
SectorOperations & Manufacturing
Start Date
AdvertiserMary King
Job Ref1003325
Job Views54
Description

Team Horizon is seeking a  Snr Associate Contract & Development Manager Manufacturing for our client based in Dublin however this role can be done remotely.


 


 


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 in Dublin, helping to ensure continuity of supply of our medicines as they expand internationally.


 


What you will be doing:



  • This position will report to the Contract & Development Manager Manufacturing. The ideal candidate will have previous experience in aseptic processing in a sterile manufacturing facility with cGMP and Quality System knowledge.

  • The candidate will have excellent troubleshooting skills using standard industry techniques

  • Position will be responsible for managing and executing nonconformance, CAPA, SICAR, Change Control and metrics oversight responsibilities for the External Supply organization

  • Determines situations which require escalation to management          

  • Communicate with all levels of the organization, facilitate development of solutions to critical business issues, and effectively define objectives to enable effective metric generation and reporting.

  • Facilitate daily scheduling meetings. Ensure current schedule is maintained, accurate, and up to

  • Be responsible for compiling, maintaining and reviewing all necessary reports

  • Assist, plan and implement continuous improvement ideas / opportunities

  •  Contribute and assist with Corporate, FDA, IMB Auditors and other regulatory bodies during company audits.

  • Complete any other duties as requested by Site Manufacturing Management.


 


What you need to apply:



  • Be a results-oriented person with excellent organizational, communicational and team development skills with an ability to successfully interact with people, create a team environment and generate co-operation

  • Demonstrated ability to deliver to team, site and personal objectives

  • Able to successfully manage workload to timelines       

  • Familiarity with basic project management tools        

  • Demonstrated understanding and use of RFT techniques and lean manufacturing concepts         

  • Strong ability to lead, challenge and positively influence in an interactive team environment       

  • Strong computer skills - knowledge Quality tracking system (QMTS).  

  • Master’s degree OR  Bachelor’s degree & 2 years of directly related experience

  •  2+ years of quality and manufacturing experience in biotech or pharmaceutical industry       

  • Understanding of the applicable manufacturing/testing processes (i.e. API, Drug Substance, Drug Product, Packaging, Device manufacturing processes


 


 

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