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Senior IT Technical Architect

Reference ID : 0791MQ
Category :
  • Pharma / Biotech
Date Posted : Sep 17, 2018
Job Location
:
  • Leinster
- Dublin
Experience : 7+ years
Salary : Negotiable - DOE
Employment Type
:
Contract
Consultant
:
Michael McQuade
Contact Number : 086-0435195
Seeking a Senior IT Technical Architect for our clients biopharma facility in Dublin.

Principal Responsibilities

Senior IT Technical Architect 

This person will be primarily responsible for the delivery of new and updated integration functionalities for Manufacturing Information Systems for use in production. Also responsible for oversight on alignment of Manufacturing Information Systems with Global Operating Specifications. 

Key Duties 

  • Responsible for the development, configuration and testing for integration components of Master Batch Records (MBRs) from initial to final design. 
  • Responsible for leading integration development design reviews including liaising with Automation, Operations, Process Development, Validation and Quality functions. 
  • Responsible for any applicable equipment integration design, configuration and testing to allow MBR interaction with shop floor equipment and lab equipment for in-process testing. 
  • Responsible for liaising with Plant Support, System Owner and Operations teams regarding documentation changes in an effective and timely manner. 
  • Responsible for support and updates to Recipe Control system – an in-house online recipe management system.
  • Responsible for the MBR design oversight, support and ongoing development of the MES system. 
  • Responsible for training of Electronic Batch Record (EBR) designers and end-users on MES integration activities and development of job aids. 
  • Responsible for support and to assist in fast Manufacturing Execution System (MES) issue resolution where required and as directed by Operations leadership.
  • Responsible for the development, review and update MES Standard Operating Procedures and Design Specifications. 

Qualifications & Requirements

  • Degree-qualified in a relevant engineering discipline.
  • Working knowledge of drug product manufacturing and packaging in pharmaceutical/biotech industries or aseptic processing. 
  • Knowledge of regulation requirements (including cGMP, 21CFR Part11). 
  • Knowledge of Quality Systems (e.g. CCMS, EDMQ, NC/CAPA). 
  • MES experience with focus on workflow, S95 & S88 standards and integration from the control layer to MES in pharma & bio-pharma industries.
  • Strong capabilities in S95 level 2 and level 3 systems and their integration. 
  • Strong working knowledge of OLE for Process Control.
  • Experience of Supervisory Control and Data Acquisition (SCADA), Process Control Systems (PCS), Recipe Managers - Siemens, Rockwell, Kepware OPC Server, OSI Pi, RT Reports, OSI PI Asset Framework, Laboratory benchtop equipment, Learning Management Systems. 
  • Strong exposure to MES technologies, including automated data collection, historian applications (OSI PI), visualization, quality and efficiency in manufacturing. 
  • MES experience in implementing stable and scalable solutions for 
    o Continuous Data Retrieval from Level 2 and Level 3 systems 
    o Creation / Loading of Level 2 Recipes 
    o Retrieval of Alarms and Events (Batch Context Information) into MES for Annotation, Review and Trending. 

For further information please contact Mick on 086-0435195 or forward details in confidence to jobs@headcount.ie



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