Foxboro IA DCS Engineer

DCS Engineer    Reference:  TPS116
SALARY Negotiable   LOCATION Cork, Ireland
JOB TYPE Contract (12 months)   DATE POSTED 18/07/2019
INDUSTRY        
         
DESCRIPTION        
 

Client:  Provider of complete automation solutions for the process and manufacturing industry. Key emphases includes the design of control and process control systems and the vertical integration of these systems in the overall corporate process.

Industries: Automotive, Chemical, Pharmaceutical / Biotech, Food & beverages, Consumer goods, Oil & gas / Energy, Primary industry.

 

Role Requirements: The chosen candidate would typically be accountable for the following activities (but not exclusively);

  • Design, specification, programming and testing of control systems, Preferably Foxboro IA, other system experience considered e.g. Delta V, Allen Bradley Plant PAX, Siemens PLC), SCADA, Wonderware) and HMI.
  • Specification, design, development, and testing of industrial SCADA, DCS and PLC based applications, including S88 Batch, to meet customer requirements.
    Responsible for industrial automation/control system integration and related support systems such as Data Historian, EBR’s, Alarm Management, PI, etc.
  • Actively participate among cross-functional teams to ensure projects are delivered on time and to required quality standards.
    Knowledge and familiarity the development and execution of C&Q documents as well as CSV deliverables such as; Planning, User/Functional Requirements, Design Specifications, Design Qualification (DQ), testing development and execution (Loop Checks, ULT, ILT, SLT) and Final Reporting.
  • Knowledge of ISA’s S88 standard, pharmaceutical and biotechnology equipment and processes desired.
    Configuration/ coding experience with Foxboro I/A HLBC

 

Education: Bachelor’s degree in Engineering (preferably Electrical, Automation, Instrumentation or Chemical.Work Experience: From six (6) years up to ten (10) years of industrial automation experience. Industrial controls experience in the life sciences industries is preferred.

 

Required Soft Skills:

Excellent analytical and problem-solving skills to be applied programming and troubleshooting of process systems.

  • HLBC Coding experience on Foxboro IA
  • Deals well with uncertainty and pressure.
  • Works well with others, within a team and takes accountability.
  • Result driven and self-motivated.
  • Strong interpersonal and communication skills (verbal and presentation).
  • Organised, with strong computer literacy such as MS Project, Excel, etc.
  • Valid European Union work permits.

 

Get in touch with us for full brief on this position.

 

Charlie Burgess +442081236574 Agent UK & Ireland  

Automation Engineering Manager

 

Automation Manager    Reference:  TPS112
SALARY Negotiable   LOCATION Cork, Ireland
JOB TYPE Contract (10 – 12 months)   DATE POSTED 15/07/2019
INDUSTRY BioPharma      
         
DESCRIPTION        
 

Client: Provider of complete automation solutions for the process and manufacturing industry. Key emphases includes the design of control and process control systems and the vertical integration of these systems in the overall corporate process. End client – BioPharma manufacturer based in Cork.

 

Role Summary: The role would ideally suit an experienced controls engineer who has moved into the project management space and has a number of years’ experience in a highly regulated Pharma environment. Project is to upgrade a number of obsolete control systems on site.

 

Role Requirements: The chosen candidate would typically be accountable for the following activities (but not exclusively);

  • Engineering background and comfortable with the technical aspects of the project.
  • Previous experience with the upgrade of obsolete control systems.
  • Manage a cross functional diverse team to deliver against the project plan.
  • Manage the cost, schedule and resourcing elements of assigned projects.
  • Experienced in highly regulated pharma environments.
  • Create regular weekly and monthly reports.
  • Strong communication skills.
  • Ability to effectively communicate upwards and at peer level.
  • Excellent written communication skills.
  • Communicate effectively with vendors.
  • Highly organised
  • Maintain the project plan and risk register.
  • Manage a diverse group of vendors.
  • Capable of co-ordinating multiple vendors to tight timelines.

 

Get in touch with us for full brief on this position.

 

Charlie Burgess +442081236574 Agent UK & Ireland Specialist

Delta V Engineer

Delta V Engineer    Reference:  TPS113
SALARY €55,000 +   LOCATION Ireland, Cork
JOB TYPE Staff   DATE POSTED 08/07/2019
INDUSTRY Pharmaceutical      
         
DESCRIPTION        
 

Client: Provider of complete automation solutions for the process and manufacturing industry. Key emphases includes the design of control and process control systems and the vertical integration of these systems in the overall corporate process.

 

Role summary: Automation engineer/Senior Automation Engineer will be involved in the design, configuration, implementation, testing, commissioning and validation of Pharmaceuticals client projects as well as day-to-day support and maintenance of the client automation systems. The successful candidates would be required to have a minimum of 5+ years’ pharma/biotechnology and Emerson DeltaV DCS experience.

 

Role Requirements: The chosen candidate would typically be accountable for the following activities (but not exclusively);

  • Experience implementing Emerson DeltaV automation solutions for clients in the Pharmaceutical and/or Biotechnology industries.
  • Full Delta V upgrade experience.
  • Good knowledge of GAMP lifecycle and quality management processes employed in the pharmaceutical and biotechnology sectors.
  • Experience with design, development and testing of DeltaV DCS
  • Preparation of functional specification and design specification documentation, and testing of automation systems
  • Configuration and programming experience – CMs, EMs, Unit Classes, Recipes, Controllers and Graphics
  • Knowledge of virtualization is added advantage
  • Experience in supporting client/sites for NC, CAPA, Root cause analysis and automation Change control management
  • Good analytical & problem solving skills
  • Excellent communication skills
  • Must work well in a team environment
  • Self-starter who can get the job done despite obstacles
  • Requires a Bachelor’s degree or foreign equivalent in Chemical, Electrical or Bio-Process Engineering, or related field
  • Minimum of 3-8 years of progressive experience as an Automation Engineer, DCS Software Engineer or related occupation

 

Get in touch with us for full brief on this position.

 

Charlie Burgess +442081236574 Agent UK & Ireland  

CSV Engineer

CSV Engineer    Reference:  TPS085
SALARY Negotiable   LOCATION County Cork, Carringtohill
JOB TYPE Contract (12 months)   DATE POSTED 08/04/2019
INDUSTRY Medical Device and Equipment manufacturer      
DESCRIPTION        
Client; Medical Devise and Equipment manufacturing company.

Responsibilities

Development of Validation Plans, Installation Qualifications (IQs), Operational Qualifications (OQs) and Summary Reports.

  • Prepare, execute, document and report validation protocols in line with GMP’s and other regulatory requirements and standards.
  • Assure that all validation test procedures are in line with current technology, corporate and governmental regulations.
  • Ensure that the Validation Strategy meets the quality requirements of its customers and applicable regulations FDA, EU & International Standards
  • Review and Approve validation protocols and assessments from a quality system documentation perspective.
  • Liaise with Engineering / Automation and external vendors regarding equipment documentation, HDS, SDS, FDS, User Requirement Specifications (URS’s), and any other associated validation issues.
  • Participate and communicate as required in project activities.
  • Develop procedures to manage computerised systems where required
  • Develop and present project plans to project management senior staff

Requirement

  • Bachelor of Science/Engineering degree or equivalent.
  • Knowledge of cGMP’s and other worldwide regulatory requirements.
  • Problem solving ability and excellent oral and written communications skills
  • Understanding of the computer system validation lifecycle

Preferred Qualifications

  • Candidates must have demonstrated experience in the delivery and management of IS / Automation systems in addition to a working knowledge of GAMP software development lifecycle, ANSI/ISA-S88 industry standards.
  • The successful candidate will have a least 3 years experience validating IS Automation systems for manufacturing organisations in the biotechnology or pharmaceutical industries.

 

Get in touch with us for full brief on this position.

 

Charlie Burgess +2081236574 Recruiter Agent in Automation UK & Ireland

Automation Engineer

Automation Engineer   Reference:  TPS082
SALARY Negotiable LOCATION Dublin, Ireland
JOB TYPE Contract (12 months) DATE POSTED 05/03/2019
INDUSTRY BioPharma
 
DESCRIPTION
 

Client; Supplier of Control Integration Services with 5 core focus area’s; Controls System Integration, Cyber Security for ICS, IOT, Functional Safety & 24/7 support.

 

End client; Pharmaceuticals corporation.

 

Responsibilities;

 

• Responsible for delivering automated solutions.

• Designing, coding and testing automation software solutions.

• Working closely with the Process Design Engineers and other project team members to meet key software delivery requirements and milestones.

• Design, develop and test software code in accordance with site coding standards and adherence to good engineering practice.

• Ability to read and understand P&IDs and Process Descriptions for various plants,       processes, and/or equipment.

• Design, program, implement, test and document process control applications.

• Understanding and implementing the validation life cycle for automated systems.

 

Qualifications;

 

• Degree qualified, experienced automation engineer with a minimum of 3 years experience.

• Knowledge of Siemens and/ or Rockwell automation platforms.

• Experience with automation system implementation and validation.

• Experience in some the following: Automation applications from Siemens S7, Rockwell and/or Wonderware, PLC Controls, Siemens and/or Allen Bradley, WinCC, PCS7.

• Experienced in all of the following project phases: Requirements documentation, detailed design generation, implementation, system integration, testing and on-site commissioning.

 

Get in touch with us for full brief on this position.

 

Charlie Burgess Recruiter 02081236574 Agent UK

CSV Engineer

CVS Engineer   Reference:  TPS081
SALARY Negotiable LOCATION Dublin, Ireland
JOB TYPE Contract DATE POSTED 04/03/2019
INDUSTRY BioPharma
 
DESCRIPTION
Client; Engineering company focused on Process Automation delivery of Process Automation Solutions to Global Brands. Distilleries | Breweries | Blending Plants | Food Production | BioPharma.

End client; BioPharma corporation.

Responsibilities

Development of Validation Plans, Installation Qualifications (IQs), Operational Qualifications (OQs) and Summary Reports.

  • Prepare, execute, document and report validation protocols in line with GMP’s and other regulatory requirements and standards.
  • Assure that all validation test procedures are in line with current technology, corporate and governmental regulations.
  • Ensure that the Validation Strategy meets the quality requirements of its customers and applicable regulations FDA, EU & International Standards
  • Review and Approve validation protocols and assessments from a quality system documentation perspective.
  • Liaise with Engineering / Automation and external vendors regarding equipment documentation, HDS, SDS, FDS, User Requirement Specifications (URS’s), and any other associated validation issues.
  • Participate and communicate as required in project activities.
  • Develop procedures to manage computerised systems where required
  • Develop and present project plans to project management senior staff

Requirement

  • Bachelor of Science/Engineering degree or equivalent.
  • Knowledge of cGMP’s and other worldwide regulatory requirements.
  • Problem solving ability and excellent oral and written communications skills
  • Understanding of the computer system validation lifecycle

Preferred Qualifications

  • Candidates must have demonstrated experience in the delivery and management of IS / Automation systems in addition to a working knowledge of GAMP software development lifecycle, ANSI/ISA-S88 industry standards.
  • The successful candidate will have a least 3 years experience validating IS Automation systems for manufacturing organisations in the biotechnology or pharmaceutical industries.

 

Get in touch with us for full brief on this position.

 

Charlie Burgess Recruiter 02081236574 Agent UK

 

Support Automation Engineer

Support Automation Engineer    Reference:   TPS079
SALARY Negotiable   LOCATION Dublin, Ireland
JOB TYPE Shift based contract (12 months)   DATE POSTED 19/02/2019
INDUSTRY BioPharma      
         
DESCRIPTION        
Client; Engineering company focused on Process Automation delivery of Process Automation Solutions to Global Brands. Distilleries | Breweries | Blending Plants | Food Production | BioPharma.

End client; BioPharmacuticals corporation.

Requirements

  • Packaging technician / FLS automation resource
  • Shift based assignment
  • 5 + years’ experience supporting the automation aspects of Packaging Equipment.
  • Experience in Siemens PLC/ HMI, Elau, Systech and Packaging Equipment including knowledge of OSIsoft PI Data Historian
  • Excellent control systems automation background and proven ability to support several automated control systems, preferably with Packaging OEM equipment
  • Strong network architecture or engineering proficiencies including TCP/IP, Routing, Switching, Network IDS/IPS.
  • Independent, self-motivated, organised, able to multi-task in demanding environments and skilled in communication and collaboration
  • Team player, prepared to work in and embrace a team-based culture that relies on collaboration for effective decision-making
  • Shift Rota – 7am to 2pm and 2pm to 10pm (Mon to Fri)

 

Get in touch with us for full brief on this position.

 

Charlie Burgess Recruiter 02081236574 Agent UK