CSV Engineer

CSV Engineer    Reference:   TPS121
SALARY Negotiable   LOCATION Grangecastle, Ireland
JOB TYPE Permanent   DATE POSTED 23/09/2019
INDUSTRY Pharmaceutical      
         
DESCRIPTION        
 

Client; Industry leading systems integrator for Automation Systems in the pharmaceutical, food & beverage, utilities, power and built environment markets.

 

Role Summary; CSV Engineer

 

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

Basic Qualifications: 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 5 years’ experience validating IS Automation systems for manufacturing organizations in the biotechnology or pharmaceutical industries.
• Candidates should have experience using a paperless validation system such as HP ALM.
• Experience in the validation of one or more of the following system types from project conception to delivery; DCS/SCADA/MES/Historian

 

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Charlie Burgess +442081236574 UK & Ireland Agency  

(Intermediate) Control Systems Engineer

Intermediate Control Systems  Engineer   Reference: TPS015  
SALARY Negotiable   LOCATION Dublin, Ireland
JOB TYPE Staff   DATE POSTED 12/08/2019
INDUSTRY Pharma/Bio      
         
DESCRIPTION        
 

Client: Engineering company offering controls, and validation solutions to manufacturing facilities across Ireland & Europe. Innovative approach to Automation, Involving in implementing Industry 4.0 and Smart Factory technologies. A rapidly growing, exciting, and fast-moving sector.

 

Role summary: As a Control Systems Engineer, your role will be the development, commissioning and support of automation and control systems. You will be responsible for automation and control systems design, specification, programming, simulation, testing and start-up assistance.

 

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

  • Software development of bespoke manufacturing systems.
  • Acquire a detailed understanding of the client’s automation systems (distributed control systems, programmable logic controllers, SCADA systems).
  • Ability to interact with the customers on technical requirements.
  • Ability to assess existing technologies and process.
  • Ability to design robust solutions.
  • Investigate and provide technical advice and support to manufacturing and other engineering disciplines on automation related issues.
  • Operate according to SOP’s developed for site engineering and maintenance.
  • Partner with different disciplines to deliver automation projects in accordance with GAMP guidelines.
  • Generate documentation and SOP’s associated with each of the Automation systems as required.

Proven experience with one or more of the following technologies will be an advantage:

  • Allen Bradley (Logix 5000)
  • Siemens (Step7)
  • Delta V DCS
  • MES
  • .Net, C#, Java, SQL (MS entity framework), Web Services (WCF), Azure DevOps:

 

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

 

Charlie Burgess +442081236574 Agent UK & Ireland  

Senior Controls Engineer

Senior Controls Engineer   Reference:  TPS120
SALARY Negotiable   LOCATION Dublin, Ireland
JOB TYPE Staff   DATE POSTED 08/08/2019
INDUSTRY Pharmaceutical

BioTech

     
         
DESCRIPTION        
 

Client: Engineering company offering controls, and validation solutions to manufacturing facilities across Ireland & Europe. Innovative approach to Automation, Involving in implementing Industry 4.0 and Smart Factory technologies. A rapidly growing, exciting, and fast-moving sector.

 

Role Summary: As a Senior Control Systems Engineer you will operate as an active member of the Engineering team and will have a responsibility to mentor more junior resources in the group based on your years of experience.

 

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

  • You will have an elevated position of authority as a Senior Engineer and will be required to give direction, inspiration and technical knowledge to fellow and junior resources.
  • Your role will involve the development, commissioning and support of automation, control systems and custom developed software programs.
  • You will be responsible for automation and control systems design, specification, programming, simulation, testing and start-up assistance.
  • You must possess the technical expertise to maintain, develop, troubleshoot and validate these systems in a compliant and competent manner
  • You will be required to self-manage agreed project goals and interact with the customer to achieve these goals
  • You should be at a sufficient level of expertise to take front line interactions with the customer for assigned project work and possess the ability to report to management on progress and any road blocks that present themselves over the course of your duties
  • You will also be required to manage the delivery of project development work and goals assigned to junior and fellow engineers if requested
  • You will require strong software development skills across multiple platforms to accommodate the vendor neutrality that currently exists. Over the course of the role you will be expected to specialise in a core group of platforms to be agreed with management and to become a system expert in those platforms for the overall group
  • You will be responsible for always representing the company in a positive light with potential and current customers and where possible interacting with the customer and management to potentially acquire and procure new work and new opportunities.
  • You will have demonstrated the ability to become a code designer in at least one software platform, i.e. Allen Bradley PLC, SQL
  • You must have proven experience in PLC logic and programming with one or more of the following PLC’s, programming languages or SCADA systems:

 

  • Allen Bradley (Logix 5000)
  • Siemens (Step7)
  • Elau
  • Bosch
  • Omron
  • Modicon
  • GE Fanuc
  • B&R
  • Mitsubishi
  • VB
  • SQL
  • Wonderware InTouch
  • RS View
  • Siemens
  • Labview
  • GE Cimplicity

 

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  

Automation Engineer

Senior Automation Engineer    Reference:  TPS111
SALARY Up to €65,000   LOCATION Cork, Ireland
JOB TYPE Staff   DATE POSTED 02/07/2019
INDUSTRY Pharmaceutical      
         
DESCRIPTION        
 

Client: Medical technology company, providing medical imaging, software & IT, patient monitoring and diagnostics to drug discovery, biopharmaceutical manufacturing technologies and performance improvement solutions.

Location: Carrigtohill

 

Role Summary: This position will be part of the Automation / IT Team and be responsible for the Design, Maintenance and management of all Automation systems onsite. The Automation Engineer reports to the Automation Manager. The candidate will have knowledge and proficiency in the use of statistical analysis tools, continuous improvement methodologies, problem solving and applied engineering relating to control systems.

 

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

  • Process improvement work to ensure operational and engineering targets are achieved in relation to output, quality, cost, and yield.
  • Ownership of issues in the operation control system field.
  • All design reviews associated with equipment purchases.
  • Project Management of small to medium sized site specific projects through conception, approval, planning, execution, and validation in all parts of the plant including Production and Packaging, Utilities, and Warehouse.
  • Continuous improvement programs and all performance improvement projects.
  • Designing, executing, implementing and directing engineering or process projects which significantly contribute to attaining high system performance.
  • Set up of specifications and standard procedures to align with industry standards.
  • Risk assessments and mitigation projects relating to system performance.
  • The development and execution of FAT, SAT and IOQ protocols in Ireland and abroad.
  • Representing manufacturing on site based teams involved in implementing new technology, products or business processes to the site.
  • Reviewing and approval of changes to operating procedures and the change control process relating to the system.
  • Working in a collaborative manner within the Process Teams structure and contributes to investigations, NC and CAPA closure.

 

Qualification Requirements

  • Advanced Degree in Engineering or Life Sciences or equivalent knowledge or experience.
  • Significant experience in engineering in biotech/pharmaceutical industry supporting manufacturing (quality, process development, manufacturing, clinical manufacturing.
  • Significant experience in executing engineering projects.
  • Experience in cGMP maintenance, operations or engineering.
  • Excellent verbal and written communication skills.
  • Very strong control system and automation skills.
  • Strong analytical problem solving skills.
  • Ability to understand and perform code changes on Siemens PLC and Rockwell PCS.

 

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

 

Charlie Burgess +442081236574 Agent UK & Ireland  

Delta V Engineer

Delta V Engineer    Reference:  TPS089
SALARY Negotiable   LOCATION Swords, Ireland
JOB TYPE Contract (12 months)   DATE POSTED 11/04/2019
INDUSTRY        
         
DESCRIPTION        
 

Client: Development and Manufacturing organisation actively operating a pharmaceutical ingredients manufacturing facility.

 

Role: Senior Automation Engineer ( Delta V DCS) required to join department to aid in designing and implementation of automation programs for large-scale biologics manufacturing facility in Dublin North.

 

Job Responsibilities

  • Senior Automation Engineer will join the automation site sustaining team
  • Work on DeltaV software and hardware.
  • All software must be fully compliant with S88 standards.
  • Supporting of PLC systems and interfacing with the primary DCS system
  • Generate, Review and approve design and test documentation.
  • The Automation Engineers will also co-ordinate the development of the Automation software and hardware to ensure alignment with the suite requirements
  • Works closely together with the other Automation Engineers to ensure deliverables are ready in time for the different milestones and projects.
  • Knowledge of Siemens and/ or Rockwell automation platforms.
  • Experience with automation system implementation and validation.
  • Experience in some the following: Automation applications from Delta V, Siemens S7, Rockwell and/or Wonderware, PLC Controls, Siemens and/or Allen Bradley, WinCC, PCS7.

 

Education & Experience Requirements

  • 2-3+ Years DeltaV design, configuration and testing a requirement
  • Allen Bradley, Siemens experience an advantage
  • Candidate should be a self-starter and take ownership of workload
  • Excellent communication Skills
  • She/he should work well in a team environment
  • Certified completion DeltaV DCS training

 

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

 

Charlie Burgess Recruiter 02081236574 Agent UK & Ireland

Control Systems Engineer

Control Systems Engineer   Reference:  TPS088
SALARY €55,000 – €60,000   LOCATION Carrigtohill, Ireland
JOB TYPE Permanent   DATE POSTED 11/04/2019
INDUSTRY Utilities      
         
DESCRIPTION        
Client: Private Industrial Automation Solutions provider, focused in delivering business Process Control Systems & MES Systems for Pharma, Food & Beverages & Manufacturing Customers in Ireland & the UK.

 

Role: Automation Engineer experienced in Siemens and/ or Allen Bradley automation platforms. The role is based in Cork. The company offer a very competitive salary along with exposure of working on some interesting projects across a range of industries including Food and Beverage, Pharmaceutical, Power and Utilities and Transport Infrastructure.

 

Job 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 UK & Ireland Agent

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