(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  

Control Systems Engineer

Control Systems Engineer    Reference:  TPS113
SALARY Negotiable   LOCATION Ireland, Cork
JOB TYPE Staff   DATE POSTED 19/07/2019
INDUSTRY Materials Handling      
         
DESCRIPTION        
 

Client: Source provider of automated material handling solutions that drive fulfilment productivity for retailers, manufacturers and logistics providers through a broad portfolio of automation equipment, software, service and support.

 

Role Summary: Control Systems Engineer to aid the team that designs, develops and integrates highly complex software functions. You will be an active member of a team to achieve the completion of goals. You will also generate innovative solutions in work situations; trying different and novel ways to deal with problems and opportunities.

 

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

  • Act as technical interface with customers, establishing professional relationships to ensure that the project requirements are fully defined and agreed.
  • Ensure that required prerequisites (e.g. design inputs, tools, documentation, deliverables, schedule, and budget) are in place prior to commencing work.
  • Testing, verification, and validation of PLC Software
  • Test and Certification of PLC Software
  • PLC Software architecture and coding and Software development.
  • Ensure proper test plans (Internal, In-House, Site, Commissioning, and Acceptance) are crafted.
  • Bachelor’s degree in Engineering, or Similar qualification HNC, or HND
  • You will have working knowledge and experience with Siemens, Rockwell PLC’s
  • You will have understanding of the software development lifecycle
  • Effective communicator with the ability to convey subtle or complex messages clearly, as appropriate for the topic and audience
  • Can quickly analyse, incorporate and apply new information and concepts
  • Ability to consistently make timely decisions even in the face of complexity, balancing systematic analysis with decisiveness.
  • Materials handling sector experience

 

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

 

Charlie Burgess +44208123 6574 Agent UK & Ireland  

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

 

System Controls Engineer

System Controls Engineer   Reference: TPS080  
SALARY £60,000 +   LOCATION UK, Bracknell
JOB TYPE Permanent   DATE POSTED 04/03/2019
INDUSTRY Baggage Handling      
         
DESCRIPTION        
Client: leading provider of sophisticated automated material handling solutions for  retailers, manufacturers and logistics providers globally.

Responsibilities: Design, develop and integrate complex software functions within client’s established Automation department. You will be an active and integral member of a team to achieve the completion of set tasks. You will also generate innovative solutions in work situations to deal with problems and opportunities.

  • Testing, verification, and validation of PLC Software
  • Test and Certification of PLC Software
  • PLC Software architecture and coding
  • PLC Software development
  • Act as technical interface with customers, establishing professional relationships to ensure that the project requirements are fully defined and agreed.
  • Ensure that required prerequisites (e.g. design inputs, tools, documentation, deliverables, schedule, and budget) are in place prior to commencing work.
  • Shares technical knowledge with project team, supervisor, own discipline and other engineering disciplines.
  • Attend all project related turnover meetings and functional design reviews.
  • Design efforts in line with program requirements and standards.
  • Ensures proper test plans (Internal, In-House, Site, Commissioning, and Acceptance) are crafted.
  • Review and consult on open issues; assists with any customer customer concern.

Required

  • Bachelor’s degree in Engineering, or Similar qualification HNC, or HND.
  • Understanding various software development lifecycle.
  • Experience with Siemens, Rockwell PLC platforms.
  • Experience of working in the Automation industry.
  • Demonstrate the ability to develop efficient and high quality software.
  • You will have understanding of the software development lifecycle.
  • Effective communicator with the ability to convey subtle or complex messages clearly, as appropriate for the topic and audience.
  • Quickly analyse, incorporate and apply new information and concepts.
  • Experience in supervising, or working in a team of engineers
  • Materials handling sector experience

 

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

 

Charlie Burgess Recruiter 02081236574 Agent UK

QA Specialist

QA Specialist   Reference: TPS072  
SALARY Negotiable   LOCATION Cork, Ireland
JOB TYPE 12 – 18-month contract   DATE POSTED 24/01/2019
INDUSTRY Pharmaceutical      
         
DESCRIPTION        
Client; Engineering company providing automation solutions from 10+ location globally. It serves chemical, pharmaceutical/biotechnology, automotive, food and beverage, oil/gas, energy, water/wastewater, and other industries.  locations in Europe, North America, and Asia. As of August 31, 2014, Process Automation Solutions GmbH operates as a subsidiary of ATS Automation Tooling Systems Inc.

End Client; Pharmaceuticals

Job Title: QA Specialist. Report: Manager QA

Department: QA (QA Manufacturing and Engineering Support Team)

Requirement:

  • Acts as the day-to-day QA project contact person for the Manufacturing and Engineering departments providing guidance / feedback on quality issues related to their respective area project activities.
  • Completes the review/ approval of Manufacturing and Engineering project documentation – in particular equipment/ process/ automation validation documentation.
  • Performs a wide variety of activities to ensure compliance with applicable regulatory requirements.
  • Actively contributes to continuous improvement initiatives.
  • Builds and maintains good working relationships with Engineering, Manufacturing and
  • Quality department personnel in particular.
  • Supports the preparation for regulatory and customer GMP inspections of the site in addition to performing and co-ordinating internal audits.
  • May conduct or serve as a lead/coordinator of investigations and corrective and preventive action (CAPA) recommendations to ensure they are implemented and accurately documented in a timely manner.
  • Participates in developing Standard Operating Procedures (SOP’s) to ensure quality objectives are met.
  • Provides guidance and technical knowledge to more junior staff.
  • Participates in site cross-departmental teams as the GSIUC QA representative – Attending associated meetings ensuring QA is represented & its concerns/ issues communicated, aiding in the identification of potential improvements and participating in discussions on issues/ queries on the associated systems/process.
  • Assists with the maintenance of programs and processes to ensure high quality products and compliance with current Good Manufacturing Practices (cGMPs).
  • Ensures compliance with all site safety-related procedures and practices.

Key skills

  • Demonstrates proficient knowledge of FDA/EMA regulations, guidance and current Good Manufacturing Practices (GMPs).
  • Experience in the review/ approval of validation documentation essential.
    Demonstrates proficiency in MS Office applications (including Word, Excel and Power Point, Adobe, SharePoint) and ability to quickly learn new systems is required.
  • Demonstrates the ability to work effectively in a team environment, contributing to a positive and constructive attitude.
  • Demonstrates solid verbal, written, and interpersonal communication skills.
    Must be able to exercise judgment within generally well-defined and established procedures and practices to determine appropriate action(s).
    Demonstrates independent action and initiative in resolving issues.
    Demonstrates the ability to prioritise and meet deadlines.
    LEAN and Six Sigma philosophy are embedded in your day to day working.

Qualifications

  • Minimum of 6 years of relevant experience and a BSc.
  • Minimum of 4 years of relevant experience and a MSC.
  • Prior experience in a cGMP related industry is desirable, within Biopharmaceutical or Pharmaceutical industry preferred.
Charlie Burgess Recruiter 02081236574 Agent UK