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  

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

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