Senior Systems Validation Engineer

Systems Validation Engineer   Reference:  TPS120
SALARY Negotiable   LOCATION Dublin (N/S), Ireland
JOB TYPE Contract (12 months)   DATE POSTED 12/08/2019
INDUSTRY        
         
DESCRIPTION        
 

Client: Leading Engineering company that provides Automation, Controls and Validation solutions to the Pharmaceutical/BioPharma/Medical Device manufacturing sector.

 

Role Summary: We currently require a Senior Systems Validation Lead/Engineer to join and take complete ownership to ensure conformance to quality systems, to liaise with various departments, and give guidance, review documentation and ensure the company validation policies & procedures are being adhered to.

 

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

  • Managing and co-ordinating the preparation, review and approval of the Validation Master Plans.
  • Managing and co-ordinating of all validation strategies and deliverables.
  • Development and maintenance of internal validation policies and procedures based on best international standards and practices.
  • Auditing of internal projects against internal validation policies and procedures.
  • Managing and co-ordinating the preparation, review and issuing of validation protocols and reports.
  • Managing and co-ordinating validation documentation including risk assessments, traceability matrices, and validation reports.
  • Managing and co-ordinating the review and approval of specifications associated with Equipment, Processes, Products and Computerised Systems.
  • Managing, co-ordinating and directing all validation and revalidation activities.
  • Reviewing, managing and approving change control forms for Validation/Compliance implications.
  • Managing and co-ordinating routine Internal Quality Audits of the facility to ensure compliance, be proactive in resolving issues which may arise
  • Updating existing quality documentation related to validation activities.
  • Identifying training requirements for project team members in support of validation.
  • Bachelor’s degree in Computer Science, Electrical Engineering, Systems Engineering, Technology or a related discipline.
  • Over 5 years’ experience as a Validation Engineer (mainly computer validation) in the Pharmaceutical or related Healthcare industry.
  • Experience of GxP Computerised Systems.
  • Industry knowledge of EU GMP (IMB/FDA), Annex 11 Computerised System Validation, ISO quality requirements.

 

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  

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  

Control Systems Engineer

Control Systems Engineer    Reference:  TPS090
SALARY £70,000   LOCATION Bracknell, UK
JOB TYPE Permanent   DATE POSTED 12/04/2019
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: 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.

 

Job Requirement

  • 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 Recruiter 02081236574 UK & Ireland Agent

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

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