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PROCESS AUTOMATION ENGINEER

 

Job Reference Number

13786280

Client ID:

RI/EM10522

Posted On:

Aug 3 2009

Location:

WESTMEATH

Job Type:

Permanent

Salary:

NEGOTIABLE

Benefits:

  • TRAINING / EDUCATION
  • CAR PARKING
  • PENSION / PRSA
  • VHI
  • PAID HOLIDAYS
Process Automation Engineer with 3-5yrs experience in automation/medical device industry required for permanent role in Athlone.

Reports To: Engineering Manager or designate

Purpose of Job:

To work within a group of Process Automation Engineers to provide support and ongoing
development to a high speed automated production line in a clean room environment.

Responsibilities:

  • Preparing and executing engineering programmes associated with the development of new automated manufacturing processes. This involves new process, scale-up, optimisation and troubleshooting. Analyse the process and analytical data generated by these programmes and report on same.
  • Equipment specification, design, procurement, installation, commissioning, modification and validation.
  • Ensuring compliance with safety, environmental and quality statutory and regulatory
    requirements. Ensuring compliance with internal company policies/procedures.
  • Preparation of technical documentation such as standard operating procedures, safety
    programmes, validation protocols, technical reports, engineering calculations, change
    controls and other documentation as required.
  • Present, where appropriate, technical data to internal/external audit and inspection groups (including IMB & FDA) and commercial partners.
  • To troubleshoot process materials and equipment related problems.
  • To ensure that all manufacturing work steps are accurately reflected in the relevant documentation.
  • To establish the most effective, reliable and cost effective processing methods for manufacturing operations.
  • To provide systems support for product lines in the areas of validations, PM's engineering spares and calibration systems.
  • Assist in training of manufacturing personnel on introduction of new equipment and processes.
  • To co-ordinate specific projects as designated.
  • To prepare technical documentation such as standard operating procedures, safety programmes, validation protocols, technical reports, engineering calculations, change controls and other documentation as required.
  • To provide technical leadership for operations personnel involved in process engineering and development activities.
  • To present, where appropriate, technical data to internal / external audit and inspection groups as required.

Requirements:

  • Minimum of Degree in relevant engineering discipline.
  • Have a minimum of 3-5 years' experience in automation/medical device or similar industry
    with an established track record.
  • Established knowledge of GMP and safety standards applicable to a clean-room/controlled environment and associated manufacturing processes and procedures.
  • Ability to share technical expertise with colleagues i.e. able to express information clearly and concisely both verbally and in written format.
  • Good problem solving abilities – able to identify facts, consider a number of alternative approaches and evaluate the most appropriate course of action.
  • Team and results orientated - committed and energetic approach to work with positive attitude.
  • Proven reliability – efficient, results-orientated and manages own time well.
  • Ability to deal effectively with all employees and external business contacts while conveying a positive, service-oriented attitude.
  • Strong computer skills
  • Six Sigma/lean expertises demonstrated in the manufacturing and design of new products is highly desired.
  • Good interpersonal and communication skills.
  • Ability to work to tight project timelines and within approved budgets.
  • Excellent use of initiative and adaptable to changing priorities.
  • Proven track record in your current role is essential.


Please forward cv to Emer.Moore@icds.ie or call Emer Moore on 057-9352468