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Thermo Fisher Scientific is hiring a

Plant Engineer II, Manufacturing Engineering

Naarden, Netherlands

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Fluctuating Temps hot/cold, Loud Noises (Equipment/Machinery), Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)

Job Description

Responsibilities

  • Proactively identify and solve electrical issues of the equipment in the manufacturing facility
  • Drive continuous improvement and operational excellence culture through self-detecting and self-correcting processes, systems and instilling strong ownership & accountability
  • Plan and complete preventive maintenance and calibration of electrical equipment
  • Plan and complete the replacement of outdated sensors and field I/O
  • Collaborate with collaborators to ensure seamless completion of tasks
  • Interact with installing contractors, maintain and adhere to PM schedule
  • Manage and deliver operational projects and continuous improvement projects
  • Assist in the development of requirements of new equipment, modifications, and projects that affect the manufacturing facility
  • Respond to utility and equipment related issues during production
  • Build and maintain relationships with other sites to develop and promote standard methodology.
  • Specify and implement modifications to improve operational performance and compliance
  • Collaborate closely with the maintenance team at the Naarden site to achieve or surpass the critical metrics.

Qualifications

  • MBO / poly technical education with a focus on electrical equipment, automation and maintenance
  • 5 years of experience in process automation
  • Proven ability to work both independently and collaboratively within a team
  • Demonstrated ability to simplify technical issues for team members without a technical background
  • Experience working in an ISO9001 or cGMP environment
  • Experience with SCADA or any other automation system would be a plus
  • Experience supporting pharmaceutical manufacturing processes within a regulated environment highly desired, however consideration to other regulated industries such as food and beverage, aviation, maritime, etc.
  • Ease of working with Microsoft Windows, Excel, PowerPoint
  • Applicants should possess a basic knowledge of cGMP standards, ISO standards, and industry engineering guidelines.
  • Working knowledge of equipment/hardware/software testing and associated protocols and lifecycle documentation would be a plus
  • Excellent communication skills in English, technical, organizational, and interpersonal skills are essential
  • Flexibility to accommodate to changing priorities and deadlines

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