BAS/EMS Engineer

Blackfield Associates

Boxmeer

Presencial

EUR 60.000 - 80.000

Tempo integral

Há 3 dias
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Resumo da vaga

Blackfield Associates is seeking a BAS/EMS Engineer for a 12-month contract in Boxmeer, Netherlands. You will develop and review SDLC deliverables and collaborate with vendors to define system architecture and control strategies.

The role requires a Bachelor's degree in engineering or life sciences, 3 years in a similar role, and fluent English. You will support FATs/SATs, commissioning, and handover, ensuring cGMP compliance and effective communication with stakeholders.

Qualificações

  • Bachelor’s degree in engineering or related field.
  • 3+ years in BAS/EMS or pharmaceutical environment.
  • Fluent in English, both speaking and writing.
  • Experience with Siemens Desigo CC/WinCC/Insight, Xworks, and PX controllers.
  • Knowledge of HVAC controls and utility systems is a plus.

Responsabilidades

  • Develop and review SDLC deliverables in line with project standards.
  • Collaborate with BAS/EMS vendor on architecture, controls strategies, sequences.
  • Ensure compliance with cGMP and quality standards.
  • Participate in FATs/SATs, commissioning and handover activities.
  • Support project schedules and document trackers.
  • Attend and support project meetings; liaise with stakeholders.

Conhecimentos

SDLC knowledge
Vendor coordination
cGMP compliance
Stakeholder communication
English fluency

Formação

Bachelor’s degree in Engineering or related

Ferramentas

Siemens Desigo CC
WinCC/Insight
Xworks
PX controllers

Descrição da vaga

BAS/EMS Engineer

Staff / Contract: Contract

Start Date: ASAP

Location: Boxmeer, Netherlands

Duration: 12 months +

Role Functions

  • Develop and/or review System Development Life Cycle (SDLC) deliverables, compliant with applicable project standards.
  • Work with BAS/EMS vendor in development of systems architecture, specifications, controls strategies, sequence of operations through all design stages.
  • Work closely with the DDQ function to ensure compliance with applicable Quality standards.
  • Participate in Hardware and Software FATs and SATs, commissioning and handover activities.
  • Provide input to the development of project schedules and document trackers.
  • Participate in, and support, relevant project meetings.
  • Liaise with stakeholders on the overall project to ensure clear communication between all parties.
  • Required to comply with Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good Manufacturing Practices (cGMP) in the performance of day-to-day activities and all applicable job functions.

Knowledge, Skills, Education & Location Requirements

  • Bachelor’s Degree in Engineering, Information Systems, Computer Science or Life Sciences.
  • Fluent in English, written and verbal.
  • Minimum of 3 years’ experience in a similar role, ideally in the Pharmaceutical industry.
  • Strong experience in one or all the following systems: Siemens Desigo CC/WinCC/Insight, Xworks and PX controllers.
  • Utility systems experience would be an advantage on Chilled water, Hot water and steam generation systems, and HVAC Control.
  • Technical proficiency on controls systems including familiarity with control panels, networking, panel/field wiring and PLC control systems, tuning and start-up control.
  • Excellent computer skills, proficient in the use of the following Microsoft tools: Excel, SharePoint, Word and PowerPoint.
  • Strong interpersonal and communication skills (verbal and written).
  • Relevant Computer Science or Engineering degree or equivalent.
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