Senior Software Engineer

Senior Software Engineer    Reference: TPS035  
SALARY €65 – €75 per hour LOCATION Netherlands, Rotterdam
JOB TYPE Contract (12 months) DATE POSTED 27/03/2018
INDUSTRY Infrastructure
 
DESCRIPTION
Function; Senior Software Engineer PLC / SCADA

  • Siemens S7 As Software Engineer PLC Siemens S7 you are responsible for the automation of traffic systems.
  • Preliminary design, detailed design and execution design including the accompanying documentation based on the specifications.
  • Translate the implementation design into software for Siemens PLC (S7) and SCADA (WinCC-OA) systems.
  • During the project you are responsible for the offsets with external suppliers and for the commissioning of the systems at the customer. In case of calamities and / or malfunctions of the installations, you are available for aftercare.

Tasks / activities

  • Engineering of automation in traffic systems.
  • Making a preliminary design, detailed design and execution design including documentation. Translating implementation design into software for Siemens PLC and SCADA systems. Commissioning of systems on location.
  • Providing aftercare.

Job requirements

  • At least a completed HBO study in Electrical Engineering or Industrial Automation.
  • Relevant experience in technical automation.
  • Knowledge of PLC and SCADA systems.
  • An advantage is knowledge of CCTV, Audio, Failsafe PLCs and networks.

 

 Recruiter Charlie Burgess 0208 432 6080
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Senior Process Engineer

Senior Process Engineer    Reference: TPS034  
SALARY All inclusive Hourly rate   LOCATION Netherlands
JOB TYPE Contract (6 months)   DATE POSTED 17/01/2018
INDUSTRY Biological  
         
DESCRIPTION        
 

Purpose of function:

As Process Engineer you will work in the industrial automation team. Together with your team you will be responsible for the further automation of existing production lines and the setting up and production of new ones.  Our clients has been one of the market leaders in producing (polio) vaccines from living viruses for decades and is continuously working on tightening our existing production process. In this role you become an integral part of this improvement process. This by further automating existing as well as designing and validating new production plants. Our systems are developed and managed as much as possible internally and built by external parties. You are the key pillar between external suppliers and internal production and maintenance departments, in addition you actively contribute to the company ambition:

Tasks and responsibilities:

  • The development and implementation of new production automation systems by: analysis, defining possible improvements, preliminary research and drawing up requirements for programs
  • Inform, advise and evaluate supplier plans
  • Setting up and managing test environments; preparation and execution of test procedures
  • 2nd line management of existing process automation systems; support production and maintenance during planned and unscheduled maintenance and breakdowns. Trouble shooting where necessary to solve problems in a team or in consultation with suppliers

Profile

  • Demonstrable HBO + work and thinking level
  • Relevant experience in a comparable role. Preferably gained in the bio-technology, food or pharmaceutical industry
  • Substantive know how to organise processes in a Controlled Production Manufacturing environment.
  • Knowledge of control systems like PLC, PCS, DCS and SCADA. BBio uses Siemens S7, TIA Portal, PCS7 and Simatic Batch where possible.
  • Preferably knowledge of GMP and GaMP quality systems.
  • Good command (word and writing) of English.

 

       

CSV Consultant

CSV Consultant   Reference: TPS032  
SALARY Negotiable   LOCATION Netherlands
JOB TYPE Contract (12 months)   DATE POSTED 16/01/2018
INDUSTRY Pharmaceutical      
         
DESCRIPTION        
Validation Engineer IT

Purpose of the function:

The Validation Engineer IT is responsible for managing IT validations from start to finish (also often referred to as computerised system validation). For …………………. this concerns the validation of IT systems that are typical for pharmaceutical production companies, including ………………………………………. The so-called Process Control systems, such as SCADA systems that are used to control and monitor production lines, also belong to this category.

Main tasks and responsibilities:

Performing GMP impact assessments.
Ensure that the quality requirements from the regulations and …………… standards are translated correctly to the user requirements of a system. Consider requirements regarding Back-up & Restore, Incident Management, Disaster Recovery, Electronic Records and Electronic Signatures.
Determine and implement a validation approach for the system (including any interfaces).
Facilitating so-called Design Verification (or Design Qualification) sessions;
Managing the tests according to a structured and formally established procedure.
Assess and report the test results. Review deviations and corrective measures and coordinate possible re-tests.
Ensure that suppliers comply with Astellas standards for design, documentation and validation.

Professional profile:

Educational attainment
Minimum HBO level (or thinking level)
Knowledge of the formulation and packaging processes.
Preferably knowledge of Electronic Batch Records Systems, Laboratory Information Systems or systems that are comparable in terms of complexity and degree of integration.
Knowledge of GMP regulations (Eudralex Volume 4, 21 CFR Parts 210, 211 and 11) and ISPE Good Practice Guides (GAMP5).
Knowledge of ICT and Industrial Automation.
Knowledge of System Life Cycle methodologies.
Competences Planning and organizing.
Analytical skills.
Quality-oriented and accurate work.
Excellent communication skills in word and writing both in English and in Dutch.
Experience
Minimum 5 years experience in the pharmaceutical or medical device industry or laboratory.
Minimum 3 years experience with the validation of computer systems in the aforementioned industries.
Experience with the validation of an Electronic Batch Records Systems, Laboratory Information Systems or systems that are comparable in terms of complexity and degree of integration.
Experience with System Life Cycle methodologies.

Recruiting Consultant – Charlie Burgess – 0208 432 6080

 

 

 

       

3 x (EPLAN) Senior Hardware Engineers

3 x SENIOR HARDWARE ENGINEERS   Reference: TPS013  
SALARY Negotiable LOCATION Netherlands
JOB TYPE Permanent DATE POSTED 10/05/2017
INDUSTRY Process
 
DESCRIPTION
Responsibilities:As a Senior Engineer you have your own vision, you are firmly in your shoes, you are a real team player and have a coaching style of leadership. In addition, you are able to set priorities and anticipate unexpected situations within a hectic environment. My client provides a challenging work environment, giving you plenty of space and freedom to bring projects in various industries to a good end.

Tasks and responsibilities:

•    You are responsible for the technical and organisational coordination and management of the hardware engineering department.

•    You are the link between engineering and project management, provides structure and performs far-reaching standardisation, bringing the department to a higher level.

•    In consultation with the project managers, you make efficient planning, you distribute the projects and make the engineers responsible for the work delivered.

•    Your hardware talent will also assist you in the execution of your own projects, including the design of industrial controls.

 

Principal Automation Engineer

PRINCIPAL AUTOMATION ENGINEER   Reference: TPS012  
SALARY Negotiable   LOCATION Rotterdam – Netherlands
JOB TYPE Permanent   DATE POSTED 26/04/2017
INDUSTRY Process      
         
DESCRIPTION        
Responsibilities: 

·         Simatic Batch & Route Control experience in the process industry. Execute projects whilst mentoring mid-level Engineers.

 

Get in touch for a full brief on position.