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.

 

       
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Delta V Engineer

Delta V Engineer    Reference: TPS027  
SALARY £50,000 +   LOCATION United Kingdom
JOB TYPE Permanent   DATE POSTED 05/12/2017
INDUSTRY Process (Food & Pharma)      
Requirements  5 years AI

2 years Delta V

     
DESCRIPTION        
 

As a lead Automation Engineer you will be Reporting to the Lead Automation Commissioning Engineer, responsible for supporting CQV teams with Loop checking, troubleshooting devices on DeltaV, Fault finding, Commissioning and troubleshooting on the DeltaV software. PID Loop tuning is an important factor in the senior commissioning engineer’s role.

Requirements

  • 5 years’ Automation experience
  • DeltaV Experience 2 years
  • Knowledge of S88
  • Software design experience Base layer to Phase
  • English is of good work proficiency
  • Knowledge of GMP
  • Change management Experience
  • AMS experience
  • Loop checking
  • Minimum 3 years Commissioning experience in a plant

Desired experience:

  • Instrumentation electrical etc experience
  • Mynah VIM experience
  • Loop tuning PID tuning
  • Communication protocols Foundation fieldbus, Devicenet, Profibus and Modbus
  • Life science experience Minimum 2 years
  • HyperV

 

 

       

Controls Engineer

CONTROLS ENGINEER   Reference: TPS009  
SALARY Negotiable LOCATION Ireland (Waterford)
JOB TYPE 6 month contract DATE POSTED 13/03/2017
INDUSTRY Pharmaceutical
 
DESCRIPTION
Newly established client of TPS currently requires experienced Controls Engineers to engage on two separate projects in Ireland. The position is focused in the healthcare/nutrition space and will require you will have a minimum of 5 years’ experience working with validated Automation systems in the pharmaceutical manufacturing environment.

The suitable candidate for this position will be responsible for;

  • Development and implementation of software solutions through change control as required while understanding impact of actions to Manufacturing and Facilities equipment.
  • Ability to program, diagnose and troubleshoot Allen Bradley Rockwell PLC and HMI application for automated process equipment.
  • Provide technical and automation operational support to Engineering, Manufacturing, Validation and Facilities departments.

My client requests that your profile shows a good level of long-term commitment on previous contracts as this position will be 12 months rolling.

 

 

Controls Engineer

CONTROLS ENGINEER   Reference: TPS008  
SALARY Negotiable LOCATION Ireland (Limerick)
JOB TYPE 6 month contract DATE POSTED 13/03/2017
INDUSTRY Pharmaceutical
 
DESCRIPTION
Newly established client of TPS currently requires experienced Controls Engineers to engage on two separate projects in Ireland. The position is focused in the healthcare/nutrition space and will require you will have a minimum of 5 years’ experience working with validated Automation systems in the pharmaceutical manufacturing environment.

The suitable candidate for this position will be responsible for;

  • Development and implementation of software solutions through change control as required while understanding impact of actions to Manufacturing and Facilities equipment
  • Ability to program, diagnose and troubleshoot Allen Bradley Rockwell PLC and HMI application for automated process equipment.
  • Provide technical and automation operational support to Engineering, Manufacturing, Validation and Facilities departments.

 

 

Validation Engineer

VALIDATION ENGINEER   Reference: TPS004  
SALARY: Negotiable LOCATION: North West England
JOB TYPE: Permanent DATE POSTED: 01/03/2017
 
DESCRIPTION  INDUSTRY  Pharmaceutical
Responsibilities:

Leader in Industrial Automation requires a Validation Engineer who will be responsible for ensuring that all manufacturing processes, packing operations, equipment, cleaning, utilities/facilities, computer and analytical methods are fully validated to meet the expected and operational requirements and GMP regulatory requirements.

The suitable candidate must have at least 5 years’ experience in Validation (Computer System/Process/Project/Equipment/Cleaning etc.) within the Biotech/Med Device/ Pharmaceutical (FDA/MHRA regulated industries).