|Senior Software Engineer||Reference: TPS036|
|SALARY||£40,000 – £55,000||LOCATION||Kent, United Kingdom|
|JOB TYPE||Permanent||DATE POSTED||05/03/2018|
Main Responsibilities of a Senior Software Engineer:
Required Skills and Experience:
|Software Developer||Reference: TPS036|
|JOB TYPE||Permanent||DATE POSTED||05/03/2018|
|Responsibilities and Duties
Qualifications and Skills
|Instrumentation Engineer||Reference: TPS035|
|JOB TYPE||Contract (3 months)||DATE POSTED||26/02/2018|
|Instrumentation Engineer required for 3 month project engagement in Finland. Responsible for supervision, factory collaboration, validation and documentation on Power Generation plant.
|Automation Engineer||Reference: TPS034|
|JOB TYPE||Contract 6 months||DATE POSTED||20/02/2018|
We are recruiting for an Automation Engineer to join a leading SI, operating pharmaceutical project engagements in Ireland. Candidate must be available on short notice, open to 6 months in duration with the necessary experience;
– Siemens PLC programming experience (S7)
– SCADA experience with preference for iFix
– Pharmaceutical Documentation – FAT / SAT
– Coordination with Vendors
|Senior Scientist (Pharmaceutical)||Reference: TPS033|
|JOB TYPE||Contract (12 months)||DATE POSTED||14/02/2018|
|“Client” is an international leading diversified healthcare company, coming from different fields, different generations, but all driven by a single purpose: translating science into lasting contributions to health. The Pharmaceuticals Division helps treat some of the most pervasive and persistent health conditions around the world, providing access to some of the most trusted and proven medicines to those who need them most.
“Client” generates over 250 pharmaceutical products of which the top 20-30 products are centrally supported by the Science and Technology organisation to maximise their growth by making use of advanced knowledge in science and technology and product expertise in a cross collaborative working model.
This group is tasked with globally facilitating operational excellence and compliance on Pharmaceutical products, reducing operational costs, guaranteeing reliable supply and customer service in changing conditions, and joining forces with the Development department for innovative improvements.
The responsible applicant will maximise product quality in an efficient and timely manner, working in close collaboration with the manufacturing, Quality, supply chain and Analytical Science & Technology.
Position is a travel based contract engagement.
12 month duration with possible extension.
Based in Holland with travel 1-2 months on average.
Good command of English, Dutch highly desirable.
|WinCC OA Specialist||Reference: TPS036|
|JOB TYPE||Contract (12 months)||DATE POSTED||07/02/2018|
|INDUSTRY||Building Management Systems|
Development of complex / decentral WinCC OA (PVSS II) Systems
Development of Frameworks, Libraries and project specific WinCC OA designs
|Automation Engineer||Reference: TPS035|
|JOB TYPE||Contract (12 months)||DATE POSTED||25/01/2018|
TPS are supporting a Systems Integrator in their on-going delivery of Automation services in the end-client space (an aseptic drug product operations facility, specialising in secondary manufacturing activities Formulation, Vial/Syringe Filling, Lyophilisation and Packaging).
|Senior Process Engineer||Reference: TPS034|
|SALARY||All inclusive Hourly rate||LOCATION||Netherlands|
|JOB TYPE||Contract (6 months)||DATE POSTED||17/01/2018|
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:
|CSV Consultant||Reference: TPS032|
|JOB TYPE||Contract (12 months)||DATE POSTED||16/01/2018|
|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.
Recruiting Consultant – Charlie Burgess – 0208 432 6080
|Automation Engineer||Reference: TPS031|
|SALARY||Negotiable||LOCATION||Ireland – Limerick / Waterford|
|JOB TYPE||Contract (6 months)||DATE POSTED||04/01/2018|
|INDUSTRY||Pharma / Food & Bev|
Our clients focus is in the Pharmaceutical; Biotech / Life Science; Healthcare; Food & Beverage and Micro-Electronics Sectors.
Platform(s): Siemens S7, Rockwell SCADA(s): Wonderware, Rockwell Factory Talk Years’ Experience required: 4+ years Language required: English
• At least 3 years’ experience in achieving or maintaining compliance for a process control system.
• Experience in the qualification of large scale Distributed Control Systems.
• Ability to keep work pace and meet deadlines. Good organising and planning skills.
• Proven success working well in a team environment with flexibility to react to changing business.
• Experience with qualification and configuration of DCS systems (Foxboro I/A, Rockwell, , Siemens, 800XA, etc)
• Knowledge of databases, data historians, reporting and analytic systems.
• Familiarity with system design lifecycle and all aspects of Pharmaceutical Industry GMP Regulations.
• Strong leadership and communication skills. Problem solver with a focus on achievement of overall project goals.