Automation/ CSV Project Engineer - PSC

Wood is recruiting for Automation / CSV Project Engineers to support the delivery of engineering capital projects based at our client site in Barnard Castle on a contract (inside IR35) basis. 

This is a site-based position, working at the client's operating facility.

What we can offer

• Meaningful and interesting projects delivered to leaders of industry across renewables and emerging energy sectors 


• Commitment to Diversity and Inclusion; we are an organisation actively committed to diversity and inclusion across our business with employee networks committed to giving all employees a voice


• Global connections; join experts around the world who are at the leading edge of our industry, shaping the standards of our profession

Working on the below scopes for automation services: 

• M’ Building disinvestment


• M2 P2 various scopes


• S’ Building Filling and Assembly lines


• GSC & R&D BMS upgrades


• Smart manufacturing

Working on the below scopes for validation services:

• Work with end business users on development of user requirements and specifications.


• Approve technical design documentation supplied by vendors such as hardware/ Software / Functional Design Specifications.


• Identify and mitigate system risks through use of GSK Technical Risk Assessment process.


• Plan, develop and execute validation documentation including validation master plans, FAT/SAT documents, commissioning protocols, risk assessments, and summary reports as needed for multiple projects relating such as containment systems, roller compactors, film coaters and associated HVAC systems.


• Development and/or improvement of procedures, practices, and policies related to computer system validation of major equipment. Monitor and update the Validation Master Plan to ensure that it complies with appropriate regulatory guidelines and standard practices.


• Participate and set maintenance life plans relating to the computer systems associated with major equipment and HVAC systems.


• Utilise GSK electronic validation systems (KNEAT) to complete all validation activities.


• Act as a validation SME in different site projects, as required.


• Work collaboratively with business process owners, technical system owners, and QA validation as needed.


• Experience with Quality systems like Change control, CAPA, and deviations.

What makes you remarkable?  

• At Wood, we are committed to equal opportunities and welcome all talented individuals to consider joining our team. So even if you don't match every statement below but feel you have some of the experience, knowledge or skills needed for this role, we encourage you to apply. It will take all of us working together to deliver solutions to the world’s most critical challenges. 
  
   

Expected: 

• Degree in an appropriate discipline of Engineering or IT or HNC/D in an appropriate discipline 


• Previous site experience, working in an operational environment  


• Previous experience and competency in Automation and Control Engineering


• Previous experience in writing or modifying software


• Experience of implementing system modifications or modpacks


• A sound understanding of engineering practices, methodologies and economic principles, calculation methods, design details, international codes and standards, procedures, and specifications 


• Pharmaceutical Manufacturing and Computerised Systems and Validation


• Experience with ISPE GAMP Computer System Development Life cycle methodology


• Knowledge of Client Server environment, UNIX, NT, Windows, Data communications equipment (Routers, Switches, LAN/WAN, PLC)