Automation Engineering Manager

 

Automation Manager    Reference:  TPS112
SALARY Negotiable   LOCATION Cork, Ireland
JOB TYPE Contract (10 – 12 months)   DATE POSTED 15/07/2019
INDUSTRY BioPharma      
         
DESCRIPTION        
 

Client: Provider of complete automation solutions for the process and manufacturing industry. Key emphases includes the design of control and process control systems and the vertical integration of these systems in the overall corporate process. End client – BioPharma manufacturer based in Cork.

 

Role Summary: The role would ideally suit an experienced controls engineer who has moved into the project management space and has a number of years’ experience in a highly regulated Pharma environment. Project is to upgrade a number of obsolete control systems on site.

 

Role Requirements: The chosen candidate would typically be accountable for the following activities (but not exclusively);

  • Engineering background and comfortable with the technical aspects of the project.
  • Previous experience with the upgrade of obsolete control systems.
  • Manage a cross functional diverse team to deliver against the project plan.
  • Manage the cost, schedule and resourcing elements of assigned projects.
  • Experienced in highly regulated pharma environments.
  • Create regular weekly and monthly reports.
  • Strong communication skills.
  • Ability to effectively communicate upwards and at peer level.
  • Excellent written communication skills.
  • Communicate effectively with vendors.
  • Highly organised
  • Maintain the project plan and risk register.
  • Manage a diverse group of vendors.
  • Capable of co-ordinating multiple vendors to tight timelines.

 

Get in touch with us for full brief on this position.

 

Charlie Burgess +442081236574 Agent UK & Ireland Specialist

Delta V Engineer

Delta V Engineer    Reference:  TPS113
SALARY €55,000 +   LOCATION Ireland, Cork
JOB TYPE Staff   DATE POSTED 08/07/2019
INDUSTRY Pharmaceutical      
         
DESCRIPTION        
 

Client: Provider of complete automation solutions for the process and manufacturing industry. Key emphases includes the design of control and process control systems and the vertical integration of these systems in the overall corporate process.

 

Role summary: Automation engineer/Senior Automation Engineer will be involved in the design, configuration, implementation, testing, commissioning and validation of Pharmaceuticals client projects as well as day-to-day support and maintenance of the client automation systems. The successful candidates would be required to have a minimum of 5+ years’ pharma/biotechnology and Emerson DeltaV DCS experience.

 

Role Requirements: The chosen candidate would typically be accountable for the following activities (but not exclusively);

  • Experience implementing Emerson DeltaV automation solutions for clients in the Pharmaceutical and/or Biotechnology industries.
  • Full Delta V upgrade experience.
  • Good knowledge of GAMP lifecycle and quality management processes employed in the pharmaceutical and biotechnology sectors.
  • Experience with design, development and testing of DeltaV DCS
  • Preparation of functional specification and design specification documentation, and testing of automation systems
  • Configuration and programming experience – CMs, EMs, Unit Classes, Recipes, Controllers and Graphics
  • Knowledge of virtualization is added advantage
  • Experience in supporting client/sites for NC, CAPA, Root cause analysis and automation Change control management
  • Good analytical & problem solving skills
  • Excellent communication skills
  • Must work well in a team environment
  • Self-starter who can get the job done despite obstacles
  • Requires a Bachelor’s degree or foreign equivalent in Chemical, Electrical or Bio-Process Engineering, or related field
  • Minimum of 3-8 years of progressive experience as an Automation Engineer, DCS Software Engineer or related occupation

 

Get in touch with us for full brief on this position.

 

Charlie Burgess +442081236574 Agent UK & Ireland  

Automation Engineer

Senior Automation Engineer    Reference:  TPS111
SALARY Up to €65,000   LOCATION Cork, Ireland
JOB TYPE Staff   DATE POSTED 02/07/2019
INDUSTRY Pharmaceutical      
         
DESCRIPTION        
 

Client: Medical technology company, providing medical imaging, software & IT, patient monitoring and diagnostics to drug discovery, biopharmaceutical manufacturing technologies and performance improvement solutions.

Location: Carrigtohill

 

Role Summary: This position will be part of the Automation / IT Team and be responsible for the Design, Maintenance and management of all Automation systems onsite. The Automation Engineer reports to the Automation Manager. The candidate will have knowledge and proficiency in the use of statistical analysis tools, continuous improvement methodologies, problem solving and applied engineering relating to control systems.

 

Role Requirement: The chosen candidate would typically be accountable for the following activities (but not exclusively);

  • Process improvement work to ensure operational and engineering targets are achieved in relation to output, quality, cost, and yield.
  • Ownership of issues in the operation control system field.
  • All design reviews associated with equipment purchases.
  • Project Management of small to medium sized site specific projects through conception, approval, planning, execution, and validation in all parts of the plant including Production and Packaging, Utilities, and Warehouse.
  • Continuous improvement programs and all performance improvement projects.
  • Designing, executing, implementing and directing engineering or process projects which significantly contribute to attaining high system performance.
  • Set up of specifications and standard procedures to align with industry standards.
  • Risk assessments and mitigation projects relating to system performance.
  • The development and execution of FAT, SAT and IOQ protocols in Ireland and abroad.
  • Representing manufacturing on site based teams involved in implementing new technology, products or business processes to the site.
  • Reviewing and approval of changes to operating procedures and the change control process relating to the system.
  • Working in a collaborative manner within the Process Teams structure and contributes to investigations, NC and CAPA closure.

 

Qualification Requirements

  • Advanced Degree in Engineering or Life Sciences or equivalent knowledge or experience.
  • Significant experience in engineering in biotech/pharmaceutical industry supporting manufacturing (quality, process development, manufacturing, clinical manufacturing.
  • Significant experience in executing engineering projects.
  • Experience in cGMP maintenance, operations or engineering.
  • Excellent verbal and written communication skills.
  • Very strong control system and automation skills.
  • Strong analytical problem solving skills.
  • Ability to understand and perform code changes on Siemens PLC and Rockwell PCS.

 

Get in touch with us for full brief on this position.

 

Charlie Burgess +442081236574 Agent UK & Ireland  

CSV Engineer

CSV Engineer    Reference:  TPS085
SALARY Negotiable   LOCATION County Cork, Carringtohill
JOB TYPE Contract (12 months)   DATE POSTED 08/04/2019
INDUSTRY Medical Device and Equipment manufacturer      
DESCRIPTION        
Client; Medical Devise and Equipment manufacturing company.

Responsibilities

Development of Validation Plans, Installation Qualifications (IQs), Operational Qualifications (OQs) and Summary Reports.

  • Prepare, execute, document and report validation protocols in line with GMP’s and other regulatory requirements and standards.
  • Assure that all validation test procedures are in line with current technology, corporate and governmental regulations.
  • Ensure that the Validation Strategy meets the quality requirements of its customers and applicable regulations FDA, EU & International Standards
  • Review and Approve validation protocols and assessments from a quality system documentation perspective.
  • Liaise with Engineering / Automation and external vendors regarding equipment documentation, HDS, SDS, FDS, User Requirement Specifications (URS’s), and any other associated validation issues.
  • Participate and communicate as required in project activities.
  • Develop procedures to manage computerised systems where required
  • Develop and present project plans to project management senior staff

Requirement

  • Bachelor of Science/Engineering degree or equivalent.
  • Knowledge of cGMP’s and other worldwide regulatory requirements.
  • Problem solving ability and excellent oral and written communications skills
  • Understanding of the computer system validation lifecycle

Preferred Qualifications

  • Candidates must have demonstrated experience in the delivery and management of IS / Automation systems in addition to a working knowledge of GAMP software development lifecycle, ANSI/ISA-S88 industry standards.
  • The successful candidate will have a least 3 years experience validating IS Automation systems for manufacturing organisations in the biotechnology or pharmaceutical industries.

 

Get in touch with us for full brief on this position.

 

Charlie Burgess +2081236574 Recruiter Agent in Automation UK & Ireland