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Projects and cqv engineer student

Bray
Takeda Pharmaceuticals
Cqv engineer
Posted: 18 October
Offer description

By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda's Privacy Notice and Terms of Use.
I further attest that all information I submit in my employment application is true to the best of my knowledge.
Job Description
JOB DESCRIPTION
JOB TITLE:
Project & Commissioning, Qualification, Validation Engineer Student
REPORTS TO:
Process Specialist and/or designee(s)
JOB PURPOSE:
To support and contribute to activities in the Project Engineering & Engineering Services (CQV) Departments.
This brief demands flexibility and cross-functional liaison and co-operation, combined with competent technical ability.
RESPONSIBILITIES:
Work with flexibility within the Project Engineering Department and in co-operation with other Departments.
Support the project engineering team throughout the project lifecycle taking ownership for specific components of the lifecycle.
Preparation of documentation as required during the project lifecycle
Hands on contractor management during projects implementation stage
Practical support of planning, execution and review of the projects planned to be undertaken during the annual maintenance shutdown event.
Regular reporting of activities to direct line manager and working closely with same to achieve targets / objectives throughout the internship
Develop and maintain a strong working relationship with all the departments' customers both internally and across the site.
Participate in Safety and Environmental training programmes and initiatives.
Adhere to safe working practices as set out by the Safety Statement and other company safety rules
Maintaining compliance with site procedures and policies
Support Validation Maintenance Activities
Qualifying equipment, critical systems (utilities), facilities, computerized manufacturing systems, cleaning processes and sterilization processes, as applicable
development of protocols, coordination of validation activities, qualification/validation execution, preparing final reports and assembly of final validation packages; generation of project plans.
Preparation, review and approve documentation for cGMP / Validation of the following:
Equipment, Facility, Utility
Manufacturing Process
Cleaning
Computerized Systems and Automation Packages
IT
Support Validation maintenance activities – Requalifications and Periodic Reviews – Equipment, Facilities and Utilities
GENERAL RESPONSIBILITIES:
Drive and promote the corporate values of Takeda-ism within the workplace.
Ensure timely completion of all SOPs, reading, training and assessment.
Other duties as required and directed by the relevant Manager or other Officer appointed by the Board of Directors.
EDUCATIONAL REQUIREMENTS:
Current participation in an Honors Engineering Degree (or higher), or related, discipline
RELEVANT EXPERIENCE:
Previous experience in an engineering role is advantageous
SKILLS/COMPETENCIES:
Excellent spoken and written English is essential.
Excellent communication and interpersonal skills.
Strong organizational skills.
Excellent attention to detail.
Ability to work under own initiative with some guidance.
Well Motivated.
Locations
Bray, Ireland
Worker Type
Employee
Worker Sub-Type
Paid Intern (Fixed Term) (Trainee)
Time Type
Full time

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