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Projects and cqv engineer student

Wicklow
Takeda Pharmaceuticals
Cqv engineer
€30,000 - €45,000 a year
Posted: 19 September
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:
*
o Equipment, Facility, Utility
o Manufacturing Process
o Cleaning
o Computerized Systems and Automation Packages
o 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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