IRL - Project Scheduler - Normal

Johnson & Johnson Worksense (via Randstad Sourceright) is responsible for finding, engaging and contracting talent for the Johnson & Johnson contingent workforce.

Job Title: Project Scheduler  

Reports To: Project Controls Manager

We are currently recruiting a Project Scheduler to join our contingent workforce at the Vision Care site in Limerick. This position will initially be for 12 months.

The Role:

You will provide engineering support in developing project schedules for large Capital projects. You will join a team of schedulers and coordinators and you will report into the Project controls manager. 

Minimum Candidate Requirements:

• Project Schedule Development and Maintenance
• Perform project management tasks for large capital projects.
• Assist project managers with schedule planning, coordination of tasks, and monitoring the timelines of scheduled assignments.
• Support Quality Assessment on schedules.
• Ensure accuracy and consistency of the project schedules.
• Coordinating project timelines with internal departments and external stakeholders.
• Monitoring project timelines and deadlines.
• Identifying potential project schedule delays and facilitating intervention in a timely manner.
• Evaluating performance and preparing project schedule reports.
• Supporting updates and changes to project schedules.
• Recommending actions to keep projects within budget and completed on time.
• Keeping stakeholders & management informed of project timelines and deadlines.
• Documenting project scheduling processes and maintaining records.
• Actively interfacing with cross-functional team members, always practicing good teamwork in support of day to day operating requirements
• Assist and support to Projects Engineering Team as required

Other Relevant Information:

Essential:

• Hold a relevant degree or equivalent qualification in production, manufacturing or mechanical engineering.
• Project Management experience
• Experience in Microsoft Project

Desirable:

• 4 years’ experience in relevant engineering role
• Prior experience in a GMP or medical device manufacturing environment
• Prior experience in equipment and process validation activities
• Process development experience
• Familiar with ISO safety standards

Other Skills and Attributes:

• Develop good working relationships across the business
• Ability to motivate and lead - must be team orientated
• Ability to work on own initiative
• Good project management

In Return:

In return for this role you will receive a very competitive hourly rate. A minimum 12 month contract & an opportunity to work with a Global Leader within the Pharmaceutical sector, Johnson & Johnson.