- অভিজ্ঞতা
- 5–10 yrs
- বেতন
- —
- শূন্যপদ
- 1
- পোস্ট করা হয়েছে
- ১ ঘন্টা আগে
- Work mode
- অফিসে
- Eligibility
- Applicants with significant experience in pharmaceutical project delivery, especially those with CQV and installation/qualification expertise, are well suited for this role.
- Resume
- Required to apply
Where you'll work
কাজের বিবরণ
Role summary
An experienced Project Manager is needed to support a pharmaceutical initiative at a South Dublin facility. The assignment begins with the installation and qualification phase of an autoclave and the related clean utilities, and may later expand into wider site capital works.
Role overview
At the outset, you will work closely with the current lead and then assume full ownership of the project through to delivery. Since the work is already in the installation and CQV stage, prior hands-on experience in these phases is essential. There is also potential to move into additional engineering projects across the site in the longer term.
Key responsibilities
- Support the execution of an autoclave installation and qualification programme.
- Take over the project after handover and manage it through to closeout.
- Coordinate all project activities across installation, commissioning, and qualification.
- Drive CQV work, including the performance of IQ, OQ, and PQ protocols.
- Manage contractors and vendors working on site.
- Make sure all activities comply with GMP expectations and site procedures.
- Assist with project documentation such as URS documents, commissioning plans, and validation protocols.
- Work with Engineering, QA, Validation, and Operations stakeholders.
- Support future capital projects elsewhere on the site.
Requirements
- Between 5 and 10 years of experience in pharmaceutical project settings.
- Demonstrated CQV experience with direct execution of IQ/OQ/PQ.
- Proven background delivering work through installation and qualification stages.
- Experience with clean utility systems such as Pure Steam and Reverse Osmosis is strongly preferred.
- Exposure to autoclaves or other sterilisation systems would be an advantage.
- Solid knowledge of GMP-based manufacturing environments.
- Capability to work autonomously and take end-to-end ownership of delivery.
- Strong communication and stakeholder coordination abilities.
Additional information
This position is based on site in South Dublin, County Dublin, Ireland.
The role is a full-time position.
No salary or stipend details were provided.
No vacancy count, start date, application deadline, or duration were specified.