A leading Pharmaceutical / MedTech manufacturing company are seeking an experienced
Validation Engineer
to join their team on a
6-month contract
to support a
decommissioning project
at their Dublin site.
This role will be
heavily focused on validation documentation and reporting
, including the creation, execution, and completion of all required validation deliverables associated with equipment and/or system decommissioning in a regulated environment. The successful contractor will be comfortable working with a
high level of autonomy
and operating in a predominantly
onsite, days-based role
.
Key Responsibilities
* Support validation activities related to a
decommissioning project
* Author, review, and execute validation documentation, including but not limited to:
* Decommissioning plans and protocols
* Validation reports
* Risk assessments
* Traceability matrices
* Ensure all validation activities are compliant with
GMP and regulatory requirements
* Liaise with cross-functional teams (Engineering, QA, Manufacturing) as required
* Ensure documentation is completed accurately, on time, and to a high standard
* Provide validation input and technical expertise throughout the project lifecycle
Required Experience & Skills
* 4–5+ years' experience
working as a Validation Engineer
* Background in
Pharmaceutical, MedTech, or other highly regulated industries
* Previous experience supporting
decommissioning, equipment lifecycle, or similar validation projects
* Strong experience with
validation documentation and report writing
* Good understanding of
GMP, regulatory, and quality standards
* Ability to work independently with minimal supervision
* Strong attention to detail and documentation accuracy
Call Róisín Vaughan at, or email for more info.