Job Description
We are seeking a Quality Engineer to join one of Cork's reputable pharmaceutical companies as it expands its quality team.
This is a 12-month contract offering a competitive hourly rate, with exciting projects on the horizon as the company continues to grow.
Responsibilities
* Facilitate investigations and closure of batch-impacting deviations.
* Collaborate and contribute to investigations and CAPA closures.
* Work with cross-functional teams to address issues.
* Plan and execute projects, tracking progress against deadlines and reporting results.
* Support teams on systems such as Trackwise, Gensuite, and Veeva to ensure timely task completion.
* Support SOPs, documentation, and protocols.
* Review and approve changes to SOPs.
* Monitor and analyze quality and safety performance trends.
* Participate in internal and external audits.
* Prepare, execute, and approve project documentation.
* Contribute to continuous improvement projects.
* Manage multiple tasks effectively and meet critical deadlines.
Qualifications and Experience
* Degree in engineering (mechanical, electrical, process, or quality) or equivalent.
* Experience working in a GMP environment, preferably in quality engineering or a similar role.
* Experience generating validation protocols.
* Internal and/or regulatory audit experience.
* Project management experience.
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