Job Description
We are seeking a Quality Engineer to join the team of a reputable pharmaceutical company in Cork. This is a 12-month contract with a competitive hourly rate.
The successful candidate will be responsible for facilitating investigations and closure of batch impacting deviations, collaborating with cross-functional teams to address issues, and planning and executing projects.
Responsibilities:
* Investigate and close batch impacting deviations.
* Collaborate on investigations and CAPA closures.
* Work with cross-functional teams to resolve issues.
* Plan and execute projects, tracking progress against deadlines.
* Support various teams on systems such as Trackwise, Gensuite, and Veeva.
* Support SOPs, documentation, and protocols.
* Review and approve changes to SOPs.
* Analyze quality and safety performance trends.
* Participate in internal and external audits.
* Prepare and execute project documentation.
* Assist in continuous improvement projects.
* Manage multiple tasks and meet critical deadlines.
Qualifications and Experience:
* Bachelor's degree in engineering (mechanical, electrical, process, or quality) or equivalent.
* Experience working in a GMP environment in a Quality Engineering role.
* Experience generating validation protocols.
* Experience with internal and/or regulatory audits.
* Project management experience.
Morgan McKinley acts as an employment agency and provides indicative pay rates.
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