Compliance Engineer will support the Engineering Team in this busy Pharmaceutical company.
Hybrid option available after initial period of time.
Will suit someone with a background in Quality Assurance, Audit readiness and preparation.
Responsibilities
* Direct and lead deviations, out of tolerance conditions and unexpected results, conducting failure analysis, root cause determination and implementing corrective actions.
* Preparation and analysis of Engineering metrics reports to trend for improved operational efficiencies.
* Format, write, deliver and review necessary documentation in line with the standard approval process, and facilitate others to do so. Documents will include SOPs, SWIs, training documents, JSAs, PMs and change controls.
* Accountable for leading investigation analysis, identifying true root cause, identifying gaps and actions to close gaps.
* Collaborate with Engineering colleagues and other departments particularly IPT, Quality, EHS, Technical Engineering in completion of tasks.
* Support Audit Readiness activities.
Education
* Typical Minimum Education Diploma or higher preferred, ideally in a related discipline.
* Typical Minimum Experience Would typically have prior related work experience; ideally in a manufacturing, preferably GMP setting.
Seniority level
Associate
Employment type
Contract
Job function
Quality Assurance, Science, and Manufacturing
Industries
Pharmaceutical Manufacturing, Medical Equipment Manufacturing, and Biotechnology Research
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