Junior Quality Assurance (Pharma)

Develop your Quality Assurance career within a global pharmaceutical environment, supporting deviations, change controls and GMP compliance in sterile manufacturing operations. Junior Quality Assurance (Pharma) Job description:

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Support Quality Assurance activities related to sterile manufacturing and filling operations.
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Assist with the preparation, assessment and follow-up of change controls.
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Support deviation investigations and ensure that the related documentation is complete and accurate.
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Follow up on actions arising from deviations, change controls and other quality records.
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Review manufacturing and quality documentation for completeness, consistency and GMP compliance.
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Clarify incomplete or unclear documentation with internal stakeholders and the external manufacturing partner.
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Monitor open quality records and support their timely progression and closure.
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Maintain an overview of several ongoing quality topics and communicate outstanding actions.
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Support the evaluation of quality issues within their practical manufacturing context.
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Assist with batch record reviews following the initial onboarding period.
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Collaborate with colleagues across the global Quality Assurance organisation. About the customer: Our client is a global, research-driven pharmaceutical and biotechnology company developing innovative treatments for complex and serious diseases. To strengthen its international Quality Assurance team, the company is looking for a Junior Quality Assurance Specialist to support quality activities connected to an external sterile manufacturing partner. This position offers hands-on exposure to sterile manufacturing, biologics and third-party production within an international and highly regulated environment. It is well suited to an early-career QA professional who has gained practical manufacturing experience and would like to further develop within operational Quality Assurance. Requirements:
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Bachelor’s degree or equivalent qualification in Life Sciences, Pharmaceutical Sciences, Biotechnology, Chemistry, Engineering or a related field; relevant practical GMP experience may compensate for a different educational background.
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2–5 years of experience in Quality Assurance or manufacturing operations within the pharmaceutical, biotechnology or sterile-production industry.
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Hands-on experience in a GMP-regulated sterile manufacturing or sterile filling environment.
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Practical experience with deviations and change controls .
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Fluent English ; Italian language skills would be a strong advantage .
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Experience working with an external manufacturer, CMO or CDMO would be advantageous.
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Knowledge of TrackWise, Veeva or another electronic quality management system would be beneficial.
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