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Biopharmaceutical laboratory support specialist

beBeeLaboratory
Posted: 20 November
Offer description

About the Role

We are currently recruiting for an exciting opportunity to support laboratory operations within a leading multinational organization based in Meath. This is an excellent position for anyone looking to join a biopharmaceutical company and be part of a team that is one of the best at what they do.

Key responsibilities will include supporting equipment qualification, documentation generation, and contributing to lab and process establishment. Additionally, you will perform supporting activities for general lab operations, run business tasks such as EM, facility testing, method verifications, troubleshooting, and execution of laboratory studies when required.

You will also review, trend, and report laboratory data to support generation of batch data, collate and analyze end-of-quarter and year reports for all raw data generated. Furthermore, you will maintain and release laboratory stock, order laboratory consumables where required, manage routine cleans of laboratory equipment, ensure laboratory housekeeping standards are maintained, and identify continuous improvement opportunities in laboratory processes.

In this role, you will respond to standard requests from partners, customers, and clients (internal and/or external) and escalate to your manager when appropriate. You will also actively participate in functional meetings, facilitate cross-functional meetings where required, audits (internal and external), and support the introduction of novel, innovative solutions.


Requirements

* A degree qualification in a relevant field (biological sciences/engineering) with background in microbiology.
* A minimum of 1-3 years' experience working in a relevant academic or industry field (internships and student placements will be considered in lieu of experience).
* Some knowledge of biologics manufacturing and familiarity with microbiological testing techniques.
* Knowledge of laboratory systems (e.g., LIMS, E-logs, MODA, electronic notebooks).
* A good knowledge of GMP, familiarity with USP, EP, JP requirements.

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