Biotech Production Coordinator

LimerickCompetitiveOn-siteFull time0 applicants

About this role

Within this role you will facilitate and coordinate inventory, documentation and perform record- related activities for manufacturing. Maintain and coordinate inventory, scheduling, sampling, and documentation requirements for manufacturing.

As a Biotech Production Coordinator, a typical day might include, but is not limited to, the following:

Coordinating,

reviewing, and cataloguing various types of manufacturing documentation

Preparing routine progress reports and tracking on various KPIs

Managing lifecycle management of documentation

Maintaining inventory systems through investigations, weekly reviews, reconciliations, and other related activities to ensure accuracy

Serving as a liaison between manufacturing and other functional areas as needed

Performing analysis of GMP and GxP data

Coordinating appropriate material needs using varying systems and forms to ensure production continuity

Ensuring systematic bill of materials are created and maintained for production needs

Evaluating, initiate, and monitor deviations and other compliance events

Creating and review sampling intake for all manufacturing unit

operations and protocols per the appropriate documentation prior to operators going on the floor

This role might for you if:

You have the ability to decipher and navigate a variety of different systems, data, calculations, and documentation

You have experience within and GMP environment and have good GDP knowledge

You possess excellent verbal and written communication skills

You enjoy problem solving

You demonstrate a can-do attitude

You are proficient in Microsoft Word, Excel, PowerPoint, and Outlook

To be considered for this opportunity you should have a

Bs/BA Degree with 0-2+ years of related experience or equivalent combination of education and experience. Experience in a cGMP environment, quality assurance, project management, or inventory management desired.

EU Requirements

Job Details

Posted10 May 2026
Closes9 June 2026
Job TypeFull time
Work ModeOn-site

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