Regeneron Biotech Production Coordinator Job in Limerick, Ireland

Regeneron is hiring a Biotech Production Coordinator at its Limerick (Ireland) industrial operations site. The listing requires a BS/BA degree with 0–2+ years of related experience, and fresh graduates are eligible.

Job Details

Company: Regeneron

Position: Biotech Production Coordinator

Location: Limerick, Ireland

Days: Monday to Friday

Requisition: R52639

Qualification: BS/BA degree

Experience: 0–2+ years (Freshers eligible)

Pay: EUR 14.55–22.73 per hour

Job Description

Regeneron uses science and innovation to develop life-changing medicines for people with serious diseases. Regeneron is currently seeking a Biotech Production Coordinator to join its Manufacturing team. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

Key Responsibilities

  • Coordinate, review, and catalogue various types of manufacturing documentation.
  • Maintain inventory systems through investigations, weekly reviews, reconciliations, and other related activities to ensure accuracy.
  • Serves as a liaison between manufacturing and other functional areas as needed.
  • Navigate a variety of different systems, data, calculations, and documentation.
  • Responsible for ensuring timelines are met through effective communication and follow through with task and/or project owners.
  • Performing analysis of GMP and GxP data.
  • Review and approve bills of materials, sample studies, and other manufacturing documentation as needed.
  • Extended functional, industry and regulatory knowledge.
  • Act as a qualified trainer for new and existing employees.
  • Lead and solves technical problems by using expert critical thinking skills and verbal and written communication skills.
  • Lead and manages projects independently and with cross-functional teams.
  • Evaluate, initiate, and monitor deviations and other compliance events.
  • Ensure accurate systems are maintained related to Manufacturing operations; OPM, MES, LIMS, WMT, FMP, etc.

Eligibility Criteria

  • Requires 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.

Work Environment

The environment and physical rhythms of this role:

  • You enjoy working in a team that brings out the best in each other
  • You can adhere to the letter and spirit of policies and regulations
  • You can adapt to a changing environment and have the ability to adhere to a schedule

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