Digital Lab Records

3 days ago

county tipperary, Ireland Quanta part of QCS Staffing Full time
Digital Lab Records - South Ireland - 11-Month Contract 

An amazing opportunity has arisen for a Digital Lab Records team member.

With ultra-modern manufacturing facilities based our client is one of the largest and most successful healthcare companies in the world specialising in the development, manufacture and distribution of a broad range of innovative products designed to improve human health. The Analytical Development and Commercialisation (ADC) department is responsible for all analytical support to the site.

The position reports to the DLR Project Lead. The position offers the opportunity to work with a team of professionals responsible for the introduction of Digital Laboratory Records to our modern analytical laboratories using the most up to date technology and quality assurance procedures. The laboratory operates under Lean principles and employees the use of a wide variety of analytical techniques.

What you will do:

Bring energy, knowledge, innovation and leadership to carry out the following activities but not limited to:
Complete activities for the project plan for DLR implementation with agreed upon deliverables – such as LabX and Empower interface with GLIMS. Review and approval of plan, protocols and completion reports. Work to standards for project deliverables. Work in SAP updates for the Analytical department. Update of site procedures and standards. Liaising with vendors in relation to hardware and software. Be part of a dynamic team responsible for DLR requirements all across all the laboratories.
What skills you will need:

In order to excel in this role, you will more than likely have:
Applications are invited from candidates who have a degree in Science (Chemistry, Physics or related Life Science) and/or relevant experience. Have knowledge of GMP standards Have knowledge Laboratory safety standards Must have good communication skills, both written and verbal. Strong documentation skills are required. Must be motivated, focused and technically strong. To maintain accurate records in compliance with GMP expectations To understand and internalise procedures relevant to GMP operations Communication - written, oral Team and interpersonal skills
So, if you are ready to:

Invent solutions to meet unmet healthcare needs, Impact the future by driving one of the world’s leading healthcare companies, and inspire your team to reach their full potential and push the boundaries of science and technology, please apply today.

#LI-TE1

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