Job Title

LIMS Validation Engineer – Sligo

The Role

  • LIMS Validation Engineer
  • Longford
  • Onsite role
  • Permanent or Contractor Opportunity

Role Brief

The successful candidate will focus on using lab informatics derived from LIMS to inform decision making within a major biopharmaceutical environment. The role will have a number of deliverables across a variety of teams and play a key part in the translation of functional and business requirements into detailed technical requirements which are used to document and develop solutions.

Some Key Responsibilities:

  • Support the client with Lab systems validation requirements
  • Support CSV Deliverables generation, testing, reviewing, training & end-user support for production use
  • Support training/mentoring of junior level IT Staff/Project Core Team
  • Assist with requirements elicitation workshops/sessions with R&D Laboratory End-Users
  • Assist with project planning/scoping discussions with requirements output
  • Generating Change Controls under GxP guidelines
  • Support GxP IT Change Control Process with any maintenance support activities with production Go-Live of LIMS and/or other systems
  • Liaison with QC & RD Lab, Quality, IT & Validation to meet system requirements

Skills Brief

  • Strong lab systems validation experience is essential and experience in any of the following – equipment validation, computer systems validation (CSV), process validation would be highly beneficial
  • Ability to work in a cross functional/matrix team environment is required
  • At a sufficient level of expertise to take front line interactions with the customer for assigned project work and possess the ability to report to management on progress and any roadblocks that present themselves over the course of the work
  • Change management and project management experience in an FDA regulated environment is preferred
  • Must possess excellent oral and written communication skills, including the ability to advise and influence
  • Strong understanding of data integrity and ALCOA+
  • Strong understanding of Windows Security, and Active Directory and how these can be leveraged to ensure data security.
  • Through practical knowledge of 21 CFR Part 11, Annex 11 and PIC’s regulatory requirements is a must.

Person Brief

Candidates must have a minimum of a bachelor’s degree in a Science/Engineering discipline with at least 5 years’ experience working with automated controls systems in 
a highly automated, regulated manufacturing environment. Extensive IT knowledge is a prerequisite.

Strong labs systems and general validation experience in a GMP environment is essential for this role. The ideal candidate will have excellent communication skills and strong problem solving skills.

The role is an onsite opportunity in Longford and there you must live in or close to this area and be able to comfortably commute to the site daily.

Opportunity Brief

This is an excellent opportunity to work with clients who are global leaders in their field, helping to develop and improve upon industry leading technology solutions. SL Controls offers a supportive environment committed to employee development and wellness, along with a competitive and rounded compensation and benefits package, which rewards high performers.

Company Brief

SL Controls are experts in the area of Equipment System Integration and System Support. We specialise in assisting our customers, including many of the world’s top multinational companies in the medical device and pharmaceutical sectors, achieve their Six Sigma and OEE targets.

Over the past 20 years we have grown our business from a Sligo based enterprise into an international business with additional offices in Galway, Limerick, Leinster and Florida USA.

We pride ourselves on our expertise in industrial IT integration and regulatory compliance in support of global end users, OEM’s and Technology providers.

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