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Process Science Equipment Analyst

Ref: 81177

  • €35k - €45k in line with experience and overall suitability.
  • 10 Jul 2024
  • Limerick
  • Permanent

Process Science Equipment Analyst

About the Company

My client is a world leader in food, environment and pharmaceutical product testing. They are also one of the market leaders in testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing.

About the Position

My client is currently recruiting a Process Science Equipment Analyst to join our their team in Limerick. The primary purpose of this role is to support the Process Science department by maintaining their laboratory instrumentation in an operational, qualified state. This entails ensuring both instrument hardware and software qualifications are completed in a timely manner and keeping them in a qualified state

Key Responsibilities

  • Maintaining laboratory equipment by performing checks (i.e. calibrations, reagent replenishment) and organizing performance maintenance or services as required in conjunction with laboratory staff and project schedules.

  • Provide core technical support with preparation of, and maintenance of, day-to-day lab equipment.

  • Generate equipment risk assessments and ensure approval prior to vendors arrival on site

  • Liaise with vendors and service providers to ensure equipment maintenance / calibration programme timelines are achieved

  • Maintain and update of laboratory equipment maintenance records, electronic laboratory notebooks (ELN), and associated data files as appropriate to tasks.

  • Preventative maintenance and calibration of laboratory equipment, not limited to, pH meter, conductivity meter, osmometer, balances, glassware washer.

  • Provide assistance for other members of staff in relation to equipment as required

  • Providing training to other team members as instructed by Lead. Ensuring all training delivered is documented appropriately

  • Ensuring all required documentation and logbooks are completed on time, accurately and legibly.

  • Ensuring that clients requirements are fully met and be flexible to work in any area of the business as is required by the client

  • Requires a Degree in Chemistry or Biology; may consider another degree discipline with relevant experience

  • At least 2 years relevant experience in a cGMP environment is required

  • Experience with executing IQ/OQ/PQ protocols and administering software databases and working knowledge of change control in the pharmaceutical industry would be advantageous

The ideal candidate will be a great team player, organised, accurate, have strong documentation skills, and be passionate about quality and customer service. The successful candidate will be empowered to delight the client through excellent service, initiative, quality, integrity, productivity, kindness, innovation, teamwork, and top notch scientific contributions.

Remuneration Package

€35k - €45k in line with experience and a generous benefits package.

Please contact Charlie Bigger on 01 5927861 or email or simply click the apply button. To view all live jobs with Brightwater and market insights, please visit our website: