Engineer, Sterile Drug Product Clean Utilities Operations And Maintenance

Working with Us
Challenging. Meaningful. Life-changing. Those aren't words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You'll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more:careers.bms.com/working-with-us .

Bristol Myers Squibb Ireland
Bristol Myers Squibb has been in operation in Ireland since 1964, employing over 650 people across a range of activities and business units
Located in Dublin, Cruiserath Biologics Campus, a one billion Multi-Product Cell Culture Biologics Manufacturing facility plays a central role in the Global Product Development and Supply (GPS) network as the company's first European biologics manufacturing facility. This state of the art facility will produce multiple therapies for the company's growing biologics portfolio. Global Biologics Laboratory (GBL) responsible for the release testing of Biologics Drug product for the network, is also based on the Cruiserath Biologics Campus.
BMS Cruiserath has been awarded "Biopharma Company of the Year 2019" in the Irish Pharma Industry Awards and is certified as a Great Place to Work since 2017, including as a Great Place to Work for Women in 2020, 2021 and 2022.

PositionSummary
BMSCruiserathBiologicsisseekinganexperiencedEngineeringprofessionalto join theDrugProductmaintenanceteam.Reportingto theManager,SterileDrugProduct Clean Utilities Operations andMaintenance,theMaintenance Engineerwillassistindeliveringasafeworkingenvironmentforourcolleaguesandareliableplanttoensurecontinuityofsupplyofmedicinesfor ourpatients.

The Clean Utilities Maintenance Engineerwillbetaskedwithinitiallysupporting thefacilityduringprojectphase,supportingequipmentinstallationandcommissioning-frominitialspecificationstofinalhandover.Supportwilltransitionfromprojectphasetooperationalphasetoensureasuccessfulstartupandcommercializationofthefacility,includingGMPreadinessandNewProductIntroductions.

TheMaintenanceteamswillalsofocusoncomplyingwithgoodengineeringpractices,companypolicies,regulations,andcodes.

TheClean Utilities Maintenance EngineerwillalsosupporttheirmanagerinensuringthattheDrugProductMaintenanceteam'sobjectivesarealignedwiththewiderEngineeringandSiteObjectives.Theywillbepartofa multi-functionalteamchargedwithcommissioningofthesignificantcapitalinvestmentanduponcompletionoftheproject,theywillsupportthesustainingoperationonsite.
This is a day's role.

Key Duties and Responsibilities:
Reporting to the Manager, Sterile Drug Product Clean Utilities Operation and Maintenance to support delivery of an effective maintenance program to ensure process equipment operates in a safe and reliable manner.
Work with the project & CQV teams to facilitate delivery, validation, and safe operation of equipment associated with the Sterile Drug Product (SDP) plant.
Develop Standard Operating Procedures (SOPs), Work Instructions (WIs), Risk Assessments (RAs) etc. for the effective and safe completion of maintenance tasks.
Create Job Plans and Preventive Maintenance (PM) routines for the SDP Clean Utilities equipment.
Ensure spare parts, tools, or other services are available when required for maintenance tasks.
Working closely with the Maintenance team and Engineering Planner to schedule and oversee job assignments and lead site technicians or contractors as required.
Follow up on completed work to ensure work orders are closed to required standards.
Co-ordination with Engineering Stores to ensure spare parts are available for all work orders.
Enhance and improve Computerized Maintenance Management System (i.e. Maximo) and other site systems to ensure clear transfer of information between Engineers and Technicians.
Ensuring compliance to all regulatory GMP, safety and environmental requirements.
Lead root cause analysis exercises with support from other functions. Investigate equipment failures and system downtime to find root cause and implement effective corrective and preventive actions.
Own quality deviation investigations, change controls and SAFE investigations as required and ensure corrective and preventive actions are effectively completed.
Support Reliability Excellence initiatives by participating in local and corporate programs.
Pursue and use new technologies and methodologies to improve overall effectiveness of maintenance programs.
Deliver ongoing continuous improvement to plant and processes for a high performing team.
Support other reliability driven tasks as assigned by Line Manager.
Support condition-based maintenance methodology to investigate how data can optimize maintenance programs. Be an advocate for data visualization using Spotfire/Tableau.
Champion a safety culture within the Maintenance team. Perform Safety GEMBA walks at assigned intervals.
Ensure maintenance and calibration activities are executed in compliance with all regulatory requirements including Quality (cGDP/GMP's), EHS, Global Engineering procedures, as well as all local regulatory requirements.
Collaborate with key stakeholders such as Manufacturing Operations, Manufacturing Planners and EHS.
Driving and promoting Good Manufacturing Practices (GMP), Good Documentation Practices (GDP), and adherence with Standard Operating Procedures (SOPs) across the team.
Assist the Clean Utilities Operations and Maintenance Manager with any other maintenance work as per the business needs, including but not limited to development of training materials, vendor management, and other continuous improvement activities.
Support and participate in maintenance reliability initiatives: Continuous Improvement (CI) projects, Support Toolbox Talks, Predictive Maintenance, Surface Imperfection, gasket management, correct torquing, spare parts, etc.

Required
The successful candidate must possess at minimum a Level 8 Engineering qualification or equivalent coupled with at least 3 years' experience in a relevant role in a regulated manufacturing environment.
Experience of working with process equipment in a biologics, drug product, pharma, chemical or food manufacturing facility is desirable.
It is essential that the Maintenance Engineer prioritizes safety, quality, and reliability in every task.
Experience of maintenance optimization techniques.
Working knowledge of Maximo or equivalent CMMS system.
High level of attention to detail and strong problem-solving abilities.
Excellent communication skills and the ability to work in a team, in a cross functional collaborative environment with all levels of the organization as required.
Desire for self-development, and the development of others.
Flexible and amenable to change with ability to work independently and remotely when required.

Why you should apply

You will help patients in their fight against serious diseases
You will be part of a company that encourages excellence and innovation, respects diversity, develops leaders and values its employees.
You'll get a competitive salary and a great benefits package including an annual bonus, pension contribution, family medical allowance, 27 days of annual leave, life assurance and on-site gym

#LI-Onsite

If you come across a role that intrigues you but doesn't perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as "Transforming patients' lives through science™ ", every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol
BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:
Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

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