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We believe every person deserves a chance for a healthy life, free from illness and full of possibility. We see a world full of healing, with viable care options available to those with limited choices today. We envision new ways of providing physicians, pharmacists and nurses with technologies that not only treat chronic diseases, but also work to prevent them. We’re looking for team members who are motivated to learn, grow and innovate, while making a meaningful difference for millions of people around the world.
We are currently looking for a Project Engineer to join our high performing plant in Liverpool, on a 24-month fixed term contract. Reporting to the Plant Manager you will help support the improvement, reliability and performance of Baxter Liverpool pharmaceutical processes. Maintaining plant & equipment, as part of the capacity expansion project. The working hours are 9am until 5pm, Monday to Friday.
Essential Duties and responsibilities
Act as point of contact based in Liverpool for the capacity expansion project
Support in the definition of project scope and objectives and support the creation of a comprehensive project plans to be shared with other staff members
Develop a continuously update a detailed project plan to monitor and track progress in collaboration with the project manager
Keep under control the project performance using appropriate tools and escalate issues on time to the project manager
Create and maintain comprehensive and detailed project documentation and support tracking project performance, specifically to analyse the successful completion of short and long-term goals
Ensure that all sub-projects are delivered on-time, within scope and within budget
Perform/support pFMEA analysis, assessments for manufacturing, quality and EHS to minimise project risks
Collect all data (process, quality, validation) from archive to create URS etc.
Support the DQ, IQ, OQ, PQ, protocols preparation and validation process
Support the CC activities in Trackwise when needed
Support EHS activities in ATEX area
Verify and calculate needs for new production and validate the numbers directly investigating the process in the gemba.
Perform other related duties as assigned
Qualifications and experience
Proven working experience in project management
Experience in Pharma
Solid organizational skills with specific attention to details
Bachelor's Degree in Engineering (Chemical is preferred)
Green belt or black belt certified
Strong knowledge of validation process DQ, IQ, OQ, PQ in pharma companies
NEBOSH Diploma or equivalent in Environment Health and Safety
IOSH Membership (Chartership preferred)
Previous experience as process engineer
Knowledge of MS Office and MS Project
Developing and Tracking Budgets
Critical/Creative thinking to overcome roadblocks
Baxter is committed to working with and providing reasonable accommodations to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application or interview process, please send an e-mail to Americas_TTA@baxter.com and let us know the nature of your request along with your contact information.