Being an Engineer at Baxter means you play a critical role in helping us achieve our mission to save and sustain lives. From innovative product design through to production and patient delivery, our Engineers are key to delivering results for our customers and patients worldwide.
Responsibilities
* Ensure Site Validation Master Plan (SVMP) is strictly adhered to and that all validation activities are conducted in accordance with established protocols and procedures, including execution of validation work on a variety of equipment. (Sometimes weekend work may be required.)
* Develop and implement validation documents and protocols for a variety of processes, equipment, facilities, and systems, with a particular emphasis on aseptic manufacturing.
* Work closely with the validation team and cross‑department teams to assist with the implementation of new processes, products, and equipment at the site, developing detailed documentation including Validation Plans (VP), User Requirement Specifications (URS), Design Qualification (DQ), Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
* Actively participate in the assessment, review, and approval of changes that may impact the validation status of facilities, equipment, processes, and systems, ensuring the correct operation of the change control process.
* Conduct thorough reviews of validation execution and equipment changes carried out by external contractors and internal project team members to ensure compliance with validation requirements.
* Take ownership of project management and execution for Capital Expenditure and Process Improvement Projects within the EMEA Validation project portfolio.
* Work with Quality Assurance to react to ad hoc validation requirements.
* Support validation activities across all UK Compounding sites.
Qualifications & Skills
* Problem Solver
* Analytical Thinker
* Data Driven
* Solution Focused & Results Oriented
* Collaborative
* Innovative
* Scientific/Engineering Degree or equivalent qualification, or right experience within a validation role
* Experience working with Hydrogen peroxide decontamination systems
* In‑depth knowledge of specific validation/engineering skill sets such as temperature mapping, airflow and smoke visualization, Biological Indicator application and processing
* Demonstrated working knowledge of validation in a pharmaceutical/FMCG/medical devices environment, preferably
* Experience with Equipment/Process systems, Cleaning Validation, HVAC, QA, QC, or Cleanroom systems
* Approaches tasks with logical and practical perspective, and has a proactive approach to problem‑solving
* Displays analytical thinking and innovative problem‑solving abilities to successfully implement validation strategies
* Self‑motivated and driven to complete projects/tasks efficiently and effectively
* Excellent teamwork skills and ability to communicate effectively with individuals involved in the project
Benefits
* Support for Parents
* Continuing Education/ Professional Development
* Employee Heath & Well-Being Benefits
* Paid Time Off
* 2 Days a Year to Volunteer
* Competitive total compensation package
* Professional development opportunities
* High importance placed on work life balance
This is where your work makes a difference.
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