Validation Engineer Job at Baxter (Stockport)

Job Description

This is where your work makes a difference. At Baxter, we believe every person—regardless of who they are or where they are from—deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond. Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results. Here, you will find more than just a job—you will find purpose and pride. Baxter Healthcare Ltd North West Compounding is currently seeking an experienced Validation Engineer to join our team on site. Our company is dedicated to upholding a seamless validation process for our manufacturing facility, equipment, processes, and systems. As a Validation Engineer, you will have a vital role in ensuring our site adheres to Good Manufacturing Practices (GMP) and regulatory standards. You will collaborate closely with a diverse team, allowing you to gain exposure to various areas of our organisation. This unique aspect of the role offers exceptional prospects for career progression within our world-class company.

Job Responsibility

Ensure Site Validation Master Plan (SVMP) is strictly adhered to
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 teams from various departments to assist with the implementation of new processes, products, and equipment at the site
Actively participate in the assessment, review, and approval of changes that may impact the validation status of our facilities, equipment, processes, and systems
Conduct thorough reviews of validation execution and equipment changes carried out by external contractors and internal project team members
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 adhoc validation requirements
Support validation activities across all UK Compounding sites

Requirements

Scientific/Engineering Degree or equivalent qualification or the right experience within a validation role
Experience working with Hydrogen peroxide decontamination systems
In depth knowledge of a specific validation/engineering skill set i.e. temperature mapping, airflow and smoke visualization, Biological Indicator application and processing etc
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 would be preferred
Logical and practical perspective
Proactive approach to problem-solving
Analytical thinking and innovative problem-solving abilities
Self-motivated and driven
Excellent teamwork skills

Nice to have

Experience with Equipment/Process systems, Cleaning Validation, HVAC, QA, QC, or Cleanroom systems

What we offer

Competitive total compensation package
Professional development opportunities
High importance placed on work life balance
Support for Parents
Continuing Education/ Professional Development
Employee Heath & Well-Being Benefits
Paid Time Off
2 Days a Year to Volunteer

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Validation Engineer

Job Description

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Requirements

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