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Validation Engineer, Compounding

Baxter

Validation Engineer, Compounding

Salary Not Specified

Baxter, Croydon

  • Full time
  • Permanent
  • Onsite working

Posted 1 day ago, 25 Sep | Get your application in today.

Closing date: Closing date not specified

job Ref: f6fb79009dd84b2e8a372708170872cb

Full Job Description

  • Ensure Site Validation Master Plan (SVMP) is strictly adhered to and that all validation activities are conducted in accordance with established protocols and procedures.
  • 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 teams from various departments to assist with the implementation of new processes, products, and equipment at the site. This involves 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 our facilities, equipment, processes, and systems. This involves ensuring the correct operation of our 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., "I am registered pharmacist in the UK with experience with drug products and final product release. I am very dedicated to my work and accurate in details to ensure correct assessment is provided to our customers to ensure patients' safety."

    Detail Oriented
  • Continuous Learner
  • Courageous
  • Collaborative
  • Critical Thinker
  • Influential
    • Validation Engineer, Compounding,
  • You will have a Scientific/Engineering Degree or equivalent qualification.
  • You will be able to demonstrate 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.
  • Approach tasks with a logical and practical perspective, and have a proactive approach to problem-solving.
  • Display 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 to contribute effectively as a member of a diverse team and effectively communicate with individuals involved in the project.

    At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients.
    • Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives-where your purpose accelerates our mission. Oxford Compounding is currently seeking a Validation Engineer to join our team. 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., Baxter is committed to growing and developing an inclusive and diverse workforce - you can read more about our specific values here https://www.baxter.com/careers/inclusion-diversity.

    This is where you make a difference in our patients' safety. As a member of the Baxter Quality team, you will play an essential part in our mission of saving and sustaining lives. Quality is important throughout the entire product lifecycle and works collaboratively with all areas of the organization. Because Quality touches everything Baxter does, a role in Quality provides many opportunities for growth, learning and a successful career that has a daily impact on people's lives.
  • 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
  • Commitment to growing and developing an inclusive and diverse workforce., Our company is enriched by a diverse population of individuals in more than 100 countries that work to solve, innovate, manufacture and drive better healthcare options for patients around the world.