Quality Assurance Lead

7 days ago


East Anglia, United Kingdom Verbatim Pharma Full time

Job Summary:

Verbatim Pharma is seeking a highly experienced Validation Manager to join our team. As a key member of our Quality Assurance department, you will be responsible for ensuring the consistency and quality of our manufacturing and cleaning processes.

Key Responsibilities:

  • Develop and execute validation protocols to ensure compliance with GMP regulations.
  • Lead engineering studies on new products and components, and manage change control assessments.
  • Coordinate computer and method validations for cutting-edge products.
  • Work directly with vendors and service providers to ensure validation and installation requirements are met.
  • Develop project timelines, track progress, and ensure deadlines are met.
  • Compile, analyze, and report on validation data, offering recommendations for improvements.

Requirements:

  • Minimum 3-4 years of experience in the medical device or pharmaceutical industry.
  • Proven track record of ensuring compliance with GMP regulations.
  • Strong understanding of validation processes and procedures.
  • Excellent communication and leadership skills.

What We Offer:

  • Opportunity to take on a leadership role in Validation.
  • Working in a diverse environment with a variety of services and products.
  • Long-term progression opportunities.
  • Work with diverse leaders with a continuous improvement mindset.

Location:

Our team is based in the UK, and we are looking for candidates who are able to commute to our location.



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