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QC Stability Specialist

2 months ago


Skipton, North Yorkshire, United Kingdom Dechra Pharmaceuticals Limited Full time

Job Summary

We are seeking a highly skilled QC Stability Specialist to join our team at Dechra Pharmaceuticals Limited. As a key member of our stability program, you will be responsible for maintaining and developing our GMP compliant stability program for veterinary medicines.

Key Responsibilities:

  • Provide technical and administrative input into the design, execution, trending, and reporting of stability data.
  • Coordinate in-house and external stability testing capabilities to ensure compliance with VICH, FDA, and product license requirements.
  • Develop and implement stability protocols and procedures to ensure data integrity and accuracy.
  • Collaborate with cross-functional teams to ensure stability program alignment with business objectives.
  • Monitor and analyze stability data to identify trends and areas for improvement.

Requirements:

  • Strong understanding of GMP regulations and stability program requirements.
  • Excellent analytical and problem-solving skills.
  • Ability to work independently and as part of a team.
  • Strong communication and interpersonal skills.
  • Experience with stability data management and reporting.

What We Offer:

  • A competitive salary and benefits package.
  • Opportunities for professional growth and development.
  • A dynamic and supportive work environment.