Pharmaceutical Documentation Manager

2 days ago


Bathgate, West Lothian, United Kingdom Disability Solutions Full time
Key Responsibilities

The Quality Specialist II will be responsible for ensuring the quality of our products by carrying out functions relevant to the Quality (GMP) objectives and policies of Catalent Limited.

The key responsibilities of this role include:

  • To be responsible for the movement, control and tracking of documentation, ensuring a timely flow to adhere to the production schedule.
  • Review and approve Randomisations to ensure compliance with GMP and client requirements
  • Review and approve observation and deviation reports to ensure compliance with GMP

We offer a competitive salary of £48,000 - £58,000 per annum, depending on experience. In addition to a generous salary, we provide a range of benefits including:

  • A comprehensive training program to support your career development
  • Opportunities for professional growth and advancement
  • A dynamic and supportive work environment


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