Job Description:
Catalent is currently recruiting for a Quality Specialist II to join the Bathgate site. The Quality Specialist will carry out functions relevant to the Quality (GMP) objectives and policies of Catalent. This role will see you join the dedicated Quality function that is an integral part of our success here at Catalent.
The Role:
To be responsible for the movement, control, and tracking of documentation, ensuring a timely flow to adhere to the production schedule.
• Review and approve Material Specifications to ensure compliance with pharmacopoeia and client requirements.
• Review and approve Incoming Bulk, Intermediate, and Finished Materials to ensure compliance with pharmacopoeia and client requirements.
• Review and approve Randomisations to ensure compliance with GMP and client requirements.
• Review and approve GMP information to ensure accuracy.
Experience And Qualifications:
The Candidate:
• Educated to HNC level in a relevant scientific topic or equivalent in a pharmaceutical environment.
• Experience of Pharmaceutical/Clinical Trials Packaging and GMP Processes.
• Excellent verbal/written communication skills.
• A high level of concentration and a good eye for detail is essential.
• The ability to be decisive when required on material/product quality issues to ensure compliance.
Application Process:
Apply via the SimplyHired website using the link provided below.
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