QP/RP/RPi

Summary

Central Pharma are actively recruiting a permanent QP/RP/RPi, based on our site in Bedford. The successful candidate will cover our manufacturing and warehouse facilities in Bedford, UK; primarily supporting batch release, whilst allowing ample opportunities to be involved in a diverse range of projects ranging from the use of AI to facility design and build. The successful applicant will find their Quality expertise will be actively sought on all areas of the business. This is a rare opportunity to positively contribute to an organisation that wants to be guided by you.

Responsibilities include:

• To be eligible to act as a Qualified Person
• To act as a Responsible Person/ Responsible Person for Import
• To comply with all the requirements of the Human Medicines Regulation 2012
• To comply with EU directives/regulations 2001/83/EC and 2013/C 343/01
• To comply with Good Manufacturing and Distribution practices and the relevant codes of conduct
• To perform batch certification for pharmaceutical products as required
• To provide Quality expertise and guidance on improvement projects relating to warehouse and electronic systems
• To review documentation as part of the Central Pharma Quality Management System, including Change Control, Complaints, Deviations and Non-Conformances
• To represent Central Pharma at Key Customer meetings as required
• To be key point of liaison with Regulatory bodies
• To support the internal quality audit programme
• To audit external suppliers and certify API manufacturing sites as required
• To review all validation activity.

Benefits:

• Company pension
• Free parking on-site
• Referral programme.

Schedule:

• Monday to Friday

Job type and Location:

• In person, office based
• Full-time, Permanent