Skip to content

Orion GxP consuting

Orion Consulting

Orion GXP Consulting are hiring a Consultant QP!

  • by

Are you looking to dip your toe into contract QP work and get in at the beginning with new start-ups?
Do you want to work just 2-5 days per week with a small number of diverse clients?

Maybe you are returning to QP work following a career break or you have the qualification and ability but are not being utilised on an MIA licence?

We have a number of diverse clients from start-ups and small scale clinical trials customers, to large manufacturing plants with critical QP requirements to be able to meet batch release requirements. We also assist clients with audits, risk assessments, training and QMS development where they are looking for a safe pair of hands and a QP’s experience for the extra work.

If any of this sounds like you and you meet QP eligibility criteria as per Article 49 and 50 of Directive 2001/83/EC then please get in touch!

 Tel:  07198 10101  or email 

QP reviewing of Batch documentation and certification per Annex 16


The role of the QP as defined in Directive 2001/83/EC is critical in pharmaceutical manufacturing., virtual manufacturing and import and clinical trails in the EU