My client, a leading CRO, is currently searching for a CMC Consultant to join their team on an initial 12-month contract basis. You will ideally have 5+ years of experience and have a strong understanding of authoring CMC and have global regulatory experience.
Required Experience & Responsibilities:
? CMC (Module 3 and other relevant CMC sections i.e. Module 2.3) authoring regulatory experience in pre and/or post approval submissions of pharmaceuticals/ biologics/ biosimilars/consumer health / medical devices for EU, US, AU, CA, China and other global markets.
? Should have worked in renowned/ acknowledged core Pharma (generic or innovator), Biologics or competitor type/CRO companies in India.
? Responsible for CMC strategy making and recommending the appropriate regulatory reporting mechanism.
? Provide regulatory CMC expertise on cross-functional project teams working with suppliers and contract manufacturers as required in order to ensure alignment of development and implementation of activities with overall regulatory CMC strategies.
? Manage regulatory CMC aspects of post approval change controls, liaising with stakeholders to ensure regulatory compliance.
For further details, please contact Fandi Hatib on +44(0)1727 817 600 or email firstname.lastname@example.org
- Agency: Achieva Group Limited
- Contact: Fandi Hatib
- Phone: +44 (0)1727 811 634
- Reference: FH-2
Website: Achieva Group Limited
- Posted: 12th November 2021
- Expires: 10th December 2021