Overview
We are seeking an experienced Qualified Person (QP) for a part-time consultancy role within a UK-based pharmaceutical company that specializes in oral solid dosage forms and oral liquid medicines. The successful candidate will work remotely, engage in batch certification and release activities, and visit the North West England site once a month to ensure compliance with GMP and regulatory standards.
Responsibilities
- Undertake QP certification and batch release in accordance with applicable UK GMP and regulatory requirements.
- Provide appropriate oversight of batch documentation and associated quality processes.
- Maintain engagement with the business to support timely, compliant release activity.
- Support the ongoing requirements associated with being named on the company’s MIA licence.
Requirements
- Hold Qualified Person status, eligible to perform certification under the applicable UK regulatory framework.
- Demonstrable experience as a QP within a pharmaceutical business.
- Experience with both oral solid dosage forms and oral liquid medicines.
- Strong understanding of batch certification, release, GMP, and pharmaceutical quality systems.
- UK-based with the ability to attend the company’s North West site once per month.
- Ability to commit to a structured, ongoing part-time contract with a monthly retainer.