Contract QP: GMP Compliance for IMPs

MedPharm Ltd; Guildford; On-site; GBP 45,000 - 65,000; Part time

Job summary

A leading company in the pharmaceutical sector in Guildford seeks a Qualified Person to provide certification and compliance oversight for Investigational Medicinal Products (IMPs). The role involves batch certification, quality oversight, and collaboration with various departments. The successful candidate will have strong knowledge of EU GMP regulations and prior experience in clinical trials. This position offers flexible hours and requires occasional travel to the UK site.

Benefits

Flexible working hours

Training opportunities

Supportive work environment

Qualifications

• Extensive knowledge of EU GMP, Annex 13 and 16.
• Experience with clinical trials and compliance.
• Knowledge of GCP applicable to clinical supplies.

Responsibilities

• Perform QP certification of IMP batches.
• Provide independent oversight across manufacturing and testing activities.
• Support internal and external GMP audits.

Skills

Independent decision-making

Strong cross-functional collaboration

Excellent communication skills

Detail-oriented

Problem-solving

Education

Registered on UK QP eligibility list

Eligibility under Directive 2001/83/EC

Job description

A leading company in the pharmaceutical sector in Guildford seeks a Qualified Person to provide certification and compliance oversight for Investigational Medicinal Products (IMPs). The role involves batch certification, quality oversight, and collaboration with various departments. The successful candidate will have strong knowledge of EU GMP regulations and prior experience in clinical trials. This position offers flexible hours and requires occasional travel to the UK site.