Job Description

QA/QC Specialist

CHR Life Sciences are pleased to be working in partnership with a pharmaceutical company in the Southeast, who are seeking a QA/QC Specialist to join their growing team. As a QA/QC specialist, you will be responsible for drafting and maintaining COSH and radiation risk assessments, participating and leading root cause analysis and CAPA identification, and accurately perform quality control testing on all manufactured products at the LRP/HRP according to SmPC and EP guidelines.

Responsibilities include:

• In your role, you maintain and organize QC equipment calibration and maintenance schedules.
• You will assist the QA manager with the day-to-day activities.
• You will be responsible for validation activities, and preparation and execution of protocols.
• In your role you will, be responsible for reviewing compliance of production and analytical methods with GMP/specials guidelines.

The Successful candidate will:

• Have an understanding of ionising radiation local rules, COSSH and Health & Safety procedures.
• Have experience working within a GMP environment.
• Have previous experience with validation activities.
• Have experience working within QA/QC, preferably within a radiopharmacy environment.

Why apply:

Fantastic opportunity to join a rapidly developing business with the potential for career progression within the pharmaceutical industry.

Radiopharmaceuticals | GMP | COSSH| Quality Control | Quality Assurance