Senior Quality Assurance Officer
other jobs Reed
Added before 1 Days
- England,South East,Oxfordshire
- Full Time, Permanent
- Salary negotiable
Job Description:
Senior QA Officer
Oxford
Full time and permanent position
Excellent salary and benefits
An exciting opportunity has arisen for an experienced Senior QA Officer to join a leading radiopharmaceutical manufacturing site. This full-time, onsite role supports the delivery of high-quality products through robust Quality Assurance, GMP compliance, and continuous improvement across operations. You’ll play a crucial part in maintaining high standards, supporting audits, and ensuring the effective running of the Quality Management System.
Key Responsibilities
*Ensure site operations comply with GMP guidelines, pharmaceutical legislation, and internal quality standards
*Review and maintain documentation, including SOPs, quality records, deviations, CAPAs, investigations and change controls
*Support QC activities including review of test results, management of OOS, and environmental monitoring oversight
*Assist with inspection readiness, internal audits, and responses to regulatory findings
*Contribute to batch review activities, ensuring documentation meets licence requirements and supports QP release
Skills & Experience Required
*Degree in Pharmacy, Chemistry, Pharmaceutical Science, Biology or a related field
*Minimum 2 years’ experience working within Quality Systems in a GMP-regulated environment
*Strong understanding of GMP compliance and operation of pharmaceutical manufacturing facilities
*Excellent communication skills, attention to detail, and ability to work effectively under pressure
*Knowledge of radiation or radiopharmaceuticals (desirable) and a strategic mindset for long-term quality improvement
If this looks like an opportunity of interest, and you possess the required skills and experience, then please follow the link to apply.
Oxford
Full time and permanent position
Excellent salary and benefits
An exciting opportunity has arisen for an experienced Senior QA Officer to join a leading radiopharmaceutical manufacturing site. This full-time, onsite role supports the delivery of high-quality products through robust Quality Assurance, GMP compliance, and continuous improvement across operations. You’ll play a crucial part in maintaining high standards, supporting audits, and ensuring the effective running of the Quality Management System.
Key Responsibilities
*Ensure site operations comply with GMP guidelines, pharmaceutical legislation, and internal quality standards
*Review and maintain documentation, including SOPs, quality records, deviations, CAPAs, investigations and change controls
*Support QC activities including review of test results, management of OOS, and environmental monitoring oversight
*Assist with inspection readiness, internal audits, and responses to regulatory findings
*Contribute to batch review activities, ensuring documentation meets licence requirements and supports QP release
Skills & Experience Required
*Degree in Pharmacy, Chemistry, Pharmaceutical Science, Biology or a related field
*Minimum 2 years’ experience working within Quality Systems in a GMP-regulated environment
*Strong understanding of GMP compliance and operation of pharmaceutical manufacturing facilities
*Excellent communication skills, attention to detail, and ability to work effectively under pressure
*Knowledge of radiation or radiopharmaceuticals (desirable) and a strategic mindset for long-term quality improvement
If this looks like an opportunity of interest, and you possess the required skills and experience, then please follow the link to apply.
Job number 3436642
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