ROLE OVERVIEW
We are currently looking for a Quality Assurance Systems Officer to join a leading pharmaceutical company based in the UK. As the Quality Assurance Specialist, you will be responsible for ensuring the Quality Systems are fit for purpose, effective, and developed in accordance with current GMP, GDP, and GCP legislations and policies.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Quality Assurance Systems Officer will be varied however the key duties and responsibilities are as follows:
1. Processing Non-Conformances, CAPA, Change Control, Document Control tasks, customer complaints, and documentation archive.
2. Maintaining KPIs for training and escalating overdue training and training records.
3. Ensuring continued compliance of QA systems in terms of change control, non-conformances, CAPA, and customer complaints.
4. Providing Quality guidance in support of operations (manufacture, production, and packaging), supplier Technical/Quality agreements.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Quality Assurance Systems Officer we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific discipline.
2. Substantial industry experience in Pharmaceutical Manufacturing testing or Quality Assurance.
3. A working knowledge and practical experience with GxP regulations.
Key Words:
Quality Assurance / Pharmaceutical / GMP / GDP / GCP / Quality Systems / Non-Conformance / CAPA / Change Control / Technical Agreements / Compliance
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
We are currently looking for a Quality Assurance Systems Officer to join a leading pharmaceutical company based in the UK. As the Quality Assurance Specialist, you will be responsible for ensuring the Quality Systems are fit for purpose, effective, and developed in accordance with current GMP, GDP, and GCP legislations and policies.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Quality Assurance Systems Officer will be varied however the key duties and responsibilities are as follows:
1. Processing Non-Conformances, CAPA, Change Control, Document Control tasks, customer complaints, and documentation archive.
2. Maintaining KPIs for training and escalating overdue training and training records.
3. Ensuring continued compliance of QA systems in terms of change control, non-conformances, CAPA, and customer complaints.
4. Providing Quality guidance in support of operations (manufacture, production, and packaging), supplier Technical/Quality agreements.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Quality Assurance Systems Officer we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific discipline.
2. Substantial industry experience in Pharmaceutical Manufacturing testing or Quality Assurance.
3. A working knowledge and practical experience with GxP regulations.
Key Words:
Quality Assurance / Pharmaceutical / GMP / GDP / GCP / Quality Systems / Non-Conformance / CAPA / Change Control / Technical Agreements / Compliance
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
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