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Qualified Person (QP)
14216Permanent£80,000 - £100,000Watford, Hertfordshire, United Kingdom
We are currently looking for a Qualified Person (QP) to join a leading pharmaceutical company based in the Hertfordshire area. As the Qualified Person (QP) you will be responsible for:
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Qualified Person (QP) will be varied however the key duties and responsibilities are as follows:
1. Perform QP batch release and support the day-to-day operation of the Quality Management System.
2. Carry out the duties as described in the QP Code of Practice and Eudralex Volume 4 GMP guideline for QPs (Annex 16).
3. Undertake routine product certification as a Qualified Person in accordance with article 51 of 2001/83/EC and Annex 16 of Good Manufacturing Practice Part I (EudraLex volume 4).
4. Assist and lead in maintaining GMP & GDP standards across all site operations.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Qualified Person (QP) we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific discipline.
2. Proven industry experience in pharmaceutical quality assurance.
3. A working knowledge and practical experience with GMP and GDP standards.
Key Words:
Qualified Person / QP / Pharmaceutical Quality Assurance / GMP / GDP / Batch Release / Quality Management System / Eudralex / Regulatory Compliance / Hertfordshire
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.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Qualified Person (QP) will be varied however the key duties and responsibilities are as follows:
1. Perform QP batch release and support the day-to-day operation of the Quality Management System.
2. Carry out the duties as described in the QP Code of Practice and Eudralex Volume 4 GMP guideline for QPs (Annex 16).
3. Undertake routine product certification as a Qualified Person in accordance with article 51 of 2001/83/EC and Annex 16 of Good Manufacturing Practice Part I (EudraLex volume 4).
4. Assist and lead in maintaining GMP & GDP standards across all site operations.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Qualified Person (QP) we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific discipline.
2. Proven industry experience in pharmaceutical quality assurance.
3. A working knowledge and practical experience with GMP and GDP standards.
Key Words:
Qualified Person / QP / Pharmaceutical Quality Assurance / GMP / GDP / Batch Release / Quality Management System / Eudralex / Regulatory Compliance / Hertfordshire
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.
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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