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A leading company in the pharmaceutical industry is seeking a Qualified Person to join their dynamic team based the Leicestershire area. As the Qualified Person, you will play a pivotal role in ensuring the highest standards of quality and compliance within the organisation.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Qualified Person will be varied however the key duties and responsibilities are as follows:
1. Certifying batches of medicinal products before release, ensuring they meet all regulatory and quality standards.
2. Overseeing the quality management system and driving continuous improvement initiatives.
3. Collaborating with cross-functional teams to ensure compliance with Good Manufacturing Practices (GMP).
4. Conducting audits and inspections to maintain regulatory compliance and identify areas for enhancement.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Qualified Person we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific discipline.
2. Extensive industry experience in pharmaceutical quality assurance.
3. Experience of releasing IMP's is essential
Key Words:
Qualified Person / QP / IMP / quality assurance / GMP / batch release / regulatory compliance / quality management system / continuous improvement / audits / inspections / Charnwood / United Kingdom
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.ROLE OVERVIEW
A leading company in the pharmaceutical industry is seeking a Qualified Person to join their dynamic team based the Leicestershire area. As the Qualified Person, you will play a pivotal role in ensuring the highest standards of quality and compliance within the organisation.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Qualified Person will be varied however the key duties and responsibilities are as follows:
1. Certifying batches of medicinal products before release, ensuring they meet all regulatory and quality standards.
2. Overseeing the quality management system and driving continuous improvement initiatives.
3. Collaborating with cross-functional teams to ensure compliance with Good Manufacturing Practices (GMP).
4. Conducting audits and inspections to maintain regulatory compliance and identify areas for enhancement.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Qualified Person we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific discipline.
2. Extensive industry experience in pharmaceutical quality assurance.
3. Experience of releasing IMP's is essential
Key Words:
Qualified Person / QP / IMP / quality assurance / GMP / batch release / regulatory compliance / quality management system / continuous improvement / audits / inspections / Charnwood / United Kingdom / #LI-DNI
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.
A leading company in the pharmaceutical industry is seeking a Qualified Person to join their dynamic team based the Leicestershire area. As the Qualified Person, you will play a pivotal role in ensuring the highest standards of quality and compliance within the organisation.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Qualified Person will be varied however the key duties and responsibilities are as follows:
1. Certifying batches of medicinal products before release, ensuring they meet all regulatory and quality standards.
2. Overseeing the quality management system and driving continuous improvement initiatives.
3. Collaborating with cross-functional teams to ensure compliance with Good Manufacturing Practices (GMP).
4. Conducting audits and inspections to maintain regulatory compliance and identify areas for enhancement.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Qualified Person we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific discipline.
2. Extensive industry experience in pharmaceutical quality assurance.
3. Experience of releasing IMP's is essential
Key Words:
Qualified Person / QP / IMP / quality assurance / GMP / batch release / regulatory compliance / quality management system / continuous improvement / audits / inspections / Charnwood / United Kingdom
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.ROLE OVERVIEW
A leading company in the pharmaceutical industry is seeking a Qualified Person to join their dynamic team based the Leicestershire area. As the Qualified Person, you will play a pivotal role in ensuring the highest standards of quality and compliance within the organisation.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Qualified Person will be varied however the key duties and responsibilities are as follows:
1. Certifying batches of medicinal products before release, ensuring they meet all regulatory and quality standards.
2. Overseeing the quality management system and driving continuous improvement initiatives.
3. Collaborating with cross-functional teams to ensure compliance with Good Manufacturing Practices (GMP).
4. Conducting audits and inspections to maintain regulatory compliance and identify areas for enhancement.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Qualified Person we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific discipline.
2. Extensive industry experience in pharmaceutical quality assurance.
3. Experience of releasing IMP's is essential
Key Words:
Qualified Person / QP / IMP / quality assurance / GMP / batch release / regulatory compliance / quality management system / continuous improvement / audits / inspections / Charnwood / United Kingdom / #LI-DNI
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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