Qualified Person

Hyper Recruitment Solutions Ltd; Zuid-Holland; On-site; EUR 90,000 - 120,000; Full time

Job summary

Hyper Recruitment Solutions Ltd in Voorschoten, Netherlands, is seeking an experienced Qualified Person to join their pharmaceutical team and ensure product quality and regulatory compliance.

The role focuses on GMP oversight, batch release, audits, and continuous improvement within a multidisciplinary environment.

If you have a relevant science degree and proven QP experience, apply to contribute to patient safety and product integrity.

Qualifications

• Degree in a scientific discipline with QP experience.
• Proven industrial experience as a Qualified Person.
• Working knowledge of QP batch release and regulatory standards.

Responsibilities

• Oversee and ensure compliance with GMP and regulatory requirements.
• Review and approve batch documentation, ensuring all products meet quality standards before release.
• Conduct internal audits and inspections to maintain high-quality production processes.
• Support and review batch release of products.
• Collaborate with cross-functional teams to address quality issues and implement continuous improvement initiatives.

Skills

QP batch release experience

GMP/regulatory knowledge

Quality Assurance

Education

Relevant degree in a scientific discipline

Job description

Role Overview Are you an experienced Qualified Person looking to make a significant impact in the pharmaceutical industry? A leading company in the Netherlands is seeking a Qualified Person to join their dynamic team in Voorschoten. This role offers a unique chance to contribute to the quality and safety of pharmaceutical products, ensuring they meet the highest standards.

Role Overview Are you an experienced Qualified Person looking to make a significant impact in the pharmaceutical industry? A leading company in the Netherlands is seeking a Qualified Person to join their dynamic team in Voorschoten. This role offers a unique chance to contribute to the quality and safety of pharmaceutical products, ensuring they meet the highest standards.

Key Duties And Responsibilities

• Oversee and ensure compliance with Good Manufacturing Practices (GMP) and regulatory requirements.
• Review and approve batch documentation, ensuring all products meet quality standards before release.
• Conduct internal audits and inspections to maintain high-quality production processes.
• Support and review batch release of products
• Collaborate with cross-functional teams to address quality issues and implement continuous improvement initiatives.

Role Requirements

• Relevant degree in a scientific discipline
• Proven industry experience as a Qualified Person
• A working knowledge and practical experience of QP batch release.

This position is ideal for someone who is looking to have exposure to multiple dosage forms and who is looking for their next challenge. You will have the opportunity to work with a team of experts dedicated to innovation and excellence.

If you are ready to take the next step in your career and contribute to a company that values quality and safety, your expertise could be the key to ensuring the health and well-being of countless individuals.

Key Words: Qualified Person / GMP / Quality Assurance / Pharmaceutical Manufacturing / Batch Release / Regulatory Compliance / Internal Audits / Quality Management / Continuous Improvement / Voorschoten

We welcome applications from anyone who meets the role requirements.