ROLE OVERVIEW

A leading organisation in the pharmaceutical industry is seeking a Senior Qualified Person to join their team in the Voorschoten area. As the Senior Qualified Person, you will play a pivotal role in ensuring the compliance and quality of medicinal products before their release to the market.

KEY DUTIES AND RESPONSIBILITIES:

Your duties as the Senior Qualified Person will be varied however the key duties and responsibilities are as follows:

1. Oversee the planning, coordination, and delivery of assigned projects, ensuring objectives, timelines, and regulatory requirements are consistently met.
2. Lead New Product Introduction (NPI) activities, including oversight of technological and analytical method transfers.
3. Manage the qualification and approval of new Contract Manufacturing Organisations (CMOs) associated with new products.
4. Provide leadership and direction to team members, ensuring effective performance management, development, and alignment with organisational and compliance standards.

ROLE REQUIREMENTS:

To be successful in your application to this exciting role as the Senior 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 quality assurance for sterile products.
3. A working knowledge and practical experience with EU GMP regulations and guidelines.

Key Words:CopySenior Qualified Person / Quality Assurance / Pharmaceutical / GMP / Regulatory Compliance / Batch Release / New Product Introduction / Contract Manufacturing Organisations / Quality Management

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.