Do you want to work focuses on creating cutting-edge cancer treatments using innovative, hospital-based methods that streamline processes and improve patient outcomes?
Our client is seeking an experienced QC Consultant for their advanced laboratory team. Are you enthusiastic about the opportunity to work in a high-tech lab environment with a focus on quality control and process optimization? Apply now!
Job Description:
The QC Consultant will play a crucial role within the European Quality Control team, working closely with laboratory professionals to ensure the highest standards in clinical trial support and quality management. This position involves providing expert QC support, managing laboratory documentation, and implementing updates to quality procedures. The role is central to the company's strategy to expand and enhance its decentralized production network, ensuring compliance and efficiency in lab operations.
Responsibilities:
- Provide expert Quality Control support for clinical trials, focusing on laboratory problem-solving and QC evaluations.
- Oversee and manage quality documentation within the laboratory, including deviations, CAPAs, and change controls.
- Author and review critical laboratory documentation related to European QC processes.
- Approve and review standard operating procedures (SOPs) to ensure laboratory practices align with regulatory standards.
- Act as a backup for laboratory QC training, ensuring all staff are well-versed in quality procedures.
- Collaborate with cross-functional teams to ensure laboratory processes are aligned and effectively communicated.
- Implement and oversee laboratory process improvements that meet regulatory requirements while enhancing efficiency and simplicity.
Requirements:
- Bachelor's or Master's degree in Life Sciences, Biotechnology, or a related field.
- Minimum of five years of experience in a pharmaceutical or biotechnology laboratory industry.
- Expertise in quality record management and root cause investigation within a lab setting.
- Hands-on experience with laboratory analytical techniques, including Flow Cytometry, PCR, and cell-based assays is a pré
- Fluent in English, with excellent communication skills.
- Availability to work on site at least three days a week, with options for part-time work (32 hours minimum)
Benefits:
- Salary range: €3400-€5500,- gross per month or a consultant payrate of €50,- per hour
- Six-month employment contract with potential for extension.
- Flexible working arrangements.
- Access to a state-of-the-art laboratory with the latest technology in the field.
- Fulltime position, contract trough Oxford Global Resources
- Location: Leiden
- Vacaturenummer: 24957
