Scientist - Injectable Drug Product Process Development

Hobson Prior; Slough; On-site; GBP 80,000 - 100,000; Full time

Job summary

Ein innovatives Unternehmen sucht einen Wissenschaftler für die Entwicklung von injizierbaren Arzneimitteln. In dieser spannenden Rolle sind Sie verantwortlich für die Entwicklung und Verfeinerung von Prozessen, die sicherstellen, dass die Produkte bereit für klinische Studien sind. Sie arbeiten eng mit verschiedenen Teams zusammen, um die Herstellung zu optimieren und Qualitätsprobleme zu lösen. Wenn Sie eine Leidenschaft für Wissenschaft und den Wunsch haben, einen echten Unterschied zu machen, könnte dies die perfekte Gelegenheit für Sie sein.

Qualifications

• Erfahrung in der Entwicklung oder Herstellung von flüssigen Arzneimitteln erforderlich.
• Kenntnisse in der biopharmazeutischen Industrie von Vorteil.

Responsibilities

• Entwicklung und Verfeinerung von Prozessen für injizierbare Arzneimittel.
• Durchführung von Laborstudien und Analyse der Daten.

Skills

Entwicklung von flüssigen Arzneimitteln

Aseptische Herstellungsbedingungen

Entwicklung von sterilen Arzneimitteln

Prozessoptimierung

Job description

We are on the hunt for bold, innovative thinkers who are ready to help push the boundaries of science and make a tangible difference in the world.

Hobson Prior is seeking a Scientist for Injectable Drug Product Process Development on a 12-month contract. You will play a crucial role in developing and refining processes for injectable drug products, ensuring they are ready for clinical trials and eventual approval. This position involves working closely with various teams to design and test manufacturing processes.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

• Develop and refine processes for making injectable drug products.
• Work with different teams and organizations to ensure smooth project progress.
• Conduct lab studies, analyze data, and document findings.
• Assess risks in the manufacturing process.
• Design processes for sterile injectable products in various forms.
• Support the preparation of investigational medicines for clinical trials.
• Ensure timely production of stability and clinical batches.
• Assist in regulatory submissions and respond to authority queries.
• Investigate and resolve quality issues related to drug products.
• Help transition processes from development to commercial production.

Key Skills and Requirements:

• Experience in developing or manufacturing liquid drug products.
• Familiarity with bio-pharmaceutical industry practices is beneficial.
• Understanding of aseptic manufacturing conditions is advantageous.
• Knowledge of sterile drug product development and process optimization is a plus.

For more information, please contact Mandi Cakwe.

If you are interested in applying to this exciting opportunity, please click 'Apply' or to speak to one of our specialists visit the 'Contact Us' page.