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- Tasks: Lead and shape sterile GMP manufacturing operations in a cutting-edge facility.
- Company: Join a rapidly growing CDMO specializing in pharmaceutical development and manufacturing.
- Benefits: Be part of a positive culture with significant investment in new facilities.
- Why this job: Make a real impact in pharmaceutical development while leading a high-performing team.
- Qualifications: Degree in a relevant scientific, engineering, or manufacturing discipline required.
- Other info: This is a rare opportunity to join a company at an exciting stage of growth.
The predicted salary is between 43200 - 72000 £ per year.
Head of Sterile Manufacturing
Are you a skilled leader in sterile GMP manufacturing, ready to take your career to the next level? This is an exciting opportunity to join a dynamic and rapidly growing CDMO at the forefront of pharmaceutical development and manufacturing.
The Company
My client specialises in developing and manufacturing pharmaceutical products, covering a range of formulations. With significant investment into a new facilities, the business is undergoing an ambitious expansion.
By joining the team, you'll step into a positive, forward-thinking culture in a state-of-the-art facility that delivers innovative medicines to patients worldwide.
The Role
As Head of Sterile Manufacturing, you will shape and lead sterile GMP manufacturing operations. This includes process development, clinical batch manufacturing, technical transfers, and process scale-up activities. Building a team of operational staff, you will be responsible for operational activities within a cutting-edge sterile manufacturing facility.
You’ll ensure compliance with regulatory requirements, develop robust processes, and work closely with clients and internal teams to deliver high-quality outcomes.
Key Responsibilities
- Oversee all sterile GMP manufacturing operations, ensuring compliance with EU GMP Annex 1 and internal quality systems.
- Lead the development, qualification, and validation of sterile manufacturing processes and equipment.
- Manage the sterile GMP facility, including environmental controls, process validation, and documentation.
- Provide leadership to the manufacturing team, ensuring their performance, training, and development.
- Drive technical transfer and process scale-up activities for both in-house and outsourced projects.
- Serve as the key representative during client visits, audits, and regulatory inspections.
- Collaborate with cross-functional teams, including Project Management and Finance, to ensure commercial targets are met.
- Monitor budgets and deliverables, ensuring projects are completed to the highest standard.
About You
- Leadership: Proven track record of leading and developing high-performing teams.
- Experience: Demonstrable expertise in sterile GMP manufacturing and knowledge of EU GMP Annex 1 requirements. Practical knowledge of isolators
- Skills: Strong relationship management, communication, and problem-solving abilities.
- Qualifications: Degree-level education in a relevant scientific, engineering, or manufacturing discipline.
This is a rare opportunity to join a company at an exciting stage of growth. If you’re ready to lead a world-class sterile manufacturing team and make a real impact in pharmaceutical development, apply today!
If you're interested in the above role then please click apply or get in touch to discuss further.
Consult will endeavour to contact candidates within 14 days of application. However, if you do not hear back after 2 weeks then please assume on this occasion, unfortunately, you have not been successful.
Head of Sterile Manufacturing employer: Consult
Contact Detail:
Consult Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Head of Sterile Manufacturing
✨Tip Number 1
Fokussiere dich auf deine Führungskompetenzen. Bereite Beispiele vor, die zeigen, wie du erfolgreich Teams geleitet und entwickelt hast, insbesondere in der GMP-Umgebung.
✨Tip Number 2
Informiere dich über die neuesten Entwicklungen in der sterilen GMP-Herstellung und EU GMP Annex 1. Zeige dein Wissen in Gesprächen und Interviews, um zu demonstrieren, dass du auf dem neuesten Stand bist.
✨Tip Number 3
Netzwerke mit Fachleuten aus der Branche. Besuche relevante Konferenzen oder Webinare, um Kontakte zu knüpfen und mehr über die Unternehmenskultur und -anforderungen zu erfahren.
✨Tip Number 4
Bereite dich darauf vor, deine Problemlösungsfähigkeiten zu demonstrieren. Überlege dir spezifische Herausforderungen, die du in der Vergangenheit gemeistert hast, und wie diese Erfahrungen auf die Rolle des Head of Sterile Manufacturing anwendbar sind.
We think you need these skills to ace Head of Sterile Manufacturing
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of the Head of Sterile Manufacturing position. Tailor your application to highlight your relevant experience in sterile GMP manufacturing and leadership.
Highlight Relevant Experience: In your CV and cover letter, emphasize your proven track record in leading high-performing teams and your expertise in sterile GMP manufacturing. Mention specific projects or achievements that demonstrate your skills in compliance with EU GMP Annex 1.
Showcase Leadership Skills: Provide examples of how you've successfully developed and managed teams in previous roles. Highlight your communication and problem-solving abilities, as these are crucial for the position.
Craft a Compelling Cover Letter: Write a personalized cover letter that connects your background and skills to the company's mission and the specific role. Express your enthusiasm for joining a dynamic and rapidly growing CDMO and your commitment to delivering high-quality outcomes.
How to prepare for a job interview at Consult
✨Showcase Your Leadership Experience
Be prepared to discuss specific examples of how you've successfully led and developed high-performing teams in sterile GMP manufacturing. Highlight your leadership style and how it aligns with the company's forward-thinking culture.
✨Demonstrate Technical Expertise
Familiarize yourself with EU GMP Annex 1 requirements and be ready to explain how your practical knowledge of isolators and sterile manufacturing processes can contribute to the company's operations.
✨Prepare for Compliance Questions
Expect questions about compliance with regulatory requirements. Be ready to discuss your experience in ensuring adherence to quality systems and how you have managed audits and inspections in the past.
✨Highlight Collaboration Skills
Since the role involves working closely with cross-functional teams, prepare to share examples of how you've effectively collaborated with project management, finance, and other departments to achieve commercial targets.
