(Senior) Director (f/m/d) mRNA Manufacturing
(Senior) Director (f/m/d) mRNA Manufacturing

(Senior) Director (f/m/d) mRNA Manufacturing

Tübingen Vollzeit 72000 - 108000 € / Jahr (geschätzt) Kein Home Office möglich
CureVac AG

Auf einen Blick

  • Aufgaben: Lead mRNA manufacturing and improve production processes while ensuring compliance with GMP standards.
  • Arbeitgeber: CureVac Manufacturing GmbH is a biopharmaceutical company focused on innovative mRNA-based therapies.
  • Mitarbeitervorteile: Join a dynamic team with opportunities for growth, innovation, and a collaborative work environment.
  • Warum dieser Job: Be part of a medical revolution, driving impactful change in cancer treatment and vaccines.
  • Gewünschte Qualifikationen: Requires a degree in pharmaceutical or bioengineering, extensive production experience, and leadership skills.
  • Andere Informationen: Fluency in English and German is essential; experience in GMP environments is a plus.

Das voraussichtliche Gehalt liegt zwischen 72000 - 108000 € pro Jahr.

(Senior) Director (f/m/d) mRNA Manufacturing

Design. Progress. Together.

CureVac Manufacturing GmbH, a wholly owned subsidiary of CureVac SE, is a biopharmaceutical company producing novel drugs based on the natural molecule Messenger RNA (mRNA). Our focus is on innovative cancer immunotherapies, prophylactic vaccines and molecular therapies. Currently, all RNA people are striving to achieve our main goal: To bring multiple best-in-class mRNA drugs to market.

To strengthen our team in Tübingen near Stuttgart, we are currently looking to recruit a

(Senior) Director (f/m/d) mRNA Manufacturing

Your Responsibilities:

  1. Ensures clinical manufacturing and industrialization of products and production process improvements as well as product portfolio extensions within the APU (Autonomous Production Unit)
  2. Disciplinary leadership of Production managers & teams for the production of mRNA active ingredients, pDNA, Master Cell banking, and formulated bulk according to GMP guidelines
  3. Follows production plans and assures feasibility, making necessary corrective adjustments as needed
  4. Monitoring compliance with documentation requirements according to GMP
  5. Overseeing the qualification of premises and equipment as well as the validation of processes
  6. Committed and accountable to deliver and push for speed/excellence in execution while not compromising on quality and safety
  7. Develops long-term manufacturing strategy servicing the product portfolio
  8. Achieves financial targets by preparing and presenting budget proposals including yearly cost improvements (e.g., yield) and managing the APU budget
  9. Allocates appropriate resources within the budget perimeter
  10. Manages the APU team by understanding the big picture of the manufacturing network, connecting the dots, and giving perspective and clarity to the team
  11. Aligns resource planning with Supply Chain & Quality, Program Management, Engineering, and Technical Development departments concerning stocks, equipment, staffing, activities, etc.
  12. Maintains the working environment according to GMP & EHS standards
  13. Shares information transparently
  14. Detects and plans training needs
  15. Participates in career management initiatives
  16. Serves as the official APU representative to regulators, customers (external or internal) and acts as a business leader by navigating and influencing in a matrix organization
  17. Ensures established customer specifications concerning cycle time, delivery, quality, quantity, and costs are met
  18. Implements preventive and corrective measures in the production process to assure that compliance & customer demands are properly met
  19. Coordinates with the quality team to meet all product standards
  20. Drives continuous improvements in APU processes to raise quality, functionality/productivity, and to obtain CureVac & product project objectives

Your Qualifications:

  1. Completed university degree with a pharmaceutical, bioengineering or scientific background or a comparable qualification
  2. Extensive production experience and experienced people leader (several years team management experience) including larger teams and shift operations
  3. Positive Leadership with hands-on mentality
  4. Experience in a regulated environment of a GMP manufacturing company, Leiter der Herstellung, §15 AMG
  5. Knowledge of biotechnological methods such as TFF, HPLC, and transcription is advantageous
  6. Operational knowledge of Lean methods (Kanban, 5S, Hoshin, Daily Performance Management) and shop floor management is desirable
  7. Ability to influence heterogeneous and diverse teams in a matrix organization
  8. Good MS Office skills and experience with process control systems are advantageous
  9. Strategic thinking, Lean Mindset and strong communication skills
  10. Fluency in English and German

We offer you a challenging and varied opportunity with an innovative and dynamic company that is expanding. With much passion and sense of responsibility, we work together on the medical revolution. We pride ourselves on maintaining an honest and trusting relationship with each other which is characterized by openness to new ideas and continuous progress. Mutual respect, reliability and personal initiative are self-evident for us.

Design your future with us – become part of the RNA people !

We look forward to receiving your application via our CareerPortal.

CureVac Manufacturing GmbH

#J-18808-Ljbffr

(Senior) Director (f/m/d) mRNA Manufacturing Arbeitgeber: CureVac AG

CureVac Manufacturing GmbH is an exceptional employer that fosters a collaborative and innovative work culture, dedicated to advancing the field of biopharmaceuticals. Located in Tübingen near Stuttgart, we offer our employees meaningful opportunities for growth and development within a dynamic environment focused on cutting-edge mRNA technologies. With a commitment to mutual respect and open communication, we empower our team members to contribute to groundbreaking medical advancements while ensuring a supportive atmosphere that values personal initiative and excellence.
CureVac AG

Kontaktperson:

CureVac AG HR Team

StudySmarter Bewerbungstipps 🤫

So bekommst du den Job: (Senior) Director (f/m/d) mRNA Manufacturing

✨Tip Number 1

Make sure to familiarize yourself with the latest advancements in mRNA technology and production processes. This knowledge will not only help you during interviews but also demonstrate your commitment to staying at the forefront of the industry.

✨Tip Number 2

Network with professionals in the biopharmaceutical field, especially those who have experience in GMP environments. Attend industry conferences or webinars to connect with potential colleagues and learn about the latest trends and challenges in mRNA manufacturing.

✨Tip Number 3

Prepare to discuss your leadership style and how you've successfully managed diverse teams in a matrix organization. Be ready to provide examples of how you've influenced team dynamics and driven performance improvements in previous roles.

✨Tip Number 4

Understand CureVac's mission and values deeply. Tailor your discussions to reflect how your personal values align with theirs, particularly regarding innovation, quality, and teamwork. This alignment can set you apart as a candidate who truly fits into their culture.

Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: (Senior) Director (f/m/d) mRNA Manufacturing

Leadership Skills
Production Management
GMP Compliance
Biotechnological Methods Knowledge
Lean Manufacturing Techniques
Process Improvement
Budget Management
Strategic Thinking
Team Management
Communication Skills
Problem-Solving Skills
Project Management
Fluency in English and German
Operational Knowledge of Process Control Systems
Training and Development Planning

Tipps für deine Bewerbung 🫡

Understand the Role: Take the time to thoroughly read the job description for the (Senior) Director mRNA Manufacturing position. Understand the key responsibilities and qualifications required, and think about how your experience aligns with these.

Tailor Your CV: Customize your CV to highlight relevant experience in pharmaceutical manufacturing, team leadership, and GMP compliance. Use specific examples that demonstrate your ability to manage production processes and lead teams effectively.

Craft a Compelling Cover Letter: Write a cover letter that not only outlines your qualifications but also expresses your passion for mRNA technology and its potential impact on healthcare. Mention specific achievements that showcase your leadership and strategic thinking.

Highlight Relevant Skills: Make sure to emphasize your knowledge of biotechnological methods, Lean management practices, and your fluency in both English and German. These skills are crucial for the role and should be clearly presented in your application.

Wie du dich auf ein Vorstellungsgespräch bei CureVac AG vorbereitest

✨Showcase Your Leadership Experience

As a (Senior) Director, you'll be leading teams. Be prepared to discuss your previous leadership roles, focusing on how you've managed larger teams and shift operations in a GMP environment.

✨Demonstrate Your Technical Knowledge

Highlight your understanding of biotechnological methods like TFF and HPLC. Discuss any relevant experience with process control systems and how it can benefit the production processes at CureVac.

✨Emphasize Your Strategic Thinking

CureVac is looking for someone who can develop long-term manufacturing strategies. Prepare examples of how you've successfully implemented strategic initiatives in past roles, particularly in a regulated environment.

✨Communicate Your Lean Mindset

Familiarity with Lean methods is desirable. Be ready to discuss how you've applied Lean principles in your previous positions to improve efficiency and quality in manufacturing processes.

(Senior) Director (f/m/d) mRNA Manufacturing
CureVac AG
CureVac AG
  • (Senior) Director (f/m/d) mRNA Manufacturing

    Tübingen
    Vollzeit
    72000 - 108000 € / Jahr (geschätzt)

    Bewerbungsfrist: 2027-03-22

  • CureVac AG

    CureVac AG

    250 - 500
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