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Head of Manufacturing Operations

Barrington James

Bayern

Vor Ort

EUR 120.000 - 150.000

Vollzeit

Vor 4 Tagen
Sei unter den ersten Bewerbenden

Zusammenfassung

A fast-scaling CDMO is seeking a Head of Operations in Bayern, Germany. The ideal candidate will oversee end-to-end operations, driving excellence across manufacturing units. Responsibilities include optimizing production lines and ensuring compliance with GMP standards. Candidates should possess extensive leadership experience in pharmaceutical manufacturing and strong communication skills. A competitive executive compensation package is offered.

Leistungen

Competitive executive-level compensation package
Opportunity to shape and grow operations

Qualifikationen

  • 10+ years of progressive leadership experience in pharmaceutical manufacturing.
  • Fluent in English; German proficiency is a strong advantage.

Aufgaben

  • Lead and optimize all manufacturing operations across production lines.
  • Drive operational excellence initiatives to enhance efficiency and quality.
  • Oversee technology transfers and compliance with regulatory standards.

Kenntnisse

Leadership
Communication
Change Management
GMP Compliance

Ausbildung

Degree in Pharmacy, Chemistry or Chemical Engineering
MBA or postgraduate management qualification

Jobbeschreibung

The Role:

Reporting directly to the CEO, the Head of Operations will be responsible for overseeing end-to-end operations across multiple manufacturing units. This includes leading production (API, fill-finish, FDF), supply chain, tech transfer, engineering, and continuous improvement. The ideal candidate will have a strong background in CDMO operations, a hands-on leadership style, and a deep understanding of GMP compliance and client-centric service delivery.

Key Responsibilities:

  • Lead and optimize all manufacturing operations across API, fill-finish, and FDF production lines.
  • Drive operational excellence initiatives to enhance efficiency, quality, and scalability.
  • Oversee technology transfers, process validation, and compliance with GMP and regulatory standards (EU/FDA).
  • Partner with QA, Regulatory Affairs, and Business Development to ensure seamless client onboarding and project execution.
  • Develop and execute the strategic operations roadmap aligned with company growth objectives.
  • Manage and mentor cross-functional teams, promoting a culture of accountability, safety, and continuous improvement.
  • Ensure robust capacity planning, supply chain management, and risk mitigation across the value chain.

Candidate Profile:

  • Degree in Pharmacy, Chemistry, Chemical Engineering, or related scientific discipline; MBA or postgraduate management qualification is a plus.
  • 10+ years of progressive leadership experience in pharmaceutical manufacturing, preferably within a CDMO environment.
  • Proven expertise across API manufacturing, sterile fill-finish, and solid/oral FDF operations.
  • Deep knowledge of cGMP, EMA/FDA regulatory standards, and international quality systems.
  • Strong leadership, communication, and change management skills.
  • Fluent in English; German proficiency is a strong advantage.

What’s On Offer:

  • Strategic leadership position with high visibility and impact
  • Opportunity to shape and grow operations in a fast-scaling CDMO
  • Competitive executive-level compensation package
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