Site Head - Manufacturing & Operations

Discover International; München; Vor Ort; EUR 60.000 - 80.000; Vollzeit

Zusammenfassung

A leading biopharma company in Munich is seeking an experienced Site Head to manage operations across two key manufacturing sites. The role includes overseeing GMP-compliant biologics production and driving strategic initiatives. Candidates should have over 10 years of experience in biopharma, proven site leadership, and strong knowledge of GMP regulations. This senior position offers a chance to lead a committed team in a growing environment, ensuring high standards for quality and compliance.

Qualifikationen

• 10+ years’ experience in biopharma, ideally within a GMP-regulated CDMO environment.
• Proven track record in senior site leadership or manufacturing management.
• Strong knowledge of GMP regulations and biologics processing.

Aufgaben

• Provide overall site leadership across multiple functions.
• Ensure full GMP compliance across all operations.
• Drive site strategy and operational planning.

Kenntnisse

Leadership

GMP compliance

Strategic mindset

Communication

Operational Excellence

Ausbildung

Degree in Life Sciences, Engineering, Pharmacy, or Biotechnology

Jobbeschreibung

A rapidly growing Biopharma CDMO is seeking an experienced Site Head to lead end-to-end operations at two of its key manufacturing sites in Germany (One Munich, One Frankfurt). The facility specialises in GMP-compliant biologics manufacturing (upstream, downstream, and sterile fill‑finish) and is entering a phase of significant investment and expansion. This is a strategic senior leadership position with full responsibility for site performance, compliance, and future development.

Your Responsibilities

• Provide overall site leadership across Manufacturing, Quality, Supply Chain, Engineering, EHS, and Operational Excellence.
• Ensure full GMP compliance across all operations, including EU GMP, FDA, ICH, and internal global quality standards.
• Oversee biologics production activities , including USP, DSP, and aseptic filling / packaging.
• Drive site strategy, operational planning, and continuous improvement initiatives.
• Lead and develop the site's leadership team, fostering a culture of accountability, safety, and quality.
• Manage budget, resource planning, and site-level CAPEX projects.
• Serve as the key point of contact for authorities, corporate teams, and client audits.
• Support new product introductions, tech transfers, and scale-up activities.
• Strengthen the site’s reputation as a reliable, high-performing CDMO partner.

Your Profile

• Degree in Life Sciences, Engineering, Pharmacy, Biotechnology, or a comparable field.
• 10+ years’ experience in biopharma, ideally within a GMP-regulated CDMO environment.
• Proven track record in senior site leadership, manufacturing management, or plant leadership.
• Strong knowledge of GMP regulations, aseptic / sterile production, and biologics processing.
• Experienced leading multi-functional teams in a highly regulated environment.
• Excellent communication skills and leadership presence.
• Strategic mindset paired with operational hands‑on capability.

If this role seems interesting for you, please send your CV to [e-mail].