Head of Formulation Development - Drug Product (w/m/d)

Progressive

München

On-site

EUR 180,000 - 240,000

Full time

3 days ago

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Job summary

A leading global biopharmaceutical organization is seeking an experienced CMC Lead Formulation Development to provide scientific, strategic, and people leadership within a cutting-edge R&D environment. This role drives formulation and process development for advanced biologics, including antibody-drug conjugates (ADCs), from early development through commercialization.

You will lead a formulation development team, shape manufacturing strategy, manage tech transfer, oversee CTM manufacturing

Qualifications

PhD in Pharmacy, Pharmaceutical Sciences, Life Sciences, Engineering, or related discipline; or a Master's with substantial relevant industry experience.
Extensive pharmaceutical industry experience (10+ years) in formulation development, CMC development, biologics development, or related functions.
Proven track record in product development and progression of programs from development through commercialization.
Strong understanding of global CMC requirements, formulation sciences, technology transfer, GMP regulations, and quality systems.
Experience supporting or leading major regulatory submissions, including BLA filings.
Previous line management experience with responsibility for team development and performance.
Strong leadership, stakeholder management, and communication skills.
Experience operating within complex global matrix organizations.
Fluency in English, both written and spoken.

Responsibilities

Lead and develop a formulation development team with scientific and people leadership.
Drive formulation design, process development, and manufacturing strategy for complex biologics.
Establish robust manufacturing processes, control strategies, and product formulations to support development.
Lead tech transfer to internal sites and external CDMOs across Europe.
Oversee CTM manufacturing activities and ensure alignment with quality, regulatory, and project requirements.
Support lifecycle management and product optimization for commercial programs.
Provide strategic CMC leadership for global development programs and regulatory submissions (INDs, NDAs, BLAs).
Collaborate with R&D, Regulatory, Quality, Manufacturing, and Supply Chain teams.

Skills

Formulation Development

Drug Product Development

Biologics Development

ADC (Antibody Drug Conjugates)

Technology Transfer

Regulatory Submissions

Leadership

Project Management

Education

PhD in Pharmacy/Pharmaceutical Sciences/Life Sciences/Engineering

Master's with substantial industry experience

Job description

Head of Formulation Development - Drug Product (w/m/d)

Location: Germany | Industry: Innovative Biopharmaceuticals | Leadership Level: Senior Management

A leading global biopharmaceutical organization is seeking an experienced CMC Lead Formulation Development to provide scientific, strategic, and people leadership within a cutting-edge research and development environment. This role offers the opportunity to drive formulation and process development for advanced biologics, including antibody-drug conjugates (ADCs), while playing a key role in global development programs from early-stage development through commercialization.

Key Responsibilities

Lead and develop a highly skilled formulation development team, providing both technical and people leadership.
Drive formulation design, process development, and manufacturing strategy for complex biologic products and novel therapeutic modalities.
Establish robust manufacturing processes, control strategies, and product formulations to support successful clinical and commercial development.
Lead technology transfer activities to internal manufacturing sites and external CDMO partners across Europe.
Oversee clinical trial material (CTM) manufacturing activities and ensure execution in line with quality, regulatory, and project requirements.
Support lifecycle management initiatives for commercial products and contribute to ongoing product optimization.
Provide strategic CMC leadership for global development programs, including preparation and support of regulatory submissions such as INDs, NDAs, BLAs, and post-approval variations.
Collaborate with multidisciplinary global teams across R&D, Regulatory Affairs, Quality, Manufacturing, and Supply Chain.
Develop and execute departmental strategies, annual operating plans, resource allocation, and performance objectives.
Mentor and develop scientific talent while fostering a high-performing, inclusive, and innovative team culture.

Qualifications

PhD in Pharmacy, Pharmaceutical Sciences, Life Sciences, Engineering, or a related discipline; alternatively a Master's degree with substantial relevant industry experience.
Extensive pharmaceutical industry experience (typically 10+ years) in formulation development, CMC development, biologics development, or related functions.
Proven track record in product development and successful advancement of pharmaceutical programs from development through commercialization.
Strong understanding of global CMC requirements, formulation sciences, technology transfer, GMP regulations, and quality systems.
Demonstrated experience supporting or leading major regulatory submissions, including BLA filings.
Previous line management experience with responsibility for team development and performance management.
Strong leadership, stakeholder management, and communication skills.
Experience operating successfully within complex global matrix organizations.
Fluency in English, both written and spoken.

Why This Opportunity?

This is an exceptional opportunity to join a highly innovative biopharmaceutical company at the forefront of next-generation therapies. The position offers significant strategic influence, international visibility, leadership responsibility, and the chance to shape the future of advanced medicines that address serious unmet medical needs worldwide.

Desired Skills and Experience