Parenteral & Liquid Drug Formulations Leader

J&J Family of Companies; Beerse; Sur place; EUR 96 000 - 165 000; Plein temps

Avantages offerts par ce poste

Competitive salary

On-site sport facilities

Health/energy programs

Work-life balance

Résumé du poste

Johnson & Johnson in Beerse, Belgium, seeks a Senior Manager / Associate Director in Parenterals & Liquids Development (PLD) within Drug Product R&D. Lead formulation and process development for small molecules, peptides and oligonucleotides, manage technology transfers, and deliver regulatory filings while mentoring a team across multiple programs.

The role focuses on advanced drug delivery platforms, GMP compliance, and cross-functional collaboration with Regulatory, Quality, and Manufacturing

Qualifications

• Ph.D. or Master’s+ equivalent in relevant field.
• 10+ years developing drug products in pharma.
• Deep experience in parenterals and liquids formulation and process development.

Responsabilités

• Advance formulation and process development for small molecules, peptides and oligonucleotides.
• Run technology transfers and deliver regulatory submissions.
• Lead and mentor dedicated scientists; coordinate cross-functional programs across PLD.

Connaissances

Budget Management

Chemistry

Manufacturing, and Control (CMC)

Clinical Trial Protocols

Data Governance

Developing Others

Drug Discovery Development

Inclusive Leadership

Industry Analysis

Interdisciplinary Work

Leadership

Market Research

Process Improvements

Product Development

Product Strategies

Prototype Development

Researching

Scientific Research

Team Management

Formation

Ph.D. in Pharmaceutical Sciences, Chemistry, Bioengineering or Chemical Engineering

Master's degree plus equivalent experience

Description du poste

Johnson & Johnson in Beerse, Belgium, seeks a Senior Manager / Associate Director in Parenterals & Liquids Development (PLD) within Drug Product R&D. Lead formulation and process development for small molecules, peptides and oligonucleotides, manage technology transfers, and deliver regulatory filings while mentoring a team across multiple programs.

The role focuses on advanced drug delivery platforms, GMP compliance, and cross-functional collaboration with Regulatory, Quality, and Manufacturing