Senior Solids Development Lead, Pharma R&D

7555-Janssen Pharmaceutica NV Legal Entity

Belgique

On-site

EUR 96,000 - 165,000

Full time

3 days ago
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Benefits offered by this job

Annual bonus
Vacation days
Parental leave (12 weeks)
Bereavement leave
Caregiver leave
Volunteer leave
Well-being reimbursement
Health programs
Insurance plans

Job summary

Johnson & Johnson’s SoliD group in Beerse, Belgium, seeks a Senior Manager/Associate Director to advance solid formulation and process development for synthetic compounds. You will guide multiple programmes, ensure regulatory alignment, and lead cross-functional teams in a fast-paced, global health environment.

You will mentor scientists, plan resources, and coordinate with Pharmaceutical & Material Sciences, Regulatory, and Supply Chain to accelerate development from discovery to

Qualifications

  • Ph.D. in Pharmaceutical Sciences, Chemistry, Bioengineering or Chemical Engineering – or a Master’s plus equivalent experience.
  • Deep experience in solid formulation and process development for synthetic compounds.
  • Track record across preclinical formulations, developability assessments, clinical development, scale-up and tech transfer.

Responsibilities

  • Advance formulation and process development for synthetic molecules.
  • Explore new drug delivery systems and technologies.
  • Create patient-centred products and fresh IP.
  • Run technology transfers and deliver regulatory submissions.
  • Lead and mentor the SoliD team and align programmes with CMC objectives.

Skills

Budget Management
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

Education

Ph.D. in Pharmaceutical Sciences

Job description

Johnson & Johnson’s SoliD group in Beerse, Belgium, seeks a Senior Manager/Associate Director to advance solid formulation and process development for synthetic compounds. You will guide multiple programmes, ensure regulatory alignment, and lead cross-functional teams in a fast-paced, global health environment.

You will mentor scientists, plan resources, and coordinate with Pharmaceutical & Material Sciences, Regulatory, and Supply Chain to accelerate development from discovery to

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