Director biologic drug substances manufacturing
Location: NetherlandsThe Company
Our client is a CDMO with international clients in biopharma. They provide full drug development from early phase to clinical development.Role Description
As the BU director you will be responsible for the drug substance development group, that has direct reports from the groups of USP, DSP, QC and a prep group. You provide support to all these groups in terms of scientific knowledge, strategy and further implementing a environment of innovation and continuous improvement.Responsibilities
You will have 3/4 direct reports, all at management level. You report to the CSO.You keep an eye on market developments, which you then implement in a strategy plan, based on your own technical knowledge. The portfolio is rather broad, from CHO and microbial proteins to enzymes and vaccines. The broader your expertise, the better!You support the Technical Business manager with his client engagement.
Requirements
- Preferably a PhD in pharmaceutical, chemical, biochemical, biologics or engineering is required- 10+ years in biologics with at least 4-6 years in a lead role is needed
- Experience in both manufacturing and in early development is preferred
- GMP experience
- Broad knowledge in protein therapeutics is needed
- An open personality that likes to engage with his team
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Naut van Osnabrugge.
Opis stanowiska
The Company
Our client is a CDMO with international clients in biopharma. They provide full drug development from early phase to clinical development.Role Description
As the BU director you will be responsible for the drug substance development group, that has direct reports from the groups of USP, DSP, QC and a prep group. You provide support to all these groups in terms of scientific knowledge, strategy and further implementing a environment of innovation and continuous improvement.Responsibilities
You will have 3/4 direct reports, all at management level. You report to the CSO.You keep an eye on market developments, which you then implement in a strategy plan, based on your own technical knowledge. The portfolio is rather broad, from CHO and microbial proteins to enzymes and vaccines. The broader your expertise, the better!You support the Technical Business manager with his client engagement.
Requirements
- Preferably a PhD in pharmaceutical, chemical, biochemical, biologics or engineering is required- 10+ years in biologics with at least 4-6 years in a lead role is needed
- Experience in both manufacturing and in early development is preferred
- GMP experience
- Broad knowledge in protein therapeutics is needed
- An open personality that likes to engage with his team
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Naut van Osnabrugge.
Dodatkowe informacje
- Ostatnia aktualizacja
- Wymiar etatu
- Pełny etat
- Rodzaj umowy
- Własna działalność
- Liczba wakatów
- 1
- Min. doświadczenie
- 2 lata
- Min. wykształcenie
- Wyższe licencjackie
- Branża / kategoria
- Praca Badania i rozwój (R&D)