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Senior/ Principal Scientist - Peptide parenteral formulation development(m/w/x)
Beschreibung
You lead the development and manufacturing of innovative peptide formulations, ensuring regulatory compliance and facilitating market approvals to provide essential medicines to patients.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •Proven experience authoring NDA drug product sections
- •Strong expertise in chemistry and solid state characterization
- •Experience in peptide analytical techniques and aseptic manufacturing
- •Direct experience in writing regulatory CMC documents
- •Excellent communication and stakeholder management skills
- •Ph.D. or master's degree in chemistry or related fields
Ausbildung
Berufserfahrung
6 Jahre
Aufgaben
- •Drive development of peptide parenteral formulations.
- •Oversee manufacturing processes for peptide formulations.
- •Manage scale-up, process characterization, and validation.
- •Facilitate transfer to global commercial manufacturing sites.
- •Act as Pharmaceutical Project Leader in CMC teams.
- •Shape global regulatory submissions for all phases.
- •Impact market approvals for life-changing medicines.
Sprachen
Englisch – verhandlungssicher
- 1201 F. Hoffmann-La Roche AGVollzeitnur vor OrtManagementBasel
- 1201 F. Hoffmann-La Roche AG
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Senior/ Principal Scientist - Peptide parenteral formulation development(m/w/x)
Die KI-Suchmaschine für Jobs
Beschreibung
You lead the development and manufacturing of innovative peptide formulations, ensuring regulatory compliance and facilitating market approvals to provide essential medicines to patients.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •Proven experience authoring NDA drug product sections
- •Strong expertise in chemistry and solid state characterization
- •Experience in peptide analytical techniques and aseptic manufacturing
- •Direct experience in writing regulatory CMC documents
- •Excellent communication and stakeholder management skills
- •Ph.D. or master's degree in chemistry or related fields
Ausbildung
Berufserfahrung
6 Jahre
Aufgaben
- •Drive development of peptide parenteral formulations.
- •Oversee manufacturing processes for peptide formulations.
- •Manage scale-up, process characterization, and validation.
- •Facilitate transfer to global commercial manufacturing sites.
- •Act as Pharmaceutical Project Leader in CMC teams.
- •Shape global regulatory submissions for all phases.
- •Impact market approvals for life-changing medicines.
Sprachen
Englisch – verhandlungssicher
Über das Unternehmen
Roche
Branche
Pharmaceuticals
Beschreibung
The company is dedicated to advancing science and ensuring access to healthcare for current and future generations. With over 100,000 employees globally, Roche aims to deliver life-changing healthcare solutions.
- 1201 F. Hoffmann-La Roche AG
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