20 beste Stellen als analytical development in basel bs – aktuell auf Personalsuche

Scientist , CMC Process Chemistry
Monte Rosa Therapeutics, Inc —Basel, BS
- CHF 100’000 - CHF 130’000 pro Jahr
- 100%
- Doktorat
- Master
- Produktion
Innovation Chemical Laboratory Technician
Ecolab Inc. —Witterswil, SO
- 100%
- Englisch
- Bachelor
- Kommunikationsfähigkeit
- Aufstiegsmöglichkeiten
Scientist/ Sr. Scientist - Image Analysis (2 year contract)
Roche —Basel, BS
- 100%
- Informatik
- Doktorat
- Datenanalyse
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Sentec —Therwil, BL
- Hybrides Arbeiten
- Management-Erfahrung
- Englisch
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Manager, Knowledge Management
Colgate-Palmolive —Therwil, BL
- Google Suite
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- Doktorat
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Civil Engineer
Wayidem Engineering —Basel, BS
- CHF 6’500 - CHF 15’000 pro Monat
- 100%
- AutoCAD
- Analysefähigkeit
- Erfahrung im Bauwesen
- Kostenloser Parkplatz
- Gesundheits- und Wohlfühlprogramme
Direkt bewerben
Quantitative Systems Pharmacology Modeler
LYO-X GmbH —Basel, BS
- Doktorat
- Englisch
- Master
Project Planning Configurator
Jet Aviation —Basel, BS
- PMP
- Englisch
- Master
Infrastructure Verification Engineer
TechBiz Global GmbH —Basel, BL
- 100%
- Homeoffice
- Analysefähigkeit
- Bachelor
- Scripting
8 Std.
Allocator Intern
Tally Weijl —Basel, BS
- Teilzeit
- Englisch
- Analysefähigkeit
- Bachelor
Direkt bewerben
Solutions Analyst
Jet Aviation —Basel, BS
- Englisch
- Analysefähigkeit
- Bachelor
People Insights & Analytics Intern 80-100%
Lonza —Basel, BS
- Microsoft Powerpoint
- Microsoft Excel
- Englisch
Systems Pharmacology Internship Antibiotics Resistance
LYO-X GmbH —Basel, BS
- Englisch
- Master
- Analysefähigkeit
End of Study Internship Product Management
Swiss AviationSoftware —Allschwil, BL
- Microsoft Excel
- Microsoft Office
- Analysefähigkeit
- Mitarbeiterrabatt
- Pensionskasse
Manager Retail Operations & Store Communications EMEA (9-month maternity cover) (f/m/x)
Fossil Group, Inc. —Basel, BS
- 100%
- Englisch
- Microsoft Office
- Analysefähigkeit
Direkt bewerben
Strategic Planning Manager Supply Chain
Sobi —Basel, BS
- 100%
- Hybrides Arbeiten
- Microsoft Excel
- Management-Erfahrung
- Englisch
Direkt bewerben
Principal, Strategic Advisory Consulting (Life Sciences Supply Chain & Operations)
IQVIA —Basel, BS
- 100%
- Management-Erfahrung
- Englisch
- Master
3 Tage
Director, Clinical Development
Neurocrine Bioscience —Allschwil, BL
- 100%
- Doktorat
- Master
- Führungserfahrung
Investment Specialist (w/m/d) Parttime/Fulltime
Baloise Group —Basel, BS
- Teilzeit
- Management-Erfahrung
- Englisch
- Master
14 Tage
Head of Strategy, Biosimilars Development, Manufacturing & Supply
Sandoz —Basel, BS
- 100%
- Erfahrung mit Netzwerken
- Produktion
- Führungserfahrung
6 Tage

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Scientist , CMC Process Chemistry

Monte Rosa Therapeutics, Inc
Basel, BS

Jetzt bewerben

Details zur Stelle

100% | Pensum: 90-100%
CHF 100’000 - CHF 130’000 pro Jahr

Qualifikationen

Doktorat
Klinische Erfahrung
Master
Produktion

Vollständige Stellenbeschreibung

Overview:

In this exciting role the successful candidate will contribute to CMC tasks from discovery/preclinical stage to clinical and potentially commercial stage. This includes managing outsourcing activities for development and manufacturing of drug substance from early phase onwards, including route scouting, process development and compounds supply from pre-IND to clinics. The role might imply involvement in drug product development activities from and early formulation to development and manufacturing. Strong experience in process chemistry of small molecule APIs, the desire to work in a fast-paced dynamic environment, excellent team working and cross-functional collaboration are critical in this role.

Responsibilities:

Delivery through external vendors of drug substance including route scouting, process research and development, scale-up, manufacturing and material supply activities from preclinical phase onwards with high level of independence.
Assessment or existing routes of synthesis, bottles necks identification and design of alternatives and synthesis solutions. During manufacturing and scale-up, trouble shooting, process and analytical development.
Contribute to the development and implementation of strategies to manufacture drug substance including process development, procurement of raw materials, phase appropriate analytical activities and control strategies.
Management of timelines, resources and budgets.
On assigned projects, act as CMC lead and point of contact in cross functional project teams by participating in project meetings and provide regular updates. As CMC lead, involvement into drug product development activities might also be required.
Establish a strong interaction with medicinal chemistry to support as needed early development efforts ensuring syntheses improvements as early as possible.
Liaise withtoxicology and clinical teams to seamlessly advance our small molecule development candidates into preclinical & clinical development.
Manage physico-chemical and solid state studies of small molecule drug substances including polymorphism, solubility, early formulation studies, etc. to assess developability and formulation strategies for clinical development and commercialization.
Identify, select and manage with high level of autonomy appropriate Contract Development & Manufacturing Organizations (CDMOs) for appropriate process development work and for the GMP supply of drug substance and drug product.
Prepare, review, edit CMC regulatory and quality documents (batch records, analytical validations, reports and protocols).
Liaise with the regulatory team for drafting and reviewing documents for INDs and other regulatory submissions.
Responsible for drug supply chain in preclinical and clinical trials.

Qualifications:

PhD or MSc in Organic Chemistry, Pharmaceutical Chemistry, Pharmaceutical sciences or related scientific discipline.
2-7 years of relevant experience in the pharmaceutical or biotech industry in areas such as: process chemistry , chemical or analytical development, scale-up, manufacturing (pilot or large scale), pre-formulation/formulation with small molecule drugs.
Sound knowledge of organic chemistry and process development of small molecule API.
Understanding of technical development from preclinical stage till clinical phases.
Experience of GMP manufacturing drug substances and/or drug products.
Experience of managing CDMOs and complex supply chains.
Other desirable experience: large molecule development and formulation; experience with different pharmaceutical dosage forms (e.g. tablets, capsules, parenteral, etc.), support of clinical development (Phase 1 through Phase 3) including IND, CTA and NDA filings; FDA and EMEA regulations are considered a plus, process validation/registration experience.
Needs to be highly effective in cross-functional and cross-site teams.

Jetzt bewerben

Erweiterte Suche

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Ich möchte aktuelle Job-E-Mails für Stellen als analytical development in basel bs erhalten

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