20 beste Stellen als chemistry project in pratteln, bl – 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
Synthesis Lead I – Synthesis Research Chemistry (m/f/d)
Syngenta Crop Protection —Stein, AG
- 100%
- Doktorat
- Englisch
- Pensionskasse
Direkt bewerben
9 Tage
Innovation Chemical Laboratory Technician
Ecolab Inc. —Witterswil, SO
- 100%
- Englisch
- Bachelor
- Kommunikationsfähigkeit
- Aufstiegsmöglichkeiten
Scientist I/II Analytical CMC & QC
Monte Rosa Therapeutics, Inc —Basel, BS
- CHF 95’000 - CHF 125’000 pro Jahr
- 100%
- Doktorat
- Master
- Qualitätskontrolle
Innovation Chemical Laboratory Technician
Ecolab —Witterswil, SO
- 100%
- Englisch
- Bachelor
- Kommunikationsfähigkeit
- Aufstiegsmöglichkeiten
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PM Group —Basel, BS
- Englisch
- Microsoft Office
- Bachelor
2 Tage
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Sulzer —Allschwil, BL
- 100%
- Englisch
- Kommunikationsfähigkeit
- Kostenloser Parkplatz
Junior Process Engineer
Ecolab —Witterswil, SO
- 100%
- Englisch
- Master
- Bachelor
- Aufstiegsmöglichkeiten
7 Tage
Junior Process Engineer
Ecolab Inc. —Witterswil, SO
- 100%
- Englisch
- Master
- Bachelor
- Aufstiegsmöglichkeiten
7 Tage
Development Operations Coordinator, CMC/DMPK (Contractor)
Monte Rosa Therapeutics, Inc —Basel, BS
- CHF 45 - CHF 65 pro Stunde
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Research Chemist - Organic Chemistry.
SpiroChem AG —Basel, BS
- Doktorat
- Schreibfähigkeiten
- Englisch
Transfer/Launch Manager ASAT E2E Bio
Roche —Kaiseraugst, AG
- 100%
- Englisch
- Analysefähigkeit
4 Tage
Application Development Engineer
Lallemand —Reinach BL, BL
- 100%
- Doktorat
- Englisch
- Master
8 Tage
Technical Operational Quality Expert
Omya International AG —Egerkingen, SO
- 100%
- Schreibfähigkeiten
- Laborerfahrung
- Englisch
Direkt bewerben
21 Std.
Research Associate Proteomics
Monte Rosa Therapeutics, Inc —Basel, BS
- CHF 90’000 - CHF 110’000 pro Jahr
- 100%
- Forschungserfahrung
- Master
- Analysefähigkeit
Global Head of Research Chemistry
Syngenta Crop Protection —Stein, AG
- 100%
- Doktorat
- Englisch
- Forschungserfahrung
- Pensionskasse
Direkt bewerben
QA Deviation Management Specialist
Thermo Fisher Scientific —Allschwil, BL
- 100%
- Englisch
- Qualitätskontrolle
- Organisationstalent
14 Tage
Principal Scientist/ (Associate) Director, Medicinal Chemistry
Ridgeline Discovery —Basel, BS
- 100%
- Doktorat
- Englisch
- Kommunikationsfähigkeit
Direkt bewerben
14 Tage
Mechanical Design Engineer Pressure Equipment
Sulzer —Allschwil, BL
- 100%
- Englisch
- Microsoft Office
- Kommunikationsfähigkeit
Global OE Specialist - Lean (a), 100%
Bachem Holding AG —Bubendorf, BL
- 100%
- Management-Erfahrung
- Englisch
- Forschungserfahrung

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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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Principal Scientist/ (Associate) Director, Medicinal Chemistry

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Ich möchte aktuelle Job-E-Mails für Stellen als chemistry project in pratteln, bl erhalten

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