20 beste Stellen als chemistry project 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
Scientist I/II Analytical CMC & QC
Monte Rosa Therapeutics, Inc —Basel, BS
- CHF 95’000 - CHF 125’000 pro Jahr
- 100%
- Doktorat
- Master
- Qualitätskontrolle
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PM Group —Basel, BS
- Englisch
- Microsoft Office
- Bachelor
2 Tage
Junior Process Engineer
Ecolab Inc. —Witterswil, SO
- 100%
- Englisch
- Master
- Bachelor
- Aufstiegsmöglichkeiten
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- 100%
- Englisch
- Master
- Bachelor
- Aufstiegsmöglichkeiten
8 Tage
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- CHF 90’000 - CHF 110’000 pro Jahr
- 100%
- Forschungserfahrung
- Master
- Analysefähigkeit
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Lallemand —Reinach BL, BL
- 100%
- Doktorat
- Englisch
- Master
9 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
Principal Scientist/ (Associate) Director, Medicinal Chemistry
Ridgeline Discovery —Basel, BS
- 100%
- Doktorat
- Englisch
- Kommunikationsfähigkeit
Direkt bewerben
Director / Associate Director – Toxicology
Monte Rosa Therapeutics, Inc —Basel, BS
- CHF 150’000 - CHF 200’000 pro Jahr
- 100%
- Doktorat
- Forschungserfahrung
- Master
8 Tage
PhD Position for Synthetic Biology-Inspired Therapies
ETH Zürich —Basel, BS
- 100%
- Doktorat
Analytical Molecular Characterization Team Lead and Mass Spectrometry Scientist
Roche —Basel, BS
- 100%
- Doktorat
- Master
- Führungserfahrung
Transfer/Launch Manager ASAT E2E Bio
Roche —Kaiseraugst, AG
- 100%
- Englisch
- Analysefähigkeit
5 Tage
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- 100%
- Englisch
- Microsoft Office
- Kommunikationsfähigkeit
CMC Expert Analytical Development focus Parenterals&Devices
Roche —Basel, BS
- 100%
- Doktorat
- Forschungserfahrung
- Analysefähigkeit
Director, Toxicology
Swiss Biotech Association —Basel, BS
- Doktorat
- Forschungserfahrung
- Master
2 Tage
Global Head of Pharma Technical Development Synthetic Molecules (PTDC)
Roche —Basel, BS
- 100%
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- Doktorat
- Kommunikationsfähigkeit
Global OE Specialist - Lean (a), 100%
Bachem Holding AG —Bubendorf, BL
- 100%
- Management-Erfahrung
- Englisch
- Forschungserfahrung
Postdoc Position for Synthetic Biology-Inspired Therapies
ETH Zürich —Basel, BS
- 100%
- Doktorat
HSE Manager BSF Site Development 100% - Sisslerfeld(a)
Bachem Holding AG —Stein AG, AG
- 100%
- Homeoffice
- Management-Erfahrung
- Englisch
- Projektmanagement
- Pensionskasse

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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

chemistry project Jobs in basel, bs

Scientist , CMC Process Chemistry

Scientist I/II Analytical CMC & QC

QA Engineering Specialist

Junior Process Engineer

Junior Process Engineer

Research Associate Proteomics

Application Development Engineer

Development Operations Coordinator, CMC/DMPK (Contractor)

Principal Scientist/ (Associate) Director, Medicinal Chemistry

Director / Associate Director – Toxicology

PhD Position for Synthetic Biology-Inspired Therapies

Analytical Molecular Characterization Team Lead and Mass Spectrometry Scientist

Transfer/Launch Manager ASAT E2E Bio

Mechanical Design Engineer Pressure Equipment

CMC Expert Analytical Development focus Parenterals&Devices

Director, Toxicology

Global Head of Pharma Technical Development Synthetic Molecules (PTDC)

Global OE Specialist - Lean (a), 100%

Postdoc Position for Synthetic Biology-Inspired Therapies

HSE Manager BSF Site Development 100% - Sisslerfeld(a)

Ich möchte aktuelle Job-E-Mails für Stellen als chemistry project in basel, bs erhalten

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