13 beste Stellen als cmc regulatory in bâle 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
Expert in Drug Product Formulation and Processing for Synthetic Molecule Parenterals (CMC Advisor)
Roche —Basel, BS
- 100%
- Management-Erfahrung
- Doktorat
- Schreibfähigkeiten
Director, Global Regulatory Affairs
Mirum Pharmaceuticals —Basel, BS
- Management-Erfahrung
- Bachelor
- Mentoring
7 Tage
Laboratory Technician (temporary for 2 years)
Roche —Basel, BS
- 100%
- Doktorat
- Englisch
- Master
2 Tage
Scientist, Pharmaceutical Development & Data Analytics _2 years temporary contract
Roche —Basel, BS
- 100%
- Management-Erfahrung
- Doktorat
- Datenanalyse
Director, QMS BPO, Quality Issue Escalation, Risk & Knowledge
BeiGene —Basel, BS
- CHF 178’600 - CHF 223’300 pro Jahr
- 100%
- Microsoft Powerpoint
- Microsoft Excel
- Microsoft Outlook
15 Std.
Analytical Molecular Characterization Team Lead and Mass Spectrometry Scientist
Roche —Basel, BS
- 100%
- Doktorat
- Master
- Führungserfahrung
QA Analytical Specialist
Sobi —Basel, BS
- 100%
- Hybrides Arbeiten
- Englisch
- Bachelor
- Kommunikationsfähigkeit
Direkt bewerben
Technical Development Leader (TDL) Large Molecules
Roche —Basel, BS
- 100%
- Doktorat
- Master
- Bachelor
MSAT Technical Lead - Drug Substance - Biologics
Sobi —Basel, BS
- 100%
- Hybrides Arbeiten
- Management-Erfahrung
- Englisch
- Produktion
Direkt bewerben
Section Lead Particle Design
Roche —Basel, BS
- 100%
- Management-Erfahrung
- Doktorat
- Kommunikationsfähigkeit
Global Head of Device Technology and Strategy
Roche —Basel, BS
- 100%
- Doktorat
- Englisch
- Master

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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

cmc regulatory Jobs in bâle bs

Scientist , CMC Process Chemistry

Scientist I/II Analytical CMC & QC

Expert in Drug Product Formulation and Processing for Synthetic Molecule Parenterals (CMC Advisor)

Director, Global Regulatory Affairs

Laboratory Technician (temporary for 2 years)

Scientist, Pharmaceutical Development & Data Analytics _2 years temporary contract

Director, QMS BPO, Quality Issue Escalation, Risk & Knowledge

Analytical Molecular Characterization Team Lead and Mass Spectrometry Scientist

QA Analytical Specialist

Technical Development Leader (TDL) Large Molecules

MSAT Technical Lead - Drug Substance - Biologics

Section Lead Particle Design

Global Head of Device Technology and Strategy

Ich möchte aktuelle Job-E-Mails für Stellen als cmc regulatory in bâle bs erhalten

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