Stellenangebote für Regulatory Jobs in Bern

42 Treffer

Clinical Project Manager (CPM)

Top Job - Bülach

Clinical Project Manager (CPM) The Medical Affairs Group is responsible for the design, conduction and evaluation of international first-in-man, regulatory submission and post-marketing trials. Your Responsibilities...

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Senior Consultant Life Sciences - Life Science Informa

Top Job - Reinach (BL)

Forschung & Entwicklung, klinische Studien, Regulatory Affairs, Marketing, Manufacturing - jeweils kombiniert mit fundiertem IT Wissen Tiefgehende Kenntnisse in den Bereichen Requirements Engineering/ Business Analysis Relevante...

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Regulatory Affairs Manager

Top Job - Bern

Regulatory Affairs Manager In this role, you will report to the Head Drug Regulatory Affairs and collaborate closely with other functions such as Clinical Research, Pharmacovigilance, Biostatistics, Commercial...

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Regulatory Affairs Manager About Serendi

- Bern

The employer is a middle-size pharmaceutical company - Responsible for the maintenance of the content of regulatory submissions of the licensed products from the site of manufacture, except for the regional, parts...

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Regulatory Database Administrative Support

- Bern

Regulatory Database Administrative Support CSL Behring - the global biotherapeutics provider driven by its promise to save lives. Our more than 1'400 employees in Bern are committed to developing and delivering live...

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Manager Clinical Evaluation

- Bern

Clinical evaluation plans and reports according to the MEDDEV 2.7.> Affairs, Product Management, Launch Team and Marketing on pipeline projects...

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Project Leader Biopharmaceutics

- Bern

Understanding of regulatory requirements for the testing and characterization of proteins as part of the submission for Phase 3 clinical trials and commercialization. - Excellent written and oral communication and presentation...

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Clinical Quality Assurance Manager

- Bern

Knowledge of GCP/GPV and related EU & FDA regulatory requirements and ICH guidelines - Ability to work effectively in a fast-paced environment and work effectively as part of clinical organization team - Ability to take...

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Clinial Scientist (Inflammatory Diseases)

- Bern

Design, statistics, regulatory processes - Fluency in English (oral, written) required, knowledge of German and French a plus - Medical writing skills If the opportunity to contribute to the development of a life-threatening...

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QA IT Project Manager ? 1 year

- Bern

GCLP and all related EU & FDA regulatory requirements and ICH guidelines...

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Quality Assurance Specialist - Diagnostics

- Bern

Review and change control are conform to regulatory requirements. Your Tasks - Manage projects as project leader and participate to others as quality support - Be the process expert for internal audit, inspections, management...

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QC Compliance Specialist ? 8 months

- Bern

Swissmedic, European union agencies and other regulatory bodies to assure that our products meet all cGMP requirements together with our operations and documentation system. Your Profile Education CFC or University degree in...

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Global Benefits Manager Europe

- Bern

Plan design and benchmarked market trends. Support market review of benefits competitiveness, documenting market trend research and maintaining pulse on regulatory changes and in-country market/talent trends affecting...

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QC Compliance Specialist ? 1 year

- Bern

Agencies and other regulatory bodies to assure that our products meet all cGMP requirements together with our operations and documentation system. Your Profile Education CFC or University degree in chemistry or pharmaceutical...

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Spezialist/in Regulatory Affairs D/E/F

Top Job - Frenkendorf

DenkvermögenStilsichere Deutschkenntnisse sowie gute Englisch und Französisch-kenntnisseWünschenswert sind Kenntnisse auf dem Gebiet Regulatory Affairs sowie Erfahrungen mit "Fast Moving Consumer Goods" (FMCG)Unser AngebotHerausforderndes und...

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Expert Regulatory Compliance

Top Job - Birsfelden

Expert Regulatory Compliance Ihr Aufgabengebiet Sie erstellen und aktualisieren den technischen Teil der Registrierungsdossiers für die bei uns hergestellten Produkte. Um ein CTD (Common Technical Dokument) von...

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