12 beste Stellen als life science consultant in reinach bl bl – aktuell auf Personalsuche

Consultant Medical Product Excellence
Arcondis —Basel, BS
- Management-Erfahrung
- Doktorat
- Englisch
Director, Clinical Development
Neurocrine Bioscience —Allschwil, BL
- 100%
- Doktorat
- Master
- Führungserfahrung
Principal, Strategic Advisory Consulting (Life Sciences Supply Chain & Operations)
IQVIA —Basel, BS
- Management-Erfahrung
- Englisch
- Master
Senior QA Manager (Consultant) / GMP & CQV 100% (w/m/d)
Azimuth Quality GmbH —Basel, BS
- CHF 100’000 - CHF 135’000 pro Jahr
- Englisch
- Kostenloser Parkplatz
- Homeoffice-Möglichkeit
Direkt bewerben
4 Tage
Partner - DACH Life Sciences Consulting Lead
Wipro Limited —Basel, BS
- Erfahrung mit Netzwerken
- Führungserfahrung
- Kommunikationsfähigkeit
8 Tage
Project Engineer (Life Sciences)
agap2 - HIQ Consulting —Basel, BS
- Englisch
- Produktion
- Kommunikationsfähigkeit
Global Scientific Lead - Clinical Outcome Assessment (COA) Strategy Consulting - Multiple locations - Hybrid/Home-based
IQVIA —Basel, BS
- Management-Erfahrung
- Doktorat
- Schreibfähigkeiten
Digital Pathologist
Roche —Basel, BS
- 100%
- Doktorat
- Analysefähigkeit
- Kommunikationsfähigkeit
Validation Engineer (Life Sciences)
agap2 - HIQ Consulting —Basel, BS
- Englisch
Trainee Recruitment Consultant
Skilled – Recruitment Solutions —Basel, BS
- 100%
- Englisch
- Aufstiegsmöglichkeiten
Principal, Brand Outsourcing & HCP Engagement
IQVIA —Basel, BS
- Homeoffice
- Master
- Analysefähigkeit
- Bachelor
Senior Commissioning & Qualification (C&Q) Lead (a), 100%
Bachem Holding AG —Bubendorf, BL
- 100%
- Homeoffice
- Englisch
- Forschungserfahrung
- Master
- Pensionskasse

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Consultant Medical Product Excellence

Arcondis
Basel, BS

Jetzt bewerben

Details zur Stelle

Qualifikationen

Management-Erfahrung
Doktorat
Englisch
Forschungserfahrung
Klinische Erfahrung
Master
Analysefähigkeit
Bachelor
Kommunikationsfähigkeit

Vollständige Stellenbeschreibung

Medical Office - Basel, Frankfurt, Kosice, Boston, Malaysia, Singapore

Your profile / requirements

Master’s or Bachelor’s degree in Life Sciences, Biomedical Engineering, or a related field
MD or PhD preferred for technical areas
3–5 years (with a Master’s/Bachelor’s degree) / 1–3 years (with an MD or PhD) of experience in MedTech, regulatory affairs, clinical development, or related areas
Initial exposure to product lifecycle or regulatory projects is a must
Understanding of product lifecycle management and regulatory fundamentals
Working knowledge of medical–regulatory interface and compliance requirements
Familiarity with FDA and/or EU MDR regulations is preferred
Foundational understanding of medical device requirements engineering, medical risk analysis, and/or usability engineering.
Basic knowledge of clinical validation and evidence generation
Strong analytical skills with the ability to structure and analyse data
Ability to support problem-solving within defined scope
Developing structured and systematic thinking
Strong communication and collaboration skills
Ability to prepare structured documentation and presentations
Ability to work effectively in cross-functional and interdisciplinary teams
Fluent in English
Ability to manage tasks and deadlines with guidance
Willingness to learn, seek feedback, and continuously develop skills
Ability to adapt to new tools, technologies, and regulatory environments

Tasks and responsibilities

Contribute to project deliverables and support project leads in Medical Product Excellence engagements
Execute work packages with guidance across product lifecycle management, regulatory readiness, and validation activities
Support product lifecycle and regulatory readiness assessments
Assist in evidence-generation planning, documentation, and analysis
Contribute to clinical validation activities and technical research
Apply analytical skills to solve structured problems within defined scope
Ensure quality and compliance with regulatory and organisational standards
Perform routine tasks independently with guidance for more complex activities
Support project-related client interactions and communication
Build understanding of client needs and regulatory environments
Apply foundational knowledge in product lifecycle, regulatory, and clinical domains
Follow established processes, methodologies, and tools
Support development of templates and tools for clinical, regulatory, and product-related deliverables
Contribute to internal knowledge management and documentation of project learnings
Provide feedback on methodologies, tools, and ways of working
Identify minor process inefficiencies and suggest improvements
Support project extensions and renewals through high-quality delivery
Contribute to proposal development and preparation of sales materials
Provide input based on research, analysis, and project experience
Develop a professional voice and presence within the organisation
Maintain a professional personal brand as a subject matter expert in development within Medical Products
Contribute to internal publications, opinion pieces, and thought leadership content

Your Contact Person(s)

Merve Turhan

Senior Recruiter

Jetzt bewerben

Erweiterte Suche

life science consultant Jobs in reinach bl bl

Consultant Medical Product Excellence

Director, Clinical Development

Principal, Strategic Advisory Consulting (Life Sciences Supply Chain & Operations)

Senior QA Manager (Consultant) / GMP & CQV 100% (w/m/d)

Partner - DACH Life Sciences Consulting Lead

Project Engineer (Life Sciences)

Global Scientific Lead - Clinical Outcome Assessment (COA) Strategy Consulting - Multiple locations - Hybrid/Home-based

Digital Pathologist

Validation Engineer (Life Sciences)

Trainee Recruitment Consultant

Principal, Brand Outsourcing & HCP Engagement

Senior Commissioning & Qualification (C&Q) Lead (a), 100%

More jobs to discover

Ich möchte aktuelle Job-E-Mails für Stellen als life science consultant in reinach bl bl erhalten

Weitere Job-Standorte erkunden

Your profile / requirements

Tasks and responsibilities

Your Contact Person(s)

Merve Turhan

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