Durchschnittsgehalt: CHF120.000 /jährlich
Mehr DatenSuchergebnisse: 98 Stellenangebote
CHF 120000 pro Jahr
...Genehmigungen. Überwachung des regulatorischen Lifecycle-Managements bestehender Produkte
Enge Zusammenarbeit mit dem Hauptteam für Regulatory Affairs mit Sitz in Deutschland
Primärer Ansprechpartner für Regulatory Affairs in der Schweiz
Anforderungen:
Mindestens...
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...industry and the academic sphere.
Job Description
One of Sobi’s four strategic pillars is to “Go Global”. The Manager, Regulatory Affairs International supports our ambitious geographical expansion plans. Sobi is seeking to register some of our existing portfolio...
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Vollzeit
Job Purpose
Be a member of product development project-teams from the initiation phase, ensure implementation of quality and Regulatory Affairs requirements for Europe, US & Canada, perform product registration in EU, US & Canada.
Main Tasks and Responsibilities...
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Vollzeit
...compliance with regulations throughout product development.
- Conduct regulatory research and prepare documentation for submissions.
- Support... ...- Bachelor's degree in a relevant field.
- Prior regulatory affairs experience
- general pharma knowledge
Ausbildung
Regulatory...
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Temporär
Senior Consultant Regulatory Affairs MedTech (SaMD, AI, Robotics)
Compliance Services - Basel, Frankfurt
Apply now
About Arcondis
Arcondis is a global consulting company with an exclusive focus on the healthcare and life science industries. Headquartered...
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Ihre Aufgaben
~Mitarbeit bei der Erstellung, Einreichung und Dokumentation des regulatorischen Meldewesen EU (CoRep, FinRep, LiqRep und weitere Unterlagen gemäss Konzernvorgaben) inkl. notwendigem KnowHow Aufbau zur Betreuung der relevanten EDV-Systeme und Schnittstellen...
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Job Title: Event Manager Clinical Development & Medical Affairs
Work Location: Allschwil
Country: Switzerland
Schedule: Parttime (80%)
Desired start date: ASAP
Duration: 12 months
Contractor Rate: CHF 69.49 - CHF 77.96
RESPONSIBILITIES AND TASKS
• Plan, coordinate...
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Teilzeitarbeit
Soforteinstellung
...promising career opportunities and offer the latest in skill development training programmes.
Contract Manager within Global Medical Affairs – 5854 LBD
We are looking for a highly motivated Contract Manager within Global Medical Affairs for our client, a major...
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Homeoffice
...: #1 reducing COGS, #2. establishing a customer obsessed E2E SC, #3 increasing our competitive advantage through Quality and Regulatory affairs, #4 building capacity to support the growth, #5 delivering on the group’s ESG commitments, by #6 engaging and growing people,...
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Vollzeit
...on budget)
Establish and oversee the execution of robust integrated drug development plans that are patient focused and address regulatory commercial and access considerations
Drive decisionmaking for budget and resource commitments. Ensure the consideration of...
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Vollzeit
...oriented and analytical mindset; ability to identify potential deficiencies, propose solutions, and effectively interpret and apply regulatory requirements; excellent communication skills; ability to collaborate efficiently with interdisciplinary teams in a dynamic...
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Stundenlohn
...Bachelor degree preferred in a technical field and/or engineering.
Proven process understanding in Sterile Manufacturing (Pharma, regulatory aspects).
Familiarity with GMP requirements, quality procedures and SOP execution.
Previous exposure to any of the...
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...Scientist to provide scientific and medical expertise to various products across various stages of clinical development to facilitate regulatory submissions.
Your tasks:
Develop a thorough understanding of scientific and medical aspects to prepare key documents (e.g.,...
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Soforteinstellung
...activities in fresh markets, documenting them comprehensively
Monitor and analyse forthcoming and recently enacted tax laws, regulatory positions, legal rulings, and court cases impacting the company's direct tax position. Propose strategic action steps as required...
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...managing tests for the software they build.
Process & Operations: support test automation required by quality practices as well as regulatory compliance needs.
Fluent in English
If its an interest to you then please reply asap as we have a deadline to submit the...
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Remote job
Soforteinstellung
...innovative biopharmaceutical company are seeking a highly inquisitive, passionate, and driven Scientific Associate to ensure the regulatory compliance of late-stage development products.
What is it like to work here?Gain the opportunity to work across several therapeutic...
Soforteinstellung
...science discipline.
Ability to address GMP and logistic related questions with line unit experts.
Scientific, technical and regulatory knowledge in a specific area.
Basic knowledge of drug development.
Detailed knowledge of cGMP, working knowledge of safety...
...with internal teams to ensure timely release of GMP relevant documents and batches.
Upholding compliance with cGMP guidelines, regulatory requirements, and internal SOPs.
Why Join Us?
Location: Fully site-based in Basel, Switzerland, immerse yourself in a...
Lehrstelle
Soforteinstellung
...specifications.
Maintain records and create traceability documents for assembled components or devices, ensuring compliance with regulatory requirements.
Address assembly challenges by providing technical expertise to resolve issues and maintain process consistency....
Vollzeit
Schichtarbeit
....
Ensure a GMP/GDP compliant supply chain and GxP environment qualification status.
Write edit assess and approve relevant regulatory documents and support audits.
Actively support the organization in regulatory requirements technology and training.
Provide...
Vollzeit