- ZürichTemporary
In this challenging position you will support the CPLs for the planning, implementation, execution and compliance of operational plans for clinical study/program with multiple clinical vendors in order to maintain inspection readiness.
Short notice availability
Work in Zurich City
- Basel-CityPermanent
RA Manager to support the business with the development and implementation of a global ra strategy.
RA Manager to run day to day RA activitiesworking with Rare Diseases
upcoming swiss biotech
- Basel-CountryPermanent
Our client is currently looking for an experienced regulatory professional to support the development and implementation of global regulatory strategies.
Join one of the most recognized Pharma players
Help people around the globe leading a healthier life
- LucerneTemporary
An exciting opportunity for a Specialist Engineering with main focus to Computer System Validation (CSV) and Data Integrity (DI) to join the biological drug development and manufacturing site
Immediate availability required
Contrat of unlimited duration
- BaselPermanent
For one of our key clients in Switzerland, we are currently recruiting a QA/QC manager.
This role has been opened to strengthen the current team.
Join the Leader in the industry
Become a key member of the QA team
- InternationalPermanentCHF161,309 - CHF230,441
For one of our top clients we are recruiting for a Senior Director, Qualified Person for Pharmacovigilance (QPPV). We are looking for a candidate who has a strong analytical mind and an eye for detail. Are you flexible, accurate and do you have good planning skills? Then we might be looking for you!
Innovative work environment
Excellent annual salary up to € 200000 gross
- SchwyzPermanent
The Global RA Manager is responsible to develop and implement the global RA strategy, as well as lead the RA business unit cluster.
Market leading consumer goods industry player
Senior role with Global reach
- NyonPermanent
Our client is looking for a Technical Documentation Coordinator to support its regulatory affairs team.
Great opportunity to join a market leader in medical device
To be part of the regulatory affairs team
- ZürichPermanent
Our client is lookig for an experienced Market Access Manager to support the business in the German speaking part of Switzerland.
cutting edge technology
multinational company with many interesting development opportunitites
- NyonTemporary
- Prepare and write registration files for pharmaceutical products to be submitted in the targeted markets.
- Maintain and protect existing licenses in international, ensuring compliance with local regulations.
International company
Pharma products
- Prepare and write registration files for pharmaceutical products to be submitted in the targeted markets.
- GenevaTemporary
-Prepare submission/compliance strategy documents in line with specified timeframes.
-Ensure complaints and reportable events are processed correctly and in a timely manner.MDR transition
International company
- NyonPermanent
Prepare and coordinate various activities to make applications for product licenses.
Great opportunity to join a market leader in medical device.
To be part of the regulatory affairs team.
- LucerneTemporary
The Medical Science Liaison (MSL) is the country scientific expert for the assigned franchise (HIV, few activities within the HCV area) under the guidance of the Medical Director and provides medical/scientific information to Clinical and Scientific Leaders (CSLs) and Scientific Organizations or Collaborative Groups based on cutting-edge scientific exchange oriented towards their interests and needs.
Immediate availability required
Global pharmaceutical organization
- NyonPermanent
The Regulatory Affairs lead will have to manage CE Mark approvals and geographical expansion while managing a small team of RA Specialists.
Global Company
Multi-tasking working environment
- GenevaPermanent
In order to strengthen its sales team in Switzerland to establish a challenging new market in the Lake Geneva region, our client is looking for a Territory Manager in charge of developing the market within orthodontists.
Growing company in the dental field
New Business to establish in Romandie
- SwitzerlandPermanent
We are urgently looking for an experienced Senior Director of Quality and Regulatory Affairs to lead all aspects of regulatory assurance, quality assurance/control, and regulatory compliance.
The right candidate will be a member of the Management Board and will be responsible for driving the overall business strategy and execution.Join a leading global medical devices player
Become an active member of the Management board
- SwitzerlandPermanent
The right Candidate will lead all aspects of R&D activities for the group.
- Driving the overall R&D business strategy and execution.
- Help achieving the business growth, profitability, and quality objectives.
- Improving, supporting new product development, building, developing, and engaging a diverse global organisation.
Join a leading global medical devices player
Drive the future R&D strategies
- ZugPermanent
Become a Key member of the RA team helping clearing advertising and promotional material.
Join a leading global medical devices player
Be a key member of the Regulatory Affairs team
- LausannePermanent
The incumbent will be responsible for EMEA quality and regulatory strategies in support of consumer goods business (Oral Care Company) for drugs, medical devices, cosmetic products, foods/food supplements and commodity products.
Our client is a healthcare company with its EMEA headquarters based in Romandie
Management of a large product portfolio
- LausannePermanent
The position will be responsible for management of EU regulatory activities including management of regulatory service providers for assigned projects. The position is based near Lausanne and reports to the Director EU Regulatory Affairs.
Fast Growing start-up organization
Oncology
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