- ZugTemporary
Technical and methodological support for the management and improvement of pharmaceutical packaging, in cooperation with customers / markets, packaging suppliers, production, engineering services and registration bodies.
Immediate availability required
Global pharmaceutical organization
Save Job View Job - LucerneTemporary
The Supply Chain Specialist is responsible for reviewing and owning processes that connect with various functions within the group to drive supply chain actions arising from Network & source changes & Regulatory driven artwork changes. These functions include, but are not limited to, Master Data, Finance, Supply Network Planning, Customer Service, Market Planning, Manufacturing sites, Quality, Regulatory and Artwork.
Global pharmaceutical organization
Immediate availability required
Save Job View Job - LucerneTemporary
Manage the contractual relationship with vendors in capital investment projects.
Immediate availability required
Global pharmaceutical organization
Save Job View Job - 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
Save Job View Job - NyonPermanent
Participate in the registration activities at a global level
International exposure
Fast growing company
Save Job View Job - InternationalPermanent
For our client, an internationally established company leader in market analysis, we are looking for an experienced Senior Consultant Real World Evidence. Our client has been operating in the Life Science sector for over 30 years. Ever since, the company has been providing elaborated analysis which drove innovation and paved the way for new healthcare solutions.
Senior position in established and renowned research company
Analytical consultancy, liaise and drive internal and external KOL's
Save Job View Job - LausannePermanent
The Regulatory Affairs Consultant for MDR will be responsible for overseeing and executing MDR compliance plan to ensure all applicable technical files meet the EU MDR requirements on schedule.
Medical devices
International company
Save Job View Job - GenevaPermanent
To incorporate Medical Device information in to Module 3 for a drug-device combination product.
International company
International exposure
Save Job View Job - GenevaPermanent
1 year temporary project management position in a Regulatory Affairs team
International company
Nyon, Switzerland
Save Job View Job - LausannePermanent
The Sr Director will be responsible for managing all aspects of operational plans across a program with multiple global clinical trials and serve as a leader to the clinical operations team and a key member of the clinical development department. The position will report to the Head of Global Clinical Operations based in the US.
Fast growing biotech company
Oncology
Save Job View Job - LausannePermanent
The Clinical will assume a leadership role in overseeing the design, implementation, conduct and evaluation of oncology clinical trials to ensure data quality and integrity.
Fast growing biotech company
Oncology
Save Job View Job - VaudPermanent
We are looking for our client a Tender Specialist who will be in charge of managing individual tender submissions as part of a tender management team, while ensuring compliance with the company's policies and applicable laws, as well as contributes to the continuous improvement of tender management processes.
Work for an innovative company
Be part of a dynamic team
Save Job View Job - BernPermanent
The Regulatory Affairs Specialist is supporting the local RA team with the upkeep of RA standards as well as the submissions for new products.
Innovative global Medical Device Company
Very good opportunities for personal and professional development
Save Job View Job - SolothurnPermanent
Our client is looking for an experienced Quality Manager to support the local production team in all quality assurance related questions. You will be responsible for the management of the on site Quality Expert as well as the liaison of quality topics between several stakeholders
innovative company with gloabl reach
very good development options
Save Job View Job - LausannePermanentCHF80,000 - CHF90,000
As RAQA Specialist, you will be responsible for establishing and maintaining the company's quality assurance system and for ensuring its regulatory compliance.
Start-up company
Innovative Medical Technology
Save Job View Job - GenevaPermanent
The primary purpose of the Post Market Surveillance Specialist is to collect, analyze, and report post market events in compliance with national and international regulations and guidance.
International company
Mid-size company
Save Job View Job - SolothurnPermanent
Our client is looking for an experienced Quality Engineer to support the local production team in all quality assurance related questions. You will be responsible for all Quality Processes as well as the liaison of quality topics between several stakeholder.
innovative company with gloabl reach
very good development options
Save Job View Job - BaselPermanent
Our client is currently looking for a passionate Regulatory Affairs professional to lead the European Cluster. This position requires strategical thinking as well as a hands on regulatory approach.
innovative medical device company
good global development options
Save Job View Job - ZugPermanent
The succesfull candidate will improve operations by bringing systematic and disciplined approach to risk management, control and governance processes. A thorough knowledge of ISO 13485 and FDA QSR are required.
Join a leading global medical devices player
Help people around the globe leading a healthier life
Save Job View Job - 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
Save Job View Job
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