- LucerneTemporary
The EMEA Compliance Manager is part of the Regional Transformation team working directly with the SCM Quality team. The function oversees and supports documentation management, training management, L&D support, compliance/transformation projects deviation & related SOP reviews/approvals. The respective compliance/transformation projects are to drive Supply Chain optimization towards the Global Quality Manual Standards & the EMEA hubs to be Permanently Inspection Ready.
Global pharmaceutical organization
Immediate availability required
- LucerneTemporary
Provide ongoing support for a Quality Assurance team such as review of documents for final disposition of clinical supplies to clinics.
Review of documents for final disposition of clinical supplies to clinics, including label release, GMP batch record review for packaging activities, regulatory review for compliance against filings
Global pharmaceutical organization
Immediate availability required
- LucerneTemporary
The Associate Director Clinical Project Manager will be responsible for the oversight in compliance related matters, for conducting the cross functional Study Execution Team, and for continuous monitoring of KPIs and Metrics compliance of vendors for assigned complex clinical trials. Moreover you manage the study budget, including Task Orders, Change Orders, invoice approval and financial reconciliation process
Challeging opportunity within a global pharmaceutical organization
Interim 12- months assignment
- 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
- LausannePermanent
We are looking for an Intellectual Property Associate.
Growing Biotech Company
Intellectual Property - One Year contract
- MorgesPermanent
Oversee and support the requirements related to the EMEIA tender process, support the global regulatory intelligence and regulatory surveillance processes, advocacy with government bodies and manufacturer associations across Europe, implementation of new regulation, tender management.
Innovative Medical Company
Dynamic environment
- 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.
- 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 support the regulatory affairs team
- 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
- GenevaTemporary
S/he has the responsibility to support dossier preparation for new medicine registration application.
Great opportunity to work on a new medicine registration application
Rare diseases
- NyonPermanent
The Clinical Affairs Manager will be responsible for successful execution of assigned clinical field trials within budget and in conformance with global regulations and internal policies and procedures.
Mid-Sized organization
Global responsibilities
- MorgesPermanent
Regulatory registrations/filings, Regulatory operations support, Quality Management System implementation & coordination.
Fast growing company
Innovative Medical Technology
- ZürichPermanent
Within this function as Verification and Validation Manager you`re responsible for the effective planning and execution of all verification and validation activities within the organization.Innovative company in the field of Medical Devices
Versatile function within a dynamic environment
- ZürichTemporary
In this function you'll manage all tasks related to the verification and validation activities of software, processes, products, equipment etc.
Dynamic Medical Device organization
Immediate availability required
- OltenPermanent
The Regulatory Affairs Manager, reporting directly to the Head Medical & Regulatory Affairs / QA, will be responsible for managing and implementing the activities required obtaining and maintaining regulatory clearance with the local Authorities for the set array of products.
Join a great Company and Business in the Canton of Solothurn
Join one of the key players in the Generics and Brands arena
- 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
- ZugPermanent
Support the Global Regulatory Team
Be an expert and guide Promotion and Advertising Regulatory affairsJoin a leading global medical devices player
Be a key member of the Regulatory Affairs team
- 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
- 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
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