Manufacturing and Logistics Pharma Jobs in Europe
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Top Job
The Head Quality Biologics Visp provides strategic and operational leadership and management for the Visp Quality Biologics organization with main focus on compliance, efficiency...
Posted 3 days ago -
Top Job
As Scientist Endotoxin testing you are responsible for the scientific lead for LER studies and the Center of competence for endotoxins – you coordinate and monitor our LER...
Posted 39 days ago -
Working closely with highly experienced colleagues, you will be a key team member working hands on in the development, scale-up and technology transfer of a wide variety of...
Posted 1 day ago Deadline 20 November -
Responsible for the development of the CMC regulatory strategy for submissions. These submissions include IND/CTA, NDA, CTD and MAA regulatory filings. Collaborate with other...
Posted 2 days ago -
Your primary responsibility will be to manage overall 16 Site Regulatory Affairs teams of Teva based in Europe. You will lead a team of 3 direct reports who are heading the so...
Posted 2 days ago -
Jobs like this to
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Manage and review analytical activities (within Corden Pharma Brussels or with external partners) for the different analytical methods of the different projects; Review...
Posted 4 days ago -
Exercises sound decisions in assuring compliance by internal functions and Contract Manufacturers to regulations, practices and policies on device related development and post...
Posted 4 days ago -
In this role, you will be working as a Member of Process Development Sciences (PDS) – A focused group of senior subject matter experts (SMEs), with extensive experience in...
Posted 11 days ago -
Ensure the quality oversight of a new facility and drug substances produced therein; Be involved in transfers of manufacturing processes; maintain contact with customers,...
Posted 16 days ago -
The Supplier Quality Assurance Regional Manager must effectively develop, execute and manage the Quality Assurance Department in accordance with Corporate and Divisional policies...
Posted 16 days ago -
The Associate Director, Quality is responsible for developing, implementing and maintaining site compliance strategies and Quality Systems. The Associate Director is responsible...
Posted 19 days ago -
Manage the team with full responsibility for all aspects of human resource management such as qualification, development, coaching, hiring, pay decisions and discipline issues...
Posted 23 days ago -
As QA GMP Manager you will work in a multidisciplinary international QA team to ensure compliance to industry standards and regulations. You will be responsible for ensuring that...
Posted 25 days ago -
In this role you will perform the release of products of Mepha’s portfolio to the Swiss market, the management of quality incidents, new product launches, complaints, deviations,...
Posted 30 days ago -
In your role as Senior Manager Quality Assurance - Nordics it is your responsability to manage Nordics LRD Quality Assurance System in line with global, regional and local quality...
Posted 33 days ago -
Specialist with a scientific background in CMC process and product development. Experience in science, translational research, CMC development, and development strategies covering...
Posted 36 days ago -
Responsible for Teva api cGMP compliance by supporting all teva api sites with a focus on Quality Control for inspection readiness, remediation of critical incidents, OPEX in QC...
Posted 37 days ago -
The Sterility Assurance specialist will provide technical expertise and support to the DVM Process for all sterility assurance aspects. He/she will act as a valuable and effective...
Posted 39 days ago -
The role reports to the GMP Compliance Officer who is based in Pratteln, and will collaborate closely with other functions such as Supply Chain, Technical Development and...
Posted 40 days ago -
Performs startups of manufacturing equipment through Installation and Operational Qualification with assistance. Understands all qualifications performed on equipment and verifies...
Posted 44 days ago -
Performs startup of manufacturing equipment through Process Qualification, acts as a site lead coordinating customer activity with the product business group. Works autonomously...
Posted 44 days ago -
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Boehringer Ingelheim PharmaBiberach, GermanyPosted 38 days ago
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