Suchergebnisse: 13 Stellenangebote
...engineering (IREB certification is an advantage)
~Experience in product development of mechatronic medical devices
~Experience in medical technology or other regulated industries
~Very good communication skills
~Very good English skills, good German skills...
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...addressing customer inquiries, resolving issues and ensuring a smooth installation process.
You stay updated on industry trends, regulations, and competitive offerings to maintain a competitive edge in the market.
You manage different report on sales activities....
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...attention to detail and documentation skills.
~Exposure to Delta V or Syncade or similar automated systems
~Experience in highly regulated industry
~Languages: English B1, German and/or French an asset
Additional Information
Why Biogen?
Our mission to...
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Vollzeit
Schichtarbeit
...technical writing, presentation and communication skills.
Practical knowledge and application of cGMP and FDA/EMA compliance regulations and inspections, with experience interfacing with inspectors and/or agency personnel.
Additional Information
Why Biogen...
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Vollzeit
...years of professional experience in Regulatory Affairs with focus medical device
Expertise in Active Medical Devices related regulations and guidance documents in EU and US
Excellent organizational and people skills
Very good English knowledge (Level C2 or MT)...
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Teilzeitarbeit
Schichtarbeit
Ypsomed AG
Solothurn SO
Vor 16 Tagen
...involvement in drug substance and drug product manufacturing, including reviewing validation documents, ensuring compliance with GMP regulations, and overseeing Quality Assurance activities related to facility and equipment qualification.
Qualifications
~ Bachelor-s...
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Vollzeit
Biogen
Solothurn SO
Vor 22 Tagen
...open communication channels with site stakeholders, providing regular updates to leadership, and serving as a subject matter expert... ...practical knowledge and application of cGMP compliance and related regulations
~ Fluent in English (written and oral)
~ Practical...
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Vollzeit
Temporär
Schichtarbeit
Michael Page
Solothurn SO
Vor 21 Tagen
...4 years of professional experience in Regulatory Affairs with focus medical device
~Expertise in Active Medical Devices related regulations and guidance documents in EU and US
~Excellent organizational and people skills
~Very good English knowledge (Level C2 or MT)...
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...management experience. – required
~ PMP certification or equivalent – highly preferred
~ Experience in medical device or other highly regulated industry – highly preferred
~ Experience with Product Transfers or New Product Introduction – highly preferred
~ Exceptional...
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...systems in a large-scale data center environment.
Perform regular system maintenance and upgrades to ensure optimal performance... ...Maintain a high level of security and compliance with relevant regulations and standards
If you meet the qualifications and are interested...
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Teilzeitarbeit
Freelance
Remote job
...Technician – Paints & Coatings 100%
~ F u lly participate in HSE Omya Program and comply with all safety, health and environmental regulations.
~ Prepare, schedule, execute and monitor Paints and Coatings projects to meet the proper efficiency, time, scope, budget,...
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Omya AG
Egerkingen SO
Vor einem Monat
...responsibilities
~Management of the sustainability reporting process including tracking and implementation of the new reporting regulations
~Creation of reports (CSRD, sustainability report)
~Data delivery to internal (Management, Communications) and external parties...
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Vollzeit
Teilzeitarbeit
Weihnachten
Flexible Arbeitszeit
...Ensure compliance with regulatory requirements, including FDA regulations, ISO 11607 standards, and other relevant guidelines.
Drive... ...effectiveness of labeling and packaging processes.
Provide regular project updates to senior management and stakeholders, highlighting...
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Sensile Medical AG
Olten SO
Vor 16 Tagen
