Suchergebnisse: 10 Stellenangebote
...Minimum Education Requirements:
Bachelor's degree in biotech, pharmaceuticals, or related field.
Solid understanding of cGMP regulations and biotech manufacturing processes.
Minimum Experience Requirements:
Minimum 7 years of experience in pharmaceutical...
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...High school diploma or equivalent; Bachelor’s degree preferred.
Strong understanding of manufacturing processes and cGMP regulations.
Minimum Experience Requirements:
Minimum 6 years of experience in a GMP environment, preferably in biotech or pharmaceutical...
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...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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...perform the certification of Finished Goods for the identified Market as well as import/export release to Switzerland as per Swiss Regulation (812.212.1) and European Directive 2001/83/EC, 2017/1572 as well as delegated regulation 2017/1569. The RP release delegate is...
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...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
...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
...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)...
Empfohlen
...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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Temporär
Schichtarbeit
...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