Suchergebnisse: 13 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...
Empfohlen
...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...
Empfohlen
...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...
Empfohlen
...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....
Empfohlen
...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
Why Biogen?
Our mission to find therapies for neurological...
Empfohlen
Schichtarbeit
Biogen International GmbH
Luterbach SO
Vor 23 Tagen
...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
Teilzeitarbeit
Schichtarbeit
Ypsomed AG
Solothurn SO
Vor 23 Tagen
...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.
Why Biogen?
Our mission to find therapies...
Empfohlen
Biogen International GmbH
Luterbach SO
Vor 26 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...
Empfohlen
Vollzeit
Biogen
Solothurn SO
Vor 29 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)...
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...
Empfohlen
Schichtarbeit
...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...
Empfohlen
...continuous improvement focused on all areas of safety, quality, cost and delivery.
8. Ensure compliance with local, state and federal regulations, including health and safety standards, mitigate risks and address any compliance issues promptly.
9. Own the operational...
Empfohlen
Vollzeit
...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...
Empfohlen
Teilzeitarbeit
Freelance
Remote job
