Suchergebnisse: 30 Stellenangebote
...reports.
Conduct, and assist others, in industry and regulatory research including research into industry standards/FDA guidelines for... ...English and preferably master French language.
Experience in Health Authority inspections are highly appreciated!
Interested? We...
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...have the perfect role for you!
Benefits:
- Innovation and Research Excellence: Join a company that emphasizes cutting-edge research... ...medical needs, giving you a sense of purpose and impact on global health.
Responsibilities:
- Thorough Documentation Review:...
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...will provide expertise in statistical methods, practices, and theory to design, conduct and report RWE and clinical research studies to understand the health impact of products in our portfolio (e.g., alternative products to cigarettes or others). You will work closely...
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...manuscripts, and reports to ensure consistency in language, flow of narrative, and overall quality.
Maintain familiarity with relevant research, conduct literature reviews, and manage references.
Assist with the design, development, and selection of scientific...
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...initiatives to streamline and standardize management of stability programs
Acts as an advisor and mentor to stability staff
Support health authorities inspection internal and external
Profile
Relevant work experience required, preferable in a Pharmaceutical...
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...transfusion medicine. They are also pioneers in medical diagnostics in pathology, serving an extensive network of hospitals, nursing homes, health institutions, and medical offices. The foundation is recognized for its commitment to quality and excellence, holding ISO/IEC 17025...
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...for post-approval filings, annual reports, product renewals, Annual Product Stability Reviews, and stability related responses to health authority inquiries
Serves as stability representative for OOT/OOS investigations, Market Action Fact Finding, and other investigations...
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Temporär
...for post-approval filings, annual reports, product renewals, Annual Product Stability Reviews, and stability related responses to health authority inquiries
Serves as stability representative for OOT/OOS investigations, Market Action Fact Finding, and other investigations...
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Temporär
...for post-approval filings, annual reports, product renewals, Annual Product Stability Reviews, and stability related responses to health authority inquiries.
Serves as stability representative for OOT/OOS investigations
Leads work activities involving Change Controls...
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Temporär
...Internship in Aerosol Science
You will join Aerosol Science team with the focus on innovative tools and projects applicable to research and development of the smoke free products (SFPs). The team is combining state of the art measurement tools with computational modeling...
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Interim
Soforteinstellung
...Specialist Bulk Operations will be responsible for manufacturing products (capsules and tablets) in compliance with GMP / cGMP regulations, health and safety rules. He/she will have to comply with the procedures defined by the pharmaceutical site's quality system.
The...
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Remote job
Schichtarbeit
Description du poste :
Your mission :
You will work with several research teams, developing automated test and characterization systems for soft sensors and actuators, as well a drive electronics for our actuators.
Tasks include:
* Design, assemble and test PCBs (Altium...
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...the scientific leader for clinical studies and projects according to study planning, within the Chief Medical Officer and Clinical Research department, being also responsible to develop and review documents in line with ICH/GCP, provide scientific/clinical input and...
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...methodologies
~Work on a range of audit assignments, coordinating and taking responsibility for planning, execution and completion
~Research and resolve technical queries
~Work on ad-hoc assignments and projects
~Reviewing and supervising work of more junior auditors...
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...cGxP requirements and best practices, including 21 CFR part 11, 210 and 211, Annex 11, EU-GMP guidelines and CAMP
Experienced in Health Authority inspections (preparation, process, presentations, responses drafting, etc).
Knowledge of pharmaceutical facilities,...
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...employeur d’action positive.
En Suisse, Aon est représenté par Aon Reinsurance Solutions, Aon Wealth Solutions et Aon Commercial Risk Health & Affinity. L’entreprise compte près de 350 collaborateurs dans ses bureaux de Bâle, Locarno, Neuchâtel, Nyon, Wollerau et Zürich....
...manuscripts, and reports to ensure consistency in language, flow of narrative, and overall quality.
• Maintain familiarity with relevant research, conduct literature reviews, and manage references. Assist with the design, development, and selection of scientific illustrations...
...for post-approval filings, annual reports, product renewals, Annual Product Stability Reviews, and stability related responses to health authority inquiries.
• Serve as stability representative for OOT/OOS investigations, Market Action Fact Finding, and other investigations...
...support site Quality activities such as :
multi sites investigations, drive change controls upon requests,
client notification
health authority inspections
continuous improvement
Ensures compliance to the policy of security at work and to laws concerning...
...in relevant discipline ?
Experience Requirements:
*??? Minimum 10 years of pharmaceutical industry experience in Clinical Research or Medical Affairs or equivalent required?
*??? 3-5 years e xperience in line management (talent identification, development...