Suchergebnisse: 22 Stellenangebote
...products on the market over the next 5 years, is looking a:
Clinical Operations Coordinator
for a 12 months-contract based in Basel... ...for an assigned trials;
~Coordinating the preparation and/or review of all operational trial-related documents and the review of...
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...offer the latest in skill development training programmes.
Clinical Operations Manager SRS 5727
Our client, an innovative and dynamic... ...Authorities, submissions to Ethics Committees/Institutional Review Boards (ECs/IRBs), timely completion of electronic Case Report...
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...candidates in finding promising career opportunities and offer the latest in skill development training programmes.
Event Manager Clinical Development 100%
Our client is a pioneer in Drug Discovery and Development and one of the frontrunners in Personalised Healthcare...
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...candidates in finding promising career opportunities and offer the latest in skill development training programmes.
Event Manager Clinical Development and Medical Affairs 80%
Our client is a pioneer in Drug Discovery and Development and one of the frontrunners in...
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...specifications for external data transfer, data cleanings and review tools that will be further provided to Data Management Programmer... .... Makes sure processes are driven in collaboration with key Clinical Development (CD) stakeholders
·Generates study metrics and status...
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...efficiency and compliance
Job Responsibilities:
~Contract review and overview
~Support GMA teams with new agreements
~Liaison... ...working/residency permit or Swiss/EU-Citizenship is required
~Clinical Trial/Medical Affairs experience in a pharmaceutical company or...
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Homeoffice
...designs while supervising project-related activities.
~Draft and review protocols, scientific reports, and process documentation (e.g.,... ...and regulatory considerations in parenteral Drug Product clinical-grade manufacturing is considered a significant asset.
Would...
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Französischkenntnisse(88)
Temporär(64)
...WIPO
Corresponding with foreign IP firms to deal with Office Actions and Oppositions
Attending Trademark Watch
Drafting or reviewing cease and desist letters, Prior Rights Agreements, letters of consent
Optimizing trademark portfolio e.g. through replacement,...
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Soforteinstellung
Flexible Arbeitszeit
...Arbeitsumfeld das Controlling für dein Projektportfolio sicherstellen (u.a. Projektstruktur SAP, Absatz- und Kostenplanung, Projekt Review, Reporting)Support und Beratung der Projektleiter und Führungskräfte im operativen Tagesgeschäft sicherstellen sowie...
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...configuration management (CM) by creating the engineering bill of material (EBOM) and manufacturing bill of material (MBOM)Write and review technical documentation part of the project/product lifecycle, such as technical specifications, system requirements and system...
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Temporär
CHF 900 pro Tag
...currently looking for a System & Process Specialist for a 24-month contract based in Kaiseraugst, Switzerland.
Background:
The Clinical Distribution organization’s objective is to cost-effectively ensure the right product is in the right place at the right time...
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...~Analyzes genomics data and contextualizes results to advance understanding of drug mechanism of action and pharmacodynamics in clinical trials and pre-clinical models.
~Mines and re-analyzes published and publicly available data to support genomics study design and...
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...services:
~Legal support for contracts – 3rd party and intercompany agreements for the client's Swiss Entities, including drafting, reviewing, and proofreading as required.
~Support on various legal documents such as CDAs, PoAs, UBO, confirmations and authorizations,...
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...reconciliation of payroll accounts to financial statements and liaise with external auditors, including provisions for vacation and overtime
~Review and approve of payroll-related invoices and reconciliation with payroll accounts
~Processing of employee inquiries and requests...
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Überstunden
...development or pre-commercialized products in portfolio sent worldwide including approval of master process documentation, batch record review, resolution of investigations, and assessment of change controls, this in close collaboration and quality oversight of CMOs
~Drive...
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...and stability studies.
~Assurance of adequate maintenance and operation of analytical equipment according to GMP.
~Drafting and review of CoAs and/or Analytical results sheet.
~Drafting of SOPs, GUIs, TPLs, FRMs.
~Training of Laboratory personnel.
~Ensuring of cleanliness...
...Authentication and security framework
• Responsible for proper Design according to IT Security and QA standards and procedures conducting reviews against architecture standards
• Ensure that forward looking architectures, including new applications, move to cloud native...
Remote job
...leading new Product Technology Transfer – supporting meetings, authoring manufacturing technical instructions, facilitating/coordinating reviews, and driving manufacturing technical instructions and recipe requirements to meet production timelines.
·Experience in Initiating,...
...specified techniques, including conducting release, retest, stability studies, transfer, and (pre-) validation analyses.
~Write, review, and document analytical method protocols, reports, Certificates of Analysis (CoAs), and Standard Operating Procedures (SOPs), particularly...
...Reporting of C&Q status, progress and issues during project stakeholders meetings (e.g. Tier 1 meetings, Wall meetings).
~Generate, review, approve, CQV test scripts in accordance with Verification Plans and any applicable site commissioning or validation plans or...
