Egészségügy, gyógyszeripar állások Külföldön főiskolai végzettséggel

• Manage all lifecycle stages of M&A/PMI projects from the Service perspective, including both Due Diligence as well as Post-Merger Integration projects
• Develop and apply upside potential & risk scenario assessment frameworks for Service

JUNIOR LABORATORY TECHNICIAN (M/W/D) - BIOLOGICAL SAMPLES / GXP / SAMPLEPREPARATION / ENGLISH / GERMAN PROJECT: For our customer Roche Diagnostics International AG based in Rotkreuz we are looking for a qualified Junior Laboratory Technician (m/w/d) BACKGROUND: Department: Instrumental Analytics...

• Lead and oversee all clinical safety and vigilance processes for medical devices.
• Manage adverse event assessment and reporting in compliance with global regulations.
• Ensure accurate development and maintenance of RSI, CIP, and IB safety content.

• Lead contamination control program, risk assessments and strategies in line with cGMP, Johnson & Johnson, and regulatory standards.
• Drive initiatives to reduce contamination risks and enhance microbiological hygiene practices.

• Drive commercial success by collaborating with German sales teams and distribution partners.
• Spearhead the launch of new technologies and indications in the German market.
• Support the transition to a direct sales model and the commercialisation of UK operations in Germany.

• Plan analysis with support from supervisory staff
• Prepare standards and samples
• Perform experiments on different instruments
• Data analysis with support from supervisory staff
• Document experiments
• Escalate issues when things are not going according to plan
• Recommend next steps based on data generated

Medical Device Clinical Safety Scientist (m/f/d)- Healthcare/ Scientific/ Biomedical/ MDs/ MD Clinical Investigation/ CIP/ Protocol/ IB/ RSI/ Risk Management/ ISO/ Drug/ English PROJECT: For our customer a big pharmaceutical company in Basel, we are looking for a Medical Device Clinical Safety...

Provide expert leadership and oversight for all clinical safety and vigilance activities associated with Class II and/or III Medical Devices (MD), ensuring adherence to global regulatory requirements and internal standards throughout the product lifecycle....

• In-process controls, release and stability tests using HPLC-based analytical methods 
• DLS-based analyses; pH, IR, and wet chemical analyses
• Visual appearance test of finished drug product for batch release and stability 

• You will shape and implement C++ software systems prioritizing performance, safety, reliability, and extensibility
• By collaborating closely with other developers and engineers you ensure seamless and hands-on integration of our software into the robotic system

• Responsible for processing incoming complaints in accordance with applicable process specifications
• Independent processing and assessment of complex or critical complaint cases with potentially high risk to patient safety or regulatory compliance

• Developing and maintaining sterility assurance and contamination control strategies for aseptic processing
• Leading risk assessments for aseptic process, single use systems and critical interventions, and ensuring compliance with authorities relevant Guidance such as Annex 1

• Unlimited Earning Potential: Keep 100% of your personal training income with no cap!
• Tiered Rent System: A supportive start to help you succeed.
• Free Promotion: Showcase your skills across PureGym platforms.
• Professional Image: Receive a complete 12-piece uniform at no cost.

Networking - You enjoy maintaining and expanding your network of decision-makers in the healthcare industry. You utilise your contacts to generate leads and gather information....

• Develop and validate LC-MS methods for the quantification of impurities in complex samples
• Optimize and troubleshoot analytical methods to ensure accuracy, precision and robustness 
• Collaborate closely with cross-functional teams to drive project success

• Strategic Sourcing / CDMO Site Selections including Due Diligence
• Price Negotiation
• Contracting of CMO contracts
• SRM Activities for CMOs
• University degree a scientific or business field or similar
• Min. 5 years relevant experience CMO Management or procurement in CMO space 
• GMP Experience 

• You are responsible for quality related topics like change control, deviations and/or complaints related to DS products at CMOs
• Define together with the CMO effective CAPAs and track the timely implementation

• Focus of this position is supporting our rapidly developing in Diabetes Care (active and connected devices)
• Manage the development and implementation of RA strategies
• Support and prepare product submission documents with main focus on US
• Partner with business stakeholders on different levels

Prepare, support the creation and review and execute the release of all technical documentation for digital health and software products ensuring compliance with applicable standards and regulatory requirements such as IEC, IEC...

Strategic Influence: Shape the success of the TRICARE Overseas Program by building and nurturing high-level relationships with military and civilian partners....