Junior elemző állások, munkák egészségügy, gyógyszeripar területen

• Perform optical simulations of devices for eye care using optical simulations in Ansys/Zemax (Optic Studio)
• Interact with a modern (object oriented) python framework to automate simulations as well as investigations and visualizations

• Provide medical oversight of ongoing clinical trials, including safety review
• Contribute to protocol development, amendments, and clinical documentation
• Interpret and review clinical trial data
• Support CRF design to ensure high-quality data collection

• Lead, mentor, and empower a high-impact direct sales team within the healthcare market
• Expand our market presence strategically by leveraging your established industry network.
• Design, implement, and continuously enhance sales excellence initiatives and best practices.

• Analyse the pharmaceutical, biotech, cosmetics, and personal-care manufacturing markets to identify trends, growth opportunities, and emerging customer needs.
• Help develop and execute segment-specific go-to-market strategies.
• Map regulatory landscapes (e.g., GMP, ISO standards).

• Lead and develop the Product Risk Management team
• Own and continuously improve the risk management process according to ISOwithin our product development framework
• Ensure high-quality risk analyses and maintain consistent, audit-ready risk management documentation

You will manage a team of product managers responsible for individual products within the product group...

• Coordinate alliance management activities and ensure adherence to contractual commitments
• Support (and later) lead contract-related updates, including tracking and initiating required changes
• Contribute to achieving key alliance business objectives

• Selling/promotion/training of Abbott products as Abbott Telesales representative according to the legal conditions and internal guidelines (Code of Conduct)
• Achieve or exceed sales targets and targeted market share and promote profitable growth

• planning, management and organization of epidemiologic research projects in the area of molecular and genetic epidemiology (with emphasis on omics technologies)
• development of data analysis plans
• data analysis of complex data from phenotyping, genotyping, sequencing and other omics sources

Plan and deliver educational programs: Organize and execute Movora EMEA workshops, webinars, and conferences, including managing materials, equipment, venues, and logistics....

Direct management of Process Team Leaders: Oversee and develop the Process Team Leaders and, indirectly, their respective teams in vaccine production...

• Actively support all areas of product and workflow management in the business field of refractive laser technology
• Work closely with the respective product managers on innovation and product development projects for our hardware and software products and collaborate with the R&D interfaces

• 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 integration of our software into the robotic system.

Independent realisation of production processes: Responsible execution of filtrations and chromatographic applications in production scale (250 to 1000 litres), according to the specifications for the GMP environment...

• Timely commissioning and qualification of laboratory equipment
• Independent commissioning of equipment, including handling repairs and accompanying external service providers
• Assigning, handing over, and returning laboratory equipment to internal customers and external services

• Operate as the primary point of contact taking comprehensive care of the needs of our customers around the world
• Ensure premium customer care through regular, remote and on-site Business Review Meetings (BRM) as well as leading Weekly Business Meetings (WBM)

• Conduct HPLC analyses for release and stability testing of small molecules and professional use of various HPLC separation techniques.
• Work collaboratively on method validation and verification to support drug development program
• Data interpretation and exploitation in CDS

• Analysis, integration, and interpretation of high-dimensional omics datasets in translational research
• Bioinformatic analysis of:
• Bulk RNA sequencing
• Single-cell and single-nucleus RNA sequencing
• CITE-seq
• ATAC-seq
• NGS-based datasets
• Metabolomics and proteomics data

• Act as the OEC leader within the Affiliate and support the Affiliate General Manager and Area Compliance Director in key compliance activities.
• Lead and manage an effective Affiliate Compliance Insights Forum (ACIF) for D.A.C.H, engaging Affiliate Leadership Teams and Country Leaders as needed.

• Collaborate with cross-functional teams including IT, Quality Assurance, and Operations to ensure documentation and validation of systems according to internal procedures
• Ensure compliance with internal and external regulatory requirements and guidelines
• Maintain the inventory of software applications