Php help csv javascript jquery állások, munkák egészségügy, gyógyszeripar területen

Munkakörhöz tartozó feladatok ellátása....

• Cooperate with Store Manager on daily business a be co-responsible for the store.
• Motivate the sales team to meet sales objectives.
• Follow all the processes and procedures in the store.

We are looking for a passionate school counselor to develop and implement a counseling program to assist students in their personal, social, and academic development. The school psychologist's responsibilities include conducting assessments to evaluate students' needs and ensuring students are...

• Design and configure Master Batch Records within Rockwell PharmaSuite
• Translate manufacturing process requirements into compliant MES design solutions
• Ensure adherence to global templates, design principles, and regulatory requirements

• Lead and manage commissioning, qualification, and validation activities for pharmaceutical facilities, utilities, equipment, automation, and computerized systems
• Develop and implement C&Q strategies, C&Q Master Plans, and risk‑based qualification approaches

• 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.

• Own revenue, market share and commercial performance across the Allergan Aesthetics portfolio
• Develop and execute growth strategies that deliver sustainable business results
• Lead, coach and develop a diverse field-based sales organization

Advance science. Develop nucleic acid-based technologies from early research towards candidates for topical dermatology, bringing in your own ideas and scientific concepts into proof-of-concept....

• Lead external sterilisation activities for active ingredients, excipients, and packaging materials.
• Prepare, review, and maintain sterilisation validation documentation.
• Support SIP and bulk product validation activities.
• Manage filter validation programs and ensure regulatory compliance.

• Act as the scientific counterpart to IT for the selection, evaluation, implementation, and maintenance of GxP-relevant IT systems
• Ensure compliant computerized system validation (CSV) and drive robust data integrity practices across all scientific processes

• Design, develop, and maintain software solutions supporting ultrasound reporting and clinical workflows
• Develop and integrate structured medical reporting solutions using TypeScript, XML, JSON, and SQL databases

• Develop and execute the DSE regional eCompliance and IT Governance strategy aligned with business objectives and Quality Management System (QMS) requirements.
• Promote and maintain global standards, policies, and procedures for Computer System Validation (CSV), IT Governance, and Data Integrity.

Manage key operational quality processes, including non-conformance reports (NCRs), quarantine, quality holds, field actions, line clearance and escalation to manufacturers....

• Coordinate quality assurance activities in design and development projects
• Provide quality guidance on project and product compliance, design controls and design changes in collaboration with Development, Software, Risk Management, Regulatory Affairs and Product Care

Develop and lead process improvement initiatives to ensure positive hospital adoption of processes and products, demonstrating improved patient outcomes....

Collaborate on and execute the product strategy for selected software, SaaS, and AI products, from roadmap and development priorities to launch and continuous improvement....

• You support an advanced development team in the design, prototyping, and testing of an innovative eye implant
• Prepare and conduct mechanical and functional tests using laboratory test equipment

• Develop and refine MxR prototypes using Godot and C++.
• Implement new features for immersive clinical applications.
• Collaborate with engineers and surgeons to evaluate prototypes in real-world settings.

Coordinate and execute regulatory activities for the PT19 insect repellent business under the EU and GB BPR at active substance and biocidal product level, including authorisations, renewals, changes and other post-authorisation activities....

• Analyze customer pharmacovigilance processes, requirements, and challenges, and provide recommendations aligned with industry best practices and regulatory requirements
• Support the implementation, configuration, validation, and adoption of drug safety solutions