Pharmacy állások, munkák

• Responsible for receiving/downloading information from different channels and receiving voice calls for reporting safety information.
• Route information/safety reports to appropriate Department (e.g. medical information, quality assurance) as applicable.

• Lead the Sterility Assurance team of 9, manage their work performance, define workload priorities, organize and control their activities
• Be the Single Point of Contact (SPOC) for any topic related to Sterility Assurance and Environmental Monitoring

• Ownership: You will lead the implementation and continuous improvement of the local QMS, ensuring all SOPs and quality records are up-to-date and effective.
• Compliance: Act as the local expert for GDP and GMP requirements, safeguarding product integrity across the entire commercial affiliate.

The Regulatory Affairs Specialist is responsible for ensuring full compliance of Sunrider products with applicable Unite Kingdom, Hungarian and European Union regulatory requirements. This position supports regulatory activities across two primary regions—50% Hungary and 50% UK & Western Europe—and...

• Receipt / Download / Accept cases from Document Exchange Tool or electronically (or any other source)
• Translation of all relevant European Non-English information from source documents to English (if required) and updating relevant fields in Standard Adverse Event (AE) form

Global Market Access Manager The Global Market Access Manager will play a key role in enabling timely, sustainable patient access to mylife Diabetes care AID therapy across global markets. The mission of the role is to shape and execute the global market access strategy by anticipating payer,...

• Lead multiple projects as product owner and/or strategic advisor, ensuring delivery excellence across quality, scope, and profitability
• Drive strategic problem-solving across teams and integrate insights into project frameworks

Scientific oversight and coordination of preclinical and toxicology studies conducted in collaboration with CROs, academic partners, and scientific institutions - covering both GLP-regulated and exploratory/non‑GLP research...

• Lead the medical TA strategy within the integrated development as well as indication teams
• Establish and manage relations with international KOLs, patient organizations, and healthcare bodies etc.
• Establish global medical advisory boards and conduct regular meetings with key external experts

• Planning, designing, and performing (primary) cell–based, molecular biological, and biochemical experiments
• Conducting animal experiments using mouse models
• Establishing new project-related laboratory methods, including experimental design, implementation, and validation of results

Scientist imaging and physical characterization Ready to take on the challenge of fascinating analytics in a great team? As a Scientist specializing in microscopy imaging and physical characterization, you will play a crucial role in developing and validating robust analytical methods for a variety...

• Investigate the cellular and neuronal basis of cognitive functions using innovative experimental approaches
• Plan, conduct, and analyze complex brain experiments in genetically modified mouse models, including optogenetic and chemogenetic methods

Medical Science Liaison Oncology - Schweiz Mitte (Ref. 2754) - (BS/BE/SO/AG/Zentralschweiz) Our client is a well‑established, globally active pharmaceutical company with a strong footprint in the Swiss market and a diverse portfolio of innovative therapies across several specialty areas. As part of...

Design and implement end‑to‑end Operations and Supply Chain strategies across the Life Sciences value chain – from R&D to manufacturing, supply, and quality....

• Plan and conduct scientific experiments to develop analytical prototype studies for solid, liquid and semisolid pharmaceutical dosage forms
• Develop, optimize, and modify HPLC/ UV test methodologies to address complex analytical challenges

Providing strategic regulatory guidance developing global regulatory strategy, planning and execution of global investigational and marketed prescription drug submissions and managing lifecycle regulatory activities in alignment with the Therapeutic Area Lead under the direction of the Senior...

Provide deep medical expertise across relevant therapeutic areas, ensuring continuous awareness of scientific and clinical developments and effectively disseminating updates to Medical Affairs and, where appropriate, to commercial teams. Lead, coach, and develop a team of Medical Affairs Managers...

Management of safety operations incl. corresponding service providers, creation and maintenance of reporting rules (in collaboration with the department Global Safety Application Management) and license partner obligations with respective compliance outputs (e.g. KPIs, PSMF)...

• Global pharmacovigilance product responsibility for the medicinal products
• Monitoring of the benefit-risk profile
• Signal management: signal detection, signal validation, signal evaluation
• Risk management: preparation of risk management plans, supervision of risk minimization measures

• Planning and initiation of business cases, definition of the project scope, objectives and deliverables. This includes gathering requirements, assessing feasibility and developing a project plan that aligns with organizational goals
• Monitoring of timelines and budget