Switzerland Job Openings
Lonza
Senior Project Lead Clinical Quality Control Physico Chemical Analytics (m/f/d)
Basel
FULL TIME
October 23, 2024
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Lead and manage pharmaceutical development projects of drug entities (m AB/protein) of all levels of complexity and new modalities (e.g. ADC, m RNA) within QC from various customers and in different clinical development phases up to market authorization readiness.
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Accountable for the successful delivery of QC work-packages for assigned projects, incl. proactive risk and issue management. This includes on time close out/authorization and provision of required documents and reports (e.g. stability reports), LIMS specifications, lead of change requests, CAPAs, investigation of deviation and OOX events, representing QC in internal project meetings and customer meetings for highly complex topics as SME (Subject Matter Expert).
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Maintain the c GMP quality standard for assigned processes in Phys Chem QC according to applicable SOPs and current health authority/international guidelines (e.g. EMA, FDA CFR, USP, Ph Eur, JP, PIC/S, ICH).
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Effectively network and liaise with partner units and relevant stakeholders within the Lonza network to ensure the successful delivery of projects.
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Accountable as process owner of assigned business processes, to continuously improve and maintain compliance and act as subject matter expert in regulatory inspections and customer audits.
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Ensure Key Quality Indicators (KQI) and safety regulations are followed within the area.
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MSc or Ph D degree in Biochemistry, Pharmaceutics, Chemistry or related field incl. solid work experience in relevant area
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Advanced scientific working experience in protein analytics incl. sound understanding of protein degradation pathways/molecule liabilities preferably demonstrated by a proven track record within a c GMP regulated area in the pharmaceutical or chemical industry, in analytical quality control (QC) or Analytical Development of large molecule.
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Over 3 years’ working experience on the analytical lifecycle of biotechnology products, CMC requirements for regulatory filings required.
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Experience in c GMP Quality Control of Antibody-Drug Conjugates (ADC) and/or m RNA, either on Drug Substance and/or Drug Product level, is a strong advantage.
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Hands-on experience in management of quality records like deviations, CAPAs, Change Requests.
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Proactive and independent self-starter with strong focus on quality, agility on changing priorities and high level of resilience when coordinating multiple tasks simultaneously incl. good communication skills to all stakeholders.
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Business fluent written and spoken English.
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