Leading end-to-end tech transfer to CDMOs for biotherapeutics. Strong GMP, regulatory, and project management experience required. Focus on process, analytical, and quality knowledge transfer.
Ensuring 21 CFR Part 4 compliance for biotherapeutic combination products. Minimum 3 years medical device quality experience required. Well-being support and global team collaboration.
Driving CMC strategy and global regulatory submissions for biotherapeutics. Demonstrated CMC development and regulatory submission experience required. Well-being support, external manufacturing partner management preferred.
Loading, unloading, and sorting packages in a warehouse environment. Operating heavy machinery and stocking inventory required. Flexible shift hours, warehouse experience preferred.
Statistical analysis for biotherapeutic process monitoring and comparability assessments. Master's or PhD in Statistics or related field required. Support for product lifecycle management preferred.
Financial analysis and reporting for a global biotherapeutics leader, supporting forecasting and budgeting cycles. Several years of financial analysis experience required. Well-being support.
Developing new biotherapeutics for immunology and hematology conditions. Bachelor's degree and up to 2 years lab experience required. Well-being support and career growth opportunities.
Applying technology platforms to biotherapeutic research and development for rare and serious diseases. Postgraduate degree or 3+ years relevant experience required. Well-being support, company car for private use.
Leading global QRA team for AI medical device software, acting as legal PRRC under EU MDR. Minimum 10 years QRA leadership and 8 years SaMD experience required. Occasional travel, professional growth opportunities.
Assessing pathogen safety risks for biotherapeutics manufacturing and operations. Advanced degree in a relevant scientific discipline strongly preferred. Well-being support and global project contributions.
Developing new biotherapeutics for immunology and hematology, with focus on clinical safety standards. Postgraduate degree or relevant experience required. Daily lab support for product testing, direct regulatory authority interaction.
Leading discovery and development of biotherapeutics for immunology and hematology. PhD in scientific discipline and track record of achievement required. Oversight of cross-functional research teams, setting direction for scientific programs.
Developing innovative medicines for immunology and hematology. Bachelor's degree and up to 2 years lab experience required. On-site work with rotating shifts.
Routine analytical testing and instrument setup for biotherapeutics development. 3 years of lab experience with HPLC/UPLC or CE required. Well-being support.
Overseeing tech transfer and QC method transfers for biotherapeutics, serving as primary technical contact for external partners. Postgraduate degree or extensive experience in Life Sciences required. Full-time employment with CSL benefits.
Automating laboratory systems and workflows for biotherapeutics development. 3+ years in lab automation with Python scripting skills required. Well-being support, collaboration with AI/automation teams.
Managing deviations, CAPAs, and change controls for biotherapeutic development and manufacturing. At least 3 years of GMP manufacturing or QA experience required. Well-being support and career development opportunities.
Routine and complex lab tasks for biotherapeutics development, generating high-quality data. Up to 2 years of lab experience required. Well-being support.
Designing and implementing experimental processes for biotherapeutics research and development. Bachelor's degree or vocational training with biomedical research experience required. Well-being support and team activity integration.
Leading global Tech Ops projects in biotherapeutics, translating strategy into operational plans. 8+ years in biotech/pharma and 3-5 years managing global, cross-functional projects required. PMP certification preferred, well-being support.
Developing pathogen safety strategies for biotherapeutics, defining virus testing, and overseeing reduction in manufacturing. Postgraduate degree in Life Sciences required. Focus on adventitious agent control in global biopharma operations.
Global analytical strategy development for biotherapeutics, including LC-MS/MS and immunogenicity testing. PhD or MSc with extensive experience required. Well-being support.
Global biotherapeutics technology transfer strategy execution and leadership for complex programs. 12+ years in biopharma development, manufacturing, or Tech Transfer required. Well-being support.
Designing and executing laboratory experiments for plasma protein purification and raw material evaluation. Minimum 5 years of plasma protein experience and DoE knowledge required. Well-being support and company car for private use.
Biomolecule characterization using LC-MS for rare disease therapies. 3+ years biopharmaceutical industry experience required. Well-being support, training team members on advanced techniques.
Characterizing biomolecules and developing fit-for-purpose analytical assays for biotherapeutics. 3+ years biopharmaceutical industry experience in protein characterization required. Well-being support, training on state-of-the-art instrumentation.
Developing binding, enzymatic, and cell-based bioassays for biologics, with focus on ELISA, SPR/BLI, and MoA-linked assays. PhD and industry experience in assay development required. Well-being support and mentoring opportunities.
Developing and implementing novel analytical methods for biomolecule characterization using biochemical and biophysical techniques. Postgraduate degree in biological sciences, biophysics, or analytical chemistry required. Well-being support and company car for private use.
Leading recombinant product process development and lifecycle management for biotherapeutics. PhD in Life Sciences and recombinant product expertise required. Well-being support.
Global QMS strategy and harmonization for vaccine development. Extensive international GxP compliance experience required. Focus on operational excellence and quality culture.