
5001 - 10000 employees
🏥 Healthcare
🏭 Manufacturing
💊 Pharmaceuticals
Healthcare • Manufacturing • Pharmaceuticals
Chiesi Group is a global pharmaceutical company that focuses on the research, development, and commercialization of innovative medicines. Known for its commitment to improving the lives of patients, the company specializes in areas such as respiratory diseases, special care, and rare diseases. Chiesi Group emphasizes sustainability and corporate responsibility, aiming to enhance health and well-being across the globe while also being dedicated to environmental stewardship.
🕒 August 12
Improve your chances of getting an interview by checking your resume score before you apply.

5001 - 10000 employees
🏥 Healthcare
🏭 Manufacturing
💊 Pharmaceuticals
Healthcare • Manufacturing • Pharmaceuticals
Chiesi Group is a global pharmaceutical company that focuses on the research, development, and commercialization of innovative medicines. Known for its commitment to improving the lives of patients, the company specializes in areas such as respiratory diseases, special care, and rare diseases. Chiesi Group emphasizes sustainability and corporate responsibility, aiming to enhance health and well-being across the globe while also being dedicated to environmental stewardship.
• Provide scientific and technical leadership for analytical method development, method qualification and validation, analytical control strategy, comparability, technology transfer, stability strategies, and lifecycle activities • Lead an extended technical team and align analytical CMC deliverables with project objectives, regulatory expectations, quality requirements, timelines, and budget • Build and retain product knowledge within GRD • Support effective decision-making and external partner oversight • Establish fit-for-purpose ways of working for rare disease development • Act as subject matter expert for analytical and CMC technical areas involving biological products such as protein therapeutics • Lead or contribute to CMC strategies from candidate selection through clinical supply, technology transfer, process characterization, validation, regulatory submission, launch, and lifecycle management • Provide guidance on expression systems, cell line development, clone selection, cell banks, media and feed development, upstream process development, harvest, clarification, purification, impurity clearance, scale-up, and process control • Translate scientific and analytical data into risk-based CMC strategies and development decisions • Lead identification and management of critical quality attributes and key product quality attributes • Drive phase-appropriate control strategies covering process parameters, in-process controls, release testing, characterization, comparability, specifications, and lifecycle knowledge management • Lead technical risk assessments, process change assessments, comparability strategies, troubleshooting, investigations, deviations, CAPAs, and continuous improvement activities • Lead technical discussions with internal stakeholders, CDMOs, CROs, academic partners, and external consultants • Support selection, evaluation, and oversight of external development and manufacturing partners • Contribute to technical and regulatory documentation, business development and due diligence assessments, and GRD CMC ways of working
• A university degree in biotechnology, biochemistry, chemistry, biology, pharmacy, engineering, or a related scientific discipline • Advanced degree is an advantage • Significant experience in analytical method development, method qualification and validation for biologics • Experience with analytical control strategy, stability testing, comparability, technology transfer, or lifecycle management within CMC development • Strong scientific understanding of analytical techniques relevant to biologics development • Understanding of assay performance, robustness, method lifecycle, data interpretation, and regulatory expectations for validated methods • Strong understanding of GMP, regulatory expectations, quality systems, and development requirements for clinical and/or commercial manufacturing • Experience working with CDMOs, CROs, external partners, or outsourced development and manufacturing models • Ability to translate complex technical information into clear recommendations, fit-for-purpose plans, and practical decisions • Experience leading technical discussions, coordinating cross-functional activities, and influencing stakeholders in a matrix environment • Excellent written and verbal communication skills in English • Proactive, solution-oriented, and comfortable taking responsibility when priorities evolve
• Annual bonus scheme, subject to company and individual performance • Pension • Private medical insurance • Wellbeing programme • Flexible benefits programme • Comprehensive healthcare programs • Work-life balance initiatives • Relocation support • Flexible working arrangements • Remote work options • Tax assistance services for foreign colleagues • Access to resources and training • Performance bonuses
Apply Now🕒 July 31
Clinical Data Manager handling large volumes of clinical data for trials at PSI, a leading CRO. Requires proficiency in Clinical Data Management systems and collaboration with project teams.
🕒 July 22
Clinical Data Manager overseeing data management responsibilities for clinical trials at PSI. Ensuring data integrity and compliance with established standards.
🕒 July 14
Data Manager for Clinical Trials at PSI focusing on managing clinical data for pharmaceutical research projects. Requires proficiency in data management systems and independent work style.
🕒 July 11
Data Manager handling clinical data for pharmaceutical trials at PSI with an inclusive culture. Aiming for quality and timely management of clinical data across projects.
🕒 July 9
Clinical Research Associate managing site qualification, monitoring, and study close-out visits in Oncology and Hematology for a global CRO in Italy.