Manager CMC, Injectable Drug Product Development
POSTULER
Emplacement
Lyon69000
Rhône-Alpes
France
Contrat
À plein temps, Durée indéterminéeDate de publication:
2025-03-24Online to:
2025-05-23EUR 20.00 HOUR
Manager CMC, Injectable Drug Product Development
- TN France
- Rhône-Alpes
- Management & Opérations
- 3 jours il y a
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Client:
Alexion Pharmaceuticals Location:
Lyon, France Job Category:
Other EU work permit required:
Yes Job Reference:
050cbd88be18 Job Views:
4 Posted:
13.03.2025 Expiry Date:
27.04.2025 Job Description:
Location: Lyon, France Reporting to the Vice President CMC based in France, the CMC (Chemistry Manufacturing and Controls) Manager will take responsibility for Drug Product design, development, manufacture and control to support Alexion clinical development programs from early project up to Process Validation activities following company strategies and corporate objectives. Key activities: Design, conduct and coordinate development and optimization of Drug Product Formulation Provide technical expertise/scientific input on formulation development strategies and formulation solution to develop phase-appropriate drug product for preclinical, clinical and future commercial use Execute drug product formulation and process development including characterization of the process and finished product. Participate in developing drug product development and delivery strategies through internal/external partnerships as well as product integration into drug/device combination products Investigate, troubleshoot, and resolve formulation and process related issues from development and throughout clinical studies Act as technical interface to guide CRO/CDMO to design formulation and manufacture Alexion drug product Provide onsite support during production/transfer at CMOs to ensure overall compliance, appropriate resolution to critical issues, and timely progress updates. Develop finished product specifications and ensure product compliance Author/review drug product development reports and related sections in IND and NDA filing Collaborate with QA functions and associated functions to ensure implementation of the highest possible quality standards throughout manufacturing and process development impacting drug products Participate in cross-functional process risk analysis using appropriate tools such as FMEA, leading to the identification of CPPs and CQAs Ensure consistency, completeness, accuracy, and adherence to regulations and applicable guidelines (ICH, GMP, ISO, etc.) Support technology transfer, review of master batch records, change control process, technical manufacturing deviation investigations, and review of executed batch records. Develop project scopes, deliverables, budget, milestones, resources, and timelines with project leaders/managers to deliver successful CMC package Maintain accountability for project success and results delivery Communicate research and development findings internally and externally Qualifications: PhD in pharmaceutics, chemistry, material science with 2-4 years or M.S. with 6-8 years of relevant CMC development experience and a deep understanding of pharmaceutical sciences Experience in parenteral formulation/delivery at various stages of development Experience in managing and working with CROs and CDMOs In-depth knowledge of cGMPs and familiarity with US and EU regulations and quality standards applicable to build CMC dossier (IND and NDA) for regulatory submissions Demonstrated technical aptitude working on complex problems with creative problem solving and application of experimental design Ability to manage projects in a fast-paced environment and effectively collaborate in a dynamic, cross-functional environment Experience leading a team of scientists and engineers, ensuring their individual and organizational development Strong organizational skills and attention to detail and accuracy Excellent written and verbal communication skills and ability to communicate and present results and ideas to upper-level management in a clear, concise, and timely manner Date Posted:
15-Jan-2025 Closing Date: Alexion is proud to be an Equal Employment Opportunity and Affirmative Action employer. We are committed to fostering a culture of belonging where every single person can belong because of their uniqueness. The Company will not make decisions about employment, training, compensation, promotion, and other terms and conditions of employment based on race, color, religion, creed or lack thereof, sex, sexual orientation, age, ancestry, national origin, ethnicity, citizenship status, marital status, pregnancy, (including childbirth, breastfeeding, or related medical conditions), parental status (including adoption or surrogacy), military status, protected veteran status, disability, medical condition, gender identity or expression, genetic information, mental illness or other characteristics protected by law. Alexion provides reasonable accommodations to meet the needs of candidates and employees. To begin an interactive dialogue with Alexion regarding an accommodation, please contact. Alexion participates in E-Verify.
#J-18808-Ljbffr
Alexion Pharmaceuticals Location:
Lyon, France Job Category:
Other EU work permit required:
Yes Job Reference:
050cbd88be18 Job Views:
4 Posted:
13.03.2025 Expiry Date:
27.04.2025 Job Description:
Location: Lyon, France Reporting to the Vice President CMC based in France, the CMC (Chemistry Manufacturing and Controls) Manager will take responsibility for Drug Product design, development, manufacture and control to support Alexion clinical development programs from early project up to Process Validation activities following company strategies and corporate objectives. Key activities: Design, conduct and coordinate development and optimization of Drug Product Formulation Provide technical expertise/scientific input on formulation development strategies and formulation solution to develop phase-appropriate drug product for preclinical, clinical and future commercial use Execute drug product formulation and process development including characterization of the process and finished product. Participate in developing drug product development and delivery strategies through internal/external partnerships as well as product integration into drug/device combination products Investigate, troubleshoot, and resolve formulation and process related issues from development and throughout clinical studies Act as technical interface to guide CRO/CDMO to design formulation and manufacture Alexion drug product Provide onsite support during production/transfer at CMOs to ensure overall compliance, appropriate resolution to critical issues, and timely progress updates. Develop finished product specifications and ensure product compliance Author/review drug product development reports and related sections in IND and NDA filing Collaborate with QA functions and associated functions to ensure implementation of the highest possible quality standards throughout manufacturing and process development impacting drug products Participate in cross-functional process risk analysis using appropriate tools such as FMEA, leading to the identification of CPPs and CQAs Ensure consistency, completeness, accuracy, and adherence to regulations and applicable guidelines (ICH, GMP, ISO, etc.) Support technology transfer, review of master batch records, change control process, technical manufacturing deviation investigations, and review of executed batch records. Develop project scopes, deliverables, budget, milestones, resources, and timelines with project leaders/managers to deliver successful CMC package Maintain accountability for project success and results delivery Communicate research and development findings internally and externally Qualifications: PhD in pharmaceutics, chemistry, material science with 2-4 years or M.S. with 6-8 years of relevant CMC development experience and a deep understanding of pharmaceutical sciences Experience in parenteral formulation/delivery at various stages of development Experience in managing and working with CROs and CDMOs In-depth knowledge of cGMPs and familiarity with US and EU regulations and quality standards applicable to build CMC dossier (IND and NDA) for regulatory submissions Demonstrated technical aptitude working on complex problems with creative problem solving and application of experimental design Ability to manage projects in a fast-paced environment and effectively collaborate in a dynamic, cross-functional environment Experience leading a team of scientists and engineers, ensuring their individual and organizational development Strong organizational skills and attention to detail and accuracy Excellent written and verbal communication skills and ability to communicate and present results and ideas to upper-level management in a clear, concise, and timely manner Date Posted:
15-Jan-2025 Closing Date: Alexion is proud to be an Equal Employment Opportunity and Affirmative Action employer. We are committed to fostering a culture of belonging where every single person can belong because of their uniqueness. The Company will not make decisions about employment, training, compensation, promotion, and other terms and conditions of employment based on race, color, religion, creed or lack thereof, sex, sexual orientation, age, ancestry, national origin, ethnicity, citizenship status, marital status, pregnancy, (including childbirth, breastfeeding, or related medical conditions), parental status (including adoption or surrogacy), military status, protected veteran status, disability, medical condition, gender identity or expression, genetic information, mental illness or other characteristics protected by law. Alexion provides reasonable accommodations to meet the needs of candidates and employees. To begin an interactive dialogue with Alexion regarding an accommodation, please contact. Alexion participates in E-Verify.
#J-18808-Ljbffr
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