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- Full time
- Permanent
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Associate Director, R&D - Process Chemistry
Salary Not Specified
Jazz Pharmaceuticals, Inc., Sittingbourne, Kent
- Onsite working
- Full time
- Permanent
Posted 2 weeks ago, 9 Jun
Job ref: 12be2e86d53d41d9ae19c043506861db
Full Job Description
- Lead a group of scientists and is accountable for the development activities in the Process Development Team.
- Analyse Evaluate medicinal chemistry synthetic procedures to redesign and/or identify scalable processes covering supply of early development activities up to GLP Tox.
- Plan, agree, resource and execute the optimization of a synthetic route identifying clear deliverables and milestones in accordance to with the overall molecule project plan.
- Identifies intellectual property generation opportunities and drives innovation within the team.
- Presents regularly project updates to the department and CMC teams with a clear focus on prioritization and delivery.
- Acts as the Drug Substance Lead and SME, working closely with other early CMC functions as including analytical, preformulation, biopharmaceutics Medicinal Chemistry and toxicology.
- Promotes a purpose driven team environment, with a focus on safety within the department.
- Identifies procedural and technical gaps within the department and drives implementation of optimized procedures.
Relevant pharmaceutical industry experience within a Discovery/Early Development setting with a broad theoretical and practical understanding of early drug development and drug candidate nomination criteria. - Good understanding of the key attributes that make a potential drug suitable for IND-enabling / clinical development.
- Scours relevant scientific literature within field and surveys broadly beyond own discipline/field.
- Excellent management skills, including planning and resource allocation.
- Excellent verbal and written communication skills, including the ability to communicate effectively with external partners.
- Strong IT skills and an ability to use key software packages to produce, present and analyse data and produce compelling materials for internal and external use
- Demonstrated ability to lead projects from inception to completion, coordinating the efforts of a team within budget, timelines and regulatory requirements.
- Partner with Pharmaceutical Development on API development approaches to mitigate risk as candidates progress.
- Displays the attributes encompassed in Jazz's values and encourages their development in others., MSc/PhD in a chemical or pharmaceutical subject, ideally with postgraduate qualification in chemical synthesis, drug substance development or related discipline.
- Knowledge of quality and regulatory standards within the Pharmaceutical Industry in early phases and experience of applying those into drug development projects.
- cGxP awareness and experience applying this within an R&D environment.
- Will have Ideally has experience with statistical procedures and software, particularly DoE and multivariate analysis.
Jazz Pharmaceuticals is a global biopharma company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases - often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines, including leading therapies for sleep disorders and epilepsy, and a growing portfolio of cancer treatments. Our patient-focused and science-driven approach powers pioneering research and development advancements across our robust pipeline of innovative therapeutics in oncology and neuroscience. Jazz is headquartered in Dublin, Ireland with research and development laboratories, manufacturing facilities and employees in multiple countries committed to serving patients worldwide. Please visit www.jazzpharmaceuticals.com for more information. This role requires you to be onsite full time based at our site on Kent Science Park in Sittingbourne.
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