Expert Science & Technology- Oral Solid Dosage

<p style="text-align:left"><b>Job Description Summary</b></p>Design, plan, perform, interpret, and report results of scientific experiments for the preparation and timely delivery of drug substances (DS), drug products (DP), processes and procedures within global ARD. Lead and manage all project/local network activities, support/coach team members, participate in sub-teams and contribute to overall TRD.<p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Job Description</b></p><p><b>Major accountabilities: </b></p><ul><li><p>Provide analytical and technical support to PHAD/project team at various stages of product development (eg. CSF, FMI and LCM).</p></li><li><p>Design and author analytical documents (e.g., Analytical methods, Stability protocols/reports, Excipient compatibility (EC) protocol/reports; APS protocols/reports, etc.).</p></li><li><p>Support Analytical project leader for setting analytical development strategy.</p></li><li><p>Support in data interpretation, results compilations and sharing the information with critical observations and proposals to project team.</p></li><li><p>Responsible for project related sample handling (e.g., sampling plans, issuance, storage, dis-tribution, reconciliation/destruction of the samples).</p></li><li><p>Support planning for assigned project activities. Accountable to meet KQI (Key quality indi-cators) and KPI (Key performance indicators) for all assigned project activities.</p></li><li><p>Provide requests for lab activities to the associates and stakeholders.</p></li><li><p>Manage project activities including logistics at third parties and external testing laborato-ries.</p></li><li><p>Proactively communicate key issues and any other critical topics in a timely manner to the appropriate management level and/or to any other relevant project team member(s).</p></li><li><p>Single point of contact for PHAD/project team and other stakeholders (e.g, BioPharm, Mate-rial science and CPP, etc.) for project execution activities.</p></li><li><p>Support internal and external audits and ensure no critical findings within the assigned pro-jects.</p></li><li><p>Actively contribute to team goals.</p></li><li><p>Work according to appropriate SOPs, GMP, GLP, QM, HSE, ISEC &amp; Novartis Guidelines.</p></li></ul><p></p><p><b>Minimum Requirements: </b></p><p><span>Ph.D in Chemistry/Pharmaceutical sciences with a minimum of 1 years of experience, or M. pharm/M.Sc. with 6 plus years of experience within the pharmaceutical industry, specifically in analytical development. </span></p><p><br /><b>Work Experience: </b></p><ul><li><p>HPLC method development</p></li><li><p>Chiral separation</p></li></ul><p></p><p><b>Languages :</b></p><ul><li><p>English.</p></li></ul><p style="text-align:inherit"><br /> </p><p style="text-align:left"><b>Skills Desired</b></p>Environment, Experiments Design, Health And Safety (Ehs), Laboratory Instrumentation, Manufacturing Processes, Materials Science, Process Simulation, Standard Operating Procedure (SOP), Technical Writing, Waterfall Model