SUMMARY This leading global pharmaceutical company is looking for a strong Formulation Scientist to join their R&D team in support of one of the fastest growing portfolios of pharmaceutical drug products across a wide range of therapeutic areas. The ideal candidate will have at least 1-2 years of hands-on experience with parentals (injectables) and scale-up from lab scale to commercial manufacturing batches in a cGMP environment.
RESPONSIBILITIES Lead formulation development activities as the SME for sterile-injectables Develop robust lab-scale, pilot-scale and commercial-scale manufacturing process based on Quality by Design (QbD) principles using design of experiments (DOE). Conduct GMP stability studies & analysis using the relevant industry-standard modeling tools to ensure purity and shelf life of products throughout scale-up processes. Manage tech transfers to CRO/CDMO/CMO’s in collaboration with project management teams in accordance with project timelines & deliverables. Participate in cross functional meetings and provide input on strategy implementation for various projects. Author & review relevant technical documents/SOP’s & FDA submissions Mentor junior staff on formulation techniques
QUALIFICATIONS Masters in Pharmaceutical Sciences (Or equivalent/relevant degree) with 3-5 years of drug product/formulation experience in the pharma industry At least 1-2 years of experience with sterile injectables/parentals and scaling up to manufacturing-scale is a MUST. Strong communication skills (written & verbal) Prior experience with tech-transfers or management of CRO’s/CMO’s is a PLUS Experience with additional dosage forms (nasal, solid-oral, topical, solutions, etc.) is a major plus!
ADDITIONAL Fully on-site position Relocation & Sponsorship available 10-15% Annual Bonus + Strong Benefits Package
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