Formulation Development Specialist x4

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• Design and develop new pharmaceutical formulations with focus on bioavailability, stability, and manufacturability. • Conduct pre-formulation and compatibility studies for APIs and excipients. • Execute laboratory-scale and pilot-scale trials and evaluate process parameters for scale-up. • Prepare development reports, formulation compositions, batch manufacturing records (BMRs) and technology transfer documents. • Evaluate and interpret data from dissolution, assay and stability studies in line with ICH Q8–Q10 guidelines. • Support the selection and qualification of excipients, packaging systems and equipment for product development. • Troubleshoot formulation-related issues during development, scale-up and commercial production. • Collaborate with Regulatory Affairs for dossier preparation, especially CTD Module 3 (P.2, P.3, P.5). • Participate in risk assessment, design of experiments (DoE) and quality-by-design (QbD) initiatives. • Ensure documentation and practices comply with cGMP, GLP and regulatory requirements. • Minimum of 4–6 years of hands-on experience in pharmaceutical formulation development in an R&D or tech-transfer role. • Proficient in formulation techniques for tablets, capsules, suspensions, syrups, gels and other dosage forms. • Sound knowledge of QbD principles, DoE tools and ICH guidelines (Q1–Q10). • Demonstrated experience with scale-up, optimization, and technical documentation. • Familiarity with GMP requirements and regulatory documentation for product registration.