GM

Job Description : Head (GM) - R&D (PFI & Formulation Products) SWEDEN Open to International candidates Experience: Min. 25 years of progressive R&D experience in pharmaceutical formulations, with at least 5 years in a senior leadership role. Qualification: PhD in Pharmaceutics / Pharmaceutical Sciences / related discipline Total Molecules : 40+ Products Look for candidates who have exposure of Commercialization Reports To: Managing Director / CEO 1. Proven track record in developing and commercializing complex dosage forms including injectables, oncology, ophthalmic, and inhalation products. 2. Strong knowledge of nano-encapsulation and advanced drug delivery systems. 3. Demonstrated expertise in handling regulatory submissions for regulated markets. 4. Excellent leadership, project management, and cross-functional collaboration skills. Role Overview: The General Manager – R&D will lead the company’s research and development initiatives across diverse dosage forms and technology platforms, with a focus on nano-encapsulation, oral finished dosage forms (FDFs), injectables, oncology formulations, ophthalmology, inhalation therapies, and external preparations. The incumbent will drive innovation, ensure regulatory compliance, and translate scientific expertise into commercially viable products to strengthen Murli Krishna Pharma’s leadership in specialty formulations. Key Responsibilities Strategic Leadership * Develop and implement the R&D roadmap aligned with the company’s strategic objectives. * Identify new opportunities in nano-encapsulation and novel delivery systems for differentiated products. * Oversee end-to-end product lifecycle from concept to commercialization. Product Development Lead formulation development of: * Oral Solid Dosage (OSD): tablets, capsules, oral liquids. * Injectables: general and oncology segments. * Ophthalmic and inhalation formulations. * External preparations and pre-finished formulations. * Ensure innovation in drug delivery, stability, and bioavailability enhancement. * Guide teams in scaling up from lab to pilot to commercial batches. Regulatory & Compliance * Ensure adherence to global regulatory standards (USFDA, EMA, MHRA, WHO, etc.). * Prepare, review, and approve technical documentation (CTDs, dossiers, regulatory submissions). * Work with QA/QC to ensure data integrity, cGMP, and GLP compliance. Team & Collaboration * Lead, mentor, and grow a multidisciplinary R&D team. * Collaborate with CROs, CMOs, academic institutes, and technology partners. * Provide technical expertise for business development, licensing, and partnerships. Innovation & IP * Drive patentable research in nano-encapsulation and novel formulations. * Protect company IP and contribute to building a strong patent portfolio. * Strategic thinker with strong scientific acumen. * Innovation-driven mindset with commercial orientation. * Deep regulatory knowledge and compliance rigor. * Ability to lead high-performance teams. Strong communication and stakeholder management skills

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