We have urgent opening for Executive/ Sr.Executive - FR&D (liquid orals) JD for Liquid Oral dosage form: 1. Experience in formulation & Development of liquid oral dosage form (Solutions & Suspensions) in regulatory market (US/EU/Aus). 2. To conduct literature search, patent search of assigned project and should be familiar with regulatory guidances. 3. To prepare application for form 29, form 11, RLD import license, form 25 etc. 4. To procure raw materials (API/Excipients), Packing material and Innovator samples in consultation with packaging/Regulatory & Purchase department. 5. To execute pre-formulation and formulation optimization trials with QbD approach and develop a robust formulation. 6. To manufacture batches for stability studies and perform other studies on optimized formulation. 7. To review analytical reports and prepare compilation sheet and discuss with superiors. 8. To co-ordinate with cross functional departments like Analytical, Regulatory, QA, MS&T etc. 9. To prepare Technology transfer documents like MFC, PDR, Stability Protocols, Risk assessment and execute scale up and Exhibit batches. 10. Address the regulatory queries. Interested Candidate may send their resume on email Id : audrey.fernandes@marksanspharma.com Regards, Audrey Fernandes Asst.Manager-HR

Urgent opening for Executive/Sr.Executive- FR&D (Topical Dosage) Roles & Responsibilities: 1. Experience on Topical dosage form formulation development Conduct Develop prototypes trials, proof-of-concept models, and experimental formulations to evaluate feasibility, performance Conduct literature reviews, patent searches, and market analyses to assess the feasibility Maintain accurate and detailed records of experimental procedures, results, and observations, and prepare technical reports like MFC, BMR, PDR, Stability protocol etc Experience on Technology transfer (TT) from R&D to commercial manufacturing site. Raw material indenting, packaging material, dies & punches stock management. Preparation & review of Scale up, Exhibit &Validation batch documents such as BOM, BMR, BPR, PVP & PVPR. Collaborate with cross-functional teams to gather and analyze data. Assist and support to plant team and cross functional team in scale-up of new products technology Summarize and document results in LNB , prepare technical reports Maintain clean working laboratory environment and suitable working equipment. Perform general lab assignments (e.g. raw material inventory review, lab instruments) as assigned. Interested Candidate may send their resume to audrey.fernandes@marksanspharma.com