Role & responsibilities Good Experience in lab chemicals and equipments Should work in API and good experience in Negotiation. Good Excel knowledge Interested Candidates can share your CVs @kavya.c@viyash.com

We are looking for Jr. Executive/Executive for R&D Work Location: Shapur, Jeedimetla Departments: Synthesis R&D Qualification: M.Sc Organic Chemistry experience: 01-05 yrs Exp in API process development with good organic chemistry and spectral characterisation (NMR, IR, Mass) knowledge. CTC: Negotiable No. Positions: 6 Note: Applicants must be from API Background Interested applicants can Walkin directly on 07-06-2025 from 10.00am to 3.00pm Regards Sireesha

Role & responsibilities Good Knowledge and experience in Variant Analysis, MIS Reporting, Finance Reporting, IND As Interested Candidates can share your CVs @ kavay.c@viyash.com

Requirements: Front end experience (~6-8 years) from Business Development or Project Management specifically executing projects for Innovators (OR) CROs for innovators. Experience of executing projects in Phase II and Phase III in the API and intermediates space, preferably. Relevant experience in handling pre-IND submission projects and phase I projects will also be considered. Few years of initial career (~3-4 years) in process or analytical development will be an added advantage for the applicant. Experience in handling lifecycle management programs with innovators will be added advantage. Strong oral and written communication is expected, with more importantly well-presented persona. Any other relevant experience in pharmaceutical R&D manufacturing will be considered. Strong ability to screen RFQs and pick/ prioritise the right ones by understanding and presenting the potential to evaluate whether such RFQs will be a value add for Viyash in the long run. Job Responsibilities: Creating customer and opportunities pool for CDMO projects by liaising with appropriate contacts at customer end. Marketing Viyash capabilities and creating win-win opportunities by understanding external opportunities and internal capabilities. Prepare Business proposals for relevant RFQs by liaising with R&D, Manufacturing and SCM teams. Lead the techno-Commercial discussions between customers and Viyash. Based on the performance and traction of the projects, support team will be added to the candidate.

Experience in US FDA regulatory submission and query response along with handling of Control correspondence. Good Knowledge in Current US FDA Guidelines and MAPP Preparation of Module 1-5, Review and submit through eCTD software. Exposure to 505(j) and 505(b)(2) NCE-1 based submission. Experience in DMF review. Prepare, review, and submit regulatory submissions for Product life cycle management. Collaborate with cross-functional teams (R&D, Quality, Clinical) to ensure regulatory compliance. Develop and implement regulatory strategies to support product approvals and lifecycle management. Monitor regulatory intelligence and assess the impact of regulatory changes on the business. Working knowledge of clinical trial regulations and GxPs. Proficiency in regulatory software or document management systems Please share your CVs @ Kavya.c@viyash.com

Responsible for API dispatches as per customer requirement and committed timelines. Coordinate with cross functional teams and close the customer deficiencies and regulatory deficiencies as per committed timeline. Coordinating the MS Teams and Zoom meetings between customers and Cross functional teams on quality issues and ensure to resolve them within in the timelines. Involved as per planned schedule and coordinating to the external / regulatory audits. Implementation of Corrective & Preventive actions effectively and its review for effectiveness. Need to provide sales forecast quarter wise and month wise for production inventory planning. Follow up to get sample from respective stake holders and send samples to customers. Ensure that every quality concern is handled amicably and promptly by actively engaging both parties' QA and regulatory. Ensure to work in a direction to meet monthly targets and annual targets should be have good technical knowledge to mange customers

We are looking for a candidate having experience in Project management in Pharma Industry with EU , US experience. any science background can be considered with the below description Identification of milestone for each for project Discuss with customer for the execution plan and timelines Coordinating with customer and internal teams from development till validation. Maintaining Project tracking sheets along with identifying targets Coordinating for licensing, qualification and various regulatory filing procedures.