Responsibilities Own end?to?end supplier quality management, including qualification, monitoring, and documentation for external suppliers. Draft, negotiate, and maintain quality assurance agreements with suppliers and service providers. Evaluate supplier change notifications and manage related quality records and change controls. Perform quality risk assessments for new and existing suppliers Prepare regulatory statements, annual monitoring reports, and quality contributions to product quality reviews. Support audits, deviations, corrective and preventive actions, and discrepant material investigations. Collaborate closely with manufacturing sites, service delivery teams and cross?functional stakeholders on quality topics. Qualification & ExperienceUniversity degree (Bachelor’s or Master’s) in a scientific field, such as chemistry, pharmacy, or a related discipline. Several years of experience in supplier quality management or quality operations in a regulated environment. Proven ability to draft and manage Quality Assurance Agreements with suppliers and service providers. Hands?on experience with supplier qualification, quality risk assessments, and annual monitoring for incoming materials. Strong collaboration skills and confident communication in English with suppliers and internal stakeholders.

Responsibilities Regulatory Strategy- Provides input to global program regulatory strategy, including regulatory designations & innovative approaches Coordinates regulatory readiness with other line functions, Country Organizations & regions?, Represents RA or leads regional or cross-functional activities, provides strategic input to cross functional deliverables (e.g. protocols, IB, safety reports etc) Contributes to the development and maintenance of the Core Data Sheet (CDS) Determines requirements and coordinates activities for Health Authority (HA) interactions. May facilitate HAs meetings together with RA program lead.? May serve as local HA liaison (e.g., FDA or EMA). Regulatory Submissions-Leads planning, preparation and submission of clinical trials. Leads implementation of the defined global registration strategy into regional submissions worldwide by country organizations. Coordinates, plans, and prepares for submission of initial registration and post-approval applications, including authoring of Module 1 documents, contributes to preparation, review and maintenance of local product information in their assigned region Qualification & ExpeirenceScience based BS or MS. Advanced degree (e.g., MD, PhD, PharmD, regulatory) preferred Understanding of?pharmaceutical development, clinical trials, analysis and interpretation of scientific data ?2 years?involvement?in regulatory?and?pharmaceutical development in 1 or more major regions Experience in working in cross-functional teams Strong collaboration and communication, problem solving skills. Basic organizational awareness (e.g., interrelationship of departments, business priorities). 

Responsibilities Clinical Pharmacology Portfolio Leadership Lead and manage multiple FiH and Clinical Pharmacology studies simultaneously with medical, scientific, and operational excellence Provide expert Clinical Pharmacology input into Study Concept Sheets, protocols, Informed Consent Forms, Statistical Analysis Plans, and TLF shells Oversee medical and safety aspects of studies, including Site Initiation Visits, ongoing safety reviews, medical coding, and safety reporting Drive development of Clinical Study Reports and contribute to dissemination of study results (e.g., abstracts, posters, manuscripts, plain?language and technical summaries)  Clinical Pharmacology Strategy & Cross?Functional Collaboration Provide strategic Clinical Pharmacology guidance to ensure optimal study design aligned with program objectives Partner with project?level TMEs to align on compound background and program strategy Lead or contribute to strategic initiatives, process optimization, and capability?building efforts within TM Clinical Pharmacology Strengthen collaborations with internal stakeholders across early and full development, as well as with external CRO partnersQualification & ExperienceMedical degree (MD) combined with a PhD/post?doctoral training, board certification, or relevant Clinical Pharmacology research experience Significant experience in FiH and Clinical Pharmacology studies—either in biotech/pharma, as a PI/sub?investigator at a CRO, or at an academic medical center Proven track record of contributions to drug development, regulatory submissions, or high?quality scientific publications Experience within a TM therapeutic area is an asset Full professional proficiency in English (spoken and written)

ResponsibilitiesFormulation development of NCE projects, generic projects and line extension projects Preparation/review of literature summary and development report to the assigned product. Involve in execution and/or supervision of formulation development, process development and manufacturing of GMP batches of assigned product. Preparation/review of technical documents, which includes but not limited to MFC, BMR, BPR and Stability protocol following GDP. Representation in departmental audit Follow GxP (GMP, GDP etc.) for all processes and train the subordinates to follow the same. Execution and/or supervision of scale up/pilot scale batches in pilot plant under GMP condition. Preparation and/or review of technology transfer documents and technology transfer to manufacturing site, whenever required. Preparing/reviewing of QMS includes but not limited to change control, deviation, SOPs and OOS Communication with cross-functional team and client via mails, meetings and oral communication Provide training on but not limited to SOPs, technology, guidelines and project specific activities Performing and/or supervision calibration and maintenance of R&D instruments and equipment Procuring materials and machines change parts related to concern projects Maintain safe and hygienic condition in respective department Ensuring the use of personal protective equipment whenever required during batch execution Attending training related to FD, EHS, QA or any other department (if applicable) Ensure comply with EHS requirements while working in FD lab and Pilot plant. Support to proposal preparation for upcoming new projects Support to any additional responsibility/activity within or other department as and when required

Responsibilities                             Discover opportunities for experienced clinicians to contribute their expertise across multiple specialties at USSH.                                                                         

Qualification & Experience                     OPD Billing Executives – Minimum 2 years hospital experience                                               

Qualification & Experience           Education Qualification/Certification : B.SC Nursing/ GNM Nursing                 Experience : 1 Years above         

Qualification & Experience       Qualification : B.Sc/ M.Sc (Nursing) - Tutor            Years of Experience : Minimum one year of Teaching Experience         

Qualification & Experience                Qualification : B.Sc (Urology Technology)                             Years of Experience : Fresher or Experienced               

Qualification & ExperienceEdu, qualification : MBB S/BHMS/BAMS with MBA/MHA Experience: Minimum 5 years in hospital clinical administration