Mujeeb Mohammed Email & Phone Number

Hyderabad, In

Hyderabad, Telangana, India

• Leading a team of Documentary Standards Acquisitions for South Asia for Small molecules, Complex Generics, Excipients.• 70%of the standards are acquired from South Asia occupying first rank in global pie of USP Presence.• Managed territory and customer segmentation for over 3,000 accounts in the South Asia region, including CDMO, CMO, CRO, and manufacturers.• Identified strategic partners for CGx, PAIs, impurities, and E&L projects in the South Asia region.• Ensured collaborative partnering across USP program units internally and with suppliers.• Conducted successful vendor audits for evaluating CGx projects for USP.• Quality champion for RPO for South Asia, successfully completed audits for RPO without any observations.• Approved Internal Auditor for USP labs and share report to QA related to quality Audits.• Successfully completed audit for RSL Lab, Finance and Purchase and IT Departments.• Imparted training about to QMS, Workflows, Risk Register, and change controls to all RPO staff and monitor their training records as per the Annual plan .• Conducted Brainstorming session for generating new ideas in the team and share the report to management about the outcomes and successfully implemented in India.• Led key account management, standards acquisition, procurement, cross-functional teams, and authorized distributor staff.• Identifying Key Contacts in India: Focused on identifying key stakeholders and experts in India to acquire monograph proposals and reference materials essential for supporting monograph submissions.• Guiding Monograph Source Acquisition: Administering the acquisition process of potential monograph sources, offering guidance on USP procedures, and collaborating with the source to co-develop a comprehensive monograph submission.• Building Relationships with Technical Experts: Establishing and nurturing relationships with technical experts to facilitate the development of high-quality monographs.

 Development of various analytical methods like Assay, Related Substances, Dissolution, Swab and Residual solvents methods of Finish products using HPLC, Dissolution, UV, GC as per customer requirements Method validations of Analytical Methods like Residual solvents, related substances, Dissolution, and Assay by HPLC, Dissolution and GC. Preparation of Method validation protocols to perform Method validation and also to prepare the summary of validation report. Discriminatory dissolution media Development for formulations Development. Analysis of Stability Samples in different storage conditions. Evaluation of the Stability data of drug products in different storage conditions by analyzing the drug products as per stability schedule. Dissolution profiling for Formulation Development support. Analysis of raw materials, compatibility study samples, in process, finished products and analytical sample under GLP. Evaluation and trouble-shooting of problems in the area of analytical method developments. Ensure that equipment/instrumentation HPLC etc is calibrated and maintained and that laboratory records/documentation comply with cGMP’s. Faced USFDA audit and number of Customer audits (Project related audits) Handled projects from Pre-clinical to Phase-III level and also ANDA projects. Handled projects various dosage forms like Solid Orals (Tablets & Capsules), Ophthalmic Mini tablets, Ophthalmic Solutions, Lyophilized Injections, Tropical Creams, Floating Tablets etc., Received award from Dr. Reddy’s, “Best Customer Delight Team”

Qms Internal Auditor Training Course (Iso9001:2015), Quality Control Technology/Technician, A

Activities and Societies: QMS Internal Auditor Training Course (ISO9001:2015)

Diploma Of Education, Sales And Marketing Operations/Marketing And Distribution Teacher Education, A

Sales, A

Generative Ai For Business Leaders

Mdp On Leadership Development

Mdp On Leadership Development

Mba, Marketing Finance And Project Management

Activities and Societies: Completed the British Council test for English and presentation modules. PMP Member. Participated in BDMA,IDMA.