Biocon

Key Responsibilities 1. Co-ordination with planning for delivery schedules 2. PRN to PO conversion as per SOP within 2days 3. Obtaining OA within 3days 4. On time delivery of materials with 90% OTIF 5. Inform stake holders on delay in supplies on time and take action to rectify the issue and ensure the delivery. Educational Qualifications: Required Education Qualification: Bach

Perform routine and non-routine tests and analyses using the appropriate technical equipment and instruments Receive or collect, as well as process, samples Calculate test results, and log and report results using a computer Prepare and supervise experiments Perform quality control and calibrate equipment if necessary Maintain equipment in proper working order and maintain a clean work area P

Characterization of waste water followed by detailed analysis. 2. Treatability assessment based on rigorous lab as well as simulation studies and solution mapping based on customer requirement. 3. Collection and analysis of the data as a prelude to solution scale-up 4. Assure proper documentation of procedures; technical data-analysis-recommendations for the studies carried out 5. It i

Roles and Responsibilities 1. Should have knowledge of method development and analysis of Mass, IR and UV-Vis spectroscopy, HPLC, GLC 2. Knowledge in quantitative and qualitative analysis must. 3. Sample preparation, operation of sophisticated analytical equipment such as HPLC, GC, spectro photometer etc 4. Documentation of data in analytical format to interpret result 5. Making qual

Responsible for the quality and workmanship of every activity, thorough knowledge of all phases of engineering construction relating to Civil, Architectural and Structural discipline interfacing the multidisciplinary operations. - Taking care of QA/QC documents of the entire project including certificates, calibration, test results, inspection requests, non-compliance reports and site instructi

The successful candidate will have relevant clinical research/pharmaceutical industry experience, preferably in pharmacovigilance/drug safety, with knowledge of medical terminology and coding systems. Must be fluent in written and verbal English with good communication skills and basic computer skills. Detail orientated and capable of working effectively within a team environment. Medical/science

Analysis Ø Analysis of in process, intermediate & finished product samples Ø Periodic calibration of HPLC instruments as per schedule Ø Maintaining clean working surroundings Ø To Follow all safety standards while working 2. Tech Transfer Ø Method Transfer at different locations of Hikal Ø To support analysis part of plant validation batches as and when required 3. Scale Up Ø Support the

Medical Writer Roles and Responsibility Creating, proofreading and editing regulatory and clinical documents, Investigator brochures. Directly involved in medical marketing of new FDA drugs, pharmaceutical products, equipment through writeups, blogs, information handouts/leaflets, etc. Coordination with physicians, scientists and healthcare professionals for whereabouts of ongoing research and

Assess clients needs and present suitable promoted products Present product information and deliver product samples Communicate with and persuade targeted doctors to prescribe our products utilizing effective selling skills and performing cost-benefit analysis Attend sales meetings, conference calls, training sessions and symposium circuits Keep detailed records of all contacts Manage budgets

Job description: Analyst/Chemist-Quality Control: High-Performance Liquid Chromatography (HPLC), Ultraviolet-visible Spectroscopy (UV) Education PG :M.Pharma in Pharmacy

Handling Formulation Development - OSD / Solidi Orals • Keeps abreast of current trends, practices, developments, and regulatory changes, which would affect products, procedures or formulation • Execution of experiments timely in meticulous manner Pharmaceutical Product/ Technology/Formulation Development for Drugs from conceptualization to proof of concept, technology transfer for regulatory fi

Roles and Responsibilities Onsite and Remote Support for the resolution of incidents encountered in the use of hardware and software. Familiar will All Networking (Both LAN, WAN and MAN). Familiar will All version of Windows OS (XP, 7, 8,10) and server OS. Installation, Troubleshooting and deployment of standard software and hardware. Assembling and Disassembling computers, Laptops, and serv

Provide SAS programming support to all clinical projects (Phase 1 to 4). Manage programming CROs providing oversight for programming deliverables. Create programming related SOPs, as necessary. Works in tandem with CRO' s Biostatistics and SAS Programming and Data Management teams on various clinical projects. Provide statistical input into and review of statistical deliverables (i.e. analysis pla

uthor, reviewer and approver of GMP relevant documents Setup, use, help to direct technician on maintaining and troubleshooting laboratory accelerated environmental resistance equipment such as fog chambers, UV and Xenon weatherometers, and temperature-humidity chambers Become in-house SME on existing environmental resistance testing by participating in, reviewing and updating Guardian’s current

Key Responsibilities Handling of Finished product/ Intermediates/ In-process/ Raw material analysis By HPLC/GC/UV/IR/KF Autotitrators and wet analysis, sampling of Finished product/ Intermediates/ In-process/ Raw material. Preferable exposure on Working standard management and instruments calibrations(HPLC/GC/UV/IR/KF Autotitrators). Roles and Responsibilities Training on Receipt of Inp

Department / group: Clinical R&D - Global Scientific Communications and Medical Writing job description: Write, edit, review, format all regulatory (clinical and nonclinical) documents and dossier sections in a manner compliant with FDA, EMA, CDSCO and ICH guidelines. Write, edit, review, clinical publications (systematic reviews, meta-analysis, manuscripts primary and secondary, abstrac

Job description Roles and Responsibilities Responsible to manage the all the initiatives in SAP MM and WM along with the Cross Function team. Manage/control all the changes carried out in the existing SAP system, by way of authorizing and timeline management. Facilitate workshops to collect business requirements from Finance teams Map business requirements, processes, and objectives; develop

Job description Roles and Responsibilities Architect and implement day-to-day SAP basis administration activities in a complex multi-tier SAP landscape. Provide operational and project support keeping focus on meeting project milestones. Ensure SAP based systems operate reliably and efficiently in a secure environment. Ensure the adherence of standards and SAP best practices. Maintain close