241 Osd Jobs - Page 7

Alembic Pharmaceuticals Ltd. is looking for a potential candidate for the position of Research Associate in our MS&T (Technology Transfer) department based at sites nearby Vadodara . Position Criteria : B.Pharm or M.Pharm (Pharmaceutics) Minimum 1 to 5 years of relevant experience. Willingness to work at site in shifts Job Description : Execution/monitoring of Feasibility, scaleup, Validation and Verification batches. Troubleshooting of problems faced during manufacturing of post-approval change batches. To monitor all critical variables using statistical analysis. Initiation /preparation of MRS, sample request, and GMP document as per SOP. Review and Preparation of Technology transfer batch documents like BMR, MFR, Scale-up batch protocol, Scale-up batch report, Additional testing protocol (ATP), Pre-Approval Investigation Annexure and Hold time report. Assist in the Challenge study, GOP study and Critical process parameter at time of execution on shop floor. Handle Software like SAP, CONDOR, MONITOR and MES. Interested candidates can share their cv to " msnt@alembic.co.in " with a position title "RA-Tech Transfer)

We have been retained by a reputed Pharmaceutical Consulting firm working in the area of GMP, Global Regulatory Affairs & Product Development to hire a "Junior GMP Consultant - QC & QA" to be based at their HO located at Navi Mumbai. Details of the position are mentioned below: Company: Our Client is a reputed Pharmaceutical Consulting firm working in the area of GMP, Global Regulatory Affairs & Product Development. They have their head office in Mumbai and subsidiaries in Europe, Singapore, Australia and Malaysia. They have been providing high quality & credible consulting services to the Pharmaceutical Industry in India and internationally. They have a young and committed team of GMP and Regulatory Experts. Role & responsibilities: Adequate experience and well versed with Quality Control and Quality Assurance systems and procedures in accordance to regulatory standards. Hands on experience in handling HPLC, GC, UV, FTIR, etc., worked on LIMS, audit trail, CSV , familiarity with GMP, GLP, EUGMP and ICH guidelines, Should have exposure working in formulations like oral solids dosage form (OSD), injectables, etc. Experience: Min 5-10 years experience in quality control & Quality Assurance in pharmaceutical industry. Knowledge & Skills Candidate should have exposure working in QC/QA laboratory in Regulated companies. Well versed with Quality Management systems/procedures Thorough knowledge of testing Raw materials, finished product, Packing materials and handling of key instrumentation like HPLC (auto sampler), GC, dissolution testing. Well versed with QC systems & procedures, audit trail review of HPLC, GC and have knowledge of computer system validation related to QC instruments. Familiarity with GMP, GLP, EUGMP and ICH guidelines. Familiar with stability management and calibration Well versed in carrying out Analytical Method validation/verification, Analytical tech transfers. Fluency in English and good communication written and verbal. Job responsibility: 1)To assist project lead in reviewing the QC systems, documentation and practices for client. 2) Participate in Supplier audits at various sites 3) Maintaining GMP data base and preparation of SOPs 4) Ready to do extensive travelling to visit Client sites and supplier audits (domestic & international) Preferred candidate: Candidates based only in Mumbai/Navi Mumbai will be preferred. 6. Qualifications: Education: A masters degree in Pharmaceutical Sciences or a master's degree in Analytical Chemistry Skills and Competencies: Strong analytical and problem-solving skills. Attention to detail and accuracy in testing and documentation. Proficient in the use of laboratory equipment and software. Those of you whose profile matches the above mentioned description and would like to apply for this position shall forward their updated CV to sudhirvinayak@gmail.com In case of a query, please feel free to speak to the undersigned: Sudhir Vinayak, Director, Pharma Placements Inc. Mobile: 98202 34987 / 81307 24980

We are hiring for the following 2 positions: Senior Executive- Quality Control RM Section Head- 5-8 Years of Experience Executive- Quality Control- Analytical Method Validation- 4-6 Years of Experience 1. Senior Executive- Quality Control- RM (Raw Material) Section Head Raw Material Testing and Release: Supervise and ensure the testing of raw materials (active pharmaceutical ingredients, excipients, packaging materials) according to approved specifications. Lead the RM team in the timely testing and release of raw materials for production use, ensuring no delays in manufacturing. Ensure that the testing of raw materials is compliant with GMP (Good Manufacturing Practices), GLP (Good Laboratory Practices), and other relevant regulatory standards. Supervision and Team Management: Lead, guide, and mentor a team of QC analysts in the RM section, ensuring effective training and development. Allocate tasks and manage workload distribution within the team to ensure smooth and efficient operations. Conduct regular performance appraisals, set objectives, and ensure team productivity and morale. Raw Material Specifications and Documentation: Review and ensure the accuracy and completeness of raw material specifications, test protocols, and related documents. Approve the testing methods and ensure compliance with the established standard operating procedures (SOPs). Ensure the proper maintenance of records related to raw materials, including stability studies, inventory control, and release certificates. Compliance and Regulatory Adherence: Ensure all raw materials and testing activities comply with the Indian Pharmacopeia (IP), USP, BP, and other regulatory standards. Ensure that all QC raw material processes are aligned with FDA, EMA, and other regulatory guidelines as applicable. Assist in audits (internal and external), and provide necessary data and reports during regulatory inspections. Equipment and Instrument Management: Oversee the calibration, maintenance, and qualification of equipment used in the RM section, ensuring accurate and reliable results. Ensure that the laboratory instruments and equipment are well-maintained and functioning optimally. Quality Control & Troubleshooting: Address any deviations, out-of-specification (OOS) results, or out-of-trend (OOT) findings related to raw material testing. Investigate and resolve any quality control issues, and recommend corrective and preventive actions (CAPAs). Lead root cause analysis and support the investigation of quality incidents related to raw materials. Vendor Management & Raw Material Supplier Interaction: Liaise with suppliers and vendors to ensure the timely and quality supply of raw materials. Participate in the selection and qualification of raw material suppliers and ensure they meet quality standards. Continuous Improvement and Efficiency: Identify opportunities for process optimization and recommend improvements to enhance operational efficiency. Ensure that the QC RM section continuously adheres to cost-effective practices, reducing wastage and improving turnaround time. Training and Knowledge Sharing: Train QC team members on analytical techniques, equipment usage, and quality control standards for raw material testing. Keep the team updated on industry trends, new regulatory guidelines, and best practices. Executive-Quality Control- Analytical Method Validation (AMV) Analytical Method Validation (AMV) : Conduct validation of analytical methods as per ICH, FDA, and other regulatory guidelines. Perform method development, optimization, and validation for raw materials, in-process materials, and finished products. Ensure adherence to validation protocols and documentation. Testing & Documentation : Oversee the execution of analytical testing for stability, release, and in-process samples. Review and verify analytical data, ensuring accuracy and completeness. Prepare and review validation reports, SOPs, and other related documentation. Compliance & Quality Assurance : Ensure compliance with GMP, GLP, ISO, and other relevant standards in laboratory activities. Support the QC team in audits (internal and external) and address any non-conformities. Ensure proper handling, storage, and disposal of chemicals, reagents, and samples in compliance with safety protocols. Equipment Maintenance : Coordinate with the maintenance team for the calibration and qualification of laboratory instruments. Perform routine checks and calibration of instruments used in testing and validation. Continuous Improvement : Actively participate in continuous improvement initiatives and training programs. Suggest and implement improvements in analytical methods and processes to enhance efficiency. Cross-Department Collaboration : Liaise with R&D, production, and regulatory teams to resolve technical issues. Assist in troubleshooting analytical issues in collaboration with the technical team

Project Role : Technology Architect Project Role Description : Review and integrate all application requirements, including functional, security, integration, performance, quality and operations requirements. Review and integrate the technical architecture requirements. Provide input into final decisions regarding hardware, network products, system software and security. Must have skills : Microsoft Intune Good to have skills : Microsoft Endpoint Configuration Manager Minimum 7.5 year(s) of experience is required Educational Qualification : BE BSc or equivalent Summary :As an Intune Architect, you will be responsible for the design, build, configure MECM infrastructure, application deployment, patch management process, OSD. Design and build Windows 10/11 SOE image, Intune configurations for Autopilot deployment, Configuration policies, MDM, Endpoint Security, Proactive Remediations, Reporting & Compliance Roles & Responsibilities:a)Ability to build new greenfield infrastructures for MECM.b)Able to build new solutions for modern device management.c)Design and plan Windows Servicing approach.d)Day to day administration of MECM environment to include engineering new solutions as needed.e)Providing technical guidance to MECM team and customer.f)Provide Tier 3 support for MECM Intune.g)Creating and updating technical documentation as required.h)Design and build Intune configurations for Windows 10 Autopilot, Configuration policies, endpoint security.i)Experience with PowerShell and OSD (Operating System Deployments)j)Configuring WDS, configuring PXE, configuring the VM build environment, and integration with MDT.k)Experience in performing large scale upgrade from windows to windows 11.l)Experience is managing deployment of device drivers. m)Experience in servicing MECM current branch infrastructures. Professional & Technical Skills:a)Should have strong experience on MECM & Intuneb)Ability to design, build and configure MECM environment.c)Design and build Windows 10 image, provide support in image rollout.d)Should be able to design policies in Intune for Windows 10/11e)Should have strong hand on Autopilot enrolments and associated configurations and rollout. Additional Information: The candidate should have a minimum of 8+ years of experience in Microsoft Endpoint Configuration Manager & Intune. The ideal candidate will possess a strong educational background in computer science or a related field, along with a proven track record of delivering impactful solutions Qualifications BE BSc or equivalent

1. Responsible for overall engineering functions of OSD & Injectable plant. 2. Responsible for O&M of utility, HVAC, Water system & process maintenance. 3. Responsible for PM/Calibration/Facility maintenance and department safety function. 4. Responsible for regulatory / statutory audit compliance at site. 5. Responsible fo preparation of maintenance reports, budget & expense control. Work Experience 18 to 22 years Education B.Tech in Mechanical Engineering Competencies

Join our EUX Technology teams and collaborate with other technology teams to ensure Infor s workstations are up-to-date using our BigFix management and Jamf for MacOS. Youll be part of our global Software Deployment team, working closely with three consistent team members in the US and Poland, with opportunities for collaboration across various IT and non-IT teams where English is the primary language. You will also be part of the MacOS Apple team with members in the US, EMEA and APAC. Enjoy a flexible workday with the ability to plan your tasks individually, focusing on tasks such as package building, BigFix system administration, Jamf Pro Administration, deployments and scripting. Regular working hours apply, with occasional exceptions with a focus on the EMEA/US work hours. (as there is where the majority of the team members are located) Essential Tasks: Software Deployment, incl BigFix MacOS Apple team, incl Jamf. Software deployment, packaging. Windows OSD team: Intune admin, Autopilot, CloudPC s Contact and collaborate with different business partners. BigFix, Intune and Jamf admin Creating packages with Bigfix, scripting,. Bash and powershell scripting 3rd line support for Windows / Apple MacOS Clients MacOS Updates and features. Windows OS Features Basic Qualifications: Resourcefulness: As a IT EUX Endpoint professional, youll need to be able to search for information and apply solutions quickly and efficiently. Were looking for individuals who can think critically and creatively to find the best solutions. Technical skills: We require good knowledge of MS Technologies, as well as experience with automation and scripting tools such as Bash scripting, BigFix relevance or other scripting languages. Communication skills: good communication skills in English, both verbal and written, are essential. We value team members who can collaborate effectively and clearly communicate technical information. Remote work adaptability: Demonstrated ability to thrive in a remote work environment, exhibiting self-motivation, independence, and proactive communication skills. Able to effectively manage tasks and responsibilities in a distributed team setup. Preferred Qualifications: Continuous learner: Proven track record of actively seeking out opportunities to expand technical knowledge and skillset. Demonstrated enthusiasm for embracing new technologies and methodologies. Adaptability and flexibility: Ability to adapt to evolving priorities and requirements in a fast-paced, dynamic environment, while maintaining a positive and proactive attitude.

Greetings from Natco Pharma Limited We are conducting Walk-in interviews for the following requirements for our formulation division in Kothur. Job Requirements Department: QA (IPQA / AQA / Qualifications / Micro QA / Documentation) - 1 to 10 Years Positions: Sr Executive / Executive / Officer / Assistant Officer Qualification: M. Sc / B. Pharmacy / M. Pharmacy Hands-on experience in IPQA activities for OSD / Sterile operations. Experience in Qualification activities for all Equipments, Utilities, Instruments, and Facilities. Experience in Analytical QA & Micro QA and handling OOS, OOT, incidents, Investigations, and GLP activities. Department: Microbiology (OSD / Injectables) - 3 to 12 Years Positions: Assistant Manager / Sr Executive / Executive / Officer / Assistant Officer Qualification: M. Sc (Microbiology) Experience in QMS & GLP activities and Analytical Doc review Experience in Media Preparation and Method Validations of MLT & BET Experience in Vitek-2 Operation/Culture handling/Water Sampling / Analysis Experience in Environmental monitoring activities. Preferably Male candidates Department: Engineering (QMS / Process / Electrical) - 4 to 10 Years Positions: Executive / Officer / Assistant Officer / Sr Assistant / Assistant / Trainee Qualification: Diploma / B. Tech Hands-on experience in QMS, Documents & OQ protocol execution. Experience in Process maintenance and vendor follow-up activities. Experience in OSD Process / Packing Maintenance and Qualifications. Experience in Electrical Maintenance & Electrical substation. Should have knowledge about AutoCAD Department: Warehouse (OSD / Sterile) - 0 to 6 Years Positions: Assistant Officer / Sr Assistant / Assistant / Trainee Qualification: B. Com / B. Sc Handling of Raw / Packing Materials Knowledge of SAP & Isolator handling Experience in Dispensing & Material Management

Roles and Responsibilities Plan Production activities Weekly, Daily & Monthly/ manager the shift production on time Preparation of all production related documents, i.e. SOPs, production formats, Machine qualifications, BMR, BPR etc. Control over quality production & production norms Guide subordinates and production operators to achieve trouble free production target Guide about GMP & its compliance Improve Productivity and cost reduction using minimum manpower Process Validations & Cleaning verification of Products for Registration Review Batch Manufacturing Record and Batch Packing Record Review online records during production operation To face Internal as well as External Agency Audits Supervising packing material and ensuring on time product delivery Categories: Allopathic and Herbal/Nutraceuticals tablets/capsules Preferred candidate profile B.Pharma /Bsc Chemistry with minimum 5 years of experience Must be good at team management production planning and execution Must be comfortable traveling to Ranjangaon MIDC, Pune If Interested, please share your updated CV on email: hr@tuliplab.com

Walk-in at Matoda We are hiring multiple positions for our manufacturing facility at Matoda as mentioned below. Please find our current job requirements and venue details mentioned, If any of the requirement is matching your current job profile, kindly walk-in with your latest resume. Role & responsibilities Injectable - Manufacturing & Packing & Visual Inspection (Senior Executive / Executive / Senior Officer / Officer / Associate) Experience - 01 to 09 Years Qualification - B. Pharmacy/ M Pharmacy / Msc /Bsc / Diploma / ITI with relevant functional experience in injectable manufacturing/ Aseptic area operations / Packing / Visual inspection / QMS activities OSD Manufacturing ( Executive / Senior Officer / Officer / Associate) Experience - 01 to 09 Years Qualification - B. Pharmacy/ M Pharmacy / Diploma with relevant functional experience in OSD manufacturing and Packing operations / QMS activities Time and Venue : 05th April 2025, 09:30 Hrs to 14:00 Hrs SATURDAY ______________________________________________________ INTAS, Matoda facility Plot No. 457, 458 Sarkhej Bavla Highway, Matoda Village, Sanand, Taluka, Ahmedabad, Gujarat 382210 ______________________________________________________ We would be pleased if you forward or refer any of your colleagues matching the desired job roles. Preferred candidate profile *Having relevant qualification as mentioned above can attend the scheduled walk-in. Perks and benefits

Role & responsibilities Good knowledge of QMS documents, SOP preparation, Change control initiation as per GMP norms. Good knowledge and preparation of Equipment qualification documents URS, DQ, IQ, OQ and PQ. Preparation and maintain daily log book of utility equipment, water system and HVAC system. Handling of breakdown and operation of water system and HVAC system Handling breakdown of pharma process equipment and Preparation of Preventive maintenance schedule/planner. Schedule Preparation and performing HVAC validation, Instrument calibration. Knowledge and handling of utility equipment, DG, Transformer, Air compressor, Boiler and PCC and MCC panel. Good Knowledge of deviation and CAPA documents

Exciting Career Opportunity Alert! HETERO is conducting a Walk-in Interview for Formulation (OSD / Injectable) roles! We are hiring for: OSD: Production: Compression, Coating, capsule filling, Granulation. Quality Control (QC): HPLC, GC, IP,FP,RM, Validation, Method Development. Warehouse: Ram Material, Packing Material, Finished Goods. Injectable: Production: Autoclave, Filling, Sealing, Lyo, Vial washing, Visual Inspection. Packing: Blister packing, Bottle Packing, Vial Labelling. Experience & Qualifications: 1 to 7 years of relevant experience in ITI, DIPLOMA, B.Com, BSc, B.Pharma, MSc. Freshers with B.Com, B.Sc., or Diploma can apply for Warehouse/Production Dept. Interview Location: PHARMA JOBS: Talent Acquisition Center, Bhagyaradhi Degree College, 1st Floor, Near IDPL X Road, Hyderabad. Work Location: Polepally, Jadcherla. Date & Time: 06th April 2025 (Sunday) 09:00 AM to 03:00 PM Contact Information: HR: +91 9010203989 / 8121005416 Join our team and be a part of an innovative and dynamic work environment!

Breakdown investigations and Implementation of appropriate corrective and preventive actions. Installation, Qualification, Trouble shooting, Speed Optimization of Production and Packing Equipment's. In-Depth Knowledge on maintenance of Process & Packing equipment like RMG, FBD, compression, capsule filling machines, Auto coaters & Softgel Encapsulation, blister packing, Bulk Packing, Sachet Packing machine. Explore automation opportunities to improve the line efficiency. Manpower Planning, Training & Preparation of Monthly Reports

Role & responsibilities Oversee and manage the Quality Control department to ensure efficient laboratory operations. Develop, implement, and maintain QC protocols and Standard Operating Procedures (SOPs) in compliance with GMP, FDA, MHRA, and other regulatory standards. Supervise and mentor QC staff, providing training and technical support to maintain high performance. Conduct routine and non-routine testing of raw materials, intermediates, and finished pharmaceutical products. Ensure timely and accurate analytical testing, stability studies, and method validations. Investigate and resolve out-of-specification (OOS) and out-of-trend (OOT) results, implementing corrective and preventive actions (CAPA). Coordinate with Production, Quality Assurance, and R&D teams to ensure smooth manufacturing and compliance processes. Review and approve analytical data, reports, and COAs (Certificates of Analysis). Ensure proper calibration, validation, and maintenance of laboratory instruments and equipment. Manage laboratory documentation, ensuring compliance with data integrity guidelines. Participate in regulatory inspections, audits, and customer visits, providing necessary documentation and responses. Stay updated on industry trends, regulatory changes, and advancements in analytical techniques. Preferred candidate profile Bachelor's/Masters degree in Pharmacy, Chemistry, Microbiology, or a related field. Minimum 12+ years of experience in Quality Control within the pharmaceutical industry. Strong knowledge of GMP, GLP, ICH guidelines, and regulatory requirements (FDA, MHRA, WHO, etc.). Hands-on experience with analytical techniques such as HPLC, GC, FTIR, UV-Vis Spectrophotometry, etc. Experience in handling QC audits, deviations, OOS investigations, and CAPA implementation.

Role & responsibilities Keen Knowledge on Regulatory guidelines for finished product registration. Dossier compilation as per guidelines. Compilation and review the product dossiers for submission in CTD, ACTD . Gap analysis of the dossier and addressing the gaps before submission to MOH. Handling the customer and MOH queries . Life cycle management of the product. Development report, scale up report , specification, COA, stability protocol and Process validation protocol. Documents review (Specification, STP, Analytical method validations, Development report and validation reports, BMR, BPR, PVP/R and stability). Post approval experience to file the applicable variations timely. Knowledge on EAEU, ICH and EMEA guidelines. Re-registration (Renewal) procedures. Administrative documents requirements (COPP, Mfg. License and Import License) . Registration information management system updates on regular basis.

Project Co-ordination Design, Planning & execution in pharma specific injectable & solid dose project HVAC with its classification, process water system, plant utilities pharma process in injectable as well as OSD URS of all process equipment's

Role & responsibilities Analytical Development Laboratory (ADL) Position: Executive Experience: 03-08 Years Qualification: M.Pharm / M.Sc Job/ Skill Set HPLC/GC/IC method development, feasibility, verification, equivalency, validation for complex OSD products, oncology products, topical products having exposure to regulated, Semi Regulated & India markets Comparative evaluation of methods with alternative vendor methods versus existing primary vendor and regulatory impact analysis Dissolution development, comparative dissolution, multimedia dissolution and statistical evaluation and report preparation Good understanding and hands on experience of analytical instruments like HPLC,IC, GC etc. NI/GI & NDSRI with LCMS/GCMS expertise, Solid state characterization and API sameness study Hands on experience on in-vitro Studies, E&L, Solid State characterization, IVPT/IVRT, Impurity characterization, sameness study Welversed with USP/EP/BP/IP and various current regulatory guidelines (ICH/EMEAVFDA) Perform maintenance and calibration of lab instruments / equipment Contact Details: Email : nitinsingh@torrentpharma.com

Vijaya Diagnostic Centre P. Ltd. is looking for TECHNICIAN - MRI to join our dynamic team and embark on a rewarding career journey Positioning: Position the patient correctly on the MRI table to obtain the best imaging results and ensure patient comfort. Safety Measures: Adhere to safety protocols to minimize risks associated with magnetic fields, ensuring that no ferrous objects are present in the MRI room during scans. Injection of Contrast Agents: Administer contrast agents intravenously when required to enhance the visibility of certain tissues or organs in the images. Monitor Vital Signs: Continuously monitor the patient's vital signs, such as heart rate and oxygen levels, during the scan to ensure their well-being. Image Quality Assurance: Review the acquired images to verify their quality and accuracy, making any necessary adjustments or re-scans. Maintenance and Troubleshooting: Perform routine maintenance and troubleshoot minor technical issues with the MRI machine. Report any major malfunctions to the appropriate personnel. Patient Comfort: Maintain patient comfort and reassurance throughout the imaging process, especially if the procedure takes an extended amount of time. Documentation: Maintain accurate records of patient information, scanning procedures, and images obtained.

Vijaya Diagnostic Centre P. Ltd. is looking for TECHNICIAN - MRI to join our dynamic team and embark on a rewarding career journey Positioning: Position the patient correctly on the MRI table to obtain the best imaging results and ensure patient comfort. Safety Measures: Adhere to safety protocols to minimize risks associated with magnetic fields, ensuring that no ferrous objects are present in the MRI room during scans. Injection of Contrast Agents: Administer contrast agents intravenously when required to enhance the visibility of certain tissues or organs in the images. Monitor Vital Signs: Continuously monitor the patient's vital signs, such as heart rate and oxygen levels, during the scan to ensure their well-being. Image Quality Assurance: Review the acquired images to verify their quality and accuracy, making any necessary adjustments or re-scans. Maintenance and Troubleshooting: Perform routine maintenance and troubleshoot minor technical issues with the MRI machine. Report any major malfunctions to the appropriate personnel. Patient Comfort: Maintain patient comfort and reassurance throughout the imaging process, especially if the procedure takes an extended amount of time. Documentation: Maintain accurate records of patient information, scanning procedures, and images obtained.

Vijaya Diagnostic Centre P. Ltd. is looking for TECHNICIAN - CT SCAN to join our dynamic team and embark on a rewarding career journey Patient Interaction: Explain procedures to patients, ensuring their understanding and cooperation. Prepare and position patients for imaging procedures. Administer contrast agents, when necessary, to enhance image quality. Equipment Operation: Operate CT and MRI equipment according to established protocols. Adjust and control imaging parameters to obtain optimal images. Monitor patients during procedures and make adjustments as needed. Safety and Compliance: Adhere to radiation safety guidelines and protocols. Ensure proper patient positioning to minimize radiation exposure. Follow infection control and safety procedures in the imaging area. Image Quality and Analysis: Evaluate images for quality and clarity, ensuring diagnostic relevance. Collaborate with radiologists and other healthcare professionals to interpret results. Equipment Maintenance: Perform routine maintenance on CT and MRI equipment. Report malfunctions or issues to the appropriate personnel for repairs. Documentation: Maintain accurate and complete patient records. Document relevant information regarding procedures and patient history. Continuing Education: Stay informed about advancements in imaging technology and techniques. Participate in continuing education to enhance skills and knowledge.

Vijaya Diagnostic Centre P. Ltd. is looking for TECHNICIAN - CT SCAN to join our dynamic team and embark on a rewarding career journey Patient Interaction: Explain procedures to patients, ensuring their understanding and cooperation. Prepare and position patients for imaging procedures. Administer contrast agents, when necessary, to enhance image quality. Equipment Operation: Operate CT and MRI equipment according to established protocols. Adjust and control imaging parameters to obtain optimal images. Monitor patients during procedures and make adjustments as needed. Safety and Compliance: Adhere to radiation safety guidelines and protocols. Ensure proper patient positioning to minimize radiation exposure. Follow infection control and safety procedures in the imaging area. Image Quality and Analysis: Evaluate images for quality and clarity, ensuring diagnostic relevance. Collaborate with radiologists and other healthcare professionals to interpret results. Equipment Maintenance: Perform routine maintenance on CT and MRI equipment. Report malfunctions or issues to the appropriate personnel for repairs. Documentation: Maintain accurate and complete patient records. Document relevant information regarding procedures and patient history. Continuing Education: Stay informed about advancements in imaging technology and techniques. Participate in continuing education to enhance skills and knowledge.

Vijaya Diagnostic Centre P. Ltd. is looking for SENIOR TECHNICIAN - CT AND MRI to join our dynamic team and embark on a rewarding career journey Patient Interaction: Explain procedures to patients, ensuring their understanding and cooperation. Prepare and position patients for imaging procedures. Administer contrast agents, when necessary, to enhance image quality. Equipment Operation: Operate CT and MRI equipment according to established protocols. Adjust and control imaging parameters to obtain optimal images. Monitor patients during procedures and make adjustments as needed. Safety and Compliance: Adhere to radiation safety guidelines and protocols. Ensure proper patient positioning to minimize radiation exposure. Follow infection control and safety procedures in the imaging area. Image Quality and Analysis: Evaluate images for quality and clarity, ensuring diagnostic relevance. Collaborate with radiologists and other healthcare professionals to interpret results. Equipment Maintenance: Perform routine maintenance on CT and MRI equipment. Report malfunctions or issues to the appropriate personnel for repairs. Documentation: Maintain accurate and complete patient records. Document relevant information regarding procedures and patient history. Continuing Education: Stay informed about advancements in imaging technology and techniques. Participate in continuing education to enhance skills and knowledge.

Vijaya Diagnostic Centre P. Ltd. is looking for SENIOR TECHNICIAN - CT AND MRI to join our dynamic team and embark on a rewarding career journey Patient Interaction: Explain procedures to patients, ensuring their understanding and cooperation. Prepare and position patients for imaging procedures. Administer contrast agents, when necessary, to enhance image quality. Equipment Operation: Operate CT and MRI equipment according to established protocols. Adjust and control imaging parameters to obtain optimal images. Monitor patients during procedures and make adjustments as needed. Safety and Compliance: Adhere to radiation safety guidelines and protocols. Ensure proper patient positioning to minimize radiation exposure. Follow infection control and safety procedures in the imaging area. Image Quality and Analysis: Evaluate images for quality and clarity, ensuring diagnostic relevance. Collaborate with radiologists and other healthcare professionals to interpret results. Equipment Maintenance: Perform routine maintenance on CT and MRI equipment. Report malfunctions or issues to the appropriate personnel for repairs. Documentation: Maintain accurate and complete patient records. Document relevant information regarding procedures and patient history. Continuing Education: Stay informed about advancements in imaging technology and techniques. Participate in continuing education to enhance skills and knowledge.

Project Role : Infra Tech Support Practitioner Project Role Description : Provide ongoing technical support and maintenance of production and development systems and software products (both remote and onsite) and for configured services running on various platforms (operating within a defined operating model and processes). Provide hardware/software support and implement technology at the operating system-level across all server and network areas, and for particular software solutions/vendors/brands. Work includes L1 and L2/ basic and intermediate level troubleshooting. Must have skills : Microsoft Intune Good to have skills : NA Minimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Infra Tech Support Practitioner, you will be responsible for providing ongoing technical support and maintenance of production and development systems and software products, both remote and onsite. You will work on various platforms, implementing technology at the operating system-level and performing basic and intermediate level troubleshooting tasks. Roles & Responsibilities: Expected to be an SME Collaborate and manage the team to perform Responsible for team decisions Engage with multiple teams and contribute on key decisions Provide solutions to problems for their immediate team and across multiple teams Implement technology at the operating system-level Perform hardware/software support Troubleshoot at L1 and L2 levels Professional & Technical Skills: Must To Have Skills: Proficiency in Microsoft Intune Strong understanding of IT operations Experience with server and network areas Knowledge of software solutions/vendors/brands Hands-on troubleshooting experience Additional Information: The candidate should have a minimum of 5 years of experience in Microsoft Intune This position is based at our Bengaluru office A 15 years full time education is required

Title: Business Development Head - (CMO / CDMO) - Pharmaceutical Human Health Industry (DOMESTIC MARKETING & BUSINESS DEVELOPMENT ONLY) Summary: We are currently seeking a dynamic and experienced Business Development Head (FOR DOMESTIC MARKETING) to spearhead our business development initiatives in the pharmaceutical human health sector. This pivotal role requires a focus on B2B marketing and contract manufacturing, particularly in oral liquids and nutraceuticals. The ideal candidate will bring a strong background in multinational corporate environments, with a demonstrated track record of success in generating new B2B orders and selling developed products within the human pharmaceutical industry. Qualifications: Masters degree in business, Marketing, Pharmaceutical Sciences, or a related field is mandatory. A minimum of 08 to 15 years of progressive experience in business development within the human pharmaceutical industry, specifically in multinational corporations. Demonstrated expertise in B2B marketing and contract manufacturing, with a focus on OSD formulations and nutraceuticals. Proven ability to develop and execute successful business development strategies in the pharmaceutical sector. Strong understanding of market dynamics, regulatory requirements, and product development in the pharmaceutical industry. Exceptional negotiation, communication, and interpersonal skills. Proven track record of meeting or exceeding business development targets. Ability to work collaboratively in a team environment and lead cross-functional initiatives. Core Responsibilities: Lead and strategize business development activities in the pharmaceutical human health sector with a specific focus on oral liquids and nutraceuticals. Identify and secure new business opportunities in the B2B market, ensuring they align with the company's strategic objectives. Secure and manage comprehensive contracts for CDMO and CMO services with multinational corporations, leveraging market insights and strategic partnerships. Maintain and enhance relationships with existing clients while actively pursuing new partnerships in the pharmaceutical industry. Collaborate with internal teams to develop and propose tailored solutions for clients, ensuring compliance with industry standards and customer satisfaction. Negotiate and finalize business deals, focusing on profitability and sustainable growth. Stay abreast of industry trends, competitor activities, and regulatory changes to inform and adapt business strategies. Provide leadership and mentorship to the business development team, setting clear goals and tracking performance. Regularly report on business development activities and progress to senior management, providing insights and recommendations for continuous improvement. (NOTE: CANDIDATES WHO ARE HAVING RELEVANT EXPERIENCE IN THE PHARMACEUTICAL INDUSTRY AS PER THE ABOVE JOB DESCRIPTION ONLY SHOULD APPLY FOR THIS POSITION)

Designing and developing new pharmaceutical formulations based on project objectives. Modifying existing formulations to improve performance or address specific needs.