8 Pk Jobs nearby Mysore

**Role Overview:** You will be working as a Java Developer for LINEN.Cloud, collaborating with cross-functional teams to translate business requirements into high-quality, scalable, and maintainable code. The ideal candidate should possess a strong foundation in Java development, excellent problem-solving skills, and a passion for building innovative solutions. **Key Responsibilities:** - Designing, implementing, and Unit testing Java applications. - Aligning application design with business goals. - Debugging and resolving technical problems that arise. - Recommending changes to the existing Java infrastructure. - Ensuring continuous professional self-development. **Qualifications Required:** - Experience developing and testing Java Web Services RESTful (primary), XML, JSON, and supporting integration and enabling access via API calls. - Experience with Tomcat, Apache, and similar web server technologies. - Hands-on experience working with RabbitMQ and Kafka. - Experience with the Spring Boot framework. - Hands-on with Angular/Node.js is preferred. - Working knowledge of ELK (Elasticsearch, Logstash, and Kibana) or Solr is a big plus. - Experience with virtualization like Cloud Foundry (PCF), Kubernetes (PKS), Docker, etc, is a big plus. - Agile/Scrum expertise. - Experience establishing and enforcing branching and software development processes and deployment via CI/CD. **About Uplers:** Uplers aims to make hiring reliable, simple, and fast, supporting talents in finding and applying for relevant contractual onsite opportunities to progress in their careers. They are committed to helping individuals overcome any grievances or challenges they may face during the engagement. If you are prepared for a new challenge, a great work environment, and an opportunity to advance your career, Uplers encourages you to apply today for this Java Developer position with LINEN.Cloud. They are looking forward to welcoming you onboard!,

As a Biology expert, you will be responsible for the following key responsibilities: - Expertise in handling HPLC and LCMS, including troubleshooting techniques. - Proficiency in different extraction procedures and independent handling of bioanalysis for various matrices in PK and ADME studies. - Good understanding of various column chemistry and its application in method development. - Ensuring data integrity and maintaining good documentation practices, including recording data in LNB and completing studies as required. - Operating and maintaining laboratory equipment. - Ensuring all instruments are maintained in a calibrated status. - Managing consumables and chemicals necessary for the smooth conduction of PK studies without delays. Your required experience and skills include: - Master's degree with 6-10 years of experience in Pharmaceutical/Biotechnology/CRO industry in Bioanalysis, focusing on NCE, peptides, nucleosides, etc. - Solid knowledge and broad experience in Bioanalysis of various DMPK samples. - Familiarity with troubleshooting problems during Bioanalysis. - Excellent interpersonal skills and ability to work effectively in a team. - Proficiency in computer skills and a good understanding of statistics. - Demonstrating a strong sense of responsibility and work ethics.,

As an AI Drug Discovery Scientist at our company, you will play a crucial role in developing innovative approaches to support our internal drug development pipeline and external partnerships in the field of oncology drug development. Your primary focus will be on accelerating the path from target identification to therapy through the application of cutting-edge AI and ML tools. **Key Responsibilities:** - Expand, select, and apply datasets and AI/ML tools to integrate preclinical and clinical data for understanding mechanisms of action (MOA) and therapeutic potential - Analyze genomic contexts of cancer pathways to optimize MOA-indication matching - Identify biomarkers that enhance molecular selectivity by evaluating relationships between MOA, therapeutic potential, and cancer genomics - Evaluate molecular features to support modifications for new chemical entities (NCEs) with improved pharmacokinetics (PK) and efficacy - Utilize AI-driven analysis to uncover the therapeutic potential of existing molecules and guide combinatorial strategies - Extract actionable insights from preclinical data to inform drug discovery strategies - Apply AI methodologies for novel targeting of cancer drugs, including antibody-drug conjugates (ADCs) and other targeted modalities - Build and maintain in silico molecule pipelines to support AI/ML drug discovery projects - Collaborate with research teams to design proof-of-concept studies and contribute to scientific publications and grant applications **Qualifications Required:** - 3+ years of experience in AI-directed drug development environments - Ph.D. in Computational Biology, Bioinformatics, Computational Chemistry, Cancer Biology, or related field (consideration for exceptional experience with Bachelor's or Master's degree) - Publication record in AI-based drug development - Skills in ML-based in silico discovery of cancer drug response pathways and biomarkers - Knowledge of deciphering MOA from complex genomic studies and utilizing AI for drug development strategy - Familiarity with genomic and cancer pathway data sources and experience in drug candidate prioritization - Strong communication skills for presenting scientific data - Proficiency in programming languages such as Python, R, or similar **Additional Company Information:** - Job Type: Full-time - Work Location: In person Apply now to be part of our dynamic team driving innovation in AI drug discovery for oncology drug development.,

As a Specialist, Application Support Engineer (Splunk) at Fiserv, you will play a crucial role in managing and maintaining the ESF/Communicator Open application to ensure the reliability, availability, and performance of systems. Your responsibilities will include collaborating with cross-functional teams, implementing automation processes, and continuously improving efficiency to reduce downtime. You should have a strong background in scripting, Dynatrace, Splunk, Azure, Kubernetes, and be adept at analyzing and resolving complex production issues. Key Responsibilities: - Resolve production incidents by analyzing issues, coordinating with necessary parties, and taking ownership of the situation. - Monitor alerts using Splunk and Dynatrace. - Discuss technical issues with business analysts and developers. - Optimize SQL queries to efficiently run on large databases. - Analyze network issues, understand flows and dependencies, and communicate with network engineers. - Install, configure, and maintain PKS Kubernetes Web Services environments. - Conduct Root Cause Analysis. - Participate in application performance testing and troubleshooting across the entire software and hardware stack. - Recreate problems locally, debug code, and identify underlying defects. - Perform technical evaluation of defects. - Understand the impact of changes across applications. - Identify potential points of failure in infrastructure/applications and improve/resolve vulnerabilities. - Create Confluence Knowledge articles and documentations. - Automate repetitive tasks to minimize manual efforts. Qualifications Required: - Bachelor's degree in Information Technology, Computer Science, Electrical/Computer Engineering, or related field. - 6-10 years of overall experience. - Experience with Web Services based architectures, PKS Kubernetes, or Cloud environments. - Proficiency in monitoring tools like Splunk, Dynatrace, and Moogsoft. - Strong troubleshooting and problem-solving skills. - Experience with scripting languages like Python. - Knowledge of CI/CD processes, Agile methodologies, Jenkins, Git, and Middleware Technology. - Automation and scripting proficiency in SQL Optimization, scheduled jobs, Splunk, Python, Selenium. - Experience in the Fintech market. - Familiarity with Network architecture (Apigee, Firewalls, Network diagrams). - Ability to multi-task, adapt to changing business priorities, and generate reports. - Awareness/experience of ITIL standard methodologies, ITIL Foundations certification a plus. - Willingness to work shifts or weekends based on business demand. Thank you for considering employment with Fiserv. Make sure to apply using your legal name and complete the profile step-by-step while attaching your resume. Please note that Fiserv does not accept resume submissions from agencies outside of existing agreements. Be cautious of fraudulent job postings not affiliated with Fiserv, as they may target your personal information or financial details. All communications from Fiserv representatives will come from legitimate Fiserv email addresses.,

As a Scientist in Pharmaceutical Development, you will be responsible for planning and executing various tasks related to the development, scale up, and manufacturing of drug products for monoclonal antibodies (mAb), bi-specific, tri-specific antibodies, and Antibody Drug Conjugates (ADC) of New biological entities (NBE). Your key responsibilities will include: - Significant experience in development, scale up, and manufacturing of drug products for mAbs, ADCs, etc. - Experience in parenteral delivery systems development like Nanoparticulate delivery systems, Lipid based delivery systems. - Proficient in pre-formulation studies of mAbs and ADCs along with physiochemical & Solid-State characterization. - Proficiency in interpreting in silico output on mAb developability and strategically using it for experimentation. - Hands-on experience in preclinical formulation development of mAbs and ADCs. Qualifications required for this role include: - Proficiency in planning and executing preclinical formulation development of mAbs and ADCs. - Ability to plan and execute pre-formulation studies, stability studies, etc., for mAB and ADC projects. - Experience in formulation development of New biological entities from mAB and ADC platform for human clinical studies. - Proficiency in executing approaches and strategies for scale up, tech transfer of mAB and ADC drug products to manufacturing facilities. - Coordination and execution of drug products of mAB and ADC under GMP set up for clinical trials with appropriate documentation. - Support development of enabling formulations for improving the bio-pharmaceutical properties and bioavailability of New Chemical Entities (NCEs). In addition to the above, you will also contribute scientifically to overall pharmaceutical development processes, prepare protocols, guidelines, SOPs for lab equipment/instruments and processes, and adhere to systems and processes pertaining to safety, health, and the environment. If you are selected for this role, you will be expected to demonstrate competencies in Presentation & Communication Skills, Interpersonal Skills, Excel Skills, Scientific Report Writing, and Team Management.,

As a Biostatistician, you will play a crucial role in contributing to trial design, protocol development, analysis planning, interpretation of results, and preparation of regulatory submissions. You will collaborate with various stakeholders such as the GBDS Biostatistics Lead, medical monitor, protocol manager, data manager, PK scientist, and other members of the study/indication team. Your responsibilities will include: - Driving the selection of optimal study designs, data collection methods, and analytic approaches. - Providing strategic and scientific input at the indication/protocol/integrated analysis level to enhance the understanding of the asset being studied and improve development decisions. - Developing a broad understanding of the clinical, regulatory, and commercial landscape by researching medical literature and regulatory documents. - Preparing the development strategy to facilitate the effective and safe utilization of the product. - Leading the development and execution of statistical aspects for multiple complex studies independently. - Playing a key role in filing activities, including planning and executing integrated analyses. - Defending protocols and Statistical Analysis Plans (SAPs) during reviews and providing independent assessments. Qualifications required for this role include: - Possession of a Master's degree in Statistics or equivalent. A Ph.D. in Statistics or equivalent combined with 6 years of industry-related experience is preferred. - At least 9+ years of experience demonstrating a deep understanding of statistical and clinical trials methodology as it pertains to clinical development. Your role as a Biostatistician will significantly impact the success of clinical trials, regulatory submissions, and market access strategies. Your dedication to upholding quality standards, adherence to processes and SOPs, and continuous learning of applied statistical methodology will be key to your success in this role.,

As a candidate for the position, your role will involve performing and analyzing in vitro and in vivo DMPK studies to support drug discovery and development projects. This includes planning, designing, and setting up DMPK experiments, handling instruments, maintaining the laboratory, preparing and reviewing protocols, writing reports, communicating with the project team, and presenting DMPK data in project meetings. Key Responsibilities: - Perform and analyze in vitro and in vivo DMPK studies - Plan, design, and set up DMPK experiments - Handle instruments and maintain the laboratory - Prepare and review protocols - Write reports, communicate with the project team, and present DMPK data in project meetings Required Qualifications: - Ability to set up and perform physiochemical assays such as solubility and logP - Experience in conducting in vitro DMPK assays (microsomal and hepatocyte stability, plasma stability, CYP inhibition, blood/plasma ratio) - Development and validation of bioanalytical methods across various biological matrices - Analysis of in-vivo pharmacokinetic samples - Knowledge of sample processing techniques (protein precipitation, liquid-liquid extraction, solid-phase extraction) - Proficiency in handling LC-MS/MS for quantitative analysis - Protocol preparation, report writing, and presentation of DMPK data in scientific team meetings Additional Details: - Experience in animal handling and conducting pharmacokinetic (PK) studies is beneficial - Working with cell lines such as Caco-2 - Ability to interpret pharmacokinetic data using Phoenix WinNonlin - Experience in a GLP or GLP-like environment Basic Skills Required: - Ability to work independently with enthusiasm and self-motivation - Strong decision-making and problem-solving skills - Effective collaboration and teamwork across multidisciplinary functions - Knowledge of drug discovery and development processes - Excellent oral, written, and interpersonal communication skills with proficiency in English - Proficiency in computer applications including word processing, spreadsheets, and presentation tools Qualifications: - M.Pharm or MS (Pharm) or PhD degree - Industry experience of 2 to 5 years - Candidate must be an Indian citizen - Salary will be commensurate with experience,

As a Biostatistician at the company, you will play a vital role in cross-functional development teams by contributing to various aspects of trial design, protocol development, analysis planning, interpretation of results, and regulatory submissions. Your main responsibilities will include: - Developing collaborative relationships with team members such as the GBDS Biostatistics Lead, medical monitor, protocol manager, data manager, and PK scientist. - Making strategic and scientific contributions at the indication/protocol/integrated analysis level to enhance understanding of the asset being studied. - Driving the selection of optimal study designs, data collection methods, analytic approaches, and interpretation of trial data. - Interacting with external vendors, key opinion leaders, and regulatory agencies. - Expanding expertise by researching medical literature and regulatory documents. You will also be tasked with: - Contributing to the development strategy to ensure effective and safe product utilization. - Designing innovative and efficient clinical trials, selecting study populations and endpoints. - Translating scientific questions into statistical terms and vice versa. - Ensuring all analyses have clearly articulated hypotheses and are supported by trial design and data. - Effectively communicating with clinical, regulatory partners, and external opinion leaders. - Collaborating with clinicians and medical writers to prepare summaries for regulatory documents and scientific articles. Furthermore, you will be involved in: - Authoring and/or reviewing various study level documents such as protocol synopsis, statistical analysis plan, clinical study reports. - Employing cost-disciplined science in trial sizing and analysis planning. - Ensuring compliance with company processes, global standards, and maintaining deliverable quality. - Leading statistical aspects for multiple or complex studies independently. - Leading filing activities, including planning and executing integrated analyses. Your contributions will be essential in ensuring alignment at the study team level and maintaining quality in all assignments associated with the assigned protocol or project. It is expected that you stay updated with the latest applied statistical methodology and have a good understanding of CDISC standards and implementation guides.,

As a Post Graduate Teacher (PGT) Physical Education, your role will involve instructing students in physical activities and sports, developing age-appropriate lesson plans, organizing events, and assessing student performance. Your essential qualification for this position is a Master of Physical Education (M.P.Ed.) degree. Your key responsibilities will include: - Teaching theory and practical lessons in physical education - Promoting health and fitness among students - Managing sports equipment and facilities - Preparing students for competitions - Maintaining records of student performance The job offers the following benefits: - Food provided - Provident Fund Please note that the work location for this role is in person.,

As a Coordinator for in-vivo studies, your role involves planning and coordinating the initiation of research study protocols. You will be responsible for establishing operating policies and procedures, ensuring adherence to pre-established work scope, study protocol, and regulatory requirements. Developing and maintaining recordkeeping systems, as well as coordinating multiple data collection efforts with collaborating agencies or institutions, will also be part of your duties. Additionally, you will be involved in writing and editing reports and manuscripts, maintaining financial records for in vivo studies, and ensuring the availability and preparation of necessary supplies as specified by protocols and/or SOP. Key Responsibilities: - Coordinate the preparation of labels, labeling of sample collection tubes, and other laboratory reagents - Coordinate the preparation of shipment packages for dispatching activities Qualifications Required: - Master's in Lifescience with 3-5 years of working experience in in-vivo studies - Excellent time management skills to handle multiple tasks, manage deadlines, and respond to urgent needs - Strong technical knowledge with exceptional attention to detail - Excellent data analysis and interpretation skills - High self-motivation to work independently under aggressive deadlines - Exceptional communication skills and ability to build relationships with stakeholders - Organizational skills to thrive in a fast-paced team environment The company is located in Ahmedabad, Gujarat, India.,

Join an industry leader and make a positive change in the sustainable use of the world's natural resources. Together, we will transform the business and drive the industry toward a greener future. At Metso, you will be supported by our inclusive culture and a network of colleagues from around the world. With us, you will embark on a personal growth journey and are encouraged to realize your potential. This is your invitation to rise above the possible. **Role Overview:** As a Technical Support Specialist at Metso, you will be responsible for providing technical assistance and support to customers, solving on-site issues, and improving equipment performance to enhance customer satisfaction. This role also involves reducing warranty claims by addressing process gaps and driving improvements. There may be a requirement for 50% or more travel time to sites across India and abroad. **Key Responsibilities:** - Provide prompt responses to customer inquiries and complaints. - Diagnose and troubleshoot mechanical equipment problems. - Track equipment issues through to resolution within agreed time limits. - Offer accurate feedback to customers. - Maintain records of customer issues and solutions for future reference. - Support the roll-out of new mechanical equipment and train users. - Document technical knowledge and drive process improvements. **Qualifications Required:** - Bachelor's degree in mechanical engineering. - 10+ years of experience with screening equipment. - Proven experience as a Technical Support Specialist or similar role. - Self-driven and proactive in planning and achieving goals. - Excellent problem-solving and communication skills. - Ability to work independently and manage multiple tasks. - Customer-oriented mindset. - Adaptable and flexible to support customers and coordinate with cross-functional teams globally, involving different time zones. - Language skills in French and Portuguese are advantageous. - Engineering experience with vibrating equipment is highly desirable. - Proficiency in CAD tools (Inventor & Team Center) is an advantage. - Familiarity with SAP S4/HANA. At Metso, you will benefit from occupational healthcare, a generous benefits plan, healthy living rewards, mental well-being services, meal benefits, and engagement surveys. You can also avail global incentive programs tied to business and performance targets. Extensive learning opportunities include ongoing growth dialogues, internal mobility, mentoring programs, education assistance, ambitious projects, and global opportunities. You will have worldwide support through the network of peers across the world, offering valuable assistance. The company culture is committed to developing an inclusive culture that enables everyone to do their best and reach their full potential. A culture that is courageous, compelling, and caring, uniting people to build a sustainable future together. Join us at Metso, a frontrunner in sustainable technologies, end-to-end solutions, and services for the aggregates, minerals processing, and metals refining industries globally. Improve customers" energy and water efficiency, increase productivity, and reduce environmental risks with our product and service expertise. Metso is headquartered in Espoo, Finland, with close to 17,000 employees in around 50 countries. Sales in 2024 were about EUR 4.9 billion. Make a difference with Metso! *[Job posting end date: 05/06/2025]* Hiring Manager: Santhosh PK metso.com,

Role Overview: As a Statistical Programmer II (SDTM/ADaM/TFLs/PK-PD) at Novanal Science & Technologies, you will be a key member of the SAS programming division specializing in providing value-focused services for clinical trials. Your primary responsibility will be to develop, test, validate, and document SAS programs in support of clinical research. This remote role will require you to program SDTM and ADaM datasets, TFLs, and PK-PD analyses, collaborating closely with biostatisticians, data managers, and other team members to ensure the accuracy and compliance of statistical outputs. Key Responsibilities: - Develop, test, validate, and document SAS programs for clinical research - Program SDTM and ADaM datasets, TFLs, and PK-PD analyses - Collaborate with biostatisticians, data managers, and team members to ensure accuracy and compliance of statistical outputs Qualifications: - Proficiency in Statistical Programming and SAS programming - Strong skills in Statistics and Data Management - Experience with creating macros in SAS - Excellent problem-solving and analytical skills - Ability to work independently and remotely - Experience in the clinical research or pharmaceutical industry is a plus - Bachelor's degree in Statistics, Computer Science, Mathematics, or related field,

As an Audit Assistant at P.K. Jayan & Co., Chartered Accountants, located in Thrissur, you will play a crucial role in the preparation and review of financial statements and audit reports. Your responsibilities will include conducting financial audits, applying analytical skills to assess financial information, and ensuring compliance with relevant standards and regulations. You will also collaborate with team members and clients while providing support in various audit-related tasks assigned by the management. Key Responsibilities: - Assist in the preparation and review of financial statements and audit reports - Conduct financial audits to assess the accuracy of financial information - Coordinate with team members and clients to ensure compliance with relevant standards and regulations - Provide support in other audit-related tasks assigned by the management Qualifications Required: - CAS, Inter CA, CMA, CS inter with experience - Ability to prepare and review Financial Statements and Audit Reports - Proficiency in conducting Financial Audits - Strong Analytical Skills - Background in Finance - Excellent written and verbal communication skills - Ability to work both independently and in a team-oriented environment - Bachelor's degree in Accounting, Finance, or related field - Experience in audit or accounting firms is a plus,

Role Overview: You will be supporting the Study Lead in TCO studies to ensure all trial deliverables are met according to timelines, budget, operational procedures, and quality standards. Additionally, you will assist TCO CSD, CSaD, and CSTL in various tasks related to the management of clinical study materials, development of study tools, guidelines, and training materials. Key Responsibilities: - Develop specific sections of selected study documents and study tools - Manage clinical study material and implement issue resolution plans - Contribute to the preparation of CSR appendices under supervision - Set up and maintain appropriate study tracking forms including enrollment log, site and vendor contact lists, drug shipping logs, and team membership lists - Assist in managing interactions with relevant functions including Global Clinical Supply and Novartis country organizations - Track drug supply at central hubs, local CPOs, and sites, ensuring adequate supply and monitoring expiry dates - Create and maintain HQ TOC, ensure timely completion and maintenance of TMF, and assist in trial data analysis and reporting - Support in meeting scheduling, distribution of meeting agendas/minutes, and archiving of study tools - Track PK and biomarker sample tracking, act as a liaison with sites for sample shipment and reconciliation - Assist in financial management, forecasting, and vendor management activities - Support other ClinOps functions as required Qualifications Required: - Prior experience in clinical trial operations or related field - Strong organizational and multitasking skills - Excellent communication and collaboration abilities - Familiarity with drug tracking and supply management - Proficiency in data analysis and reporting - Ability to work effectively in a fast-paced environment with attention to detail Please note that Novartis is committed to providing reasonable accommodation to individuals with disabilities if needed during the recruitment process. Additionally, the company values diversity and inclusivity in the work environment to better serve patients and communities.,

You will be responsible for providing advanced expert support and functional leadership to ensure scientific integrity and validity for clinical development, early development, and/or research projects. Your role will involve developing and applying biostatistics and programming methods to ensure valid conclusions. Additionally, you will provide statistical support for regulatory submissions, including planning, analysis, and reporting of clinical safety and efficacy summaries. You may also provide statistical support in research or other R&D areas. Independently, you will lead special projects focusing on innovative tools and systems, supporting the Director of Clinical Data Standards. **Key Responsibilities:** - Responsible for all statistical tasks on assigned clinical or non-clinical trials, including protocol development, statistical analysis plan development, and reporting activities. - Contribute to planning and execution of exploratory analyses, innovative analyses for publications, pricing & reimbursement submissions, PK/PD analyses, exploratory biomarker and diagnostic analyses, and statistical consultation. - Provide statistical expertise for submission activities and documents, meetings with Health Authorities, pricing agencies, and other drug development activities. - Lead interactions with external review boards/ethics committees, external consultants, and other external parties. - Collaborate with cross-functional teams, explain statistical concepts to non-statisticians, and ensure effective communication within the clinical trial team. - Provide strategic statistical input into projects, collaborate with other functions to drive quantitative decision-making, and ensure timeliness and quality of statistical deliverables. **Qualification Required:** - MS in Statistics or equivalent with 10+ years of relevant work experience, or PhD in Statistics or equivalent with 6+ years of relevant work experience. - Fluent in English (oral and written) with strong interpersonal and communication skills. - Proven expertise in statistics, pharmacokinetics, exposure-response modeling, and statistical software packages such as SAS and R. - Strong understanding of drug development, Health Authority guidelines, and regulatory activities. - Demonstrated leadership skills in building partnerships, mentoring associates, and facilitating quantitative team contributions.,

You will be working as a Research Scientist/ Sr. Research Scientist (L1/L2) in the DMPK department of Jubilant Biosys located in Greater Noida. Your responsibilities will include ADME representation, lab management, mentorship, and publishing results. - Understand the broader ADME requirements of various projects and guide chemistry teams towards improving duggability of the NCEs - Design DMPK strategy and implementation plan - Conduct PK and PK/PD analysis through early pre-clinical development - Interact with cross-functional teams and contribute to project progression - Design tailor-made ADME protocols for projects - Collate results and prepare presentations for internal and external meetings - Contribute to the design of the critical path for projects - Address queries from clients In terms of lab management, you will be responsible for: - Developing methods and troubleshooting analytical issues - Generating data, compiling reports, and maintaining lab records - Optimizing lab resource utilization - Tracking FTE utilization in projects - Monitoring CAPEX and OPEX requirements Your role will also involve mentorship where you will: - Guide team members on work planning and execution - Develop team skill sets for project activities - Mentor and train juniors on assays and technologies - Ensure ethical guidelines are followed in all aspects Additionally, you will be involved in publishing results by communicating scientific work to peer-reviewed journals. For Fee-for-service (FFS) projects, you will: - Understand client requirements and design appropriate experiments Qualifications required for this position are: - Ph.D./M.Sc./M.Tech in Biochemistry, Pharmaceutical Chemistry, or Biotech background Experience needed includes: - 1 to 8 years post-PhD or 10-12 years post M.Sc./M.Tech - Experience in a drug discovery industry/CRO in the DMPK department Jubilant Biosys is an equal opportunity employer, and all qualified applicants will be considered without regard to various characteristics as per local laws and regulations.,

As a Drug Safety Scientist, your role involves evaluating and monitoring the effectiveness and safety of prescribed drugs in patients. You will be responsible for analyzing pharmacokinetics (PK), pharmacodynamics (PD), and bioavailability data to ensure the efficacy of medications. Additionally, you will collaborate with regulatory authorities for drug approvals and ethical clearances to uphold medical standards. Key Responsibilities: - Collaborate with physicians to provide guidance on rational and evidence-based prescribing practices. - Customize drug treatments according to individual patient characteristics such as age, genetics, renal/liver function, etc. - Offer consultation on complex cases, particularly those involving polypharmacy. - Provide recommendations on appropriate dosing and therapeutic regimens based on clinical data. - Assist in managing adverse drug reactions (ADRs) and drug interactions effectively. Qualifications Required: - Bachelor's or Master's degree in Pharmacy or related field. - Prior experience in pharmacovigilance or drug safety. - Strong understanding of pharmacokinetics and pharmacodynamics. - Excellent communication and collaboration skills. The company offers benefits including health insurance, Provident Fund, and a yearly bonus. This is a full-time position that requires in-person work at the specified location. As a Drug Safety Scientist, your role involves evaluating and monitoring the effectiveness and safety of prescribed drugs in patients. You will be responsible for analyzing pharmacokinetics (PK), pharmacodynamics (PD), and bioavailability data to ensure the efficacy of medications. Additionally, you will collaborate with regulatory authorities for drug approvals and ethical clearances to uphold medical standards. Key Responsibilities: - Collaborate with physicians to provide guidance on rational and evidence-based prescribing practices. - Customize drug treatments according to individual patient characteristics such as age, genetics, renal/liver function, etc. - Offer consultation on complex cases, particularly those involving polypharmacy. - Provide recommendations on appropriate dosing and therapeutic regimens based on clinical data. - Assist in managing adverse drug reactions (ADRs) and drug interactions effectively. Qualifications Required: - Bachelor's or Master's degree in Pharmacy or related field. - Prior experience in pharmacovigilance or drug safety. - Strong understanding of pharmacokinetics and pharmacodynamics. - Excellent communication and collaboration skills. The company offers benefits including health insurance, Provident Fund, and a yearly bonus. This is a full-time position that requires in-person work at the specified location.

As a Medical Transcriptionist at Dr. P.K. Saha Hospital, your role will involve accurately transcribing medical reports, discharge summaries, and operative notes dictated by physicians and specialists across various departments. Your attention to detail and experience in medical transcription will be crucial in ensuring the maintenance of patient record confidentiality and timely delivery of reports to respective departments. Key Responsibilities: - Maintain confidentiality of patient records at all times - Coordinate with consultants to clarify any inconsistencies - Ensure timely delivery of reports /discharge summaries to the respective departments Qualifications & Skills: - Proven experience in medical transcription (minimum 1 year preferred) - Good typing speed and attention to detail At Dr. P.K. Saha Hospital, you will have the opportunity to work in a high-volume, fast-paced multispecialty environment and be a part of a mission-driven team serving thousands of patients across the region. Join us and grow with our rapidly expanding hospital.,

As a Hotel Reservation Executive, you will be responsible for handling incoming reservation requests, confirming bookings, managing cancellations, and ensuring smooth guest experiences by accurately processing and updating reservation data. Your role may also involve upselling and promoting hotel services to maximize revenue. Key Responsibilities: - Handling Reservation Inquiries: Answer phone calls, emails, and online inquiries from guests, travel agents, and other sources. Provide information about room availability, rates, packages, and amenities. - Confirming Reservations: Send confirmation details to customers, ensuring they have all the necessary information for their stay. - Managing Cancellations and Modifications: Handle cancellations, changes to existing reservations, and address guest inquiries or requests promptly and efficiently. - Maintaining Accurate Records: Keep reservation records and customer information up-to-date and organized. - Coordinating with Other Departments: Work with front desk, housekeeping, and other hotel departments to ensure smooth operations and guest satisfaction. - Upselling and Promoting Services: Identify opportunities to upsell and promote hotel amenities, packages, and services. - Resolving Guest Concerns: Address guest concerns and feedback in a professional and timely manner. - Maintaining Confidentiality: Handle guest information and property data with discretion and confidentiality. - Updating Room Vacancies: Keep online booking platforms and other channels updated with accurate room availability information. Qualifications Required: - Previous experience in hotel reservations or a similar customer service role is preferred. - Strong communication skills and the ability to interact effectively with guests and colleagues. - Attention to detail and the ability to maintain accurate records. - Ability to work collaboratively with other departments to ensure guest satisfaction. - Knowledge of upselling techniques and strategies is a plus. Please note that this is a full-time position with benefits including cell phone reimbursement and provided food. The work schedule is on day shift and the location is in person. If you are interested in this opportunity, you can speak with the employer at +91 7290044436.,

As a professional in the field of biotechnology and biochemistry, you will have the following responsibilities: - **For Protein Characterization - Analytical:** - Hold an M.Sc. / M. Tech. in Biochemistry / Biotechnology with at least 5 years of industrial hands-on experience. - Demonstrate sound knowledge in analytical method development, validation, technology transfer activities, and scientific report writing skills. - **For Upstream Process Operations:** - Hold an M.Sc. / M. Tech. with Biotechnology with 1 to 3 years of experience or a Ph.D. / M. Tech. with more than 10 years of experience. - Capable of handling mammalian cell culture processes, microbial fermentation, and equipment such as Bioreactors, CEDEX Bioanalyzer, etc. - Possess good documentation skills including SOP, STP, etc. - **For Downstream Processing and Antibody Drug Conjugate:** - Hold a PhD / M.Sc. / M. Tech. in Biochemistry / Biotechnology / Life sciences with 2 - 8 years of hands-on experience. - Proficient in protein purification techniques and handling equipment such as AKTA Avant, AKTA Pure, etc. - Capable of resin screening, process optimization for Mab and ADC at small-scale and pilot scale. - **For In-process Analysis and Stability Group:** - Hold a Ph.D., M.Sc., M. Tech, M. Pharm in Biotechnology / Biochemistry or equivalent with 3 - 10 years of experience. - Responsible for the development and qualification of analytical methods, in-process analysis, degradation / stability studies, etc. - **For Formulations Group:** - Hold a Ph.D., M.Sc., M. Tech. in Biotechnology / Biochemistry or M. Pharm in Biotechnology / Pharmaceutics with 3 - 5 years of experience. - Responsible for planning and execution of formulation development, stability / degradation studies, and technology transfer. - **For Molecular Biology:** - Hold an M. Sc. in any field of life sciences with 3-4 years of experience or a Ph.D. in life sciences. - Experienced in molecular biology techniques, cell and gene therapy development activities, and basic bioinformatics. - **For Mammalian Cell Culture:** - Hold an M.Sc. / M.Tech / M.Pharm with Biotechnology as a fresher or with 3-5 years of experience. - Capable of handling various cell lines, optimization & execution of stable/transient transfections, clone screening, etc. - **For Upstream Analytics:** - Hold an M.Sc. / M. Tech / M. Pharm with Biotechnology as a fresher or with 2-4 years of experience. - Proficient in protein binding studies using SPR, purification of therapeutic proteins, and protein characterization techniques. - **For PK/ PD/ Immunogenicity:** - Hold an MSc. in any life sciences area or M. Pharm in Biotechnology / Pharmacology as a fresher or with 3-7 years of experience. - Experienced in activities like development, validation & execution of PK/PD/Immunogenicity/Nab assays to support pre-clinical & clinical studies. Qualification Required: - **For Protein Characterization - Analytical:** - M.Sc. / M. Tech. in Biochemistry / Biotechnology with at least 5 years of industrial hands-on experience. - **For Upstream Process Operations:** - M.Sc. / M. Tech. with Biotechnology with 1 to 3 years of experience or Ph.D. with more than 10 years of experience. - **For Downstream Processing and Antibody Drug Conjugate:** - PhD / M.Sc. / M. Tech. in Biochemistry / Biotechnology / Life sciences with 2 - 8 years of hands-on experience. - **For In-process Analysis and Stability Group:** - Ph.D., M.Sc., M. Tech, M. Pharm in Biotechnology / Biochemistry or equivalent with 3 - 10 years of experience. - **For Formulations Group:** - Ph.D., M.Sc., M. Tech. in Biotechnology / Biochemistry or M. Pharm in Biotechnology / Pharmaceutics with 3 - 5 years of experience. - **For Molecular Biology:** - M. Sc. in any field of life sciences with 3-4 years of experience or Ph.D. in life sciences. - **For Mammalian Cell Culture:** - M.Sc. / M.Tech / M.Pharm with Biotechnology as a fresher or with 3-5 years of experience. - **For Upstream Analytics:** - M.Sc. / M. Tech / M. Pharm with Biotechnology as a fresher or with 2-4 years of experience. - **For PK/ PD/ Immunogenicity:** - MSc. in any life sciences area or M. Pharm in Biotechnology / Pharmacology as a fresher or with 3-7 years of experience.,