2398 Pharmacy Jobs - Page 30

PV Reporting Associate We are currently seeking a Pharmacovigilance Associate to join our diverse and dynamic team. As a Pharmacovigilance Associate at ICON, you will play a vital role in monitoring and ensuring the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event information. Your attention to detail and understanding of regulatory requirements will be essential in supporting the organization s commitment to patient safety and compliance. What You Will Be Doing: Collecting and reviewing adverse event reports to ensure accurate and timely reporting in accordance with regulatory guidelines. Conducting signal detection and risk assessment activities to identify potential safety issues. Collaborating with cross-functional teams to support safety-related inquiries and investigations. Maintaining up-to-date knowledge of pharmacovigilance regulations and industry best practices. Assisting in the preparation of safety reports and regulatory submissions. Your Profile: Bachelors degree in life sciences, pharmacy, or a related field; advanced degree preferred. Experience in pharmacovigilance, drug safety, or a related area, preferably within a clinical or pharmaceutical environment. Strong analytical skills with attention to detail in data collection and reporting. Excellent communication and interpersonal skills, enabling effective collaboration with team members and stakeholders. A commitment to maintaining high standards of quality and compliance in all pharmacovigilance activities. Visit our careers site to read more about the benefits ICON offers. At ICON, inclusion & belonging are fundamental to our culture and values. We re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here . Interested in the role, but unsure if you meet all of the requirementsWe would encourage you to apply regardless there s every chance you re exactly what we re looking for here at ICON whether it is for this or other roles. Are you a current ICON EmployeePlease click here to apply

PV Reporting Associate ICON plc is a world-leading healthcare intelligence and clinical research organization. We re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development We are currently seeking a Pharmacovigilance Associate to join our diverse and dynamic team. As a Pharmacovigilance Associate at ICON, you will play a vital role in monitoring and ensuring the safety of pharmaceutical products by collecting, analyzing, and reporting adverse event information. Your attention to detail and understanding of regulatory requirements will be essential in supporting the organization s commitment to patient safety and compliance. What You Will Be Doing: Collecting and reviewing adverse event reports to ensure accurate and timely reporting in accordance with regulatory guidelines. Conducting signal detection and risk assessment activities to identify potential safety issues. Collaborating with cross-functional teams to support safety-related inquiries and investigations. Maintaining up-to-date knowledge of pharmacovigilance regulations and industry best practices. Assisting in the preparation of safety reports and regulatory submissions. Your Profile: Bachelors degree in life sciences, pharmacy, or a related field; advanced degree preferred. Experience in pharmacovigilance, drug safety, or a related area, preferably within a clinical or pharmaceutical environment. Strong analytical skills with attention to detail in data collection and reporting. Excellent communication and interpersonal skills, enabling effective collaboration with team members and stakeholders. A commitment to maintaining high standards of quality and compliance in all pharmacovigilance activities. What ICON can offer you: Our success depends on the quality of our people. That s why we ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. Our benefits examples include: Various annual leave entitlements A range of health insurance offerings to suit you and your family s needs. Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family s well-being. Life assurance Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others. Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless there s every chance you re exactly what we re looking for here at ICON whether it is for this or other roles.

Division Department Sub Department 1 Job Purpose Monitor and execute the production activities in an area during the shift by maintaining cGMP and safety norms to achieve production targets Key Accountabilities (1/6) Execute production activities in a shift by managing available resources to achieve production target Execute assigned tasks as per planned production activity to meet production targets for a shift Regulate usage of consumables in the production process at optimum levels to save costs Increase the efficiency of area by utilization of equipment and by reducing downtime in manufacturing area Key Accountabilities (2/6) Maintain standard process parameters as per BMRs and other supporting documents for achieving production target and maintaining quality Ensure all operations are performed as per GMP & Safety norms by reviewing all processes and documents for compliance Ensure equipment, facility and block premises are maintained as per regulatory compliance Maintain system integrity by updating documentations and deviations on CipDox while performing operations Perform validation, qualification and calibration as per schedule and update output of all activities in the systems Prepare new documents and update existing documents as per GMP requirement Key Accountabilities (3/6) Prepare manufacturing records and update online documentation to meet production and cGMP requirements Maintain online documentation and timely entries in BMR and supporting documents Prepare new documents and update existing documents as per GMP requirement Operate software such as SAP, CipDox and QMS Key Accountabilities (4/6) Follow safe work processes and ensure safety appliances are utilised during production activities in shifts to create a safe working environment Ensure safety systems and procedures followed by the operators in the shift Ensure availability and usage of PPEs in the shift by coordinating with HSE department for requirements and shift schedule Key Accountabilities (5/6) Execute production activities in a shift by managing available resources to achieve production target Execute assigned tasks as per planned production activity to meet production targets for a shift Regulate usage of consumables in the production process at optimum levels to save costs Increase the efficiency of area by utilization of equipment and by reducing downtime in manufacturing area Key Accountabilities (6/6) Major Challenges Meeting shift targets due to unavailability of adequate resources. Overcome by efficient work load distribution and resource optimisation Meeting production targets due to lapses in knowledge transfer between shifts. Overcome by bridging gaps between inter-shift communication Maintaining cGMP requirements during system downtime. Overcome by coordinating with the engineering team and technical support team Key Interactions (1/2) QA/QC for scheduling of batches, issues in product (Daily) Engineering & Utility for system related queries (Daily) Formulation Technical Support for troubleshooting in products (Case Basis) Formulation Technology Transfer for support in new products (Project Basis) Stores and Warehouse for RM/PM related activities (Daily) Safety for safety rounds and PPE requirement (Daily) Key Interactions (2/2) Maintenance Contractor and vendors for any machine repairs and spares (Case Basis) Equipment manufacturer: For troubleshooting in machine (Case Basis) Dimensions (1/2) Direct Reports : 12 (dotted reporting in shift) Number of areas managed : 3 Number of dosage forms : 2 Number of tech transfer supported per month : 2 Number of batches executed per month : 35-40 Achieve internal OTIF more than 90% YOY improvement in shift operations efficiency Achieve Zero reportable accidents / incidences during manufacturing Achieve set target for batch failure reduction Achieve 0% errors in online documentation Meet 100% compliance to SOP and safety regulations Dimensions (2/2) Key Decisions (1/2) Resource allocation for each shift Workload distribution in each shift Key Decisions (2/2) Up-gradation in Facility and Documents (To Section Head) Modification in plant and equipment (To Section Head) Deviation and implementation of CAPAs (To Section Head) Education Qualification Bachelor in Pharmacy Relevant Work Experience 3-4 years of experience with 2 years of experience in pharmaceutical manufacturing Knowledge of cGMP practices, equipment operations required for Formulation Production

Facilitate the care team in coordinating care for visits and for future healthcare needs and ensure that proper care has been provided to each patient as per plan. Handle calls from patients if needed. Resolve the reason for the call or route to the appropriate party. Provide an effective communication link between patient and medical staffincluding relaying messages from providersgathering information from patients for providersetc. Support in the medication refill process. Ensure that information goes when and where it is needed. Ensure that all patients are tracked and data entered into systems for follow-up and reporting. Coordinate with the medical staff to ensure that case management services are provided to patients with complex medical and/or psychosocial problems. Work with the medical staff to developimplement and carry out improvement programs Ensure that disease and other registry data entry is up to date and use registry Use and update the directory of resources in the service area to meet basic health and human needs. Be facile at using the resources available within the Center. Act as a back-up to other Patient Care Coordinator or to other Care Team members as needed. Facilitate the admission and discharge process as per policy. Act proactively in quality improvement program. Perform other duties as assigned by relevant authorities. Candidate Requirements: Proficiency in verbal communication in English and understanding of basic written English. Demonstrated ability to work effectively in a team environment. Demonstrated problem solving skills in a complex environment. Demonstrated effective interpersonal relationships and customer service skills. Good organizational and time management skills Good working knowledge of local social service resources or skills to acquire and use this knowledge and information expeditiously. Ability to work effectively with people from diverse cultures and diverse socioeconomic situations. Basic level of skill with Microsoft WordExcel and ability to use other computer programs and applications in ways that facilitate panel management. Behavioral Competencies: Accountability: For the relevant processes Customer-Focus: Listen to the voice of the customer and strive to delight them by exceeding their expectations Teamwork: If someone needs helphelp them Initiative: Be innovativeapply fresh ideasand continuously improve how you do your work Confidentiality: Maintain strict confidentiality and respect the privacy of others Ethical: Demonstrate integrityhonestyand stewardship in all encounters at work Respect: Demonstrate consideration and appreciation for co-workers and patients Communication: Demonstrate the ability to convey thoughts and ideas as well as understand perspective of others

Noida Institute of Engineering & Technology (NIET), Greater Noida invites talented educators and researchers for walk-in interviews and applications for the position of Research Associate in the Department of Computer Science & Engineering and Allied Technologies. Position: Research Associate Qualification: Master s degree in a relevant field required; Ph.D. preferred. Experience: Previous research experience in Emerging Technologies/Trends preferred. Key Responsibilities: Research Design & Implementation: Design and implement research methodologies and experiments. Publications & Reports: Contribute to research papers, reports, and publications. Collaboration: Collaborate on interdisciplinary research projects. Patent and IPR Management: Identify, document, and protect intellectual property arising from research, including potential patent applications. Literature Reviews: Conduct literature reviews to support ongoing research projects. Grant Writing: Assist in writing grants and securing research funding. Data Analysis: Collect, organize, and analyze data using research tools and software to interpret findings. Record Keeping: Maintain detailed records of research activities and outcomes. Presentations: Present research findings to internal and external stakeholders. Compliance: Ensure adherence to safety and ethical research standards. Contact Person: Chetan Teotia 9311337162 chetan.teotia@niet.co.in recruitment@niet.co.in Documents Required: Updated Resume Passport-size Photograph Copies of Educational Certificates Experience Certificates (if any) Valid ID Proof (Aadhar, PAN, etc.) Why Join NIET? First Engineering Institute in UP with UGC Autonomous Status NAAC Accredited with CGPA 3.23 Highest in UP NIRF 2024 Rankings: Pharmacy Rank 40, Engineering & Management Band 101 150 NBA Accredited B.Tech (IT, BT, ECE, ME, CSE), B.Pharm, MBA, PGDM, MCA Certified Excellent by ARIIA 2020 21 QS I-Gauge Gold Certified

Were Hiring: Hospital & Retail Pharmacists Location: Bangalore, Hyderabad, Chennai, Dehradun Industry: Healthcare & Pharmacy Employment Type: Full-Time Are you a passionate pharmacy professional looking to make a real impact in patient care? Join our growing team as a Hospital or Retail Pharmacist , where youll play a vital role in ensuring safe, effective, and patient-centric medication services. Who Can Apply? Diploma in Pharmacy (D.Pharm) Bachelor of Pharmacy (B.Pharm) Doctor of Pharmacy (Pharm.D) Freshers & Experienced Candidates Welcome Responsibilities Dispense medications and counsel patients Ensure accuracy in prescription processing Monitor drug interactions & stock inventory Collaborate with healthcare teams for optimal care Maintain pharmacy standards & compliance

Applications are invited for the post of Project Research Scientist I ( Non-Medical ) for the Indian Council of Medical Research (ICMR) funded project in School of Bio Sciences and Technology, Vellore Institute of Technology (VIT) Vellore- 632014, Tamilnadu. Title of the Project : 3D printed nano-engineered sublingual patch with viral-mimetic nanoparticles for non-invasive delivery of Insulin Qualification (Essential) : First Class Post Graduate Degree, including the integrated PG degree in Nanomedicine / Pharmaceutics / Nano-formulations / Chemical engineering/Chemistry and other related fields. Qualification ( Desirable) : Candidates with Ph.D., having hands-on experience in the area of nano-formulations / drug delivery systems esp. lipids / polymers-based nanoparticulate systems will be preferred. Candidates with above research area with animal handling experience will be given high preference. Stipend : Rs. 56,000/- + 10 % HRA per month Sponsoring Agency : Indian Council of Medical Research (ICMR) Duration : 1 year extendable to one more year maximum based on the performance of the candidate. The post is temporary and co-terminus with the duration of the project. Principal Investigator Co-Principal Investigators : : Dr. Sankar Ganesh Devaraj, Assistant Professor Senior, School of Bioscience and Technology (SBST), Vellore Institute of Technology Vellore- 632014, Tamilnadu. Dr.Arunkumar Palaniappan, PhD, MRSC. Associate Professor, Department of Biotechnology, BITS Pilani - Dubai Campus, Joint Appointment with Department of Pharmacy, BITS Pilani -Hyderabad Campus. Dr. Sunil P M., Director, Centre for Stem Cells and Regenerative Medicine Oral and maxillofacial pathology, Sri Anjaneya institute of Dental Sciences. Send your resume along with relevant documents pertaining to the details of qualifications, scientific accomplishments, experience (if any) and latest passport size photo etc. on or before (30/07/2025) through online http://careers.vit.ac.in To apply online http://careers.vit.ac.in , Indicate project title, and the post applied for in the application. No TA and DA will be paid for appearing in the interview. Shortlisted candidates will be called for an interview at a later date, which will be intimated by email. The selected candidate will be expected to join at the earliest. JOB Location: VIT Vellore, Tamil Nadu.

Job Title: Analytical Technical Writer Employment Type: Full-time Location: Mumbai Experience: 2-4 years Job Description: Preparation & review of analytical technical documents from the laboratory data such as and but not limited to, Product specifications, analytical test methods, analytical method validation protocol, method validation reports, analytical method transfer protocol, method transfer reports, stability study protocol and stability study report etc. Coordinate with client stakeholders and external laboratories to collate required documentation. Change control management from initiation to approval in coordination with cross function teams and drive to implement the changes timely. Ability to read the analytical laboratory data and summarize the contents into report format. Experience to ensure completeness and accuracy of the technical reports. Experience in managing the lifecycle of technical reports/documents. Supporting cross functional team in sharing the technical documents for submission requirements. Follow client documentation standards and best practices. Qualifications and desired skills: Minimum M. Sc. Chemistry, M. Pharmacy, or related scientific field. 2-4 years of working experience in Quality Control/QA documentation/R&D or/and Analytical Quality Assurance, with strong analytical thinking.

Job Summary: Drug In charge will be responsible for preparing and administering appropriate pharmaceuticals to patients. She/he achieves this by executing a physician s order. The job entails a high level of responsibility and knowledge. A Drug In charge does not merely hand out prescribed medicine; he/she has the expertise and willingness to assist people and provide them with information and solutions. Duties and Responsibilities: Ensuring that all pharmacy staff are knowledgeable about the THF s policies and procedures about medicines management Conducting regular medicines audit to verify the stock, expiry dates and optimal usage of the medicines/consumables/reagents. Participating in continuing education programs regarding new drugs and drug interactions Recommending and implementing medicines management systems to improve workflow efficiency and patient care Recommending changes to pharmacy procedures to improve workflow efficiency Assisting the pharmacist/lab technicians preparing indents, collecting them and preparing the final indents and sharing it with seniors. Assisting the pharmacist/lab technicians and SPO preparing the GRNs to ensure proper medication dosages are being administered Assisting Project coordinators for proper dispensing and upkeep of the medicines at the block level. Monitoring inventory levels of all drugs in order to ensure that there is an adequate supply available for patient care Controlling the inventory on a daily basis. Enforcing best practice protocols when storing prescription drugs and controlled substances. Maintaining an approved drug and controlled substances list and verifying expiry dates. Monitoring product displays and shelves, as well as the general appearance of the warehouses at block level. Training of new pharmacists. Prepares weekly opening and closing balance report for the medicines. Education and experience M. Pharma or B. Pharma and permanent register in Pharmacy council 3-5 years of experience required Excellent skills in MS-Office Experience in Drug and warehouse management

Cigna Medical Group is looking for HIH - Software Engineering Senior Analyst to join our dynamic team and embark on a rewarding career journey. Software Design and Development : Software engineers are involved in designing and developing software solutions. They analyze requirements, create system architectures, and write code using programming languages such as Java, C++, Python, or JavaScript. Programming and Coding : Software engineers write and maintain code to implement software functionalities and features. They follow coding best practices, use software development frameworks and libraries, and ensure code quality, readability, and maintainability. System Analysis and Requirements Gathering : Software engineers work closely with stakeholders to understand business needs and gather software requirements. They analyze user requirements, functional specifications, and system constraints to determine the scope and objectives of software projects. Testing and Quality Assurance : Software engineers perform software testing to ensure the functionality, reliability, and performance of software systems. They develop and execute test plans, conduct unit testing and integration testing, and debug and fix issues to ensure high - quality software. Software Documentation : Software engineers create documentation, including system requirements, design specifications, user manuals, and technical guides. Documentation helps other team members understand and maintain the software and provides valuable references for future enhancements or updates.

This position will: - Develop, integrate, and deploy Gen AI/Agentic AI solutions leveraging AWS for data engineering and Azure OpenAI for LLM-based applications - Translate business and technical requirements into robust, scalable, and maintainable code - Collaborate closely with architects, data engineers, and data scientists to deliver high-quality solutions - Maintain high standards for code quality, documentation, and testing - Continuously learn and apply new tools and techniques in AI/ML and cloud development - Support troubleshooting, optimization, and enhancement of existing AI solutions - Work collaboratively with ServiceNow and Workday teams to ensure AI components integrate smoothly with the virtual assistant and HR workflows - Understand and respect the boundaries of responsibility, providing technical support for integrations without direct development on ServiceNow or Workday - Implement Gen AI/Agentic AI use cases for the HR function - Develop and maintain data pipelines on AWS for ingestion, transformation, and storage of structured and unstructured HR data - Integrate Azure OpenAI LLMs with AWS-based data sources and HR applications, ensuring secure and efficient data flow - Build and maintain APIs and microservices to support AI-driven HR processes and system integrations - Collaborate with data scientists to operationalize models, including fine-tuning, evaluation, and deployment - Write unit, integration, and end-to-end tests to ensure solution reliability and performance - Document technical designs, code, and deployment processes for maintainability and knowledge sharing - Participate in code reviews, provide constructive feedback, and contribute to team best practices - Support the integration of AI outputs with ServiceNow and Workday and other HR solutions by developing and maintaining well-documented APIs and data exchange mechanisms - Engage in joint troubleshooting and validation sessions with ServiceNow and Workday teams to resolve integration issues Education: - Bachelor degree in Computer Science, Engineering, or a related field Experience: - 3+ years of experience in AI/ML or software development, with exposure to cloud-based environments Required Qualifications: - Proficiency in Python and relevant ML libraries (e.g., PyTorch, TensorFlow, Hugging Face) - Experience with AWS data engineering tools (e.g., S3, Glue, Redshift) and pipeline development - Hands-on experience integrating and consuming Azure OpenAI or similar LLM APIs - Familiarity with RESTful API development and microservices architecture - Understanding of data security, privacy, and compliance considerations - Experience working in collaborative, multi-team environments, especially on projects with platform integrations Preferred Qualifications: - Certifications in AWS or Azure cloud platforms - Experience with Gen AI frameworks (e.g., LangChain, LlamaIndex) - Knowledge of HR domain processes and integrations with systems like Workday - Experience with CI/CD pipelines and DevOps practices - Strong problem-solving, analytical, and communication skills - Exposure to agile development methodologies - Familiarity with ServiceNow and Workday integration concepts is a plus

Requirement Education/Training: Bachelor s degree in pharmacy. Work Experience: Minimum six years experience in the pharma industry, acquired in Quality Assurance departments. Experience in pharmaceuticals, cosmetics and medical device Good skill and experience for handling of customer complaints, Deviation and QMS management. Be familiar with GDP, ISO9001, ISO13485 requirements and internal audit. Well verse with Excel, MS Word & Powerpoint, Trackwise, PATH & eDMS Required pre-requisites skills for this position: awareness of the local regulatory Guidelines and Corporate Standards and applicable laws, Expert in presentation preparation & delivery Analytical skills Good, positive and proactive communication skills, English. commitment to continued improvement in department processes and performance. Duties and Responsibilities Main Responsibilities Designated as Responsible Person (RP) for ensuring Good Distribution Practice (GDP) in complied with for products imported and wholesaled by Affiliate. GMP responsible person for the Affiliate as applicable Handling of customer complaints, processing the case in Trackwise and work / ensure compliance in accordance with respective SOP. Perform quality and compliance specific tasks including but not limited to end to end management of customer complaints, lias with customer care teram, internal stake holders , review of information about secondary packaging/redressing, ensure proper labelling of products at the distributor, and product recall coordination. Participate in the creation/update of local SOPs to reflect local practices in accordance with Corporate Policies and SOPs Implementing and maintaining the QMS to ensure that required processes are established and effective. Support in quality systems processes such as, but not limited to; internal audits/self-inspection, change control, management reviews, 3rd party vendor management, deviation management and CAPA Compile and update training manuals, undertake induction training and refresher training related to QMS for local affiliate staff Maintenance, analysis and reporting of Quality KPIs Ensure local repackaging of products is performed in accordance with specifications and required licenses. Review all packaging artworks from a local regulatory perspective as per internal / Corporate and local SOPs in place. Managing imported shipment, review of data loggers, and review all redressing artworks from a quality prospectives. Ensure proper system utilization for eDMS / PATH / Trackwise/Smartcockpit- participate as admin for mentioned software. To Support cross functional team in review and approval of GMP documents Execute assigned task by line manger on time-to-time basis.

Our Role The Meeting Governance Contracts and Project Administrator will provide support for the Corporate Shared Services team, focusing on Group Meeting governance and Sponsorships contract review, negotiation, and execution. This includes the use of technology to support the contract intake, as well as reporting for enterprise spend and negotiated savings. This position will work closely with internal business areas to clarify precise business needs and act as the point person throughout the contracting process. In addition, the role will assist the Corporate Shared Services team as it relates to project management for key initiatives. Not only does this include support of the internal expense audit process to align with policy, but also the continuous improvement opportunities within the organization, supporting process change and the implementation of technology tools and best practices. The position will work closely with our key travel partners and suppliers on a global scale. Must have a keen sense of corporate culture with the ability to effectively communicate and interact with all levels of senior leadership and conduct themselves in a highly professional manner. This position will support the Senior Manager of Global Travel, Policy & Group Meeting Governance. Additionally, the Meeting Governance Contracts and Travel Projects Administrator is responsible for: Supports monthly contract reporting and ad-hoc reporting requests as needed. Works closely with the Policy, Communications and Meeting Governance Contracts Advisor on contract management and execution. Execute a high-volume of contracts, for both Meetings and Sponsorships, in a timely manner ensuring adherence to Global T&E Policy. Supports the internal expense audit process, including review of rejected or flagged reports for alignment to policy. This includes working closely with our internal expense team to support. Assists the Corporate Shared Services team with projects to support the enterprise, including HIH support. Our Ideal Candidate Will Offer: 5 to 8 years professional work experience Contract management and project management experience working in a large, global organization. Bachelors degree or equivalent strongly preferred This experience should include an in-depth understanding of contracts management, including demonstrated success in negotiations and ability to influence internal/external constituencies. Project management experience with the ability to remain agile in a rapidly changing industry Customer service background, with experience managing responses to internal SLA. Knowledge and/or experience in the meetings, sponsorship and travel industry Expert level computer skills to include Microsoft Office, Excel, and PowerPoint. Competency profile: Extraordinary communications capability across all levels of the organization, and strong interpersonal skills. Relentless focus on service needs and consistently rise the bar on service excellence. Strategic thinking, superb time management, judgment, and problem-solving skills. Demonstration of a high level of integrity and ethics. Ability to work collaboratively to meet deadlines with accuracy, attention to detail, and strong organizational, written, and verbal communication skills. Versatility, flexibility, and ability to work within constantly changing priorities with enthusiasm. Innate ability to exude our values and preserve our culture as we grow.

This position will: Lead the architectural design and strategic planning for Gen AI/Agentic AI solutions, integrating AWS data engineering and Azure OpenAI LLMs Serve as the primary technical authority and decision-maker for AI solution design and delivery Ensure all solutions align with organizational goals, scalability, and best practices in data engineering and AI Collaborate cross-functionally with business stakeholders, product owners, and technical teams to translate requirements into technical solutions Maintain up-to-date knowledge of advancements in cloud platforms, AI/ML, and HR technology trends Champion security, privacy, and compliance standards throughout the solution lifecycle Coordinate closely with ServiceNow and Workday teams to ensure seamless integration of AI solutions with the virtual assistant and HR workflows Responsibilities: Define integration requirements and data exchange protocols for connecting Gen AI/Agentic AI solutions with ServiceNow, Workday and other HR solutions while respecting boundaries of responsibility Design end-to-end technical architectures for HR AI use cases, specifying data flow, integration, and security modelsOversee the development and optimization of AWS-based data pipelines, ensuring efficient ingestion, transformation, and storage of HR dataArchitect seamless integration between AWS data sources and Azure OpenAI LLMs, defining API contracts and data exchange protocolsEstablish standards for model deployment, monitoring, and lifecycle management, including versioning and rollback strategiesDefine and enforce data governance, security, and compliance requirements, including role-based access and data encryptionLead technical reviews, provide mentorship to engineering and data science teams, and ensure adherence to architectural guidelinesEvaluate and recommend tools, frameworks, and platforms to enhance solution capabilities and maintainabilityTroubleshoot complex technical issues, perform root cause analysis, and drive continuous improvement in system performance and reliabilityWork with ServiceNow and Workday teams to understand integration points, data flows, and system constraints, ensuring AI components fit seamlessly into the broader HR technology ecosystem Qualifications: Support integration testing and validation efforts involving ServiceNow, Workday and other HR solutions, collaborating with respective teams as needed Education: Bachelor or Master degree in Computer Science, Engineering, or a related field Experience: 8+ years of experience in software architecture, with at least 3 years focused on AI/ML solutions Required Qualifications: Deep expertise in AWS data engineering services (e.g., S3, Glue, Redshift, Lambda) and data pipeline design.Demonstrated experience integrating and deploying LLMs, preferably with Azure OpenAI.Strong understanding of API design, microservices architecture, and cloud integration patterns.Proven track record of leading cross-functional teams and delivering complex technical projects.Experience with security, privacy, and compliance in cloud and AI environments.Experience working in environments with multiple platform teams, and ability to define clear integration boundaries and collaboration models Preferred Qualifications: Certifications in AWS (e.g., Solutions Architect) or Azure (e.g., AI Engineer)Experience with HR systems (e.g., Workday) and enterprise SaaS integrationsFamiliarity with Gen AI frameworks such as LangChain or LlamaIndexKnowledge of MLOps best practices and tools for model deployment and monitoringStrong analytical, problem-solving, and communication skillsExperience with agile methodologies and DevOps practicesFamiliarity with ServiceNow platform concepts and Workday HR workflows is a plus

Summary Oversee all aspects of quality management and ensure the highest level of compliance across our projects About the Role Major accountabilities: Oversee & support all areas of quality management for GxP/non GxP Systems. Drive the validation process, including validation planning, testing (IQ/OQ/PQ), and validation reporting. Support Authoring, reviewing, and approving of CSV deliverables for accuracy, consistency, clarity and completeness. Ensuring all the validation SOP/Work Procedures are followed during the application development. Coordinate with project managers and teams to ensure the alignment of project outputs with quality standards. Evaluate data and QM processes to identify improvements to enhance efficiency and accuracy. Manage change control processes for tool updates and deployments while driving continuous improvements in validation and quality workflows. Support in audits and inspections to ensure adherence to compliance regulations and industry standards. Create and maintain documentation of processes and validation activities and provide training to teams on quality standards and procedures. Oversee root cause analysis, corrective actions, and preventive actions to address quality issues. Ensure all systems and software used meet industry regulations and data integrity rule Minimum Requirements: Minimum of 10 years experience in Quality Management, ideally within the Pharma or any regulated industry. Proven experience in managing GxP/non GxP projects from requirement definition to retirement. Working experience in all lifecycle stages of IT system(including System retirement) would be preferred. Ability to drive innovative validation strategies for business initiatives Knowledge of IT systems and software used within the Pharma industry. Exceptional leadership skills with the ability to drive a team towards meeting quality standards. High attention to detail with the ability to identify potential risks or issues. Solid interpersonal skills, including the ability to build and maintain effective working relationships. Ability to influence and drive collaboration across all levels of the organization. Bachelors degree in IT, Pharmacy or related field.

Promote and sell pharmaceutical products, medical equipment, and medical products to doctors, pharmacists, and hospitals within the assigned territory. Conduct regular visits to healthcare facilities and engage with healthcare professionals to present product information and address concerns. Offer complete product knowledge, including usage, dosage, and benefits. Build strong relationships with healthcare professionals to enhance product awareness and achieve sales targets. Actively listen to customer needs and concerns, offering appropriate product recommendations. Gather insights on market trends, customer feedback, and competitor activities and report to internal departments. Collaborate with the sales team and marketing departments on promotional strategies and campaigns. Attend seminars, workshops, and other events to expand professional knowledge and networks. Maintain detailed records of customer interactions and sales performance using CRM software. Ensure compliance with pharmaceutical industry regulations and ethical standards.

Job Title: R&D Senior Executive Softgel Formulation Department: Research & Development (R&D) Softgel Formulation Job Summary: A reputed softgel manufacturer in Gujarat is seeking an accomplished R&D professional with 8-10 years of experience in softgel formulation and drug development. The ideal candidate will demonstrate expertise in pharmaceutical or nutraceutical softgel product development, process optimization, technology transfer, and the creation of QA/QC documents from scratch. Willingness to relocate to Gujarat is essential. Key Responsibilities: Softgel Formulation Development: Lead the complete development process for softgel products, including excipient compatibility, fill and shell formulation for pharmaceuticals and nutraceuticals. Process Scale-up & Optimization: Design, execute, and optimize laboratory and pilot scale batches using rotary die or relevant softgel encapsulation technologies. Product Development (NCE & Generics): Drive projects involving both new chemical entities and generic softgel drugs, ensuring robust formulation and regulatory compliance. QA & QC Documentation: Independently develop and implement all necessary Standard Operating Procedures (SOPs), batch manufacturing and packing records, product specifications, method validation documents, and stability protocols. Technology Transfer: Prepare required documentation and ensure smooth transfer of technology and processes to manufacturing, QA, QC, and regulatory teams. Cross-Functional Collaboration: Coordinate with Quality Assurance, Quality Control, Regulatory, Procurement, and Production teams for successful project execution. Regulatory & Compliance: Support global regulatory filings, address queries, and maintain compliance with cGMP, ICH, and international regulatory standards. Continuous Improvement: Keep abreast of industry trends and proactively recommend improvements in formulation and manufacturing processes. Qualifications & Requirements: Educational Qualification: M.Pharm in Pharmaceutics, Pharmaceutical Sciences, or a related discipline. 8-10 years of hands-on experience in softgel formulation and product development within the pharmaceutical or nutraceutical industry. Strong technical expertise in softgel encapsulation, fill/shell composition, and process troubleshooting. Proven ability to create all QA and QC documentation from the ground up. Solid knowledge of cGMP, ICH, FDA, and other global regulatory requirements. Experience in analytical method development and stability studies is an advantage. Excellent teamwork, communication, problem-solving, and documentation skills.

Seeking a motivated Medical Sales Associate with 4-5 year experience in B2B/B2C sales. D Pharm/B Pharm preferred. Candidates with strong sales background in online pharmacy or related sectors are welcome to drive growth & deliver healthcare solutions Required Candidate profile Drive B2B/B2C sales strategy to boost revenue Build ties wt HCPs, pharmacies, hospitals, consumers Demo product knowledge & educate customers Submit sales reports, forecast & activity update

Seeking a motivated Medical Sales Associate with 4-5 year experience in B2B/B2C sales. D Pharm/B Pharm preferred. Candidates with strong sales background in online pharmacy or related sectors are welcome to drive growth & deliver healthcare solutions Required Candidate profile Drive B2B/B2C sales strategy to boost revenue Build ties wt HCPs, pharmacies, hospitals, consumers Demo product knowledge & educate customers Submit sales reports, forecast & activity update

Eden Hospital 120 Bedded NABH Hospital is urgently requiring Pharmacists for our Hospital Pharmacy. Senior Pharmacist with suitable experience is preferred. Walk-in Interviews - Eden Hospital #115, Phase-1, Industrial Area, Chandigarh

Coordinate and manage clinical trials from initiation to completion, ensuring compliance with regulatory guidelines and study protocols Recruit, screen, and enroll study participants while maintaining accurate documentation and records Required Candidate profile Maintain study supplies, track data collection, and support data analysis, ensuring high-quality and ethical research practices throughout the study

Join one of the best names in healthcare! We are currently hiring Pharmacists for the following locations: Chennai Bangalore Hyderabad Requirements: Minimum 6 months of experience Valid State Pharmacy License (for respective location) If you're passionate about patient care and ready to be part of a growing healthcare team, apply now!- Contact No- 8884852696

Clin Infotech is offering the internship opportunity for BDS MDS Dental Graduates Should have Knowledge in Pharmacovigilance Should Have knowledge on Argus & MEDDRA Applicants Should Complete Certification in Pharmacovigilance Required Candidate profile B.Pharm / M.Pharm/Pharm D/Life sciences degree With Hands On Experience On Argus Safety Database and Med DRA coding, Argus, Narrative Writing, Triage

Should have knowledge in clinical research studies Monitoring of Clinical studies conducted at various CROs located globally as per ICH/GCP, applicable regulatory requirements, protocols and SOPs. Perform Site visits (i.e. Site Selection Visit) Required Candidate profile Strong understanding of clinical trial processes and regulatory requirements. Excellent clinical assessment skills and a commitment to patient safety and ethical research practices.

Clin Infotech is offering internship Opportunities for B.Pharm and M.Pharm Freshers who are willing to start a career in Clinical Research Pharmacovigilance clinical data management sas Medical writing and Medical coding Required Candidate profile Clinical Research Internship includes of Hands on Experience on softwares in Clinical Research Pharmacovigilance clinical data management Domain. B.Pharm M.Pharm and Pharm D Are Eligible to Apply