Hiring Female Dermatologist for our clients in Mumbai, Chennai, Hyderabad, Bangalore, Coimbatore, Delhi & Ludhiana. Job Role: - Skin & Hair Consultation - Procedures - Treatment Plan & Supervision Whatsapp CV, Location, Exp, Salary on 7207991555

JOB TITLE: Assistant Research Scientist (Product Engineering) JOB FUNCTION: Research and Development WORK LOCATION: Unilever Bangalore With 3. 4 billion people in over 190 countries using our products every day, Unilever is a business that makes a real impact on the world. Work on brands that are loved and improve the lives of our consumers and the communities around us. We are driven by our purpose: to make sustainable living commonplace, and it is our belief that doing business the right way drives superior performance. At the heart of what we do is our people - we believe that when our people work with purpose, we will create a better business and a better world. At Unilever, your career will be a unique journey, grounded in our inclusive, collaborative, and flexible working environment. We don t believe in the one size fits all approach and instead we will equip you with the tools you need to shape your own future. Unilever is reimagining the future of cleaning, and it starts with reinventing a century-old history of chemistry. Billions of people around the world are asking for products that are tough on germs and stains, and ever more convenient to use. But now, people also want these products to be kinder to the planet. CATEGORY OR FUNCTION INTRODUCTION The Purpose of the Science & Technology, Home care team is to provide Unilever with world class capability to develop next generation formats like powders, bars, liquids, capsule products with superior performance, great value, and sustainable technology. Within the S&T, team is responsible for exploring upstream/novel process and product technologies. This includes the development of new analytical methodologies to create data spaces and digital models of previously unknown interactions. These technology insights are used to develop deep domain expertise that ultimately supports the product design and delivers competitive advantage. JOB PURPOSE: The role requires individuals to develop a comprehensive understanding of product engineering principles, as well as in-depth knowledge of manufacturing technology and the interactions between materials, processes, and products in the home care sector. Areas of expertise should include product microstructure, rheology, and structure-property relationships. This knowledge must then be translated into decisions, actions, and initiatives that align with and support the divisional strategy, targets, and plans. Material Engineers are not merely technology specialists; they are integrators who combine consumer and business needs into effective technical solutions. JOB RESPONSIBILITIES: 10+ years experience in materials, polymers background either in FMCG or extended industries like Pharma Experience in basic unit operations, processing and product engineering is preferred Strong analytical including physio-chemical characterization is critical for this role. 10+ years experience in materials, polymers background Work with international and interdisciplinary teams (Unilever R&D, Academics, material and equipment suppliers) to develop next generation solid formats. Develop a deep understanding of how-to materials/process/structure products that deliver against consumer needs. Generate ideas for new products and for improvement of existing products. Must have a hands-on approach to pilot plant and laboratory scale-up activities. Need to be able to work in a safe, disciplined manner. Lead workstreams/projects WHAT YOU NEED TO SUCCEED: In depth knowledge of material science, thermodynamics, equipment principles and practices Computer literate and digital savvy (experience of DoE and statistical data analysis) Project management (communication and presentation) Experience in product/process development, and technology transfer desirable. EXPERIENCES AND QUALIFICATIONS Essential Experience: ME, MTech in Materials/Chemical Engineering with specialization in Polymer Science from reputed institutes Our commitment to Equality, Diversity & Inclusion Unilever embraces diversity and encourages applicants from all walks of life! This means giving full and fair consideration to all applicants and continuing development of all employees regardless of age, disability, gender reassignment, race, religion or belief, sex, sexual orientation, marriage and civil partnership, and pregnancy and maternity.

Hiring Anesthesiologist - Consultant !!! No.of Position - 2 Qualification - MD Anaesthesia / DNB Experience - 2-7 years Location - Narayana Multispecialty Hospital, HSR layout , Bengaluru Interested Candidates can drop their Cvs at preety.kumari@narayanahealth.org / 9508366041

e are hiring Staff Nurse in Multiple locations of Hyderabad and Peripheral; Bandalaguda Jagir ECIL Gachibowli Kukatpally Chandrayangutta Uppal Job Description :- Clinical Work Provide direct & indirect patient care in emergency care situations. Provide any & every detail about the procedures, medications, and answer patient queries & subsequent follow-up. Reporting & documenting USG findings/treatment plan in File/Portal. Documenting the prescribed mediation/Stimulation/HRT drugs etc. & in file/portal/ providing Trigger time. Executing all Donor Related Activity, in association with Donor Coordinator. Administer injection to patient/donor, as prescribed in file. Maintain stock of all required injections/drugs. Elicit accurate & relevant patient/donor medical history Co-ordinate procurement of necessary documents from patient/donor, per PCPNDT regulations. Update all patient records in both physical, as well as digital format. File all regulatory forms/consents before each procedure. Submit PCPNDT forms timely, as required by PCPNDT office. Identify & provide for physical, emotional, and developmental needs of patients. Counsel patients & their families; explain procedures planned for them. Ensure all procedures are carried out as per the SOP, and are compliant with the Policies on Universal Protection, Biomedical Hazard & Infection Control. Should have valid Telangana state registration Only immediate joiners apply for the role Interested candidates can share their profile on sneha.shetty@indiraivf.in / Careers@indiraivf.in

Job Description Designation : Executive Role: QC Pharmacist Department: Warehouse Operations Location: Bangalore/South About Tata 1mg Tata 1mg is a trusted health partner for end consumers and large institutions. Our Mission is to make healthcare understandable, accessible, and affordable for all Indians. Over the past three years, we've worked to build a healthcare platform that guides customers to the right and affordable care. Today, Tata 1mg is present in 1000+ cities And were just getting started. Leading the chart as one of the top consumer health platforms through ePharmacy, eDiagnostics, e-consult and offline stores, Tata 1mg has delivered over 15M ePharmacy orders, 2M eDiagnostics orders & 1M+ organic users/day in 2022 and we are just getting started. Our strongest asset is our 6400+ people enabling us to deliver on our mission consistently. Know more about us: https://www.1mg.com/aboutUs Brief about the Team The warehouse operations team is within the supply chain vertical of Tata 1mg. The team works closely with the org-wide leadership team, business, product, growth, and category teams to drive operational excellence and strategic initiatives. The team works on special projects and innovations that aim to deliver high impact. The projects span across business verticals including e-pharma, e-diagnostics, and retail. What will you do Customer Support Read & validate prescriptions (Rx) + OTC orders Contact customers for clarification or information required to process the order Inventory Management Keep check of Inventory in the warehouse. Drive vendors to ensure adequate inventory levels are maintained. Compliance Ensure strong quality checks while packing/ dispensing medicines Ensure 100% compliance per the process guidelines What we are looking for 1+ year of relevant experience (pharmacist). Diploma or Bachelor (D. Pharma or B. Pharma). License for that state. Should be comfortable working in shifts and on weekends. Why Join Us? Tata 1mg provides one of the most exciting and high-growth environments to work. You get the added benefit of working in a prestigious legacy brand like Tata and a highly dynamic and versatile startup like 1mg. Being an integral part of the Warehouse Operations will provide you to closely work with the Operations and Logistics team which is spread PAN India. Disclaimer Tata 1mg is proud to be an Equal Opportunity Employer. All employment decisions at Tata 1mg shall be made without discrimination, harassment or less favorable treatment of any employee or job applicant, either directly or indirectly, on the grounds of age, color, physical ability, ethnic origin, nationality, religion, gender, family status, marital status, prenatal status, gender reassignment, or sexual orientation. All employment decisions are based on business needs, job requirements, competence, and merit

Skill required: KYC Screening - Sanctions Screening Designation: Regulatory Compliance Associate Qualifications: BCom Years of Experience: 1 to 3 years What would you do? Help clients transform their compliance function from reactive to proactive through an intelligent compliance operating model – powered by data, intelligent technologies and talentLooking for someone with KYC experience along with ECDD/OCDD knowledgeAbility to effectively and efficiently conduct the process of screening individuals, entities, or transactions against lists of sanctioned or restricted parties. Sanctions screening involves using specialized software, understanding relevant regulations, and maintaining a proactive approach to mitigate the risk of engaging with sanctioned entities. What are we looking for? Collaboration and interpersonal skills Problem-solving skills Strong analytical skills Numerical ability Ability to meet deadlines Roles and Responsibilities: In this role you are required to solve routine problems, largely through precedent and referral to general guidelines Your expected interactions are within your own team and direct supervisor You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments The decisions that you make would impact your own work You will be an individual contributor as a part of a team, with a predetermined, focused scope of work Please note that this role may require you to work in rotational shifts Qualifications BCom

CONTROLLERS Controllers ensure that the firm meets all the financial control and reporting obligations of a global, regulated, and public financial institution. Our professionals measure the profitability of, and risks associated with, every aspect of the firms business. Controllers also ensure that the firms activities are conducted in compliance with the regulations governing transactions in the financial markets. OUR IMPACT Were a team of specialists charged with managing the firm s liquidity, capital, and risk, and providing the overall financial control and reporting functions. Whether assessing the creditworthiness of the firm s counterparties, monitoring market risks associated with trading activities, or offering analytical and regulatory compliance support, our work contributes directly to the firm s success. The business is ideal for collaborative individuals who have strong ethics and attention to detail. BUSINESS UNIT The Controllers group is responsible for safeguarding the firms assets: to help maintain the integrity of Goldman Sachs finances and expenditures. Through careful consideration and analyses of firm finances, objectives and strategies, we ensure that the firms businesses continue to be profitable and efficiently run. Controllers also ensure that all business practices are in compliance with financial and regulatory requirements worldwide. Since contact with virtually every part of the firm is essential to Controllers, professionals in the department experience Goldman Sachs businesses, products, and sophisticated technology systems in depth. Direct Hedge Funds, Hedge Funds Strategies, Private Equity Group teams within Controllers support the alternative investments within Goldman Sachs Asset Management division with oversight over complex private funds. ABOUT GOLDMAN SACHS We believe who you are makes you better at what you do. Were committed to fostering and advancing diversity and inclusion in our own workplace and beyond by ensuring every individual within our firm has a number of opportunities to grow professionally and personally, from our training and development opportunities and firmwide networks to benefits, wellness and personal finance offerings and mindfulness programs. Learn more about our culture, benefits, and people at GS.com/careers. We re committed to finding reasonable accommodations for candidates with special needs or disabilities during our recruiting process. Learn more: https: / / www.goldmansachs.com / careers / footer / disability statement.html Please note that our firm has adopted a COVID 19 vaccination requirement for employees who work onsite at any of our U.S. locations to safeguard the health and well being of all our employees and others who enter our U.S. offices. This role requires the employee to be able to work on site. As a condition of employment, employees working on site at any of our U.S. locations are required to be fully vaccinated for COVID 19, and to have either had COVID 19 or received a booster dose if eligible under Centers for Disease Prevention and Control (CDC) guidance, unless prohibited by applicable federal, state, or local law. The Goldman Sachs Group, Inc., 2023. All rights reserved. Goldman Sachs is an equal opportunity employer and does not discriminate on the basis of race, color, religion, sex, national origin, age, veterans status, disability, or any other characteristic protected by applicable law. ",

CONTROLLERS Controllers ensure that the firm meets all the financial control and reporting obligations of a global, regulated, and public financial institution. Our professionals measure the profitability of, and risks associated with, every aspect of the firms business. Controllers also ensure that the firms activities are conducted in compliance with the regulations governing transactions in the financial markets. OUR IMPACT Were a team of specialists charged with managing the firm s liquidity, capital, and risk, and providing the overall financial control and reporting functions. Whether assessing the creditworthiness of the firm s counterparties, monitoring market risks associated with trading activities, or offering analytical and regulatory compliance support, our work contributes directly to the firm s success. The business is ideal for collaborative individuals who have strong ethics and attention to detail. BUSINESS UNIT The Controllers group is responsible for safeguarding the firms assets: to help maintain the integrity of Goldman Sachs finances and expenditures. Through careful consideration and analyses of firm finances, objectives and strategies, we ensure that the firms businesses continue to be profitable and efficiently run. Controllers also ensure that all business practices are in compliance with financial and regulatory requirements worldwide. Since contact with virtually every part of the firm is essential to Controllers, professionals in the department experience Goldman Sachs businesses, products, and sophisticated technology systems in depth. Direct Hedge Funds, Hedge Funds Strategies, Private Equity Group teams within Controllers support the alternative investments within Goldman Sachs Asset Management division with oversight over complex private funds. ABOUT GOLDMAN SACHS We believe who you are makes you better at what you do. Were committed to fostering and advancing diversity and inclusion in our own workplace and beyond by ensuring every individual within our firm has a number of opportunities to grow professionally and personally, from our training and development opportunities and firmwide networks to benefits, wellness and personal finance offerings and mindfulness programs. Learn more about our culture, benefits, and people at GS.com/careers. We re committed to finding reasonable accommodations for candidates with special needs or disabilities during our recruiting process. Learn more: https: / / www.goldmansachs.com / careers / footer / disability statement.html Please note that our firm has adopted a COVID 19 vaccination requirement for employees who work onsite at any of our U.S. locations to safeguard the health and well being of all our employees and others who enter our U.S. offices. This role requires the employee to be able to work on site. As a condition of employment, employees working on site at any of our U.S. locations are required to be fully vaccinated for COVID 19, and to have either had COVID 19 or received a booster dose if eligible under Centers for Disease Prevention and Control (CDC) guidance, unless prohibited by applicable federal, state, or local law. ",

Job Description Designation: Senior Research Investigator Job Location: Bangalore Department: Discovery Chemistry - Synthetic Chemistry About Syngene: Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit. Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene s quality standards at all times Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Role Requirements: Ph.D. degree with post-Doctoral research with excellent communication skills is preferred with minimum 2 years experience in CRO industry. The candidate should manage a team of 7-12 scientists and be capable of designing scheme, troubleshoot, problem solve independently and execute high-profile project(s). The person should be flexible working shifts as per the organizational policy. The candidate should be excellent in cross functional teamwork and in customer engagement. Strategic Responsibilities Safety: Commitment to safety (self, team, lab and the organization) always Ensuring ZERO safety incidents in the lab/organization Ensuring ZERO safety non-compliances at workplace. Reporting incidents (or near-misses) and learnings from those incidents to avoid recurrence Near miss reporting 1 per year per employee, Reduction in number of first aid injuries reported compared to previous FY, Review SOPs and checklists for completeness of information related to safety Quality: Ensure to comply with Syngene s quality standards and services (self and team) always ZERO data integrity incidents Adhere to the ALCOA+ principles in all data generated. Ensuring adherence to all Syngene policies related to data integrity by all team members. Maintain confidentiality Zero repeat audit observations, Zero major and critical observations in external audits, SOP s vs Practices: Review and implement necessary refinements for continuous training, testing, and tracking SOP compliance Deviations Delivery Responsible for Project Health Index: Project planning, Execution, Deliverables including tracking of KPIs for his/her team and Quality of services (internal/client metrics) Achieve per-quarter improvement in key FY25 KPIs, per OU per plan, 18-20 steps per FTE per month, 6 compounds/FTE/month, 70% targets TAT within 30 days for deliverables 0.1 g scale. Help the Group Leaders and Head of the department in managing the process of governance tools for effective, transparent, and collaborative management of the projects. Engagement: Good in engaging the customers (weekly reports, experimental for completed final compounds etc). Zero flaw in presentations and report, real time and flawless communication 0% business attrition w.r.t scientific environment and work culture Support in implementing comprehensive client feedback collection and response platform in collaboration with PMO as service management piece. Demonstrate consistent, sustainable technical and operational improvements per RCA/CAPA process in Synthetic chemistry Excellent in team and cross-functional engagement Cost: Manage lifecycle of various lab infrastructure, instruments. Ensure optimum resource utilization and cost efficiencyManage FH to chemist ratio. Maintain above 50 % of Scientist-1 in the team and around 25 % of Scientist-2 employees. Compliance: Adhere to the ALCOA+ principles in all the experiments and data generated. Ensuring adherence to Syngene policies related to data integrity by all team members. ALCOA+ deviations Gemba walk compliance at 100%, Timesheet compliance at 100% Confidentiality compliance Ensuring all assigned mandatory training related to data integrity, health, and safety measures are completed on time by all team members. People: Leadership Next and Succession planning for critical roles - Reduce critical talent attrition by Build competencies and skills that are required to achieve current and future business needs. Technical/functional Skills: The candidate should have excellent knowledge of modern synthetic methodology including asymmetric synthesis, heterocyclic chemistry, catalysis and the reaction mechanism is expected. Should be expert in synthetic problem solving/troubleshooting skills. Excellent communication skills including face to face and virtual interactions with team and clients. Must have exceptional Presentation skills. The candidate should maintain an accurate scientific notebook, draft concise written reports for publications. Managerial Skills: Expertise in handling multiple collaborations. Demonstrated in handling a team size of 7-12 FTEs Worked effectively with interdisciplinary teams. Efficient Lab management skills The Leader must demonstrate the essential qualities of People Management. Giving receiving performance-enhancing feedback Setting clear performance expectations Conducting challenging performance conversations Coaching individuals toward improved performance Delegating tasks Creating accountability Lead the change Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Accountabilities as a Syngene Leader (only for Leadership Hires) Champion effective Environment, Occupational Health, Safety and Sustainability (EHSS) practices for the company and oversee compliance with those practices within Biologics business. Play an active leadership role in monitoring and verifying safety performance through Gemba walks and other safety-led activities. Foster a corporate culture that promotes an environment, occupational health, safety, and sustainability (EHSS) mindset as well as the highest standards of quality, integrity, and compliance. Put people at the heart of our success by providing clear, active leadership defined by the Syngene leadership framework setting high standards of people management, career planning and talent retention as a priority. Specific requirements for this role Experience Demonstrated Capability Education Experience: 3 - 12 Years Skills and Capabilities: Technical/functional Skills: The candidate should have excellent knowledge of modern synthetic methodology including asymmetric synthesis, heterocyclic chemistry, catalysis and the reaction mechanism is expected. Should be expert in synthetic problem solving/troubleshooting skills. Excellent communication skills including face to face and virtual interactions with team and clients. Must have exceptional Presentation skills. The candidate should maintain an accurate scientific notebook, draft concise written reports for publications. Education: Phd + Post Doc Equal Opportunity Employer: It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

Job description Job Role: Medicincal Chemistry Scientist Job location: Bangalore/Hyderabad About Syngene: Syngene ( www.syngeneintl.com ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, Safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and sops, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams, and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self Compliance to Syngene s quality standards at all times Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time Core Purpose of the Role: Personnel handling this profile will be responsible for performing reactions as per the requirement of the project. They are also responsible for documenting the observations in relevant note books. They are to follow instructions from the supervisor and work in a group (or individually) to accomplish the tasks in a timely and efficient manner Role Accountabilities: Perform synthetic chemistry reactions, reaction workups, purification of the compounds by column chromatography, crystallization, re-crystallization techniques, preparative TLC and operating lab equipment s Ensure that the samples generated during synthesis are given for analysis and record subsequent results obtained and update the supervisor / group leader on the progress of synthesis and ensure samples are packed appropriately for shipment Record the observations of experiment/reaction, results, utilization of resources and other activities related to the reaction in the laboratory or e-notebook following guidelines and in timely manner and ensure that the same is handled safely and confidentially. Ensure that the instrument / equipment is calibrated, undergone preventive maintenance and are kept clean before use and in case of any breakdown, report to maintenance immediately Ensure that they know the MSDS of the chemicals they are handling and aware of emergency response procedures in case of accidental spillage, leakage or fire and ensure proper waste segregation as per EHS norms Always follow EHS and quality system requirements in the workplace ensuring individual safety and lab safety Attend all mandatory trainings and update training records as and when trainings are completed Always ensure confidentiality Syngene Values All employees will consistently demonstrate alignment with our core values Excellence Integrity Professionalism Specific requirements for this role Experience: 3-12 years Education: M.Sc/ M.Pharm Skills and Capabilities: Should be familiar with concepts of chemical synthesis Familiar with operations of relevant apparatus - instrument / equipment.

Provide necessary input / guidelines to the Structural Consultant. Review the design along with the subordinates to ensure codal compliance and safety in all areas of civil / structural design. Develop exhaustive guidelines / checklist for the review of civil / structural design. Holistic review of the structural model and design to ensure functional requirements are being satisfied. Ensure that the Civil / Structural Design is safe, economical and compliant with relevant codes / standards Requirements 10 -16 years of professional experience in Civil & Structural Design of Buildings. Experience in Industrial / Commercial / residential Projects. Looking for Female candidates.

Job Title: iCMC Regulatory Affairs Manager I Career Level - D1 Introduction to role As an iCMC RA Manager I, you will effectively handle the production of Chemistry, Manufacturing, and Control (CMC) documentation for designated product ranges to meet the needs of both AstraZeneca and our customers. You will project manage international CMC regulatory submissions, ensuring that project activities and documentation are delivered to the required standards across the product lifecycle. You will chip in to and lead the regulatory CMC components of business-related projects, maintaining effective communication with collaborators and project team members to ensure relevant timelines and regulatory commitments are met. Additionally, you will ensure the application of international CMC regulations and guidance within AstraZeneca and chip in to the development of new guidance, policy, and processes. Accountabilities Manage the timely preparation (including authoring) and delivery of CMC contributions to regulatory submissions linked to medicinal products throughout the lifecycle, including marketing authorization applications and all post-approval activities. Accountable for delivering submission ready CMC modules to internal and external regulatory team members in compliance with relevant AstraZeneca systems and procedures, ensuring submission quality. Document maintenance and communication of Health Authority approval status. Develop and build expertise in regional regulatory requirements to ensure compliance of CMC submissions. Demonstrate project management expertise with the ability to adapt to changing situations to ensure on-time delivery. Share learnings from own projects with colleagues/within functions. Support the agreed strategy to employ fit-for-purpose content applying regulatory intelligence and optimize proposed submission content. Participate in regulatory execution and delivery meetings, providing relevant updates to the CMC team. Contribute to business process optimization activities to reduce waste and ensure efficiency. Continually evolve and develop regulatory expertise through proactive recording and communication of Health Authority interactions, responses, and commitments. Apply GxP principles according to the stage of the product lifecycle. Responsible for organisational change as assigned. Understand the application of appropriate risk management across own activities. Demonstrate research skills in understanding regulations and guidance from different regulatory agencies. Essential Skills/Experience University degree in a science or technical field such as pharmacy, biology, chemistry, or biological science. Minimum 8 years of proven experience from the biopharmaceutical industry or other relevant experience. Breadth of knowledge of manufacturing, project, technical, and regulatory management. IT skills. Collaborator & project management. Professional capabilities: Regulatory knowledge. Desirable Skills/Experience Knowledge of the drug development process and regulatory submissions. Understanding of current regulatory CMC requirements. Direct/indirect Regulatory Affairs CMC experience with submissions for synthetics and/or biologic and biotechnology-derived products such as monoclonal antibodies or complex biologic products. Understanding of regulations and guidance governing the manufacture of biotechnology products, especially monoclonal antibodies. Lean capabilities. When we put unexpected teams in the same room, we fuel ambitious thinking with the power to inspire life-changing medicines. In-person working gives us the platform we need to connect, work at pace, and challenge perceptions. Thats why we work, on average, a minimum of three days per week from the office. But that doesnt mean were not flexible. We balance the expectation of being in the office while respecting individual flexibility. Join us in our unique and ambitious world. At AstraZeneca, we are committed to turning our drug development strategies into reality. We work at all stages of development to translate our life-changing science into medicines that achieve the best results for patients in need and healthcare professionals. Our innovative mindset drives us to think broadly about patients and what it takes to prevent and treat diseases. We are a diverse and open-minded team that values different skills and experiences, empowering us to make quick decisions and influence drug development strategies. Our science-driven approach ensures that our regulatory strategy is appreciated and valued, allowing us to bring life-changing medicines to patients. Ready to make a difference? Apply now to join our dynamic team! Date Posted 18-Mar-2025 Closing Date 22-Apr-2025

Minimum of 5 years experience managing data in support of clinical research. Experience working with complex external data e.g., Biomarkers, Genomics, imaging or similar. Demonstrated project management skills. Coordinates external Data stream set-up and post-production changes, ensuring quality and timely delivery according to established timelines. Collaborates with External Data Provider and key stakeholders to ensure that data capture aligns with requirements. Provides input on data collection Strategy. Sets up data transfer specifications and data transfer mechanisms for external data streams. Follows up on data transfer issues with (E)DP s. Identifies potential risks and communicates with study team in collaboration with the GDM. Acts as point of contact for GDM, DAE and CP on the standardization of external data. Candidate should have worked in Oncology, Cross TA , Immunology or Medical affairs Therapeutic area. Should have hands on experience on DTA/DTS, tsDTA preparation. Test Concept Mapping. Test transfer file review.

You will be working closely with internal Product Management and Project Management teams, as we'll as external stakeholders, to ensure Product Launches for our Life Science Business are executed on time You must understand the laws and regulations governing GHS, Safety Data Sheets (SDS), Trade Compliance, and Chemical Registration across the globe Your responsibilities will include collaborating with various business teams globally to ensure detailed compositional and physical property data, along with any other relevant primary and secondary information needed for regulatory assessments, are provided You will utilize various MS Suite applications, SAP modules, and Big Data platforms to prepare and deliver the gathered data to downstream processing teams Additionally, you will apply basic Project Management skills to run your own projects Your role will also involve examining and understanding product formulation, consolidating the regulatory teams decisions regarding the feasibility of sales, and ensuring proper documentation for hazardous characterization Partnering with internal processing teams using the information provided will also be part of your responsibilities Who You Are: Master s degree in Natural Sciences or Toxicology More than 2 years of experience with Regulatory data and laws Basic knowledge in Data Analytics Sound understanding of product data, specifically chemical composition Knowledge of SAP EHSM Module; excellent Microsoft suite skills Basic/Minimum Qualifications: Effective communication skills Basic support towards Project ManagementTeam-oriented work style Vendor negotiation skillsPreferred Qualifications: Medium to advanced Project Management skills

Greetings from Aashvi Infotech.! We have urgent requirement for our client, it's Diagnostics Center . Requirement : Medical Transcriptionist (Female) WORK FROM OFFICE ONLY Job Locations : Jayanagar, Yelahanka & Whitefield Job Role: You have to type CT MRI & ultrasound reports based on doctor's conversation. Interested candidates can WhatsApp CV on 9979304590

SUMMARY Home Care Nurse in Qatar About the Client Our client is a prominent provider of alternative live-in home care support for elderly, disabled, and individuals recovering from accidents or illnesses. Job Summary The Home Care Nurse will be responsible for delivering direct patient care, assessing patient needs, and evaluating care plans in home or clinical settings. Key Responsibilities & Accountabilities Develop and assess nursing care plans Monitor vital signs and holistic patient needs Collaborate with healthcare team members Administer medications and maintain medication safety Document nursing care and ensure client safety Conduct client assessments using approved tools Attend training and seminars Key Competencies Nursing Care Knowledge Critical Thinking Problem-Solving Attention to Detail and Quality Multi-Tasking Emotional Self-Awareness Proactivity and Assertiveness Optimism Organizational Awareness and Commitment Required Qualifications Bachelor's Degree in Nursing Licensed nurse from the country of origin Minimum 2 years of experience as a Registered Nurse Note: Only FEMALE candidates willing to relocate to Qatar should apply. Requirements REQUIRED QUALIFICATIONS: A Ho der of Bachelors Degree in Nursing Licensed nurse from the country of origin At least 2 years of working experience as a Registered Nurse Benefits BASIC PAY 3,000.00 QR OVERTIME 1,200.00 QR FOOD ALLOWANCE 550.00 QR TRANSPORTATION ALLOWANCE PROVIDED BY THE COMPANY ACCOMMODATION ALLOWANCE PROVIDED BY THE COMPANY TOTAL MONTHLY SALARY Up to 4 ,750 QAR

We are hiring Pharmacist in Multiple locations of Hyderabad and Peripheral; Bandalaguda Jagir ECIL Gachibowli Kukatpally Chandrayangutta Job Description :- Issue & Return of Material against Patient indents from Stores and against Departmental indents Direct Issue of drugs/ medical consumable to Patient Issue of Narcotics as per protocols Receiving the material at Receiving Bay & Processing of Invoices Emergency Cash Purchase Receipt of consignment goods & Processing their Invoices on Consumption Physical Stock Verification. Should have valid Telangana state registration Only immediate joiners apply for the role Interested candidates can share their profile on sneha.shetty@indiraivf.in / Careers@indiraivf.in

Narayana Hrudayalaya Hospital Group, India's leading healthcare provider, invites dynamic and passionate healthcare professionals to join the group. We invite applications for the following positions: Position: Consultant, Cardiology Qualification: DNB/DM (Cardiology) Location: Bangalore A medical professional with 2 to 8 years' experience would be preferred. Interested medical professionals can contact Raghavendra and forward updated resume to raghavendra.h01@narayanahealth.org Thanks & Regards Raghavendra +919513314873

Check the medical admissibility of claim by confirming diagnosis and treatment details Verify the required documents for processing claims and raise an information request in case of an insufficiency Approve or deny claims as per T&C within TAT If candidates are interested please drop your update resume/CV on my WhatsApp no - 8951865563 Thanks & Regards Sarika Email - Sarika.pallap@mediassist.in

JOB DESCRIPTION Designation: Associate Scientist (8-I) Job Location: Bangalore Department: In vitro Pharmacology (LE), Department of Discovery Biology About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&D productivity, speed up time to market and lower the cost of innovation. Job Purpose (1-2 Lines) BBRC is seeking an experienced scientist (MS/MTech/MPharm) with expertise in Neuroscience to join their Molecular Pharmacology group in their mission of discovery and validation of therapeutic targets and participation in drug discovery programs. Applicants with expertise in neurodegenerative diseases like Alzheimers/Multiple Sclerosis etc and other neurological conditions like Schizophrenia are particularly encouraged to apply. Key Responsibilities: Design and conduct rigorous experiments including cell based (cell-lines, primary neurons and human iPSCs) and biochemical assays, aimed at execution of discovery programs focused on neuropsychiatric diseases Routinely perform occupancy assays etc to analyze changes in target engagement from cell cultures, brain and peripheral tissues Independently determine in-vitro pharmacologic methods and procedures to study modulation of GPCRs/neurotransmitter receptors in the primary neurons/human iPSC neurons etc Develop and troubleshoot assays independently, record, analyze and communicate scientific data; ensure the accuracy and reliability of data Search and review the scientific literature independently on the target biology Educational Qualification: MS, MTech or MPharm in enzymology, biochemistry, molecular biology or related discipline Experience: 5-6 years Technical/functional Skills: Experience in neuropharmacology/small molecule pharmacology at therapeutically relevant GPCRs/neurotransmitter receptors at the molecular level in the CNS Demonstrated technical proficiency in biochemical, cellular, and/or radioligand binding assay systems to assess drug target engagement Ability to perform ex-vivo receptor occupancy assays in the brain tissues to understand receptor targeted drug efficacies Hands-on experience in complex cellular models/ex-vivo systems, including designing and executing mechanistic/pharmacological characterization of lead candidates Must be independent and able to follow pre-established experimental designs, as well as develop new methods, protocols, and technologies based on existing literature Behavioral Skills: Strong problem-solving and data analysis skills, excellent written and verbal communication skills, good presentation skills, and the ability to handle multiple projects simultaneously and meet aggressive project timelines. Must demonstrate integrity and take accountability for their work Equal Opportunity Employer: It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.

Body & Mind - Physio & Pilates Studio, located in Bengaluru, is a holistic wellness centre that specializes in physiotherapy, pilates, manual therapy, mat pilates, reformer pilates, and mindful movement. We are dedicated to providing comprehensive wellness solutions to our clients, focusing on the connection between the body and mind. Role Description This is a full-time on-site role for a Physiotherapist at Body & Mind - Physio & Pilates Studio. The Physiotherapist will be responsible for providing physiotherapy treatments, conducting assessments, developing treatment plans, implementing therapeutic exercises, performing manual therapy techniques, and offering guidance and support to clients on their wellness journey. Qualifications Strong knowledge and experience in physiotherapy techniques and practices Proficiency in conducting assessments and developing personalized treatment plans Expertise in implementing therapeutic exercises and manual therapy techniques Knowledge of pilates and mindful movement practices Excellent communication and interpersonal skills Ability to work effectively with clients of all ages and fitness levels Proactive and compassionate approach to client care Valid certification and licensure in physiotherapy Additional certifications in pilates or manual therapy are a plus

Designation: Pharmacist Department: Pharmacy Supply Chain Location: Bangalore, Karnataka About Tata 1mg Tata 1mg is a trusted health partner for end consumers and large institution. Our Mission is to make healthcare understandable, accessible, and affordable for all Indians. Over the past three years, we've worked to build a healthcare platform that guides customers to the right and affordable care. Today, Tata 1mg is present in 1000+ cities And were just getting started. Leading the chart as one of the top consumer health platforms through e Pharmacy, e Diagnostics, e-consult and offline stores, Tata 1mg has delivered over 15M e pharmacy orders, 2M e Diagnostics orders & 1M+ organic users/day in 2022 and we are just getting started. Our strongest asset is our 6400+ people enabling us to deliver on our mission consistently. Know more about us: https://www.1mg.com/aboutUs` What will you do Accurately dispense prescribed medications. Manage medication on inventory, storage, handling, and disposal in compliance with safety regulations. Verify the accuracy and appropriateness of prescriptions. What we are looking for Bachelors or Diploma of Pharmacy degree from an accredited institution. Valid pharmacist license and registration of Karnataka state. Prior experience in pharmacy Excellent communication, collaboration, and adherence on to detail. Ability to handle high-stress situations and prioritize tasks in a fast-paced healthcare environment. Why Join Us? Tata 1mg provides one of the most exciting and high-growth environments to work. You get the added benefit of working in a prestigious legacy brand like Tata and a highly dynamic and versatile startup like 1mg. Being an Integral part of the team will provide a great opportunity to scale up a business to great heights leveraging the existing capabilities of Tata 1mg. Disclaimer Tata 1mg is proud to be an Equal Opportunity Employer. All employment decisions at Tata 1mg shall be made without discrimination, harassment or less favorable treatment of any employee or job applicant, either directly or indirectly, on the grounds of age, color, physical ability, ethnic origin, nationality, religion, gender, family status, marital status, prenatal status, gender reassignment, or sexual orientation. All employment decisions are based on business needs, job requirements, competence and merit.

Responsibilities: Provide expert nursing care in ICU setting Manage critically ill patients' needs Collaborate with interdisciplinary team on patient plans Administer medications and treatments accurately

1. Patient Care Clinical Responsibilities The Staff Nurse will provide direct patient care, including monitoring vitals, administering medications, wound dressing, IV therapy, catheterization, and post-operative care. They will assist patients with mobilization, rehabilitation, and pain management, ensuring holistic recovery. Nurses will also support doctors during rounds, respond to critical changes in patient conditions, and educate families on disease management and medication adherence. 2. NABH Compliance Quality Assurance The nurse is responsible for maintaining accurate medical documentation in line with NABH standards, ensuring seamless patient care handovers. They must strictly follow infection control protocols, biomedical waste management, and patient safety guidelines. Participation in quality audits and training programs is essential to uphold the hospital s accreditation and compliance with healthcare standards. 3. Inventory Medication Management The nurse will oversee the safe storage, administration, and stock-keeping of medicines and medical supplies. They must maintain updated inventory records, coordinate with the pharmacy for replenishment, and ensure the crash cart and emergency drugs are always stocked. Strict adherence to hospital drug administration protocols is mandatory to prevent medication errors. 4. Medico-Legal Documentation Compliance The role requires strict compliance with Indian medico-legal requirements, including handling medico-legal cases (MLCs) such as assault, poisoning, and accident cases. Nurses must ensure proper documentation of consent forms, treatment records, and forensic evidence, following legal protocols. They are expected to work in alignment with The Clinical Establishments (Registration and Regulation) Act, 2010, ensuring complete legal compliance. 5. Ward Management Housekeeping Duties The nurse will oversee bed-making, linen changes, infection control, and equipment maintenance to ensure a hygienic and safe patient environment. They must report any malfunctioning medical equipment and ensure proper patient area sanitation. Nurses will also provide basic patient assistance, including feeding, personal hygiene, and mobility support. 6. Emergency Critical Care Responsibilities The nurse will actively respond to medical emergencies, including cardiac arrests, trauma cases, and Code Blue situations. They must be trained in Basic Life Support (BLS) and Advanced Cardiac Life Support (ACLS), assisting in ICU, NICU, and emergency wards as required. Prompt decision-making and teamwork are crucial to saving lives in critical situations. 7. Communication Patient Education Effective communication with patients, families, and the medical team is essential to providing high-quality care. Nurses will educate patients on post-hospital care, lifestyle modifications, and follow-up treatments. They will also handle patient concerns professionally, ensuring empathy and confidentiality in every interaction. Coordination with social workers and counselors will be required for comprehensive patient support. Qualifications Requirements: 1. Education: Diploma / B.Sc. / M.Sc. in Nursing from a recognized institution. 2. Registration: Valid registration with the State Nursing Council (mandatory). 3. Experience: Minimum 1-3 years of experience in clinical nursing (freshers with strong commitment to quality care may apply). 3. Certifications: Basic Life Support (BLS) / Advanced Cardiac Life Support (ACLS) preferred. Skills: 1. Strong clinical skills in patient care and medical-surgical nursing. 2. Knowledge of NABH standards, infection control, and quality assurance. 3. Familiarity with medical records management and medico-legal documentation. 4. Ability to work in a team-based, community healthcare setting. 5. Good communication skills in English and at least one local languages (Tamil/Telugu/Kannada). Compensation Benefits: 1. Salary: As per industry standards hospital pay scale. 2. Benefits: Health insurance, paid leave, professional development opportunities. 3. Work Schedule: Rotational shifts, including weekends holidays as per hospital policy.

Laboratory Technician Mission: The mission of the position Laboratory Technician is to drive sustainable growth and foster strategic partnerships, through innovative approaches, relentless pursuit of new opportunities, and a commitment to customer success, our Laboratory Technician play a pivotal role in positioning our organization as a market leader. Guided by integrity, collaboration, and a passion for excellence, we strive to create lasting value for our customers, stakeholders, and the company as a whole. Job Responsibilities: 1. Sample Handling and Processing: Specimen Collection and Preparation: Collect, label, and prepare patient samples with utmost accuracy and adherence to protocols. Ensure proper handling and storage of specimens to maintain sample integrity. Laboratory Testing: Conduct a variety of diagnostic tests following established procedures and safety protocols. Operate laboratory equipment such as analyzers, microscopes, and centrifuges proficiently. Perform quality control checks to ensure accuracy and precision of test results. 2. Analysis and Reporting: Data Analysis: Analyze test results meticulously, recording and interpreting findings accurately. Document and maintain comprehensive records of all tests conducted and results obtained. Report findings promptly to supervisory personnel for further review or action. 3. Equipment Maintenance and Calibration: Instrument Maintenance: Perform routine maintenance on laboratory equipment to ensure proper functioning. Calibrate and troubleshoot equipment issues promptly or report them to the appropriate personnel. Maintain inventory of reagents, supplies, and equipment, ensuring adequate stock levels. 4. Quality Assurance and Compliance: Quality Control: Adhere strictly to quality control and quality assurance procedures, following regulatory guidelines. Participate in proficiency testing programs to validate laboratory procedures and maintain accuracy. Assist in the implementation of quality improvement initiatives to enhance laboratory operations. 5. Safety and Hygiene: Safety Protocols: Maintain a clean and sterile laboratory environment, following safety protocols at all times. Dispose of bio hazardous materials and waste in accordance with established procedures. Adhere to infection control measures and ensure compliance with safety regulations. *This job description provides a general outline of responsibilities and qualifications and is not exhaustive. The role may be required to perform additional duties as necessary for the smooth functioning of the business. Qualification A diploma or associate degree in Medical Laboratory Technology, Clinical Laboratory Science, or a related field. Previous experience (1-2 years) in a laboratory setting, especially in diagnostic or clinical laboratories, is advantageous. Proficiency in conducting various laboratory tests and operating laboratory equipment. Knowledge of laboratory procedures, protocols, and safety measures. Ability to perform quality control checks and maintain accurate records of tests conducted. Strong analytical and problem-solving skills to interpret test results accurately. Attention to detail and precision in handling and processing specimens. Capability to manage multiple tasks efficiently in a fast-paced laboratory setting. Flexibility to adapt to changing priorities and work schedules. Good communication skills to interact effectively with colleagues and superiors. Ability to work collaboratively in a team-oriented environment.