2389 Pharmacy Jobs - Page 14

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 : Responsible for product development for parenteral drug products, which includes pre-formulation, formulation design, process optimization & characterization, and technology transfer from R&D to different manufacturing sites. Lead all activities for transferring lab process to GMP manufacturing site and facilitate drug product manufacturing in GMP fill finish facility, in coordination with production and quality team. Responsible for optimization of manufacturing processes (right first time approach) to support drug product supply for clinical trials

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: He should expertise in granulation and coating area is mandatory. Exposure to packaging will appreciable, The candidate should have 6 to 9 years of experience in any pharmaceutical organization and qualification should be Diploma in pharmacy or Diploma in any engineering segments or Graduation in any stream. The handling of machine setup, troubleshooting, operation, change over, and cleaning of manufacturing equipment s like FBP, RMG, Roller Compacter, Fluid bed Wurster granulator/coater, and tablet coating machine are the key requirements. He should handle the IQQC instruments like Halogen moisture analyser, Tap density apparatus, sieve shaker, Hardness tester etc. He should have good knowledge on data integrity concept (ALCOA+), GDP and cGMP norms. He should have good communication skill. He should have experience on audit handling. He should have good knowledge on housekeeping, area maintaining as per client visit, internal and external audits.

Contact potential customers to verify interest and coordinate/schedule meetings with local sales representatives (direct or through channel partner) Document and qualify incoming leads using Salesforce Customer Relationship Management (CRM) software Respond to basic products and services inquiries and collaborate with the sales and marketing teams to optimize processes The essential requirements of the job include: 2+ years experience in customer service or client interaction role (e.g., healthcare, pharmacy, pharmaceuticals, sales, or support) Fluency in English, both spoken and written in addition to fluency in one of the following languages: Spanish, German, or French Strong computer literacy and experience working in a PC environment It would be a plus if you also possess previous experience in: Working knowledge of Customer Relationship Management (CRM) systems (preferably Salesforce) Previous experience working in biomedical, pharmaceutical, or healthcare-related fields

Design, conduct and or supervise formulation development, process development, process optimization, scale up and manufacturing of product. Prepare and review documents such as batch records, Batch Packaging Records, Product Development reports, SOPs, Stability protocols, Raw material specifications, Packaging material specifications and In-process/ Finished product specifications, labelling and stability loading. Review of test results in alignment with the project goals, identify causes of variances and recommend solutions to achieve goals. Schedule experiments and prioritize assignments to meet project objectives and deadline. Maintain laboratory equipment and follow company safety standards. Conduct laboratory experiments and prepare reports with conclusions and recommendations. Follow current laboratory procedure and develop new laboratory procedures or improvise existing procedures to meet project objectives. Identify and manage the potential risks within complex projects in a timely fashion. Record accurate and complete experimental methods and results in compliance with good documentation practices. Act as primary scientific contact to external collaborators. Check and manage inventories of supplies and raw materials. Ensure completion of all the training on time. Qualifications and Education Requirements M. Pharm or Ph.D. in Pharmacy with minimum industrial experience of 3 to 6years in pharmaceutical development and scale-up of products. Preferred area of expertise is oral dosage forms precisely in Modified Release/ extended release/ targeted release/immediate release solid/Suspensions/Solutions. Global Product Development Experience with markets like US/EU/China/ROW. Experience of developing branded and differentiated products 505(b)(2) category would be preferred. Experience of working with CROs/CDMOs would be preferred. Should be well versed with Microsoft office applications.

PON PURE CHEMICAL INDIA PRIVATE LIMITED is looking for Senior Manager R&D (Pharma) to join our dynamic team and embark on a rewarding career journey Analysis for the current business practice. Find out the different operational strategies. Work on developing the current operational strategy applied to the company with the most recent technology. Coordinate with the operations manager to take the required steps after brainstorming and research. Optimize the operations in the company. Put the suitable operational strategy to fit with the companys culture. Implement the operational strategy in the different departments of the company. Supervise the strategy, and make sure that all the employees respect this strategy. Work regularly in improving the companys operations performance. Also, the deputy operations manager works in certain cases in touch with the clients to make sure that they receive the required service with the highest quality. In Customer service company, the deputy operations manager works with his team to make the clients satisfied by offering to his team the required training and courses to be able to communicate correctly with the customers. Follow up with the running project daily in order to make sure that they follow the right operation process. Check the logistics operations. Monitor t Show to the employees the company strategies and regulations in order to maintain the operation process. Solve all the different problems that could face the operations, to ensure the operational strategy. Issue a weekly, and monthly report for the operations manager to see all the updates realized on

Reveleer Global Capability Center is looking for Healthcare Business Analyst (BA) to join our dynamic team and embark on a rewarding career journey Evaluating business processes, anticipating requirements, uncovering areas for improvement, and developing and implementing solutions. Leading ongoing reviews of business processes and developing optimization strategies. Staying up-to-date on the latest process and IT advancements to automate and modernize systems. Conducting meetings and presentations to share ideas and findings. Performing requirements analysis. Documenting and communicating the results of your efforts. Effectively communicating your insights and plans to cross-functional team members and management. Gathering critical information from meetings with various stakeholders and producing useful reports. Working closely with clients, technicians, and managerial staff. Providing leadership, training, coaching, and guidance to junior staff. Allocating resources and maintaining cost efficiency. Ensuring solutions meet business needs and requirements. Performing user acceptance testing. Managing projects, developing project plans, and monitoring performance. Updating, implementing, and maintaining procedures. Prioritizing initiatives based on business needs and requirements. Serving as a liaison between stakeholders and users. Managing competing resources and priorities. Monitoring deliverables and ensuring timely completion of projects.

PrimeVigilance is looking for a Medical Information Associate to be responsible for supporting the Medical Information team in handling initial adverse event and medical information inquiries in English and French. Responsibilities To provide approved responses to medical enquiries (healthcare professionals, patients, pharmaceutical clients) including call handling To accurately identify, document and report adverse events/side effects, pregnancy and other special situation events, and product quality complaints within required timeframes To ensure that all medical information enquiries are tracked and fully documented within the Medical Information database accurately and completely To participate in the out-of-hours provision of medical information for clients who have contracted a 24/7 enquiry handling service Providing management with regular updates regarding project status and metrics concerning enquiries Assisting in departmental regulatory inspection preparedness for the company pharmacovigilance system and actively participating in PV inspections or audits; Life science / bio medical background healthcare related degree (chemistry, biology, biotechnology, pharmacy, nursing) Customer service or call centre experience preferred Comfortable receiving enquires by phone

Job Opportunity: MEDPLUS Pharmacy & Customer Service Roles Company: MEDPLUS (Leading Pharmacy Retail Chain) Industry / Department: Medical / Pharmacy Services Location: Across Karnataka Within District: Gulbarga (Kalaburagi) District Eligibility: Education: SSLC / PUC / Degree / D. Pharmacy / B. Pharmacy Gender: Male & Female candidates eligible Age Limit: 18 35 years Number of Openings: 300 positions Job Role & Responsibilities: Selected candidates will be responsible for handling day-to-day operations in MedPlus outlets. Dispensing Medicines accurately as per prescriptions. Customer Handling at the counter (guidance, support, and billing). Auditing Medicines (stock management, expiry checks, compliance). Maintaining proper records and ensuring smooth pharmacy operations. Skills Required: Good communication skills (reading and understanding). Willingness to work for a long-term period with the organization. Salary & Benefits: Salary Range: 15,500 25,000 per month Structured training and career growth opportunities. Note: Same-day offer letter will NOT be issued. Why Join MEDPLUS Be part of one of India s fastest-growing medical retail chains. Attractive salary package with career progression. Stable and respected role in the healthcare sector.

Please find below the Job Description of Business Development- International market/ Formulation 1. Handling New Inquiries: Evaluate customer inquiries by understanding project requirements. Provide quotations and relevant documentation to support customer engagement and project progression. 2. Sample and Agreement Management: Coordinate with the R&D team to arrange and dispatch product samples to customers. Handle the post queries related to sample Review customer agreements and coordinate with the legal team to finalize terms. Ensure all agreements are accurately documented and stored. 3. Regulatory Support: Manage and track regulatory submissions (e.g., Dossier, DMF) via Salesforce. Coordinate with the Regulatory team to obtain required documentation, artwork, and respond to customer or authority queries. 4. Lead Generation & Market Research: Identify and develop new business leads through analysis of data Conduct in-depth analysis of customer and product data as well as MoH data for targeted markets to support strategic expansion. 5. Customer Relationship Management: Build and maintain strong relationships with clients. Follow up with customers post-registration to secure initial orders and ensure ongoing engagement. Required Skills & Qualifications: Bachelors degree in Pharmacy 1 3 years of experience in business development, preferably in the pharmaceutical. Proficiency in Salesforce or similar CRM tools. Strong communication and coordination skills. Knowledge of regulatory documentation (DMF, Dossiers, COA, MSDS) is a plus.

Job Category: Healthcare Procurement Procurement Supply chain management Job Type: Full Time Job Location: Bangalore Qualification: B Pharmacy D Pharmacy Experience: 2 to 5 Years Identify potential suppliers and evaluate their offerings based on quality, price, delivery schedules, and service levels. Issue RFQs (Request for Quotations), RFIs (Request for Information), and RFPs (Request for Proposals) to suppliers. Negotiate prices, contracts, and terms with suppliers to ensure cost-effective procurement. Prepare and maintain purchase orders and procurement records. Coordinate with various departments to understand their procurement needs and ensure timely fulfilment. Monitor supplier performance and conduct periodic reviews. Maintain a database of suppliers, price lists, and procurement documentation. Ensure compliance with company policies and procurement procedures. Track and analyse market trends to identify new sourcing opportunities. Resolve any issues related to procurement and delivery.

About 2070 Health - W Health has set up India s first healthcare focused Venture Studio called 2070 Health - an innovation platform that builds transformative healthcare companies from scratch by discovering disruptive opportunities in whitespaces. Distinct from the accelerator approach, our venture studio is closely involved in idea generation, day-to-day operations, and strategic decisions of growing the new business. Companies incubated in the last 15 months include Elevate Now , Nivaan Care , Reveal Healthtech and BabyMD . About the Company - Everhope Oncology Everhope Oncology is on a mission to transform cancer care by making high-quality treatment more accessible, patient-friendly, and closer to home . Backed by Narayana Health , one of Indias leading hospital systems, W Health Ventures , a healthcare venture capital firm, and 2070 Health , a healthcare-focused venture studio, Everhope has secured $10 million in seed funding to establish a nationwide network of medical and surgical oncology facilities . Starting in Delhi and Mumbai , Everhope plans to expand to 10 cities over the next three years , bringing expert-led early diagnosis, daycare chemotherapy, and surgical oncology to locations where patients need them most. India faces a growing cancer burden, with over 150 million people expected to be diagnosed in their lifetime . Everhope is tackling this challenge head-on by creating smaller, strategically located centers that eliminate the logistical and emotional barriers to care . If youre passionate about shaping the future of oncology and want to be part of a high-impact, patient-first organization , join us in building a new era of cancer treatment one that prioritizes convenience, empathy, and innovation . Read more: ET | Business Standard | The Hindu We are hiring for a Pharmacist with a strong background in chemotherapy drug procurement, checking, and mixing. The ideal candidate will play a vital role in ensuring safe and effective medication use for oncology patients, contributing to personalized treatment plans, and enhancing overall patient care in a collaborative clinical setting Responsibilities - 1. Chemotherapy, Targeted Therapy, and Immunotherapy Preparation and Compounding: Responsible for accurately mixing and compounding chemotherapy, targeted therapy, and immunotherapy drugs, ensuring precise dosing and adherence to safety protocols. Follow strict sterility and handling guidelines for hazardous drugs, ensuring optimal patient safety and regulatory compliance. 2. Pharmacokinetics Analysis & Drug-Interaction Assessment: Review patient medical histories to adjust drug dosages, ensuring efficacy while minimizing side effects. Assess potential drug interactions, especially with complex cancer regimens, to ensure safe and effective treatment. 3. Patient Counselling and Education: Provide comprehensive counselling on chemotherapy and other oncology drugs, educating patients on proper use, managing side effects, and fostering adherence to treatment regimens. Offer emotional support to patients and families coping with cancer treatment challenges. 4. Medication Safety and Clinical Protocols: Ensure the accuracy of chemotherapy administration by closely monitoring treatment and minimizing errors. Collaborate in the development and implementation of clinical protocols, ensuring they align with best practices and regulatory standards for optimal oncology care. Report medication errors and adverse drug reactions, conducting Root Cause Analysis (RCA) and implementing Corrective and Preventive Actions (CAPA) to prevent recurrence. 5. Pain Management and Palliative Care: Collaborate with oncologists to manage pain and other symptoms in cancer patients, optimizing therapy to improve quality of life. Support palliative care initiatives, addressing patient comfort through appropriate pharmacological interventions. 6. Immunotherapy and Targeted Therapy Management & EHR: Stay up-to-date with advancements in targeted therapies and immunotherapies, integrating these treatments into patient care plans. Utilize Electronic Health Records (EHR) to track treatments and ensure accurate documentation, coordinating care effectively with the healthcare team. 7. Clinical Trial Support: Provide key support for oncology clinical trials, ensuring the correct preparation and administration of investigational drugs. Adhere to trial protocols, monitor patient responses, and maintain accurate records for regulatory compliance. 8. Research and Evidence-Based Practices: Engage in research activities to evaluate new therapies and treatment regimens. Integrate the latest evidence into clinical practice, ensuring that patient care is continually improved and aligned with current research. 9. Collaboration and Team Training: Work closely with oncologists, nurses, and other healthcare professionals to ensure patients receive appropriate and safe treatments. Collaborate on treatment plans, patient monitoring, and adjustments to therapy as needed, ensuring a comprehensive and coordinated approach to patient care. Provide monthly training to nursing staff and Resident Medical Officers (RMOs) on drug safety, medication management, and adherence to NABH guidelines to ensure consistent and high-quality care across the team. 10. Escalation Management: Actively manage and resolve any medication-related issues or adverse events that arise, ensuring that appropriate steps are taken to resolve the issue promptly. Collaborate with the clinical team to escalate issues appropriately, ensuring the safety and well-being of patients. 1. Bachelor of Pharmacy (B.Pharm) or Master of Pharmacy (M.Pharm) or Doctor of Pharmacy (Pharm.D) from a recognized institution. 2. Active pharmacy license. 3. Minimum of 5 years of experience as a pharmacist.

Why This Role Matters: The complexity of healthcare benefits makes decision automation critical. As a Rules Engine Engineer , you ll be at the heart of this challenge designing and implementing rules that determine what members can buy with their benefits. Your work directly shapes member experience, prevents misuse, and ensures compliance with Medicare regulations. If you enjoy building high-performance, logic-driven systems that solve tough real-world problems, this role is for you. What You ll Do: Own the rules layer : Design, implement, and optimize decision logic using Sparkling Logic SMARTS . Build real-time adjudication flows for transactions at grocery and pharmacy point-of-sale systems. Translate complex requirements into executable rules by collaborating with US-based product and compliance teams. Debug, test, and tune rules to handle edge cases, scale to high transaction volumes, and minimize false rejections/approvals. Version, deploy, and maintain rules with best practices for governance, traceability, and rollback. Continuously improve accuracy, performance, and maintainability of the adjudication rules engine. What We re Looking For: 2+ years hands-on experience with Sparkling Logic SMARTS (preferred) or other business rules engines (Drools, ODM, Blaze, etc.). Strong grasp of decision modeling (DMN), rule authoring, and lifecycle management . Solid programming/scripting skills for integration (Java, Python, or similar). Ability to debug distributed systems and reason through complex rule interactions. Experience in fintech, healthcare, or other transaction-heavy, regulated domains is a big plus. Strong communication skills comfortable working with US teams across time zones. A mindset that balances engineering precision with business pragmatism . What You ll Get: The chance to work on mission-critical systems where every rule you write has immediate impact. Exposure to both fintech scale challenges and healthcare compliance complexities . A collaborative global engineering culture that values technical ownership and problem-solving. Competitive pay, growth opportunities, and the ability to help redefine healthcare payments .

Career Category Regulatory Job Description R egulatory Affairs, Chemistry, Manufacturing and Controls (RA CMC) facilitates product development and global registration by developing and executing regulatory strategies and managing effective regulatory agency interactions for product manufacturing and quality programs throughout product lifecycle. The Regulatory Compliance team is a part of RA CMC and is seeking to expand its capacity in India . The Regulatory Compliance team performs assessment of operational changes for regulatory reportability and maintenance of state and federal licenses for Amgen products across phases of development, modality, and countries. The team member will be responsible for maintaining U.S. state and federal commercial product licenses and will collaborate with Global CMC, Site CMC, and Device Regulatory, Operations, Quality, and Supply Chain teams on strategies and activities impacting licensed products. Roles & Responsibilities: Key responsibilities of the Regulatory Affairs Sr Associate include: Tracks license status to ensure all are current and effective. Communicates requirements to internal Amgen functional teams. Obtains supplemental documentation from internal and external partners. Prepares , reviews, and submits license applications and renewals. Maintains all State Licensing documentation, submissions, and interactions with State Authorities. Interfaces with State Board of Pharmacy ( BoP ) and/or Department of Health ( DoH ). Complete s required annual notifications to FDA What we expect of you We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a type of person with these qualifications. Basic Qualifications: Master s degree OR Bachelor s degree and 2 years of manufacture, QA/QC, or regulatory CMC in the Pharmaceutical/Biotechnology industry OR Associate s degree and 6 years of manufacture, QA/QC, or regulatory CMC in the Pharmaceutical/Biotechnology industry Preferred Qualifications: Degree in Life Science discipline Regulatory CMC specific knowledge & experience Experience in manufacture, testing (QC/QA or clinical), or distribution in Pharmaceutical/Biotech industry Working knowledge of US state and/or federal licensing requirements What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we ll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now for a career that defies imagination Objects in your future are closer than they appear. Join us. careers.amgen.com As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. .

Career Category Regulatory Job Description R egulatory Affairs, Chemistry, Manufacturing and Controls (RA CMC) facilitates product development and global registration by developing and executing regulatory strategies and managing effective regulatory agency interactions for product manufacturing and quality programs throughout product lifecycle. The Regulatory Compliance team is a part of RA CMC and is seeking to expand its capacity in India . The Regulatory Compliance team performs assessment of operational changes for regulatory reportability and maintenance of state and federal licenses for Amgen products across phases of development, modality, and countries. The team member will be responsible for maintaining U.S. state and federal commercial product licenses and will collaborate with Global CMC, Site CMC, and Device Regulatory, Operations, Quality, and Supply Chain teams on strategies and activities impacting licensed products. Roles & Responsibilities: Key responsibilities of the Regulatory Sr Associate include: Tracks license status to ensure all are current and effective. Communicates requirements to internal Amgen functional teams. Obtains supplemental documentation from internal and external partners. Prepares , reviews, and submits license applications and renewals. Maintains all State Licensing documentation, submissions, and interactions with State Authorities. Interfaces with State Board of Pharmacy ( BoP ) and/or Department of Health ( DoH ). Complete s required annual notifications to FDA What we expect of you We are all different, yet we all use our unique contributions to serve patients. The professional we seek is a type of person with these qualifications. Basic Qualifications: Master s degree OR Bachelor s degree and 2 years of manufacture, QA/QC, or regulatory CMC in the Pharmaceutical/Biotechnology industry OR Associate s degree and 6 years of manufacture, QA/QC, or regulatory CMC in the Pharmaceutical/Biotechnology industry Preferred Qualifications: Degree in Life Science discipline Regulatory CMC specific knowledge & experience Experience in manufacture, testing (QC/QA or clinical), or distribution in Pharmaceutical/Biotech industry Working knowledge of US state and/or federal licensing requirements. What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we ll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now for a career that defies imagination Objects in your future are closer than they appear. Join us. careers.amgen.com As an organization dedicated to improving the quality of life for people around the world, Amgen fosters an inclusive environment of diverse, ethical, committed and highly accomplished people who respect each other and live the Amgen values to continue advancing science to serve patients. Together, we compete in the fight against serious disease. Amgen is an Equal Opportunity employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or any other basis protected by applicable law. We will ensure that individuals with disabilities are provided with reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment. Please contact us to request accommodation. .

Optum is a global organization that delivers care, aided by technology to help millions of people live healthier lives. The work you do with our team will directly improve health outcomes by connecting people with the care, pharmacy benefits, data and resources they need to feel their best. Here, you will find a culture guided by inclusion, talented peers, comprehensive benefits and career development opportunities. Come make an impact on the communities we serve as you help us advance health optimization on a global scale. Join us to start Caring. Connecting. Growing together. Optums Applied AI team is seeking a detail-oriented and proactive Senior Data Scientist (Core in Data Analysis) with minimum 3-4 years of industry experience to support the development and maintenance of data pipelines that fuel AI/ML initiatives. You will work closely with data engineers and other data scientists to enable large scale data analysis of prior ML inferred data - structured and unstructured clinical datasets. This role blends hands-on data wrangling, transformation logic, and insight generation in a highly collaborative environment. Primary Responsibilities: Collaborate with cross-functional teams - including ML engineers, annotators, and clinical domain experts - to translate business challenges into deployable AI solutions Implement automated data labeling pipelines using techniques like active learning, weak supervision, and human-in-the-loop systems Support the design, development, and maintenance of scalable data pipelines for AI/ML workflows Perform exploratory data analysis (EDA), profiling, and validation on healthcare data to ensure readiness for downstream ML tasks Partner with data scientists to prepare datasets for model training, evaluation, and monitoring Ensure data quality, consistency, and documentation across structured (e.g., EHRs) and unstructured (e.g., scanned PDFs) sources Integrate and monitor data workflows using orchestration tools (e.g., Airflow, Step Functions) Build dashboards or reports to communicate insights, trends, or pipeline health as needed Comply with the terms and conditions of the employment contract, company policies and procedures, and any and all directives (such as, but not limited to, transfer and/or re-assignment to different work locations, change in teams and/or work shifts, policies in regard to flexibility of work benefits and/or work environment, alternative work arrangements, and other decisions that may arise due to the changing business environment). The Company may adopt, vary or rescind these policies and directives in its absolute discretion and without any limitation (implied or otherwise) on its ability to do so Required Qualifications: Bachelors degree in computer science or adjacent field Advanced degree in a field that emphasizes the use of data science/statistics techniques (e.g., Computer Science, Applied Mathematics, or a field with direct NLP application) 4+ years of experience in Data Science (Core in Data Analysis) to support the development and maintenance of data pipelines that fuel AI/ML initiatives Solid experience in Ms Excel and Version Control using GIT Proficiency in Python (Advanced), SQL(Advanced). Experience in tools like Airflow, Jupyter notebook Cloud Exposure: Basic familiarity with AWS ecosystem Visualization Tools: Power BI, Tableau, or Plotly for dashboarding and reporting Data Quality Monitoring: Experience with tools or techniques for detecting data drift or label inconsistencies Healthcare/NLP Domain Knowledge: Prior work with clinical documents, EMR data, or coding workflows Proven excellent Communication Skills Proven flexibility to provide support during critical business periods Proven ability to interpret and present complex data in various formats Proven positive team player with a drive to learn and contribute to achieving results Willingness to work in varying shifts At UnitedHealth Group, our mission is to help people live healthier lives and make the health system work better for everyone. We believe everyone - of every race, gender, sexuality, age, location and income - deserves the opportunity to live their healthiest life. Today, however, there are still far too many barriers to good health which are disproportionately experienced by people of color, historically marginalized groups and those with lower incomes. We are committed to mitigating our impact on the environment and enabling and delivering equitable care that addresses health disparities and improves health outcomes - an enterprise priority reflected in our mission. #NJP ",

Career Category Regulatory Job Description Regulatory Affairs, Chemistry, Manufacturing and Controls (RA CMC) facilitates product development and global registration by developing and executing regulatory strategies and managing effective regulatory agency interactions for product manufacturing and quality programs throughout product lifecycle. The Regulatory Compliance team is a part of RA CMC and is seeking to expand its capacity in India . The Regulatory Compliance team performs assessment of operational changes for regulatory reportability and maintains state and federal licenses for Amgen products across phases of development, modality, and countries. The team member will be responsible for maintaining U.S. state and federal commercial product licenses and will collaborate with Global CMC, Site CMC, Device Regulatory, Operations, Quality, and Supply Chain teams on strategies and activities impacting licensed products. Roles & Responsibilities: Key responsibilities of the Regulatory Affairs Manager include: Conducts periodic assessments of licenses / facilities and ensure s business practices comply with current regulations and statutes. Evaluates new and existing regulations to maintain up-to-date compliance. Communicates requirements to internal Amgen functional teams. Obtains supplemental documentation from internal and external partners. Prepar es , reviews, and submits license applications and renewals. Maintains all State Licensing documentation, submissions, and interactions with State Authorities. Interfaces with State Board of Pharmacy ( BoP ) and/or Department of Health ( DoH ). Complete s required annual notifications to U.S. FDA Obtains DUNS and FEI numbers for new U . S . sites, as required Processes Financial obligations relating to fee payment. Identifies and implements process improvements for the state licensing process Coaches and supp orts junior regulatory staff s career development What we expect of you We are all different, yet we all use our unique contributions to serve patients. The successful candidate will have the following qualifications: Basic Qualifications: Doctorate degree OR Master s degree and 3 years of manufacture, QA/QC, or regulatory CMC in the Pharmaceutical/Biotechnology industry OR Bachelor s degree and 5 years of manufacture, QA/QC, or regulatory CMC in the Pharmaceutical/Biotechnology industry Preferred Qualifications: Degree in Life Science discipline Regulatory CMC specific knowledge & experience Experience in manufacture, testing (QC/QA or clinical), or distribution in Pharmaceutical/Biotech industry Working knowledge of US state and/or federal licensing requirements What you can expect of us As we work to develop treatments that take care of others, we also work to care for your professional and personal growth and well-being. From our competitive benefits to our collaborative culture, we ll support your journey every step of the way. In addition to the base salary, Amgen offers competitive and comprehensive Total Rewards Plans that are aligned with local industry standards. Apply now for a career that defies imagination Objects in your future are closer than they appear. Join us. careers.amgen.com .

Career Category Sales & Marketing Operations Job Description ABOUT AMGEN Amgen harnesses the best of biology and technology to fight the world s toughest diseases, and make people s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what s known today. ABOUT THE ROLE Role Description: The Manager will report into the Senior Manager, Patient Data Management at our Innovation Center in India. This individual will manage Amgen s patient data assets (e. g. , data generated from Patient Support Programs and Specialty Pharmacy patient data contracts) and partner with other colleagues across the globe. This includes executing solutions to compliantly connect patient data assets that will serve as the foundation for driving patient journey analytics that inform enhanced patient experiences. This position is responsible for executing cross-functional processes, SOPs (Standard Operating Procedure), and governance to ensure secure and appropriate access to these sensitive data sets. This individual will partner with Patient Access, IS, and Commercial teams and with multiple external vendors to support patient data aggregation, integration, and ongoing operations. Roles & Responsibilities: Gather data requirements for onboarding of new patient support programs, specialty pharmacy and other patient data sources Implement end-to-end data curation processes for Amgen s new and existing PSP (Patient Support Programs) and SP (Specialty Pharmacies) data sources Implement linking of first- and third-party patient data assets to enable longitudinal analytics across the patient journey (e. g. , across SPP, Hub, and Syndicated data sets) Lead all aspects of day-to-day patient data operations for multiple brands supported by this role including the daily management of data aggregation vendor activities Respond and resolve data inquiries from cross-functional stakeholders Identify data issues across data sources, ensure checks are implemented and monitor data quality Ensure compliant processing and management of patient level data assets in adherence to all Amgen Privacy and Compliance SOPs Enforce data governance for patient data assets through data access management and business approval processes Basic Qualifications and Experience: Master s degree and 4 to 6 years of data management experience OR Bachelor s degree and 8 to 10 years of relevant data management experience Proven experience in working in global teams and across time zones and cultures Proven experience in working in Product teams and delivering high quality solution in adherence with established processes Strong stakeholder management and communication skills. Excellent English oral and written communication. Functional Skills: Must-Have Skills: Experience in Data Management, Analytics, Sales and/or Marketing Operations, Value & Access, or a related field Direct experience in analyzing large data sets and translating data into information and insights Experience with data, analytics, and technology solutions (AWS/other cloud platforms, SQL, Databricks, Tableau, SAS, Python, R, etc. ) Ability to effectively translate business stakeholder requirements to IT partners to ensure high quality, timely, integrated data assets Deliver prioritized data deliverables through agile execution and continuous improvement Demonstrated self-starter, ability to work under limited supervision Strong interpersonal skills, active listening, and relationship management skills Strong vendor management skills Prior experience in executing in major data transformation projects with global teams, including core teams located in India. Good-to-Have Skills: Experience working in the life sciences commercial data domain space, ideally in the areas of Data Platforms and Patient Data. Experience working with patient level datasets including first party sources such as Patient Support Programs & Specialty Pharmacies, Syndicated Sales & Claims data sources, Digital data sources, etc. Quick learning agility to understand new concepts such as our end-to-end Commercial data flows to identify and remediate interdependencies. Understanding of the syndicated commercial data sets and use cases Worked in multinational settings with teams from different countries. Basic understanding of compliance and data privacy requirements. Familiarity with and application of Scaled Agile Framework (SAFe). Soft Skills: Exceptional collaboration and communication skills. Strong data & analytics/critical-thinking and decision-making abilities. Able to perform well in a fast-paced, changing environment. Strong oral, written, and presentation skills, with the ability to articulate complex concepts and controversial findings clearly and compellingly. .

Career Category Sales & Marketing Operations Job Description ABOUT AMGEN Amgen harnesses the best of biology and technology to fight the world s toughest diseases, and make people s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what s known today. ABOUT THE ROLE Role Description: The Patient Data Management Senior Manager will be responsible for building and growing the Patient Data Management team and capabilities, insourcing work from external vendors to drive operational excellence in our Innovation Center in India. The Sr. Manager will collaborate with other data and analytics colleagues across the organization to manage Amgen s patient data assets (e. g. data generated from Patient Support Programs and Specialty Pharmacy patient data contracts). This also includes managing solutions to compliantly connect patient data assets that will serve as the foundation for driving patient journey analytics that inform enhanced patient experiences. This position is responsible for overseeing cross-functional processes, SOPs, and governance to ensure secure and appropriate access to these sensitive data sets. Roles & Responsibilities: Collaborate with cross-functional data & analytics leads to define use cases and deliver high quality data that supports longitudinal patient journey analytics Deliver end to end data curation including aggregation, processing, integration and secure access for new and existing patient data assets, ensuring adherence to all Amgen privacy and compliance SOPs Implement patient data connectivity across Amgens first party data and third party syndicated data assets to enable longitudinal analytics across the patient journey Drive productivity and improve cycle times with automations in data processing and data quality Drive data requirements for patient data contracting with Specialty Pharmacies and Sites of Care organizations Develop guidelines and SOPs for appropriate access and usage for Patient Data, with guidance from Legal, Privacy and Compliance leads Drive standardization of data deliverables including source data layouts, reference data and reporting solutions Manage and oversee outsourced data aggregation vendor partners, ensuring adherence to compliance guidelines, processes and documentation related to processing of Patient Data Collaborate and build strong partnerships across the organization, including Commercial Analytics, Data Platforms, Data Sciences, Patient Access, Privacy, Legal, Compliance, IS, and external vendor partners Basic Qualifications and Experience: Master s degree and 8 to 10 years of data management experience OR Bachelor s degree and 10 to 14 years of relevant data management experience Proven experience in building teams, managing, and retaining talent in India. Demonstrated success in managing complex transitions. Strong leadership, stakeholder management, and communication skills. Excellent English oral and written communication. Comfortable working in global teams and across time zones and cultures. Functional Skills: Must-Have Skills: Experience in Data Management, Analytics, Sales and/or Marketing Operations, Value & Access, or a related field Experience working in the life sciences data domain space, ideally in the areas of Data Platforms and Patient Data. Expertise with relevant data, analytics, and technology solutions (AWS/other cloud platforms, SQL, Databricks, Tableau, SAS, Python, R, etc. ) Direct experience in analyzing large data sets and translating data into information and insights Excellent communication skills, including interpersonal skills to foster collaboration and success in a highly matrixed environment; strong oral/written presentation skills Strong project management skills design, lead and manage project teams in a matrixed and, at times, ambiguous environment Prior experience in partnering with Global stakeholders and managing teams on planning and execution of multi-year programs Quick learning agility to understand new concepts such as our end-to-end Commercial data flows to identify and remediate interdependencies. Alignment with best practices and a commitment to championing new and innovative methodologies and tools to enhance patient data strategies and solutions to drive business outcomes. Good-to-Have Skills: Strong expertise and experience working with patient level datasets including first party sources such as Patient Support Programs, Specialty Pharmacies, Syndicated Claims data, Digital, etc. ) Ability to effectively translate business stakeholder requirements to IT partners to ensure high quality, timely, integrated data assets Prioritize and deliver an aggressive set of data deliveries each quarter, through agile execution and continuous improvement Demonstrated self-starter, ability to work under limited supervision Strong interpersonal skills, negotiation skills, active listening, and relationship management skills Strong vendor management skills Familiarity with and application of Scaled Agile Framework (SAFe). Soft Skills: Excellent leadership and team management skills. Exceptional collaboration and communication skills. Strong data & analytics/critical-thinking and decision-making abilities. Able to perform well in a fast-paced, changing environment. Strong oral, written, and presentation skills, with the ability to articulate complex concepts and controversial findings clearly and compellingly. .

Career Category Sales & Marketing Operations Job Description ABOUT AMGEN Amgen harnesses the best of biology and technology to fight the world s toughest diseases, and make people s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of innovation, using technology and human genetic data to push beyond what s known today. ABOUT THE ROLE Role Description: Data Management Sr Mgr will be responsible for building and leading a highly talented and data-focused team in our Innovation Center in India. This individual will be responsible for building and growing the GCO Commercial Data Management team and capabilities, insourcing work from external vendors to drive operational excellence and leading transition efforts from vendors. The Sr. Manager will also oversee operations of our core commercial data platforms in partnership with the Technology team lead in India, driving cost efficiencies of the platform, and continuous innovation. The Sr. Manager will also be responsible for managing Data Management team members in India on the execution of Operations deliverables aligned across our various Data Platforms Product teams. Roles & Responsibilities: Build and Develop High-Performing Teams Hire, onboard, and develop new talent to deliver on our Customer Data & Analytics (CDNA) organizational goals and ambitions. Lead and manage the Commercial Data Platforms and Data Management team in India partnering with the Director of Commercial Data Management Partner with peers in matrixed organization and across our four pillars Master Data Management, Data Platforms, Patient Data Management, Data Acquisition & Governance to build an aligned vision for the Data Management team in India Motivate the team, delegate effectively, champion diversity within the team and act as a role model. Partner with peers & leads in the stakeholder teams in India across Secondary Analytics, Forecasting, Incentive Compensation, Field Reporting and Technology to drive prioritization and implementation of requests across our Product teams Partner with Technology teams in India and US and peers in India to establish processes for Infrastructure governance to cover costs and performance and proactively address issues and manage costs Partner with Technology teams in conducting Proof of Concepts (POCs) on new Tools and technologies and communicate results to Leadership to gain alignment for Production scaling Lead projects to implement Gen AI solutions on our Data Platform including solutions that leverage LLMs to improve Data Quality, detect anomalies in data and processes, leverage unstructured data for insights, along with lineage detection and business rule bots, etc. Engage in design discussions with peers in stakeholder organizations around building data products leveraging data from syndicated data providers like IQVIA DDD, XPO, LAAD and internal data sets like CRM data, HR and Finance data and Digital Media data to enable customer (prescriber & patient) centric datasets Instill a culture of collaboration, continuous improvement, and accountability. Identify and resolve roadblocks, process gaps, and resourcing needs as part of continuous improvement efforts. Manage Work Transition and Insourcing Develop and oversee transition plans to migrate work to our Amgen India innovation center with minimal disruption. Lead the insourcing of our operational data management services currently delivered by external vendors, ensuring appropriate knowledge transfer, risk mitigation, and operational readiness. Ensure robust documentation during transition phase to enable onboarding the team members Facilitate Cross-Team and Organizational Engagement and Alignment Partner closely with the peers in Commercial Data Strategy core pillars and the Data Management Director to contribute to delivering against our priority initiatives and establish new ways of working, especially across time zones. Partner and collaborate with peers from stakeholder functions who have an extended team in Amgen India e. g. , Incentive Compensation Sr. Manager, Field Reporting Sr Manager, Brand Analytics Sr Managers and other peers within the Data Management organization to set up Data Products for these stakeholders Work with our Technology/IT partners to establish Agile Product Teams at our Innovation Center and work effectively across other product teams in other geographies Act as a key liaison between at the Amgen India innovation center with other Customer Data & Analytics Teams to ensure alignment of goals, processes, and success measures Basic Qualifications and Experience: Master s degree and 8 to 10 years of data management experience OR Bachelor s degree and 10 to 14 years of relevant data management experience Proven experience in building teams, managing, and retaining talent in India. Demonstrated success in managing complex transitions. Strong leadership, stakeholder management, and communication skills. Excellent English oral and written communication. Comfortable working in global teams and across time zones and cultures. Functional Skills: Must-Have Skills: Prior experience and success building high-performing data management teams, with clear demonstrations of collaboration, innovation, and continuous improvement. Prior experience managing Data Platforms operations - including managing across Agile Product teams on phased execution of Platform enhancements and innovations Prior experience in leading major data transformation projects with global teams, including core teams situated in India. Prior experience leading Proof of Concept (POC) projects evaluating new technologies and scaling from POCs to production Prior experience and familiarity with future state Data Architectures and solutions including Gen AI solutions for Data Products, Data Architectures and tools to support Insight generation on Unstructured data Prior experience leading and partnering with Technology teams in data architecture design, data modelling and data flow design Prior experience using technologies such as AWS and Databricks and in managing Infrastructure costs and leading optimization efforts Prior experience in partnering with Global stakeholders and managing teams on planning and execution of multi-year Data management programs Quick learning agility to understand new concepts such as our end-to-end Commercial data flows to identify and remediate interdependencies. Collaborate with peers, India leadership team and peer teams in the USA to stay ahead of industry trends, best practices, and emerging technologies in data acquisition and build multi-year forward looking Data platform roadmaps. Alignment with best practices and a commitment to championing new and innovative methodologies and tools to enhance data strategies and solutions to drive business outcomes. Good-to-Have Skills: Experience working in the life sciences commercial data domain space, ideally in the areas of Data Platforms and Patient Data supporting Commercial stakeholders Analytics, Reporting, Decision Sciences and Forecasting Understanding of the syndicated commercial data sets including data sets like DDD, XPO, LAAD from IQVIA, CRM data sets for Call Planning, Patient Hub and Specialty Pharmacy data sets Worked in multinational settings with teams from different countries. Basic understanding of compliance and data privacy requirements. Familiarity with and application of Scaled Agile Framework (SAFe). Soft Skills: Excellent leadership and team management skills. Exceptional collaboration and communication skills. Strong data & analytics/critical-thinking and decision-making abilities. Able to perform well in a fast-paced, changing environment. Strong oral, written, and presentation skills, with the ability to articulate complex concepts and controversial findings clearly and compellingly. .

This is where your work makes a difference. At Baxter, we believe every person regardless of who they are or where they are from deserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond. Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results. Here, you will find more than just a job you will find purpose and pride. Job Summary Baxter provides a broad portfolio of essential renal and hospital products, including home, acute and in-centre dialysis; sterile IV solutions; infusion systems and devices; parenteral nutrition; surgery products and anesthetics; and pharmacy automation, software and services. The company s global footprint and the critical nature of its products and services play a key role in expanding access to healthcare in emerging and developed countries. Baxter s employees worldwide are building upon the company s rich heritage of medical breakthroughs to advance the next generation of healthcare innovations that enable patient care. You will be responsible for the development of solutions to drive product development for new and existing components of the Medication delivery portfolio. The successful candidate will possess solid hands-on technical abilities, demonstrate excitement and energy for product development, and a passion for their work and the impact it has on meeting the needs of patients. What you ll be doing Strategizing and planning Verification activities independently/along with other leads Verification and validation of Software as a system using manual and automated test methods. Creation and execution of Verification and Validation plans, including coordinating efforts of test personnel inside and outside the Design Verification and Validation group. Reviewing test procedures, test input documents and test results Defining test setups and environment required for test execution Driving Challenging verification, sampling strategy & Non-functional req. tests Documenting any design defects (product non-conformances) discovered. Interfacing with other engineering disciplines to research, correct, and close design defects. Publishing test reports, defect summary report, performing defect analysis, driving defects to closure Managing traceability from requirements to verification Ensuring that the testing abides by the business Engineering Quality Procedures (QMS), Phased Review Discipline and regulatory needs of the applicable markets Development, implementation, and documentation of verification techniques. Participation in project meetings, project reviews, and specification reviews, Sprint Planning, Release Planning, Daily Scrums Development of new test systems and tools and maintenance of existing test systems Identifying and reporting any quality or compliance concerns and taking immediate corrective actions as required Interacting with global teams to promote consistency and maximize synergy Communicating effectively & impactfully in a cross-functional, multi-cultural, global environment Participating and driving SW FMEA, dFMEA, FTA to define Risk Based Test Strategy Demonstrating Good structured approach for DSM, DBT Leading continuous improvement activities by driving the implementation of process and product quality improvement initiatives What you ll bring Bachelors or master s degree in engineering/science or equivalent At least 10+ years of experience out of which at least 2 years of experience as a Verification Lead at system-level for products that include Hardware and Software. Good knowledge of testing methodologies and processes, including manual, automated, standards and compliance testing Demonstrated skills for planning and coordinating verification and validation activities for New Product Development programs at a sub-system level. Demonstrated abilities and skills in working, influencing and communicating in a diverse global environment Demonstrated problem-solving and leadership skills Strong influential and communication skills Knowledge of medical device software development is highly preferred including knowledge of standards such as IEC 62304, ISO 14971 Desired Characteristic Experience of having led verification for large and complex programs that includes stringent regulatory requirements and demonstrated automation implementation experience Advanced ISTQB Certification Engineer with Black BELT certification will be added advantage

We are hiring For TATA 1mg For The Role Of Pharmacist , Sr. Pharmacist , Assistant Team Lead / Store Manager for Hyderabad Locations Designation: Pharmacist & Sr Pharmacists & Assistant Team Lead Role: Retail-Senior Pharmacist, Pharmacist Qualification-D Pharma, B Pharma, M Pharma What You'll Do: Oversee daily store operations and ensure smooth functioning. Drive sales performance to meet revenue targets. Lead, train, and motivate the team for exceptional customer service. Manage Inventory, stock replenishment, and merchandising. Ensure compliance with company policies and operational standards. What We're Looking For: Bachelors degree in Pharma field. Prior experience in pharmacy store management preferred, organizational, and communication skills. Ability to multitask and work efficiently under pressure. Proficiency in MS Excel and knowledge of the pharmaceutical industry. 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, Diagnostics, e-consult and offline stores. Tata 1mg has delivered over 15M ePharmacy orders, 2M 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.Img.com/aboutUs Role: Pharmacist / Senior pharmacist Industry Type: Healthcare Employment Type: Full Time, Permanent Role: Healthcare & Life Sciences-Other industry Type: Pharmaceutical & Life Sciences Department Healthcare & Life Sciences Employment Type: Full Time, Permanent Role Category: Healthcare & Life Sciences-Other Education UG: B.Pharma in Pharmacy PG: M.Pharma in Pharmacy Role: Retail Operations Manager industry Type: Pharmaceutical & Life Sciences Department: Merchandising. Retail & eCommerce Employment Type: Full Time, Permanent Role Category: Retail Store Operations Education Doctorate: Ph.D/Doctorate in Medicine, Pharmacy

Designation : Pharmacist , Sr. pharmacist , Assistant team lead Role: Retail - Store Manager Department : B&M Retail Location : Bengaluru What You'll Do: Oversee daily store operations and ensure smooth functioning. Drive sales performance to meet revenue targets. Lead, train, and motivate the team for exceptional customer service. Manage inventory, stock replenishment, and merchandising. Ensure compliance with company policies and operational standards. What Were Looking For : Bachelors degree in medical field OR Prior experience in pharmacy store management preferred. Strong leadership, organizational, and communication skills. Ability to multitask and work efficiently under pressure. Proficiency in MS Excel and knowledge of the pharmaceutical industry. 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 Mail:- anshi.gupta@1mg.com Department : Pharmaceutical & Life Sciences Type: Full Time, Permanent Role Category: Retail Store Operations Education : Graduation

Exciting Opportunity for Non-Certified Freshers in Medical Coding! Are you a recent graduate eager to kickstart your career in the medical coding field? CorroHealth is looking for enthusiastic individuals to join our team as Trainee - Coding services. "NO VIRTUAL Only WALK-IN INTERVIEW" Eligibility Criteria: Non-Certified Candidates Only. - Qualifications: 1) B Pharm/ M Pharm. 2) BE/ME Biotechnology 3) BE/ME Bio Medical Science 4) Bsc/Msc Microbiology 5) Bsc/Msc Biotechnology 6) Bsc/Msc Applied Biology 7) Bsc/Msc Bioinformatics 8) Bsc/Msc Nursing 9) BPT/BOT - Passing Year: 2024 or 2025 - Academic Requirement: Above 60% in 10th, 12th & Graduation without any arrears or backlogs Documents Required: - Updated Resume - Government-issued ID proof Only Candidate Who are interested to come for a walk-in Contact me For registration, call Sushil- 9043979492 or Mention "Sushil " on top of your resume. Only direct walk-ins are accepted. Join us at CorroHealth and take the first step towards a fulfilling career in healthcare. We can't wait to meet you and discuss the exciting opportunities awaiting you!

Roles and Responsibilities Provide expert advice on medication use, potential side effects, and drug interactions to patients. Dispense medications accurately and efficiently according to prescriptions. Maintain accurate records of patient consultations, medication dispensed, and inventory management. Collaborate with healthcare professionals to develop treatment plans for patients. Ensure compliance with pharmacy policies and regulatory requirements.

Promote excellence in teaching, learning, and research within the department Supervise undergraduate and postgraduate teaching programs Oversee daily operations Guide PhD scholars Prepare and manage budget Manage and evaluate academic programs Required Candidate profile Ph.D. in Pharmacy Minimum 8 years of teaching/research experience