2389 Pharmacy Jobs - Page 3

Position Summary: As a Business Development Executive for Apollo tez, you will be responsible for identifying, onboarding, and managing Doctor Chambers, Resident Welfare Associations (RWAs), and Corporates to set up the Apollo tez kisok. You will lead growth efforts in your region while ensuring an excellent experience for all stakeholders. Minimum Requirements: 2 to 4 years of experience in Business Development (Healthcare experience preferred) Proficiency in the local language is mandatory Strong communication and interpersonal skills Age should be less than 35 yrs. Should be local based out of same state and speaking local language fluently. Should have experience in filed sales, meeting doctors and healthcare professionals Current location should be same as job location, relocation candidates please avoid. Roles & Responsibilities: 1. Lead Generation & Partner Acquisition: Scout and empanel Doctor Chambers, RWAs, and Corporates for the Apollo tez model 2. Target Ownership: Meet or exceed monthly onboarding and revenue targets for your assigned territory 3. Cross-functional Collaboration: Coordinate with internal teams and regional staff for seamless partner activation 4. Relationship Management: Build and maintain strong relationships with tez partners and Ensure a consistent and high-quality experience for all stakeholders 5. Service Activation & Enablement: Set up DocVerse services and ensure partner teams are fully equipped and Guide partners through infrastructure setup and operational onboarding 6. Training & Development: Organize regular training sessions for partners and their staff on all digital tools and pharmacy processes 7. Issue Management: Adhere to the escalation matrix to resolve any stakeholder issues swiftly and effectively

Zepto is hiring! Join the Zepto Team as a Pharmacist! We are seeking dedicated and knowledgeable Pharmacists to join our team! If you are passionate about patient care and enjoy working in a collaborative environment, we want to hear from you. Job Opportunity: Pharmacist Key Responsibilities: 1. Dispense medications accurately and provide patient counselling. 2. Collaborate with healthcare professionals to optimize medication therapy. 3. Maintain accurate records and ensure compliance with regulations. Qualications: 1. Bachelor or a Diploma of Pharmacy (B or D Pharm.) degree. 2. Active license. 3. Strong communication and interpersonal skills. Why Join Us? 1. Competitive salary and benets. 2. Opportunities for professional development. 3. Supportive and dynamic work environment. Location : Mumbai, Bengaluru, Delhi, Chennai and Hyderabad.

Role & responsibilities 1. Before Administration, Medication review and clinical audits on the floor. 2. Transcription / Indenting of drug and non-drug orders. 3. Responsible for medication tracking and receiving from pharmacy. 4. Auditing all the in-patient orders for drug name, strength, formulation, dosage and duration of therapy, therapeutic duplication and to check for possible drug interaction, if any as per hospital protocols. 5. Checking the Medication Administration Records in the ward and rectification of any medication error observed. 6. For clarification check the patient record at the ward / ICU discuss with Clinical Pharmacologist. 7. In case any non-formulary drugs are indented inform to the concerned doctor and substitute it with the drugs given in the formulary. 8. Responsible for checking the drugs in impress stock, crash cart, disaster kits and ambulance regularly. 9. Responsible for documentation of restricted antibiotics and report it to Clinical Pharmacologist. 10. Monitoring of adverse drug reaction. 11. Drug information resource. 12. Any other duties assigned by Reporting Manager. Preferred candidate profile * Registration is Mandatory * Qualification Required - B Pharm/M Pharm / Pharm D

Pharmacist / Production Chemist / QC Analyst / Medical Representative For further information, please call -7026629008 / 8050011327

Job Description: Pharmacists will be responsible for processing orders in the store, handling both pharmaceutical and non-pharmaceutical items. Their primary tasks include accurately selecting products from storage, preparing orders for shipment, and ensuring all items are handled with care to prevent damage. Additionally, they will ensure inbound, and inventory audits are performed in line with the company's standard operating procedures. Key Responsibilities: Inbound Responsibilities: Quality Control (QC): Ensure all received products meet quality standards. Goods Receipt Note (GRN): Verify and document all incoming products. Putaway (Storage): Store products in their designated locations correctly, for both pharmaceutical and non-pharmaceutical items. Outbound Responsibilities: Picking: Accurately and efficiently pick products from designated storage areas based on order sheets or pick tickets. Packing: Securely pack orders to prevent damage during transit. Dispatch: Ensure the timely and accurate dispatch of all products to customers. Inventory Management Responsibilities: Cycle Count (CC): Regularly perform stock counts to maintain accurate inventory records. Damaged/Expired Goods (DEQ): Identify, manage, and document any damaged or expired products. Returned Items: Document and track returned items, ensuring accurate processing and proper storage as per the SOPs. Desired Candidate Profile: Must be 18 years or older. A pharmaceutical degree (D. Pharm or B.Pharm) is mandatory. Ability to thrive in a fast-paced environment. Willingness to work in rotational shifts. Willing to handle both pharmaceutical and non-pharmaceutical operations. Commitment to adhering to store rules and regulations. Open to contract-based opportunities with flexibility and commitment to project success. Service Continuity Requirements: Submission of a valid pharmacy license for operational purposes. Successful completion of background verification (Green status).

Roles and Responsibilities * Dispense medications to patients according to prescriptions and provide guidance on usage. * Maintain accurate records of patient information, medication dispensed, and any issues that may arise. * Collaborate with healthcare providers to resolve medication-related issues and ensure optimal patient care. * Ensure compliance with pharmacy policies, regulations, and industry standards.

Hi, We are hiring for Auth profile- Healthcare process - Non voice B Pharma/M Pharma with 1 yr authorization exp can apply Salary upto 5.80 LPA 24*7 Shifts 5 Days working Gurgaon Call/Whatsapp Vishu@9810359162 Perks and benefits Both side cabs PF/ESI

Dindayal Industries Limited, under the esteemed brand DINDAYAL AYURVEDA , is a leading organization in Ayurvedic Medicines, FMCG, and OTC Products , dedicated to delivering high-quality, natural health solutions. With a legacy built on trust and innovation, we continue to enhance wellness through our diversified product portfolio. Position: Production Manager Classical Ayurvedic Medicines Department: Manufacturing / Production Location: Ajmer & Bharatpur, Rajasthan Job Description: We are seeking an Ayurveda professional with hands-on experience in manufacturing classical Ayurvedic formulations including Asava–Arishta, Avaleha, Syrup, Churna, Rasavati, Guggulu, Swarna Yog, Ghrita, Taila, and related products. The candidate should have strong process knowledge, raw material understanding, and expertise in ensuring compliance with GMP and Ayurvedic pharmacopeial standards. Key Responsibilities: Having good knowledge of Drugs & Cosmetic Act , Licensing process, Labelling Protocols etc. Supervise production of classical Ayurvedic medicines in line with authentic procedures Ensure raw material selection, processing, and standardization as per classical texts Oversee formulation processes for Asava–Arishta, Avaleha, Syrup, Churna, Rasa Vati, Guggulu, Swarna Yog, Ghrita, Taila, etc. Monitor in-process quality checks and maintain compliance with GMP standards Collaborate with Quality Control and R&D teams for consistency and innovation Prepare and maintain production documentation as per regulatory requirements Key Requirements: Education: M.Pharm (Ayurveda) Experience: Minimum 3 years in Ayurvedic manufacturing/production Expertise in preparation of classical dosage forms (liquid, semi-solid, powder, and medicated oils/ghritas) Knowledge of raw materials, pharmacopeial standards, and traditional Ayurvedic formulations Employment Type: Full Time Compensation: As per industry standards How to Apply: Interested candidates may apply directly send their updated CV to hr@dindayalgroup.com

Dindayal Industries Limited, under the esteemed brand DINDAYAL AYURVEDA , is a leading organization in Ayurvedic Medicines and OTC Products , dedicated to delivering high-quality, natural health solutions. With a legacy built on trust and innovation, we continue to enhance wellness through our diversified product portfolio. Position: Manufacturing Chemist Ras Shastra Department: Manufacturing Location: Bharatpur, Rajasthan Job Description: We are looking for an Ayurveda professional specializing in Ras Shastra for our manufacturing units. The candidate should have hands-on experience in Bhasma-Pishti , Kupi pakwa rasayana , with strong knowledge of Ayurvedic formulations and production protocols. Key Responsibilities: Lead and oversee manufacturing of Bhasma-Pishti , Kupi pakwa rasayana . Ensure quality evaluation, sourcing, and utilization of raw materials Supervise formulation processes as per classical Ayurvedic texts and GMP standards Collaborate with R&D and Quality teams for new product development and standardization Maintain compliance with all statutory and regulatory requirements in Ayurvedic manufacturing Key Requirements: Education: MD (Ayurveda) Ras Shastra specialization Experience: Minimum 3 years in Ayurvedic manufacturing/production Proven expertise in medicated oils, Bhasma-Pishti , Kupi pakwa rasayana,. Knowledge of production planning, process compliance, and quality assurance Employment Type: Full Time Experience Level: Mid-Senior Level Compensation: As per industry standards How to Apply: Interested candidates may apply directly send their updated CV to hr@dindayalgroup.com

Assist in reviewing medical records and documentation for accuracy and completeness. Learn to assign appropriate ICD-10, CPT, and HCPCS codes under supervision. Support the coding team in maintaining compliance with healthcare regulations and guidelines. Participate in training programs and workshops to build coding knowledge and skills. Ensure confidentiality and security of patient health information. Collaborate with senior coders, auditors, and healthcare staff to clarify documentation. Maintain productivity and quality standards as per organizational requirements.

About Us :- Indira IVF centre is the pioneer in providing affordable yet creditable infertility curation to the common people for the first time in India. It is armed with the state-of-the-art infrastructure, advanced equipments and a pool of renowned physicians. We started with a two room clinic back in 1988 and today we stand tall as one of the most esteemed and prestigious IVF service providers in the country and beyond. 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. Only immediate joiners apply for the role Interested candidates can share their profile on manali.yadav@indiraivf.in

Dindayal Industries Limited, under the esteemed brand DINDAYAL AYURVEDA , is a leading organization in Ayurvedic Medicines, FMCG, and OTC Products , dedicated to delivering high-quality, natural health solutions. With a legacy built on trust and innovation, we continue to enhance wellness through our diversified product portfolio. Position: Manufacturing Chemist Panchkarma Specialist Department: Manufacturing Location: Bharatpur, Rajasthan Job Description: We are looking for an Ayurveda professional specializing in Panchkarma Specialist for our manufacturing units. The candidate should have hands-on experience in medicated oils and Panchkarma oils , with strong knowledge of Ayurvedic formulations and production protocols. Key Responsibilities: Lead and oversee manufacturing of Medicinal Oils, Ointments, Panchkarma Oils , Panchkarma churna, Kwath & other products. Ensure quality evaluation, sourcing, and utilization of raw materials Supervise formulation processes as per classical Ayurvedic texts and GMP standards Collaborate with R&D and Quality teams for new product development and standardization Maintain compliance with all statutory and regulatory requirements in Ayurvedic manufacturing Key Requirements: Education: MD (Ayurveda) – Panchkarma specialization Experience: Minimum 3 years in Ayurvedic manufacturing/production Proven expertise in Medicinal Oils, Ointments, Panchkarma Oils , Panchkarma churna, Kwath & other products Knowledge of production planning, process compliance, and quality assurance Employment Type: Full Time Experience Level: Mid-Senior Level Compensation: As per industry standards How to Apply: Interested candidates may apply directly send their updated CV to hr@dindayalgroup.com

HIRING ALERT | CUSTOMER SERVICE SPECIALIST US HEALTHCARE (NIGHT SHIFT) Role: Customer Service Specialist US Healthcare Location: Airoli, Navi Mumbai (Work from Office) Shift: Night Shift | 5 Days Working We are looking for smart professionals with excellent communication skills and a great attitude to deliver outstanding customer experiences! Your Impact Handle inbound & outbound customer calls Deliver timely and accurate resolutions at high productivity Build client & domain knowledge for first-call resolution Ensure adherence to SLAs CSAT, Handle Time, Customer Effort Maintain quality & compliance standards Document queries/issues and follow up effectively Support operational improvements Eligibility Graduates in B.Com, B.A, BBA, BSc, BPharma Not Eligible: BTech, MTech, MCA, BCA, MBA, Hotel Mgmt., or other specialized/technical streams Excellent English communication skills mandatory Basic MS Office skills required Flexible to work in rotational shifts Compensation & Benefits CTC: 2.40 LPA + 3,000 Incentives + 3,000 Night Allowance 10-Day Virtual Training Defined career growth roadmap Performance-based incentives Talent development & skill enhancement programs 5-day workweek for work-life balance Collaborative & engaging work culture Insurance benefits Apply Now & Kickstart Your Career in US Healthcare! HR Contacts: Tabitha : 95142 73632 Afreen : 62060 77869

Job Summary Roles & Responsibilities Review and approval of all analytical test data of Quality control. Review and usage decision of analytical reports in LIMS, Empower and SAP. Electronic signatures level-2 for chromatography data station (CDS) and standalone instruments. Review the Analytical test report in LIMS. Review the reported results against specification and trends. Review the method validation and method transfer documents. Review the instrument calibrations and working standard qualification records. Handling the Incidents/ Deviations, Out of Trends, Out of Specification including investigations, Corrective and Preventive actions follow up and closure. Monitoring of analytical activities in Quality control laboratory. Verification of Specifications/standard test Procedures/Worksheets/Analytical Reports before Approval. Verification and review of the audit trails for Standalone, Empower and LIMS. Ensure cGMP / cGLP compliance. To follow Safety, Health and Environmental procedures and practices. Review and approval of excel sheet validations. Review results acceptance for API and Excipients and Packing material. Review of compiled of Stability Data and its verification/ Exhibit batch sampling protocols. Handling of Robotic Process Automation of Chromatography Data review (RPACD) To carry any other activities assigned by upward reporting staff. Qualification Educational qualification: A Bachelor’s/Master's degree in Pharmacy, Chemistry, Chemical Engineering, or a related field Minimum work experience : 3 to 7 years of experience in QC or AQA department is mandatory. Additional Information About the Department Global Manufacturing Organisation (GMO) At Dr. Reddy's Laboratories, we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence, we are a leading force in the pharmaceutical industry. We operate 19 state-of-the-art manufacturing plants across Hyderabad, Vizag, Baddi, Mexico, Shreveport, and Mirfield, comprising 8 OSD facilities, 3 Injectables facilities, and 8 API facilities. Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1,150+ drug master files across key therapy areas such as Oncology, Cardio-vascular, Central Nervous System and Anti-Diabetes. he World Economic Forum has recognised our largest manufacturing facility in Bachupally, Hyderabad, as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive, meeting business imperatives, and meeting our ambitious ESG goals. Building such ‘factories of the future’ is integral to innovation and to build healthcare of the future. Benefits Offered At Dr. Reddy’s we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddy’s are on par with the best industry standards. They include, among other things and other essential equipment, joining & relocation support, family support (Maternity & Paternity benefits), learning and development opportunities, medical coverage for yourself and your family, life coverage for yourself. Our Work Culture Ask any employee at Dr. Reddy’s why they come to work every day and they’ll say, because Good Health Can’t Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and we’re always attuned to the new and the next to empower people to stay fit. And to do this, we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system, they can make magic. For more details, please visit our career website at https://careers.drreddys.com/#!/

Designation : Pharmacist , Sr. pharmacist , Assistant team lead Role: Retail - Store Manager Department : B&M Retail Location : Banglore 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 e-Pharmacy, eDiagnostics, e-consult and offline stores, Tata 1mg has delivered over 15 M 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 Mail:- anshi.gupta@1mg.com Department : Pharmaceutical & Life Sciences Type: Full Time, Permanent Role Category: Retail Store Operations Education : Graduation

Dispense prescribed medications accurately, including eye drops, ointments, and ophthalmic tablets. Provide proper instructions to patients on dosage, usage, and storage of medications. Maintain up-to-date knowledge of ophthalmic drugs, surgical packs, and post-operative medications. Manage and monitor inventory levels, placing timely orders to avoid stockouts. Ensure proper storage of medicines as per guidelines (e.g., cold chain maintenance). Check for expired or near-expiry stock and dispose of them as per protocol. Cross-check prescriptions for accuracy and report any discrepancies to doctors. Maintain daily sales and stock registers as per hospital and regulatory norms. Support the surgical team with timely availability of OT medicines and consumables. Ensure compliance with NABH, pharmacy rules, and drug control regulations. Assist in audits, quality checks, and maintaining pharmacy documentation.

ASG Eye Hospitals is a chain of super specialty eye hospitals in India. It offers a comprehensive range of eye care services including treatment and surgeries of Retina, Cataract, Squint, Oculoplasty, Cornea, Lasik, ICL, Glaucoma, and Paediatric Ophthalmology. Currently, the group has 165+ Eye Hospitals across 83+ cities in India. Role - Executive - Pharmacist Location - Puducherry Job Responsibilities Provide advice about health issues, symptoms and medications in response to customer enquiries. Process prescriptions and dispense correct medication. Ordering, selling and controlling medicines and other stock. Manage inventory to ensure an adequate supply of medications. Managing budgets Keeping statistical and financial records Preparing publicity materials and displays Counsel patients on proper medication and side effects. Desired Candidate Profile D.Pharm / B.Pharm Must be a registered Pharmacist from the (Pondicherry)State Pharmacy Council . Good Communication Skills. Must have Basic computer knowledge.

As a Clinical Safety Coordinator at our Clinical Safety department in India, you will be responsible for handling and processing adverse events from various sources, including clinical trials and post marketing surveillance. Your key responsibilities will include: - Determining the plan of action for incoming calls; - Collecting, processing, and tracking incoming adverse and serious adverse events; - Writing safety narratives; - Reporting on various safety data; - Collaborating with internal departments and investigative clinical research sites to ensure compliance with safety processes. To qualify for this role, you should have: - A Bachelor's degree in a Healthcare related field such as Nursing, Pharmacy, or Pharmacology; - Clinical experience or Clinical Research, case processing, and Post marketing Pharmacovigilance experience preferred; - Proficient English language skills; - Proficient knowledge of Microsoft Office tools; - Broad knowledge of medical terminology; - Strong organizational and communication skills. About Medpace: Medpace is a full-service clinical contract research organization (CRO) offering Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, and employing more than 5,000 people across 40+ countries, we aim to accelerate the global development of safe and effective medical therapeutics. We specialize in various therapeutic areas including oncology, cardiology, metabolic disease, and more, leveraging local regulatory and therapeutic expertise. Why Medpace: Joining Medpace means being part of a team that makes a difference every day. Our work positively impacts the lives of patients and families across various therapeutic areas. We offer a flexible work environment, competitive compensation and benefits package, structured career paths, employee appreciation events, and health and wellness initiatives. Medpace Perks: - Flexible work environment - Competitive compensation and benefits package - Competitive PTO packages - Structured career paths with opportunities for professional growth - Company-sponsored employee appreciation events - Employee health and wellness initiatives Awards and Recognition: - Forbes recognition as one of America's Most Successful Midsize Companies in 2021, 2022, 2023, and 2024 - CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility Next Steps: If your qualifications match our requirements, a Medpace team member will reach out to you with details on the next steps.,

Role & responsibilities Job Description Position: Medical Coding Trainee CT : HR Priya R 9600 450 980 Job Description: Position: Medical Coder Medical coding is the process of translating patient health information, such as diagnoses, procedures, and medical services, into universal alphanumeric codes. These codes are then used for medical billing, research, health statistics, and to track patient outcomes. Key coding systems include the International Classification of Diseases (ICD) for diagnoses, and Current Procedural Terminology (CPT) codes for services and procedures. . Eligibility: All (UG/PG) Paramedical Graduates: Bsc/Msc (Nursing/DGNM0 Pharmacy (B.Pharm M.Pharm Pharm. D) Physiotherapy- (BPT, MPT) B.D.S M.D.S All (UG/PG) Life Science Graduates: Microbiology Biotechnology Biochemistry Zoology and Advanced zoology Biology Botany Medical Biochemistry Plant biotechnology Medical Microbiology (UG/PG) Allied Health Science Graduates: Physician assistant Critical Care Technology Medical Lab Technician Operation Theatre & Anaesthesia Technology Radiology & Imaging Technology Accident & Emergency Care Technology Audiology & speech Language Pathology Cardiac Technology Cardio Pulmonary Perfusion Care Technology Medical Record Science Dialysis Technology Neuro Electrophysiology Optometry Technology Respiratory Therapy (UG/PG) B.E or B.Tech Graduates: Biomedical Engineering Biotechnology Perks & Benefits : 5-Day Work Week Enjoy a consistent (Monday to Friday) schedule Fixed weekends off Saturday & Sunday) Fixed Day Shifts ( work only during daytime hours. Free Meals & Transportation Company-provided food and cab facilities for your convenience. Performance Incentives Additional earnings based on your individual performance. Attractive Starting Salary Salary ranges from 14,000 to 18,000, Gross with a hike after 6 months based on your individual performance Healthcare Coverage: Company covers medical expenses for your well-being. Provident Fund Contribution: Build your savings with company-supported PF benefits. Job Location: Chennai, Coimbatore, Trichy, Vellore, Cuddalore, Pondy Salem, Erode, Namakkal, Thanjavur, Nagercoil, Theni, Dindokal Villupuram, Karur, Tirunelveli, Kanniyakumari, Other Tamilnadu, Bangalore, Hyderabad Kerala, AP, Telangana Reach us : HR Priya .R 9600 450 980 job@omshealthcare.in , www.omshealthcare.in

Role Overview: As a Senior Clinical Research professional at Ascentrik Research Pvt. Ltd, you will be responsible for leading and managing a research team to curate accurate, timely, insightful, and comprehensive data and intelligence for Beacon Targeted Therapies. You will work closely with UK-based clients, analyze relevant information, and ensure project deliverables are met. Additionally, you will be part of a global network of life science researchers, focusing on dynamic products in cutting-edge life science areas. Key Responsibilities: - Lead and manage a research team to curate accurate, timely, insightful, and comprehensive data and intelligence - Identify and analyze the most relevant information for Beacon and its users - Coordinate with UK-based clients to understand and meet project deliverables - Manage activities towards the launch of a beacon module and provide support post-launch - Perform data management activities efficiently - Generate queries to clarify and improve data quality - Demonstrate a strong understanding of Clinical Trials and preclinical data Qualification Required: - Masters in Pharmacy (except Pharmacognosy)/Biology/Bio-Technology/Bio-Chemistry/Pharm D with minimum 2-3+ years of relevant experience - Bachelors in Pharmacy (except Pharmacognosy)/Biology/Bio-Technology/Bio-Chemistry with at least 4 years of relevant experience - Candidates with additional Clinical research diploma or relevant courses can apply - Basic computer skills, Microsoft Office & detailed Internet Knowledge - One research paper published - Ability to work in a high-pressure, deadline-driven environment - Exceptional communication and reporting skills Additional Company Details: Ascentrik Research Pvt. Ltd is a premier Research & Data Service Provider that serves Top Fortune 500 Companies and multinational companies across various industries. The company specializes in customized Research Services, providing actionable insights and quality data to clients. With offices in Pune, Navi Mumbai, and Noida, Ascentrik Research Pvt. Ltd is committed to growing its workforce and expanding its services further.,

As a Regulatory Executive within the D3I department in Bangalore at L'Oral, your role is crucial for ensuring compliance and strategic management of raw material dossiers for innovative beauty products. Your responsibilities include: - **Regulatory Intelligence & Compliance:** Stay updated on global and local regulations, guidelines, and best practices related to raw material dossier management. - **Dossier Management:** Take ownership of assigned raw material regulatory topics, meticulously building and managing comprehensive raw material dossiers to meet specific regulatory scopes and requirements. - **Stakeholder Management:** Effectively manage relationships with internal teams and external partners to gather necessary data and ensure timely dossier completion. - **Process Optimization:** Identify and implement opportunities to enhance dossier management workflows, improve efficiency, and refine document control processes. - **Quality Assurance:** Conduct quality checks on all dossiers to ensure accuracy, completeness, and compliance with relevant regulations. To excel in this position, you should have: - **Education:** Master's degree in Chemistry, Pharmacy, or Chemical Engineering. - **Experience:** Minimum of 1 year of professional experience in regulatory affairs, dossier management, or a related field. - **Technical Skills:** Ability to analyze and manage large datasets, proficiency in Microsoft Office Suite, critical assessment skills for dossier preparation. - **Soft Skills & Competencies:** Excellent communication, interpersonal skills, stakeholder management capabilities, self-motivation, and a proactive mindset. Joining L'Oral as a Regulatory Executive offers you the chance to: - **Be at the Forefront of Beauty Innovation:** Contribute to L'Oral"s legacy of blending science with beauty and inventing safe, sustainable, and responsible beauty products. - **Drive Global Impact with Innovative Ingredients:** Ensure cutting-edge raw materials meet regulatory standards, impacting the launch of new products globally. - **Lead Process Improvement & Efficiency:** Actively identify opportunities to enhance workflows, leaving a tangible impact on efficiency. - **Grow in a Culture of Continuous Learning:** Dare to challenge yourself, acquire new skills in a dynamic and supportive environment. - **Be Part of a Diverse & Inclusive Team:** Work in an environment that fosters growth and thrives on differences. (Note: The additional details about the company were omitted as they were not explicitly mentioned in the job description.),

As a part of Apollo Hospitals, a leading healthcare provider in India, you will be contributing to delivering exceptional care with compassion to our patients. Renowned for our state-of-the-art medical facilities and advanced technology, we are committed to ensuring patient satisfaction through quality care. Our organization offers comprehensive healthcare services across various specialties, equipped with cutting-edge technology, modern infrastructure, and a skilled team of healthcare professionals. Key Responsibilities: - Provide patient-centric care and prioritize patient satisfaction - Collaborate with a team of doctors, nurses, and support staff to deliver high standards of healthcare - Offer a wide range of medical services from primary care to specialized treatments - Emphasize preventive care and wellness programs to promote a healthy lifestyle - Participate in research and development activities to remain at the forefront of medical advancements Qualifications Required: - Senior Secondary (11th & 12th) education level - Full-time job schedule - Location: Plot No.1A, Ahmedabad, Gujarat, 382428, IN As part of our team at Apollo Hospitals, you will have the opportunity to embody our values of patient-centric care, teamwork, integrity, and compassion. Together, we can make a significant impact on the lives of our patients and contribute to the progress of healthcare in our community. We look forward to collaborating with you and utilizing your skills and expertise to deliver exceptional care and service to our patients. If you have any inquiries or wish to learn more about Apollo Hospitals, feel free to reach out to our team. Thank you for choosing to join the Apollo Hospitals family. We are excited to embark on this journey together towards excellence in healthcare. Sincerely, Team HR,

- Candidates with experience in managing civil works at Retail Pharma Chains - Role involves vendor co-ordination, cost estimation, installation & timely store handover. - Mandatory experience in Pharma retail chain like Apollo, Medplus, etc.

Role & responsibilities Managing Store for Retail and Wholesale Orders Managing Stock Managing shipment orders Preferred candidate profile Proficiency with Marg Software is required Min. 1 years of experience Must have KSPC registration.

Dispense prescription medications accurately and provide appropriate counseling to patients Collaborate with healthcare professionals to ensure comprehensive patient care Review and interpret prescription orders to verify accuracy and appropriateness