2398 Pharmacy Jobs - Page 29

Seeking a driven Pharma IT Sales Executive to lead growth in pharma/life sciences. Must excel in consultative sales, positioning validation, compliance, audits. Engage CXOs, QA, IT heads with trusted, value-driven solutions. Regulatory standards

Responsibilities Serve as an SME in CSV processes and best practices Develop and execute validation protocols (IQ/OQ/PQ) for computer systems, software applications, and automated processes. Create validation plans, test scripts, and summary reports. Ensure all computer systems comply with FDA regulations, GxP guidelines, and other relevant industry standards (e.g., 21 CFR Part 11). Provide training to staff on CSV processes and regulatory requirements Stay updated on industry best practices, regulatory changes, and advancements in technology related to CSV. Identify opportunities for improving validation processes and procedures. Perform Change Impact Assessments, Risk Assessments, Periodic Reviews . NOTE: Experience in IT Systems Validation is a must. Specifically experience with LMS(Learning Management System) is must. Preferred candidate profile 5-6 years of overall experience in computer system validation within the pharmaceutical, biotech, or medical device industry. Experience with validation of IT Systems(LMS). Knowledge in process required for GxP and Non-GxP systems/features. Strong knowledge of FDA regulations, GxP guidelines, and industry standards (e.g., 21 CFR Part 11, GAMP 5). Experience working with cross function teams. Proficiency in developing and executing validation protocols and related documentation. Proficient in using validation tools and software. Strong written and verbal communication skills. Education and Trainings Bachelors degree in Biotechnology, Pharmacy, Computer Science, Engineering, Life Sciences, or a related field. Advanced degrees or certifications in validation, quality assurance, or regulatory compliance are a plus.

RG Stone Clinic - Faridabad - Urology is looking for Pharmacist to join our dynamic team and embark on a rewarding career journey. Compounding and dispensing medications, as prescribed by physicians. Monitoring customers drug therapies, advising interventions, and informing customers of any potential side effects. Instructing customers on how and when to take prescribed medications. Conducting health and wellness screenings. Providing immunizations, and other medical services, such as taking blood pressure, temperature measurements, and checking blood sugar levels. Keeping accurate customer records. Ensuring a safe and clean working environment. Completing operational requirements of the pharmacy, including verifying order entries, maintaining records of controlled substances, charges, and removing expired and/or damaged drugs from the pharmacys inventory. Adhering to applicable legal rules, regulations, and procedures governing pharmaceutical practice. Performing other administrative tasks when needed.

Position Summary... What youll do... About Team: The Digital Pharmacy Team is at the forefront of transforming how pharmacy services are delivered, leveraging technology to enhance access, improve medication adherence, and streamline pharmacy operations. Our mission is to create a seamless, patient-centric digital experience that bridges the gap between clinical care and medication management. What you will do: As a Software Engineer III for Walmart, youll have the opportunity to: Develop intuitive software that meets and exceeds the needs of the customer and the company. You also get to collaborate with team members to develop best practices and requirements for the software. In this role it would be important for you to professionally maintain all codes and create updates regularly to address the customers and companys concerns. You will show your skills in analyzing and testing programs/products before formal launch to ensure flawless performance. Troubleshooting coding problems quickly and efficiently will offer you a chance to grow your skills in a high-pace, high-impact environment. Software security is of prime importance and by developing programs that monitor sharing of private information, you will be able to add tremendous credibility to your work. You will also be required to seek ways to improve the software and its effectiveness. Adhere to Company policies, procedures, mission, values, and standards of ethics and integrity What you will bring: B.E./B.Tech/MS/MCA in Computer Science or related technical field. Minimum 3 years of object-oriented programming experience using Java. Excellent computer systems fundamentals, DS/Algorithms and problem solving skills. Excellent organisation, communication and interpersonal skills. Large scale distributed services experience, including scalability and fault tolerance. Exposure to cloud infrastructure, such as Azure, GCP, or AWS Exposure to build, CI/CD ; deployment pipelines and related technologies like Kubernetes, Docker, Jenkins etc. A continuous drive to explore, improve, enhance, automate and optimize systems and tools. Experience in systems design and distributed systems. Exposure to SQL/NoSQL data stores like Cassandra, Elastic, Mongo etc.

Division Department Sub Department 1 Job Purpose Submit product documents to regulatory authorities in accordance with country specific regulatory requirements to ensure approvals and market launch in stipulated time and handle post-approval changes, maintenance, and updation of documents during the products life-cycle Key Accountabilities (1/6) Achieve timely submission of dossier/DMF and deficiency responses to regulatory authority by reviewing, collating, and compiling documents in order to ensure approvals for launch in stipulated time Co-ordinate with cross-functional teams and external stake-holders for query response discussion and distribute updated work plan *Create DMF master in LoA software & issue LoAs/CEPs Verify pre-approved documents Leverage product gap analysis #Preparation compilation and submission of the dossier documents / deficiency responses to agency as per the region specific requirements(for Para-IV -US) Preparation of M1 documents, and collate the dossier/ deficiency responses package/DMF received from CDT and submit to the regulatory authority/customer Submit online audit dossier/DMF along with queries Key Accountabilities (2/6) Submit post approval variations for changes that improves productivity, cost-effectiveness, quality of the product by reviewing, collating, compiling the variation application to meet the delivery within timelines and maintain Product Marketing Authorization, Renewals/Sunset clause to ensure continuous validity of marketing authorisations. Verify pre-approved documents/variation packages as received from LCM Prepare M1 documents, and collate variation packages and annual report packages received from LCM team and submit to the regulatory authority/customer Check for the MA business interest from stakeholders and progress with the renewal/ sunset clause filing Prepare labelling submission package to be in-line with RLD labelling updates and submit to the authority Prepare SPL and Drug listing for customer/launch products Key Accountabilities (3/6) Maintain, and update product dossier as required to meet changes in Cipla s internal systems, changes in regulatory guidelines, and to meet the need of regulatory requirements Review DMF and resolve discrepancies (if any) in co-ordination with CFTs Evaluate proposals related to changes (Facility change con/Notifications) and conveying line of action to manufacturing unit/relevant stakeholders. Update the database (PRC/SAP-RA/ table) associated with product dossier approvals by including registration details in database. *Attend launch meetings with internal and external stake-holders *Updating tracker for DMF number assigned by Regulatory Health Agencies and maintain the relevant data base (LOA software) upto date Notify cross-functional teams and external stake-holders about the approvals and approved documents Include and update registration details in databases (PRC/SAP-RA table/) # Provide details for APQR compilation Key Accountabilities (4/6) Provide Regulatory support throughout the life cycle of the product for smooth functioning Provide the approved product information (labelling) and the relevant documents as requested by the drug safety or quality teams Confirm product list and MA details for finalization of TA Provide the information on the suitability and availability of dossier for out-licensing and in-licensing Check the dossier information for due-diligence Perform drug listing and review labelling Key Accountabilities (5/6) Check with regulatory authorities (EU, NZ & TGA) for submission activity and approval status for submission done Check with authorities for safe receipt of submitted DMF/documents as and when required Communicate to authorities for regulatory support/data requirement to get approvals Maintaining the acknowledgement letters/deficiency letters received from Regulatory Health Agency Key Accountabilities (6/6) Major Challenges Delay in the availability of the documents from cross functional teams - leads to inadherence to target deadlines Changing regulatory environment, constant updates in the regulations-leads to rework and inadherence to target deadlines Change proposals affecting dossier sections leads to leads to rework and inadherence to target deadlines Inefficient software-leads to inadherence to target deadlines Key Interactions (1/2) RnD team (for formulation clarity-need basis) Manufacturing Unit-QA/QC/Production for documents procurement -daily Packaging Team (for procurement labelling documents - dailly) CPM, BD & Supply chain - for routine commercial/launch clarity (weekly basis) PV - for product approval notification and audit support (daily) Patent Team -to get the clarity on product patent and exclusivity (need basis) Key Interactions (2/2) Customers - product related queries / additional information required by customers and status updates- (daily) Regulatory consultants - submissions, queries, status (weekly) Software provider - trouble shooting (need basis) Health authorities- follow up- seek advice (need basis) Dimensions (1/2) Issuance of LoAs/CEPs: Approx. 100/Month Submission of DMFs to authorities: Approx. 14/Month Submission of AP DMFs to customer: Approx. 12/Month Legalization of documents: Approx. 20 documents /Month Dimensions (2/2) Key Decisions (1/2) Classification and type of change category for moderate and major changes confirm with group leader Key Decisions (2/2) Education Qualification B.Pharmacy, M. Pharm, Bsc or MSc Relevant Work Experience Minimum 5 years experience in regulatory activity in pharma industry preferably worked for same region/authority. Hands-on experience of eCTD submission

Summary Job Description Summary: This role focuses on independently executing Incentive Compensation (IC) operations, including detailed analytics, rigorous quality assurance, and effective project management. The incumbent is accountable for accurately managing IC reporting processes, understanding and applying IC business rules, and ensuring alignment with IC operational calendars and guidelines. About the Role Job Description: Major Accountabilities: Functional and Technical Expertise: Independently execute all IC reports, following optimized system configurations and defined processing guidelines. Clearly understand IC Business Rules and their implications on eligibility, awards, and downstream processes. Maintain rigorous quality control standards, ensuring error-free reports; independently review reports and provide actionable insights to leadership. Conduct detailed analytics autonomously, adhering strictly to prescribed KPIs, methodologies, and technical processes; perform thorough self-quality checks. IC Communications and Project Management: Deliver IC projects effectively with team support, ensuring clear communication and adherence to timelines. Accountable for consistently following IC ways of working, established processes, and adhering to the IC operational calendar. Key Performance Indicators: Zero-error IC report accuracy Timely execution and delivery of IC analytics and reports Adherence to IC operational guidelines and calendar Positive stakeholder feedback and satisfaction scores Minimum Requirements: Commercial experience in healthcare. Effective communication/knowledge/Best Practice sharing Familiarity with US Geography Able to navigate Javelin and Zaidyn suites comfortably Mandatory Tools: Javelin / Zaidyn Suites, MS Office Ability to work with multiple stakeholders Work Experience: Experience in Operations Management and Execution Project Management experience Familiarity with Incentive Compensation processes, preferably within the pharmaceutical sector Graduate / Postgraduate in Engineering/Pharmacy/ Science/Statistics or related fields Overall 2+ years of experience, with 1+ years in SFE /FFO/related analytics function with a leading pharma company/service provider Cross Cultural Experience Skills: Strong Analytical Thinking Effective Project Management Stakeholder Engagement Cross-Functional Collaboration Proficiency in Process Documentation and Quality Control Languages: English (Proficient) Benefits and Rewards: Read our handbook to learn about all the ways we ll help you thrive personally and professionally:

Summary Lead and manage a team developing drug products, processes, and procedures in line with global technical development strategy and objectives; apply scientific/technical/ GMP and/or quality-related expertise to address complex R&D issues; coach team members; manage operational aspects in lab or plant; develop strategies on science and technologies. Work according to appropriate standards for quality, ethics, health, safety, environment, protection, and information security. Foster a culture of innovation, empowerment, trust, learning, diversity & inclusion, and high performance. About the Role YOUR KEY RESPONSIBILITIES: Your responsibilities include but are not limited to: Oversee and lead all activities of assigned teams/projects: meet customer needs L ead initiatives to ensure continuous improvement; all activities have to be aligned with organizational workflows and procedures. Manage day to day operations of development lab including resource and budget planning. Evaluate and interpret results, draw relevant conclusions; supervise project related activities; perform complex tasks with or without having established procedures (establish new procedures). Oversees and may also write protocols, scientific reports, lab procedures or process r elated SOPs; write scientific documents intended for external partners or for generation of registration documents; interact with authorities. Communicate, address and solve problems within own and broader area of responsibility; communicate effectively across organizational interfaces; lead the transfer of know how to other departments or external contractors, including troubleshooting and on-site training. Lead lab automation, leverage new technologies including planning of investments and budgets, contribute to innovation and continuous improvement initiatives. Foster scientific mindset and innovation in team e.g. PAT implementation and technology knowledge foundation. Develop complex methods (lab or plant); lead the optimization of project related scientific /technical activities or processes, co-ordinate local team(s); guide development and implementation of new technologies. Lead assigned teams; represent own technical function in teams and fulfill all project tasks and responsibilities related to the own discipline. Broadly uses professional concepts in accordance with company objectives to solve complex problems in creative and effective ways. Contributes to many costs center goals and objectives; may contribute to service line goals Influences/persuades others and work according to appropriate SOPs. GLP, GMP, OQM, HSE, ISEC and Novartis Guideline. Minimum requirements WHAT YOU LL BRING TO THE ROLE: Minimum: Advanced degree in scientific or relevant discipline (Masters or equivalent) Desirable: Masters in Pharmacy or relevant discipline or equivalent. Good knowledge of English (oral and written). Desirable knowledge of site language leadership position with successful performance and track record. Minimum of 10 years of relevant experience; minimum of 2 years in a role of line/people manager in Technical R&D, or a related industrial area (e.g., TechOps, specialty chemicals) and Proven track record of successfully managing interfaces to other functions. Benefits and Rewards: Read our handbook to learn about all the ways we ll help you thrive personally and professionally:

About the job Use Your Power for Purpose At Pfizer, our Worldwide Medical and Safety colleagues are pivotal in bridging evidence-based medical decision support with stakeholders to enhance health and treatment outcomes. Whether you are developing frameworks to ensure our evidence is scientifically robust, offering unbiased and medically essential expertise, or exploring ways to address data gaps, our mission remains clear: to empower healthcare decisions regarding the safe and appropriate use of medicines for patients. Organizational Relationship(s) including to whom the position reports to: Case Processing Team Lead Position Purpose Review, preparation, and completion of reports of adverse drug experiences, to determine the safety profile of Pfizer s products and to meet regulatory requirements. Primary Responsibilities Identify and select routine cases for processing, determining appropriate prioritization criteria, and noting reasons for any delays. Assess cases to distinguish those with particular complexities and/or specific issues, and escalate appropriately. Review, rank, verify, process and document: event terms; case classifications (validity, seriousness, expectedness / listedness / labeledness); special scenarios; product complaint information; reportability with due date; and accuracy and consistency. Based on assessment of cases, process accordingly. Review case criteria to determine the appropriate workflow for case processing. Write and edit the case narrative. Generate reports, ensuring adherence to regulatory compliance timelines. Determine appropriate case follow-up, requesting follow-up letters when appropriate. Liaise with key partners, including Pfizer Country Organizations, Clinical Development, License Partners, and other stakeholders regarding safety data collection and data reconciliation. Develop and maintain expertise and knowledge of all products within the Pfizer portfolio; applicable corporate and global regulations, guidelines, Standard Operating Procedures and writing practices; data entry conventions; and search functions in the safety database. Consistently apply regulatory requirements and Pfizer policies. Qualifications (i. e. , Preferred Education, Experience, Attributes) Minimum a bachelor s degree in healthcare professional qualification (ie, Pharmacy, Dentistry, Nursing etc). 1 3-years experience in pharmacovigilance/ related domains. Work Location Assignment: Hybrid Medical #LI-PFE

Kochi, India| Bengaluru, India| India| Remote Save this job Job Description Job Overview Perform/Assist the Data Manager in managing various data management projects as per sponsor requirements and to provide efficient, quality management products. Support coordinate with other departments, sites and sponsors as and when necessary Essential Functions Perform/Assist regular Data cleaning activities to ensure clean data with quality and timely deliverables to sponsor. Serve in the role of back-up to a Sr. Data Coordinator or Data Team Lead. Manage the allocated tasks with minimum oversight. Ensure that all the deliverables are of expected quality standards and meet customer expectations with support of Senior Data Manager. Interact with Data Management team leaders to report on the quality of data collection and tasks done. Attend internal study meetings and internal/ sponsor audits. Assist in tracking and managing the projects, oversee project progress, identify risks and take corrective action to rectify any errors as recommended by DTL. Be compliant to trainings and eSOP reading. Communication with Data Team Lead and other team members across functions should be collaborative. Qualifications Bachelors Degree Graduate Science/Bachelor Pharmacy or equivalent Pref English Fluency Spoken and English Basic computer applications like Microsoft excel, word, Inbox etc Should have basic understanding of Drug development lifecycle and Overall Clinical research process IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at Save this job LEARN ABOUT HOW WE WORK Join our Global Talent Network Let s stay connected. Sign up to receive alerts when new opportunities become available that match your career ambitions.

About Medhavi Skills University Medhavi Skills University (MSU) is a government-notified private skills university established under a State Act in Sikkim, dedicated to promoting quality skill education and entrepreneurship integrated with higher education. As a pioneering institution in the convergence of the skilling ecosystem with higher education, MSU aligns with the National Education Policy, 2020 (NEP 2020). Recognized by the UGC and established in 2021, MSU collaborates with industries and Skill Development Institutes to offer work-integrated courses, embedding on-the-job internships and training within the curriculum. MSU is a recognized Awarding Body under the National Council for Vocational Education & Training (NCVET) and is empanelled with the Directorate General of Training (DGT). As an anchor university partner with the National Skill Development Corporation (NSDC) and the Project Management Unit (PMU) of NSDC International, MSU is committed to preparing youth for the future workspace by co- working with industry partners to design and implement demand-driven programs. For more information, visit https://msu.edu.in/ Role Overview: The Assistant Professor Pharmaceutical Analysis will play a vital role in delivering high-quality education and research in the School of Pharmacy at MSU Campus, Sikkim. The position involves teaching undergraduate and postgraduate courses in Pharmaceutical Analysis, guiding student research, and actively contributing to the departments academic and research goals. The faculty member will manage laboratory infrastructure, support curriculum development, contribute to institutional accreditation processes, and participate in administrative and academic committees. The role requires a blend of academic expertise, research acumen, and commitment to student development and institutional growth Key Responsibilities: Teaching & Academic Delivery: Deliver lectures and practical sessions in Pharmaceutical Analysis and related subjects as per the curriculum. Design, plan and update course materials, lesson plans, and laboratory manuals. Evaluate and assess students through exams, assignments, and presentations. Guide B.Pharm and M.Pharm students in academic and research projects. Research & Development: Undertake independent and collaborative research in the field of Pharmaceutical Analysis. Publish high-quality research papers in peer-reviewed journals and conferences. Guide postgraduate students in their thesis and research activities. Apply for research grants and projects from funding agencies. Laboratory & Equipment Management: Supervise and maintain laboratory infrastructure and instruments used in analysis (e.g., HPLC, UV-Vis Spectrophotometer, GC, FTIR, etc.). Ensure safety protocols and SOPs are followed during practical classes. Coordinate calibration and maintenance of instruments. Curriculum Development & Accreditation: Participate in the periodic review and revision of curriculum. Assist in documentation and preparation for NAAC, NBA, PCI, and other accreditations. Administrative & Institutional Activities: Serve on academic and administrative committees. Participate in faculty development programs, workshops, and conferences. Contribute to student mentoring, career guidance, and academic advising. Qualifications & Skills Required: M.Pharm in Pharmaceutical Analysis or Quality Assurance with first class. Registered Pharmacist under State Pharmacy Council. Ph.D. in Pharmaceutical Sciences (preferably in Pharmaceutical Analysis). Qualified in GPAT/NET. Minimum 1-2 years of teaching or research experience. Experience in handling analytical instruments like HPLC, UV, etc. What We Offer Being a key player in something potentially massive and world-changing Competitive salary and incentive structure, best in the industry. Opportunities for . We celebrate diversity and are committed to creating an inclusive environment for all employees.

JD: Serve as the company s subject matter expert on drug safety and pharmacovigilance Ensure compliance with Local & Global PV-relevant Heath Authority requirements Oversee PV Contracts, vendor management and PV system audits/inspections Have good understanding of signal management and benefit-risk evaluation activities Develop and implement Risk Management Plans (RMPs) and additional Risk mitigation measures Act as the primary safety liaison with country regulatory authorities and internal stakeholders Collaborate with Clinical Development, Regulatory Affairs, Medical Affairs, and Quality Assurance, marketing teams etc. Contribute to clinical trial safety strategies and protocols (e.g., protocols, safety monitoring plans, SAE reporting etc.) Mentor and develop PV team members to maintain a culture of continuous improvement and compliance Manage departmental budgets, staffing, and resourcing in line with organizational needs Qualifications: Advanced degree in Medicine or Pharmacy Minimum 10 years of progressive pharmacovigilance experience in the pharmaceutical industry In-depth understanding of Local/global PV regulations and guidance Demonstrated experience in leadership roles with proven ability to build and scale PV systems. Strong analytical, strategic thinking, and communication skills. JOB FAMILY: Product Development LOCATION: India > Mumbai : BKC Building t SIGNIFICANT WORK ACTIVITIES: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)

Job Description Role & responsibilities Consultant Cardiac Thoracic SurgeonDetermining the method of surgical procedures.Conducting medical management.Specializing in diagnoses.Reviewing patient history to determine treatment.Charting in compliance with the law and regulations.Identifying tests and the need for follow-up visits.Preferred candidate profile Qual: MBBS, MD/DNB,MCh CardiacthoracicFresher or 1+ yrs of ExperienceLocation: PallikaranaiPart Time/Full TimeDuty Coverage-8hrsImmediate Joiner

Job Title: Trainee Pharmacist Company Name: DM Hospital Job Description: As a Trainee Pharmacist at DM Hospital, you will be an integral part of the pharmacy team, assisting in the provision of high-quality pharmaceutical care to patients. You will work under the supervision of licensed pharmacists, gaining hands-on experience in medication management, patient counseling, and pharmacy operations. Your responsibilities will include preparing and dispensing medications, conducting medication therapy management, ensuring compliance with regulatory standards, and providing support in pharmaceutical services to enhance patient health outcomes. Key Responsibilities: - Assist in the preparation and dispensation of medications, including oral and intravenous formulations. - Conduct medication reviews and assist in monitoring patient medication therapy. - Provide accurate drug information to healthcare professionals and patients. - Participate in inventory management, including stock checks and ordering of pharmaceuticals. - Support the pharmacist in counseling patients about their medications, including dosage, side effects, and interactions. - Maintain accurate records and documentation of all pharmaceutical activities. - Collaborate with healthcare team members to ensure continuity of care for patients. - Uphold compliance with laws, regulations, and standards governing pharmacy practice. Skills and Tools Required: - Strong understanding of pharmacology, pharmacy law, and medication management. - Excellent communication and interpersonal skills for effective patient interaction. - Detail-oriented with strong organizational skills to manage multiple tasks. - Ability to work collaboratively in a team environment and assist in crisis situations. - Proficient in using pharmacy management software and electronic health record systems. - Basic knowledge of medical terminologies and drug classifications. - Ability to handle and resolve conflicts in a professional manner. - Willingness to learn and adapt to new challenges in a dynamic healthcare setting. - Strong commitment to patient safety and quality of care. Qualifications: - Bachelor’s degree in Pharmacy or currently enrolled in a Doctor of Pharmacy (Pharm.D) program. - Demonstrated interest in pursuing a career in hospital pharmacy. - Previous internship or experience in a pharmacy setting is a plus but not required. - Active registration as a pharmacy student or intern under the relevant pharmacy board (if applicable). Roles and Responsibilities About the Role: - As a Trainee Pharmacist at DM Hospital, you will gain hands-on experience in pharmaceutical care. - You will work under the supervision of licensed pharmacists to support medication management and patient safety. - The role involves assisting in dispensing medications and providing patient counseling on drug therapies. About the Team: - You will be part of a multidisciplinary healthcare team dedicated to improving patient outcomes. - The pharmacy team collaborates closely with doctors, nurses, and other healthcare professionals to ensure comprehensive care. - Team members are committed to ongoing education and professional development, fostering a supportive learning environment. You are Responsible for: - Assisting pharmacists in preparing and dispensing medications accurately. - Conducting medication reconciliation and ensuring patient records are up-to-date. - Providing information and guidance to patients regarding their medications and potential side effects. To succeed in this role – you should have the following: - A genuine interest in pharmacy practice and patient care. - Strong attention to detail and excellent communication skills. - A willingness to learn and adapt in a fast-paced healthcare setting.

Registered Pharmacist with state license of Bengaluru -Karnataka Chennai - Tamil Nadu Hyderabad - Telangana 1-7 yrs experience Pharmacist Sr Pharmacist Required Candidate profile Dpharma Bpharma with license

The Medical Sales Representative position is a full-time on-site role located in Ongole. As a Medical Sales Representative, you will be responsible for reaching out to potential customers, establishing and nurturing relationships with healthcare professionals, promoting and selling medical products, and delivering exceptional customer service. Your daily responsibilities will include making sales calls, delivering product presentations, engaging in contract negotiations, and addressing customer inquiries and issues effectively. To excel in this role, you should possess skills in Medical Sales and Customer Service. Strong communication abilities are essential for effectively conveying product information and addressing customer needs. A solid understanding of Medicine and Pharmacy is crucial for successfully promoting and selling medical products. You should be capable of working independently and achieving sales targets. Excellent organizational and time management skills are necessary to handle multiple tasks efficiently. The ideal candidate for this position will hold a Bachelor's degree in a relevant field such as Medicine or Pharmacy. While prior experience in sales or the healthcare industry is preferred, individuals with a strong foundation in Medical Sales and Customer Service are encouraged to apply.,

You are invited to attend a WALK-IN INTERVIEW at eNoah iSolution India Pvt Ltd. The dates for the interview are 24th & 25th July 2025 and 28th & 29th July. The interview timings are from 11 AM to 6 PM on the specified dates. To be eligible for the interview, you should hold a UG/PG degree in Pharmacy, Life Science, Microbiology, or any Medical Degree. The work hours for this position are from 8:30 AM to 5 PM with a 5-day working week (Saturday & Sunday Off). The interview will take place at NRK Business Park, No. 603-B, 6th Floor, Vijay Nagar, Behind Mangal City Mall, Indore. For more details or queries, you can contact Rashmeet at 7200902979 or Krishna at 9522220247. Make sure to bring your updated resume with you to the interview. This is a great opportunity that you wouldn't want to miss!,

You will be responsible for leading the end-to-end process of new product development, from concept ideation through to launch. You will work closely with R&D, marketing, regulatory, supply chain, and manufacturing teams to ensure that products meet the highest standards of quality, efficacy, and compliance. Develop and refine innovative skincare product concepts based on market trends, consumer insights, and brand strategy. Own and drive the NPD process, ensuring project timelines, milestones, and deliverables are met. Coordinate with R&D, packaging, procurement, regulatory, marketing, and operations to bring products from concept to shelf. Collaborate with R&D to identify key actives, test prototypes, and refine formulations to ensure performance, stability, and safety. Oversee sensory testing, focus groups, and other consumer validation methods to ensure products meet consumer expectations. Ensure all products comply with relevant regulations and guidelines (e.g., BIS, FDA, EU, etc.), including labelling and claims substantiation. Champion sustainable and ethical sourcing, packaging, and formulation practices. Monitor NPD budgets and resource allocation effectively. Qualifications: Bachelors or Masters degree in Cosmetic Science, Chemistry, Pharmacy, or a related field. Minimum of 3-5 years of experience in NPD within the skincare or personal care industry. Proven track record of successfully launching skincare products. Strong understanding of formulation chemistry, regulatory compliance, and market trends. Excellent project management, organisational, and communication skills. Passion for innovation and staying updated on beauty industry trends. Collaborative mindset and ability to lead cross-functional teams. Opportunity to shape the future of skincare innovations. Collaborative and dynamic work environment. Competitive salary and benefits package.,

Open Position: City Head Location: Bangalore (Wilson Garden) Company Name: Primecare Pharma Pvt Ltd Experience: 8 - 10 years Qualification: D Pharma/B Pharma We are hiring only Bangalore based candidate for this position. Key Responsibilities : Oversee day-to-day operations of retail pharmacy outlets, ensuring high standards of service and operational efficiency. Develop and implement strategies to drive sales growth, customer acquisition, and retention. Collaborate with the General Manager to create and execute business plans aligned with company goals. Lead, mentor, and develop a team of managers and staff, promoting a culture of accountability and excellence. Ensure all pharmacy operations comply with relevant laws, regulations, and industry standards. Manage inventory levels, procurement, and supplier relationships to maintain optimal stock levels while minimizing costs. Analyze financial and operational reports to identify areas for improvement and implement corrective actions. Drive initiatives to improve patient care, service delivery, and customer satisfaction. Identify market trends, customer needs, and competitor strategies to adapt business plans accordingly. Coordinate with cross-functional teams such as Marketing, HR, and IT to ensure seamless support to retail operations. Establish and monitor KPIs for performance evaluation, and provide timely feedback and support to meet targets. Qualifications : Diploma in in Pharmacy, Bachelors degree in Pharmacy, Minimum of 8 years of experience in retail pharmacy management, with at least 5 years in a leadership role. Strong knowledge of retail pharmacy operations, regulatory requirements, and industry trends. Excellent leadership and people management skills, with a proven track record of building and leading high-performing teams. Strategic thinking and problem-solving skills, with the ability to make data-driven decisions. Proficient in financial analysis, budgeting, and inventory management. Excellent communication and interpersonal skills. Ability to work in a fast-paced environment and manage multiple priorities effectively.

We Are Hiring! We are looking for Pharmacist for our retail outlets Gokavaram, Rajahmundry, Kakinada. Only Andhra Pradesh state candidates with Andhra Pradesh state PCI were eligible for this position. Job Responsibilities : Knowledge about medicines Reading prescriptions Be able to suggest medicines for basic ailments Suggest alternate me dicine if one brand is not available Basic Computer knowledge Manage invoicing and billing Qualification: *For Pharmacist: D. PHARM / B.PHARM / M.PHARM with Andhra State PCI Registration *For Pharmacy Assistant: SSC & above with at least 2+ years of retail pharmacy experience *For Pharmacy Trainee: Freshers with SSC & Above *Experience: Freshers / 0 to 10 years of relevant pharmacy retail experience Skills Required: Knowledge of medicines (drugs), commitment to serve the community & good interpersonal skills. Why to Join Apollo Pharmacy? Largest organized Pharmacy retail chain in India Continuous Learning & Development Transparent Career Path Rewards & Recognition Attractive Compensation & Benefits 1 Weekly off & Holidays Casual, Sick & Earned leaves PF & ESI Monthly Incentives NOTE: Eligibility for candidates with D. Pharm / B.Pharm / M.Pharm qualification with valid PCI License ONLY. Incase awaiting for PCI License apply for "Trainee Pharmacist" role on https://careers.apollopharmacy.app Venue : DOOR NO. 115-12-313, Apollo pharmacy Korukonda Rd, Side by S.B.I, Konthamuru, Rajamahendravaram, Andhra Pradesh 533105 Google Map: https://goo.gl/maps/7tGtSNiXdgMT6cSc8 Contact Details: G Rajesh - 8121026481

Dispense medications accurately, provide guidance on prescriptions, ensure compliance with healthcare regulations, manage inventory, and offer patient counseling on medication use and safety in the pathology lab and polyclinic setting. Required Candidate profile Qualification: B.Pharmacy Exp: 2-4yrs in Diagnostic/Retail/Hospital Pharmacy Male candidates with Immediate notice period Shift timings: 2PM to 11PM

Dear Candidate, Greetings from Medplus.. About Company :- Medplus - India's Largest Organized Pharmacy Retail Chain. We are immediately hiring freshers for the role Pharmacy Aide/Customer Service Associate(CSA) in Medplus Pharmacy . Qualification required:- Min 12th/Diploma/Any Arts UG Degree/B.Pharm/D.Pharm. Experience required :- Freshers or Experienced any one can apply. Work Location :- Chennai(Nanganallur/Keelkattalai/Tambaram/Kundrathur/S.Kolathur/Kovilambakkam/Urapakkam) Interested candidate can call or WhatsApp the resume to Karthick HR Mobile No :- 9789747555 Thanks, Karthick HR Medplus 9789747555

Job description Greetings from Indira IVF !!! Position - Pharmacist Qualification - D. Pharma / B. Pharma Location- Chandrapur - Maharashtra Experience - 1 to 5 Years Job Timing - 9 am to 6 pm Salary- Best in the industry Notice Period- Immediate Joiners Interested candidates - Kindly share resume on kishori.mhatre@indiraivf.in Thanks & Regards, Kishori Indira IVF Pvt Ltd. 7230068884

About Apotex Inc. Job Summary Responsible for leading Regulatory Affairs individuals accountable for management of life cycle changes including change assessments and submissions all the way to approvals of PLCM (Product Life Cycle Management) projects to support regulatory compliance continued supply of Apotex products. Also responsible for Global Regulatory practices to manage regulatory information in various databases and ensure consistent practices and compliance is maintained at Global Apotex sites. This is to be accomplished by planning and managing the activities of the group. Strong linkages need to be established with R&D, Quality, Operations and the Regulatory Market Affiliates/customers (Canada, US, EU, AUS and NZ) and Regulatory partners at Global Apotex sites. Responsible for coaching team members via sharing of technical knowledge/expertise. Job Responsibilities Responsible for planning workload / projects (i.e. change assessments, submissions, training plans, deficiency responses, audits etc.) and managing processes to ensure objectives of department and submission and approval timelines are met. Prioritizes projects in support of commercial business needs. Reviews and ensures timely submission of post-launch variations and completes any other activities as assigned, in a timely manner, to ensure supply continuity through smart regulatory strategies and quality submissions. Handling of deficiencies received from Apotex Affiliates and/or customer and health regulatory agencies for post-launch variations. Responsible for ensuring timely approval of the PLCM projects with high quality technical submissions and monitoring Agency reviews with the Regulatory Market Affiliate. Standardizing processes, guiding reviews, ensuring quality and compliance of submissions with technical expertise. Represents Regulatory Affairs in cross-functional team meetings and provides impact analysis in relevant forums associated with PLCM to support ongoing commercial supply of product. Supports Corporate Business processes (change control, compendia etc.). Develops & proposes regulatory solutions and escalates action plans for identified product issues to mitigate risks, as required. Challenges the status quo. Develops and maintains effective relationships with external vendors, suppliers, business partners and internal stakeholders in order to ensure business needs are met. Implements business objectives, R&D initiatives and regulatory strategy focusing on process improvements. Regular interactions with stakeholders to discuss on expectations, deliverables/priorities and provides solutions to regulatory issues and/or problems. Stays abreast of changes in regulatory environment / trends and escalates appropriately to ensure that regulatory practices at global Apotex sites are updated as needed. Provides guidance and participates as required in recruitment, training, developing and effective management of ongoing performance of regulatory individuals. Manages compliance activities (including but not limited to audit preparation, regulatory information management systems and regulatory info supporting quality management systems) for global regulatory affairs teams and is responsible to ensure that consistent and compliant practices are followed at all Apotex sites. Contributes and encourages team members towards the creation and promotion of an environment of teamwork and empowerment built on mutual trust and respect. Works as a member of a team to achieve all outcomes. Completion of all the assigned trainings in timely manner. Supervises work of direct reports, determining training requirements, performing regular performance reviews and executing development plans in co-ordination with Reporting Manager. Leads performance conversations, ensuring progress, support, and clear expectations, fostering a high-performance, safe work environment. Utilizes open, honest, two-way communication to build trust-based relationships with employees, business partners and direct leader while continuously improving leadership capabilities by personally seeking feedback and development. Creates a culture which values trust and provides the opportunity for Employee development and growth in pursuit of our purpose and demonstrating our core Values Collaboration, Courage, Perseverance and Passion. Attract, hire and onboard talent through networking, ensuring a consistent, value-driven experience for new employees. Ensures adherence of team members (direct reports) with all compliance programs and company policies and procedures. All other duties as assigned. Job Requirements Education A Graduate/ Post graduate degree in Chemistry, Biology, Pharmacy, Health Sciences or similar. Knowledge, Skills and Abilities Must possess detailed knowledge of the technical, quality compliance, and global regulatory requirements. Excellent communication, presentation, and interpersonal skills. Excellent Leadership, negotiation, problem-solving and conflict management skills. Demonstrated experience in supervising, influencing, and coordinating the complex activities and interaction of staff, including direct and non-direct reports. Strong organisational skills; ability to work independently as well as in dynamic team environment. Strong ability to lead a team of professionals. Demonstrated knowledge of the generic new product development and post approval management process. Excellent understanding of Project Management principles and practice in a complex environment. Excellent oral/written communication in English. Knowledge of recent updated Guidance s of Health agencies is a must. Knowledge of and experience with the MS-Office suite of products; with particular emphasis on MS-Word, MS-Excel, and MS-Project (or other PM software). Experience 15+ years progressive experience pharmaceutical industry. 10+ years regulatory filing experience with exposure to PLCM & compliance activities for Finished Dosage forms. At Apotex, we are committed to fostering an inclusive, accessible work environment, where all employees feel valued, respected and supported. Apotex offers accommodation for applicants with disabilities as part of its recruitment process. If you are contacted to arrange for an interview or testing, please advise us if you require an accommodation.

KIRTI PHARMACEUTICALS is looking for Pharmacist to join our dynamic team and embark on a rewarding career journey Compounding and dispensing medications, as prescribed by physicians. Monitoring customers drug therapies, advising interventions, and informing customers of any potential side effects. Instructing customers on how and when to take prescribed medications. Conducting health and wellness screenings. Providing immunizations, and other medical services, such as taking blood pressure, temperature measurements, and checking blood sugar levels. Keeping accurate customer records. Ensuring a safe and clean working environment. Completing operational requirements of the pharmacy, including verifying order entries, maintaining records of controlled substances, charges, and removing expired and/or damaged drugs from the pharmacys inventory. Adhering to applicable legal rules, regulations, and procedures governing pharmaceutical practice. Performing other administrative tasks when needed.

Customer Support Read & validate prescriptions (Rx) + OTC orders Contact customers for clarification or information required to process the order Inventory Management Keep check of Inventory in the warehouse. Drive vendors to ensure adequate inventory levels are maintained. Compliance Ensure strong quality checks while packing/ dispensing medicines Ensure 100% compliance per the process guidelines