1784 Pharmaceutical Jobs - Page 45

conceptualising Full job description We are seeking a proactive and detail-oriented Product Development Executive to join our team. This role will be responsible for supporting the end-to-end process of researching new products and enhancing existing ones. Key Responsibilities: Assist in conceptualizing and developing new product ideas based on market trends, customer insights, and competitive analysis. Coordinate with design team to execute product plans. Conduct market research and competitor benchmarking to identify gaps and opportunities. Track product development timelines and ensure milestones are met. Prepare reports, presentations, and documentation for internal reviews and external stakeholders. Monitor product performance post-launch and suggest improvements. Contribute to pricing strategies and go-to-market plans. Qualification : Pharmacy and Biotech Background eligible.Role & responsibilities Preferred candidate profile

Job Description Labware 7. LIMS implementation, Master data creation, Validation. Caluculation configurations. CSV documentations, Test Script review, Instrument integrations. LIMS trouble shooting and resolutions. QAMS activities, CCP, CAPA, Deviation investigation. Work Experience 4-7 years of experience in QC and LIMS Implementation Education Post Graduation in Analytical Chemistry or Analytical Chemistry Graduation in Pharmacy or Pharmacy Competencies Innovation & Creativity Result Orientation Collaboration Customer Centricity Developing Talent Stakeholder Management Strategic Agility Process Excellence

Monitor Field Force activity & sales Digitally Analyze statements & reporting the Mgt Support FF to achieve targets Monitor & Plan-trade schemes & incentives for Field force-dispatch of Stocks & Sales promotion material - gifts-brochures-posters. Required Candidate profile Exp. in Pharma - preferred. Will work @ Head Office Know reporting systems, man mgt, data analysis, planning & computer skills Must know English, Telugu or Oriya, Hindi. Pls Call - 8871829882

We are seeking a licensed and detail-oriented Pharmacists to join our team. Candidate will be responsible for dispensing prescriptions, providing medication counseling, ensuring regulatory compliance, and supporting overall patient health outcomes. Required Candidate profile Interested Candidates Drop CVs to HR Priyanshu WhatsApp: +91 99882-18886 Mail: recruitment@amandeephospital.org

Qualification: Bsc Chemistry/Bpharma Experience : 0 to 5 Years CTC: Up to 4.5 LPA Work Location : Ankleshwar Experince in Pharma Company Prefer Like OSD, Tables, API send cv on sdpbharuch@gmail.com with Sub : Production Ankleshwar Required Candidate profile Interview Venue: SDP HR SOLUTION 610, GOLDEN SQUARE BESIDE DMART ABC CIRCLE BHARUCH Share CV on sdpbharuch@gmail.com with Subject: Production Ankleshwar No Charges Share with Friends & Colleagues

Job Title: Associate - OT Pharmacy Company Name: Manipal Hospitals Job Description: Manipal Hospitals is seeking a dedicated and detail-oriented Associate for our OT Pharmacy team. The ideal candidate will be responsible for managing pharmaceutical services in the operating theater environment, ensuring safe and effective medication management. Key Responsibilities: - Assist in the preparation and dispensing of medications for surgical procedures. - Collaborate with the surgical team to optimize pharmacological therapy. - Maintain accurate inventory of medications and supplies in the OT pharmacy. - Support the implementation of safety protocols and procedures in medication handling. - Provide guidance and information to healthcare staff regarding medication use and interactions. - Participate in continuous education and training to stay updated on pharmaceutical practices. - Ensure compliance with regulatory requirements and hospital policies. Qualifications: - Bachelor's degree in Pharmacy or a related field. - Valid pharmacy license. - Experience in a hospital pharmacy setting, particularly in an operating theater, is preferred. - Strong communication and organizational skills. - Ability to work efficiently in a fast-paced environment. Join Manipal Hospitals and become part of a team committed to delivering exceptional healthcare services. If you are passionate about pharmacy and patient care, we encourage you to apply for this exciting opportunity. Roles and Responsibilities Job Title: Associate - OT Pharmacy Company Name: Manipal Hospitals Roles and Responsibilities: 1. Assist in the management and organization of the outpatient pharmacy operations, ensuring the efficient flow of medication distribution. 2. Prepare, dispense, and label medications according to prescriptions and established safety standards. 3. Collaborate with healthcare professionals to provide optimal pharmaceutical care and support patient safety initiatives. 4. Maintain accurate patient medication records and ensure compliance with regulatory requirements. 5. Conduct medication inventory management, including ordering, receiving, and conducting regular audits to prevent stock discrepancies. 6. Provide medication counseling to patients and their families, addressing any questions or concerns regarding prescriptions and dosages. 7. Support the continuous improvement of pharmacy practices by participating in training programs and staying updated on industry trends and best practices. 8. Engage in quality assurance activities to monitor the effectiveness of pharmacy services and implement necessary improvements. 9. Assist in the preparation and maintenance of pharmacy policies and procedures to align with hospital standards. 10. Contribute to team meetings and collaborate effectively with colleagues to enhance overall pharmacy operations and patient care.

Execute process development activities for pharmaceutical products at laboratory scale Design and implement experiments to optimize manufacturing processes for increased efficiency and product quality Conduct and analyze data from characterization and optimization studies Prepare the documents like PIS, sampling plan and risk matrix for pilot scale batches (Confirmatory batch and exhibit batch manufacturing) Troubleshoot process issues and implement corrective actions Collaborate with cross-functional teams including manufacturing, quality assurance, and regulatory affairs Author and review technical reports, batch records, and standard operating procedures Ensure compliance with cGMP regulations and company policies Participate in technology transfer activities to support scale-up and exhibit batches. Stay current with industry trends and emerging technologies in pharmaceutical process development Present findings and recommendations to group leader. Contribute to continuous improvement initiatives within the department Qualification M. Pharmacy Additional Information

Job Responsibilities: Picking medicines according to prescription. Checking medicine before dispense from the pharmacy Procuring outside medicines from outside pharmacy Checking returns medicine quality batch & expiry & marketing return quality in original packed bill before it goes for returning system. Stock checking every day Dispense and supply medicine based on a doctor's prescription Formulate and implement drugs policies and practices Checking expiry dates, batch no. of medicines Ensure that only quality drugs are purchased, properly stored and distributed. Billing and cash collection Receiving the medicines (i.e. stock) from the vendors In case of credit billing after dispensary the medicine bill should be handed over to billing department to the credit repaid While issuing the medicine check the expiry date and batch No. on the medicine and compare it with the bill entry Stock check at the end of the month is necessary A minimum stock has to be maintained in your category and indent to the pharmacy purchase in charge whenever necessary Any other jobs to be carried out as and when there is instruction from the HOD While taking the patient return they have to check the batch No & expiry, Quality management properly Implement drug policies

Urgent job opening for PMT (Product Management) Executive at Andheri. Experience: 3 to 5 years Qualification: Any graduate Job description To design and implement various brand promotion activities for the Product range, in line with the objectives budgetary allocations of the Company. To prepare, edit and finalize the technical write up / presentations for visual aids and other promotional activities. To conduct/ attend/ Give lectures demonstrations in various promotional events approved by the Management like Seminars, CMEs etc. To train and guide the Sales team regarding Brand promotion activities planned by the Company. To monitor the Sales team for effective execution of the promotional activities. To Collate and analyze the data received from the field force and the sales figures. To identify and report the trends and competitor's activities in the market to the top Management periodically in their respective areas . To initiate for the launch of the new products in the markets , prepare plan for new product developments . If you are interested for the above referred position, kindly revert back with your Updated Resume with Photograph along with following details: 1) Current salary 2) Expected salary 3) Notice period 4) Total experience 5) Relevant experience 6) Current location 7) Reason for job change Contact :- Snehal Mail ID:- snehal.k@jobsearchindia.in

Title: Business Development Head - (Contract Manufacturing/CMO / CDMO) - Pharmaceutical Human Health Industry (DOMESTIC MARKETING & BUSINESS DEVELOPMENT ONLY) Summary: We are currently seeking a dynamic and experienced Business Development Head (FOR DOMESTIC MARKETING) to spearhead our business development initiatives in the pharmaceutical human health sector. This pivotal role requires a focus on B2B marketing and contract manufacturing, particularly in oral liquids and nutraceuticals. The ideal candidate will bring a strong background in multinational corporate environments, with a demonstrated track record of success in generating new B2B orders and selling developed products within the human pharmaceutical industry. Qualifications: Masters degree in business, Marketing, Pharmaceutical Sciences, or a related field is mandatory. A minimum of 08 to 15 years of progressive experience in business development within the human pharmaceutical industry, specifically in multinational corporations. Demonstrated expertise in B2B marketing and contract manufacturing, with a focus on OSD formulations and nutraceuticals. Proven ability to develop and execute successful business development strategies in the pharmaceutical sector. Strong understanding of market dynamics, regulatory requirements, and product development in the pharmaceutical industry. Exceptional negotiation, communication, and interpersonal skills. Proven track record of meeting or exceeding business development targets. Ability to work collaboratively in a team environment and lead cross-functional initiatives. Core Responsibilities: Lead and strategize business development activities in the pharmaceutical human health sector with a specific focus on oral liquids and nutraceuticals. Identify and secure new business opportunities in the B2B market, ensuring they align with the company's strategic objectives. Secure and manage comprehensive contracts for CDMO and CMO services with multinational corporations, leveraging market insights and strategic partnerships. Maintain and enhance relationships with existing clients while actively pursuing new partnerships in the pharmaceutical industry. Collaborate with internal teams to develop and propose tailored solutions for clients, ensuring compliance with industry standards and customer satisfaction. Negotiate and finalize business deals, focusing on profitability and sustainable growth. Stay abreast of industry trends, competitor activities, and regulatory changes to inform and adapt business strategies. Provide leadership and mentorship to the business development team, setting clear goals and tracking performance. Regularly report on business development activities and progress to senior management, providing insights and recommendations for continuous improvement. (NOTE: CANDIDATES WHO ARE HAVING RELEVANT EXPERIENCE IN THE PHARMACEUTICAL INDUSTRY AS PER THE ABOVE JOB DESCRIPTION ONLY SHOULD APPLY FOR THIS POSITION)

Talent Acquisition (80% Focus): Must have experience in pharmaceutical industry Handle end-to-end recruitment for plant-based and field roles Conduct screening, schedule interviews, manage candidate pipeline and ensure timely closures Maintain and update hiring dashboards, trackers, and recruitment MIS Leverage job portals, social media and referrals HR Operations (20% Focus): Maintain employee database and documentation Training and development of staff as per requirement Help in preparing HR MIS and reports for audits or management reviews Job Location: Kadi, Gujarat ( Bus transportation facility available from Ahmedabad, Kalol & Kadi)

Talent Acquisition (80% Focus): Must have experience in pharmaceutical industry Handle end-to-end recruitment for plant-based and field roles Conduct screening, schedule interviews, manage candidate pipeline and ensure timely closures Maintain and update hiring dashboards, trackers, and recruitment MIS Leverage job portals, social media and referrals HR Operations (20% Focus): Maintain employee database and documentation Training and development of staff as per requirement Help in preparing HR MIS and reports for audits or management reviews Job Location: Kadi, Gujarat ( Bus transportation facility available from Ahmedabad, Kalol & Kadi)

We are excited to connect with SAP ATTP Lead Functional Consultants who are experienced in SAP S/4 HANA PP/QM with at least 1 Pharma Serialization implementation projects in ATTP to be placed with one of the largest IT Software Indian MNCs. Please note the opportunity is Work From Office. Job Role : SAP ATTP Lead Functional Consultant (PP/QM) Experience : 10+ Years Job Type : Full Time Location : Hyderabad/ Bangalore Qualification: B.Tech / B.E / MCA / M.Sc (Comp) Job Description :- Minimum 10+ years of experience in SAP S/4HANA PP/QM and at least 2 pharma serialization implementation projects in ATTP Lead the design, configuration, and implementation of the SAP ATTP solution in S/4 HANA to meet regulatory requirements for track and trace in the pharmaceutical industry Conduct workshops to understand the current as-is scenarios and define the to-be processes and should be able to recommend latest best practices and innovations Configure and optimize ATTP functionalities, including serialization, aggregation, and reporting for compliance with industry standards and regulations Demonstrate expertise in SAP ATTP, including integrations with S4/HANA, migration to S4/HANA, upgrades, rules framework, AIF configuration, and regulatory reporting for US, EU, RU, ROW, and Middle East markets Conduct FUT, system integration testing (SIT) and user acceptance testing (UAT) to ensure the solution meets business requirements Ensure seamless integration of ATTP with other SAP modules like MM, SD, PP, and EWM and Trackwise to facilitate end-to-end track and trace processes Proficiency in configuring SAP ATTP, developing custom enhancements, and integrating with third-party systems Monitor serialization data flow and troubleshoot serialization event failures, EPCIS errors, and regulatory submission issues. Supporting Site SMEs with user training and work instructions documentation Conducting change management activities for awareness of changes that are happening due to Serialization implementation Strong understanding of Life sciences industry regulations and compliance requirements Interested candidates with suitable profiles please apply with your latest updated resume to: arun.m@creenosolutions.com For more details you may reach out Arun @ 9392352955

GREETINGS ! ARE YOU LOOKING FOR A CORE ENGINEERING JOB ? SEND YOUR UPDATED CV/ RESUMES TO RECRUIT@MEDIANALYTIKA.COM FOR AN IMMEDIATE RESPONSE. WOULD YOU LIKE TO HAVE YOUR CAREER IN TECHNICAL SALES, APPLICATION SUPPORT, INSTALLATION & TO PROVIDE SERVICE SUPPORT OF HIGH TECHNOLOGY IMPORTED EQUIPMENTS ? WELCOME TO JOIN ONE OF THE THE LARGEST INSTRUMENTATION COMPANIES IN INDIA MEDI ANALYTIKA - INDIA, ESTABLISHED DURING 1994 HAS SUCCESSFULLY COMPLETED 29 YEARS IN BUSINESS. WE ARE RECOGNIZED AS THE LARGEST INSTRUMENTATION COMPANY IN INDIA SUPPLYING HIGH TECHNOLOGY EQUIPMENTS FOR VARIOUS FIELDS FROM SEVERAL WORLD LEADING INSTRUMENTATION COMPANIES FROM USA - CANADA - UK - EUROPE - JAPAN - KOREA OUR CLIENTS INCLUDE MULTI-NATIONAL COMPANIES, PHARMA MAJORS AND OTHER INDUSTRIES, IIT's, TOP UNIVERSITIES & SCIENTIFIC RESEARCH INSTITUTIONS, HOSPITALS & MEDICAL RESEARCHERS. AS A PART OF EXPANSION, WE ARE HIRING LARGE NUMBER OF ENGINEERS & PhD FOR TECHNICAL SALES, INSTALLATION AND TO PROVIDE AFTER SALES SERVICE & APPLICATION SUPPORT. MEDI ANALYTIKA HAS THOUSANDS OF CUSTOMERS. SEGMENTS SERVED INCLUDE : PHARMACEUTICAL /BIO-PHARMA /CRO : DRUG DISCOVERY - FORMULATION, PRODUCTION OF ONCOLOGY DRUGS & INJECTABLES + VACCINES +NANOMEDICINE, BIO-ANALYTICAL, , PRE-CLINICAL ANIMAL RESEARCH, ELECTROPHYSIOLOGY, ION CHANNEL RESEARCH ENVIRONMENT - OCEAN RESEARCH : AIR POLLUTION, WATER POLLUTION, UNDER WATER RESEARCH, TSUNAMI WARNING SYSTEMS, PETROLEUM EXPLORATION & DEEP OCEAN RESEARCH HOSPITALS & MEDICAL RESEARCH CENTRES : NEUROSURGERY - NEUROSCIENCE - REHABILITATION - EYE RESEARCH - BURNS - VASCULAR DIAGNOSTICS - DIABETIC RESEARCH IITs, MAJOR UNIVERSITIES & SCIENTIFIC RESEARCH SCIENTIFIC DISCOVERY : IMAGING & ADVANCED MICROSCOPY / LASERS / MATERIAL SCIENCE FOOD & BEVERAGE INDUSTRIES : LAB / PILOT / PRODUCTION SCALE MACHINES AUTOMOBILES - TEXTILES COMPANIES NANOSCIENCE - NANOTECHNOLOGY - MICROFLUIDICS RESEARCHERS GENETIC ENGINEERING, BIOTECHNOLOGY & CELL RESEARCH RESEARCHERS SPACE RESEARCH & NUCLEAR POWER ESTABLISHMENTS We have plans to recruit 50 + young experienced engineers who can market the instruments from top foreign instrumentation companies, for whom we are exclusive distributors throughout India. Growth and best salary in the industry is assured for those who continue in our company for a longer period of years... 1-5 YEARS EXPERIENCED ENGINEERS WHO ARE WORKING IN MEDICAL / SCIENTIFIC INSTRUMENTATION FIELD ARE WELCOME TO JOIN MEDI ANALYTIKA. JOB INVOLVES TRAVELLING AND SHOULD BE SELF MOTIVATED YOU WILL BE VISITING UNIVERSITIES, RESEARCH INSTITUTIONS, HOSPITALS, MEDICAL RESEARCH CENTRES, BIOTECH COMPANIES AND ALSO ALL MAJOR PHARMA-CHEMICAL-FOOD PROCESSING COMPANIES & OTHER INDUSTRIES THROUGHOUT INDIA. YOU WILL HAVE TO EXPLAIN ABOUT THE SALIENT FEATURES OF OUR IMPORTED INSTRUMENTS FROM WORLD LEADING COMPANIES (FROM USA, CANADA, EUROPE, JAPAN, KOREA) TO SCIENTISTS AND PROFESSORS, WHO ARE GENERALLY DOCTORATES IN THEIR RESPECTIVE FIELD. AFTER THE SALE, SELECT ENGINEERS WHO ARE QUALIFIED WILL BE ALSO TRAINED TO INSTALL AND ALSO PROVIDE AFTER-SALES- SERVICE SUPPORT MINIMUM QUALIFICATION : MINIMUM 60 % M.TECH/ B.E. / B.TECH (EEE, E& I, E&C, BIOMEDICAL / MEDICAL TECHNOLOGY / GENETIC ENGINEERING / BIOTECHNOLOGY/CHEMICAL ENGINEERING) OR M.SC. ( PHYSICS / CHEMISTRY / BIOPHYSICS / BIOTECHNOLOGY / MICROBIOLOGY/ BIOCHEMISTRY) VACANCY : DELHI/NCR - CHANDIGARH - LUCKNOW - MUMBAI - PUNE - AHMEDABAD - KOLKATA - BHUBANESWAR - GUWAHATI - CHENNAI - BANGALORE - TRIVANDRUM - COCHIN - HYDERABAD -GOA - VIZAG Required Candidate profile B.E./B.TECH/M.TECH/ M.SC. (MALE) ENGINEERS EXPERIENCED IN ANY FIELD ARE WELCOME TO JOIN MEDI ANALYTIKA Perks and Benefits PLUS Incentives, Travel Allowance, PF, Gratuity, ETC.

Safety tools inspection,work permits,safety compliance,day to day safety measures,documentation, SOP Preparation,Mock drill, Fire drill, first aid Conducting risk analysis and ensuring the proper solution to avoid the risk & hazard. Required Candidate profile Health & Safety, Occupational Health & Accident Investigation skills Formulate WSH solutions based on analysis of WSH reports ensuring that corrective& preventive actions (CAPA) are promptly implement

Experience: 4-8 Year Experience in manufacturing (API) as per Pharma Manufacturing GMP requirements. Responsibilities for Internal Candidates Key Roles & Responsibilities 1. Capable to handle independent projects 2. Analytical testing support to PDG synthetic group. 3. Coordinate with QA regarding method transfer, CCF and investigation reports. 4. Experience of handling of HPLC, GC, Potentiometer, Polarimeter instruments. 5. API Stability knowledge. 6. Capable to handle analytical method development, Implementation, Validation as per requirement. 7. Should have experience of Analytical method transfer to QC. 8. Experience of making documents like method transfer protocol & report, method validation protocol & report, method development report, specification, standard test procedure etc. 9. Should aware about GLP practices and 21 CFR part-11. 10. Keep the work area clean and the laboratory under controlled temperature. 11. Calibrate the instruments according to the master calibration schedule and follow GLP and SOPs. 12. Understand the safety and environmental aspect. 13. Maintain the reagents and standardize the volumetric solutions as per schedule. 14. Maintain the laboratory journals and instrument log books online. 15. Ensure compliance to Hazardous waste and chemical management. Responsibilities Qualifications Qualification : M.Sc (Analytical Chemistry), (Chemistry) & (Organic Chemistry)

We are looking for a dynamic and experienced Project Management Professional to join our pharmaceutical team. The ideal candidate will have strong experience in managing end-toend projects in formulation development and tech transfer for oral solid, semi-solid, and liquid dosage forms. This role requires excellent coordination across departments, strong technical knowledge, and the ability to lead project timelines and deliverables effectively Roles & Responsibilities: Lead and manage pharmaceutical product development projects (oral solid, semi-solid, and liquid dosage forms). Coordinate technology transfer activities from R&D to pilot scale and commercial manufacturing sites. Act as a central point of coordination across Regulatory Affairs, Quality, Supply Chain, and manufacturing partners (especially in India), to ensure technical documentation is planned, developed, and submitted in line with project timelines. Change Control & Deviation Support: Assist with the documentation and coordination of changes, deviations, and quality events as required to support the RA division. Ensure timely completion of project milestones and deliverables across multiple stakeholders. Track and report project status, identify risks, and implement mitigation strategies. Liaise with cross-functional teams to resolve site and plant-related issues. Drive project timelines and ensure all regulatory and quality requirements are met. Ensure thorough documentation and compliance with company SOPs and regulatory guidelines. Provide strategic inputs from QA, RA, and R&D perspectives to strengthen project planning and execution. Liaison with Indian Manufacturers: Establish and maintain strong working relationships with India-based suppliers to ensure their outputs meet South African regulatory requirements (preferred not desirable), with a particular focus on technical consistency, traceability, and responsiveness. Requirements: • Masters degree in Pharmacy (M. Pharm) • 7–10 years of relevant experience in project management within the pharmaceutical industry. • Experience in technology transfer of oral solid and semi-solid dosage forms is highly desirable. • Strong understanding of QA, RA, and R&D operations. • Sound knowledge of plant/site processes, compliance, and manufacturing workflows. • Demonstrate strong communication, leadership, and multitasking abilities.

The reputed pharmaceutical company engaged in development, manufacturing and marketing of oral solid dosages forms in regulated market. We are looking for competent, growth-oriented professional in Quality Assurance and Quality Control profiles for our USFDA & EU-GMP approved OSD manufacturing facility at N-32, Additional Patalganga MIDC, Tal.- Panvel, Dist.- Raigad.Roles and Responsibilities Ensure compliance with cGMP guidelines during formulation development, solid oral manufacturing, and OSD production. Conduct analytical method validation, stability studies, and quality control activities to ensure product quality. Develop and maintain documentation for batch records, test results, and equipment calibration schedules. Collaborate with cross-functional teams to resolve issues related to process deviations and CAPAs (Corrective Action Preventive Actions). Participate in audits conducted by regulatory agencies such as USFDA. Desired Candidate Profile 3-7 years of experience in pharmaceutical industry with expertise in formulation development, solid orals, OSDs, QC/QA/Qc/quality assurance/quality control. Bachelor's degree in Pharmacy (B.Pharma) or Master's degree in Pharmacy (M.Pharma) from a recognized institution. Strong understanding of GMP regulations and industry standards for pharmaceutical manufacturing.

The reputed pharmaceutical company engaged in development, manufacturing and marketing of oral solid dosages forms in regulated market. We are looking for competent, growth-oriented professional in Quality Assurance and Quality Control profiles for our USFDA & EU-GMP approved OSD manufacturing facility at Patalganga MIDC, Tal.- Panvel, Dist.- Raigad.Roles and Responsibilities Ensure compliance with cGMP guidelines during formulation development, solid oral manufacturing, and OSD production. Conduct analytical method validation, stability studies, and quality control activities to ensure product quality. Develop and maintain documentation for batch records, test results, and equipment calibration schedules. Collaborate with cross-functional teams to resolve issues related to process deviations and CAPAs (Corrective Action Preventive Actions). Participate in audits conducted by regulatory agencies such as USFDA. Desired Candidate Profile 3-7 years of experience in pharmaceutical industry with expertise in formulation development, solid orals, OSDs, QC/QA/Qc/quality assurance/quality control. Bachelor's degree in Pharmacy (B.Pharma) or Master's degree in Pharmacy (M.Pharma) from a recognized institution. Strong understanding of GMP regulations and industry standards for pharmaceutical manufacturing.

Meet&engage with doctors, end-users, procurement, purchase departments in clinics, cradles, specialty hospitals.Achieve monthly sales targets. Location: Chennai, Bangalore, Hyderabad, Delhi,Kolkata,M umbai Required Candidate profile Exp 2 to 6 yrs with a Degree in Marketing, Selling, preferably Pharma, Medical & Surgical Aggregator Business. Medical Device, Disposable & Surgical

Graduate / PG with 0 to 3 years of experience as a Personal Assistant / Executive Assistant. Arranging travel & accommodation for Directors for hotel & travel. To provide comprehensive administrative and secretarial support to our Directors. Required Candidate profile Capable of managing schedules, handling confidential information, coordinating meetings, preparing reports & ensuring smooth running of daily operations for leadership team. Handle all correspondence. Perks and benefits Negotiable - Depending Upon Candidate & Experience

Looking for a Zonal Sales Manager who has handled the Gujarat as well as Maharashtra regions and is based in Ahmedabad. Key Responsibilities: Sales Leadership: Develop and execute sales plans and strategies for the assigned zone, ensuring alignment with overall company goals. Lead and motivate a team to achieve sales targets. Conduct regular performance reviews and provide coaching and development opportunities for team members. Client Relationship Management: Build and maintain strong relationships with key accounts, including hospitals, clinics, and pharmaceutical distributors. Identify and develop new business opportunities within the zone. Address customer inquiries and concerns in a timely and professional manner. Sales & Marketing Strategy: Develop and implement targeted sales and marketing campaigns to drive product awareness and adoption. Monitor market trends, competitor activities, and customer needs to identify opportunities for growth. Collaborate with the marketing team to ensure effective execution of marketing programs. Performance Management: Set and track sales targets for the zone, ensuring accountability and progress towards goals. Analyze sales data to identify areas for improvement and optimize sales strategies. Manage the zonal budget and ensure efficient resource allocation. Compliance & Industry Knowledge: Maintain a thorough understanding of relevant regulations and industry standards. Keep abreast of new product developments, competitor offerings, and market trends. Ensure compliance with all company policies and procedures. Qualifications: Bachelor's degree in Life Sciences, Biotechnology, or a related field. Minimum 5 years of experience in pharmaceutical sales, with a proven track record of success in a managerial role. Strong leadership, communication, and interpersonal skills. Experience in team management and development. Excellent analytical and problem-solving skills. Understanding of the pharmaceutical industry, including market dynamics, key stakeholders, and product launches.

Roles and Responsibilities Provide clinical pharmacy services to patients, including dispensing medications and counseling on their use. Authorize prescriptions and monitor patient treatment plans in collaboration with healthcare providers. Participate in quality improvement initiatives to enhance patient care and satisfaction. Desired Candidate Profile 1-5 years of experience as a Clinical Pharmacist or related field (pharmacy, biotechnology). Strong knowledge of pharmacy operations, drug authorization processes, and regulatory requirements. Excellent communication skills for effective interaction with patients, families, and healthcare professionals. Ability to work independently while prioritizing tasks effectively under pressure.

What you will do The Global HEOR Systematic Literature Review (SLR) Leader oversees the development and delivery of systematic literature review activities within Amgens Global HEOR function. This operational and managerial role includes supervision of a team of Global HEOR SLR Analysts, ensuring high-quality, timely, and scientifically robust literature review outputs. The Global HEOR SLR Leader will align closely with Global HEOR TA Heads in support of global market access and value demonstration for Amgens products across their lifecycle. Lead, mentor, and handle a team of Global HEOR SLR Analysts, fostering a high-performance culture. Oversee the design, execution, and quality control of systematic literature reviews across therapeutic areas. Supervise the development of research protocols, screening strategies, and data abstraction tools. Collaborate with HEOR TA Heads to align literature review outputs with HEOR strategy. Serve as the functional guide on literature review within HEOR. Ensure consistency with PRISMA, PICOS, and other industry standards for evidence synthesis. Support integration of SLRs into HTA submissions, global value dossiers, and peer-reviewed publications. Continuously improve workflows, tools, and methodologies to enhance review efficiency and quality. Contribute to hiring, training, and performance evaluations within the SLR team. What we expect of you We are all different, yet we all use our unique contributions to serve patients. The HEOR Systematic Literature Review Leader we seek should possess these qualifications. Basic Qualifications & Experience: Doctorate degree in health economics, public health, Epidemiology, Pharmacy, life sciences or related field and 2 years of experience in systematic literature reviews and evidence synthesis in the pharmaceutical, biotech or consulting setting OR, Masters degree in Health Economics, Public Health, Epidemiology, Pharmacy, life sciences or related field and 8 to 10 years of experience in systematic literature reviews and evidence synthesis in the pharmaceutical, biotech or consulting setting OR, Bachelors degree in Health Economics, Public Health, Epidemiology, Pharmacy, life sciences or related field and 10 to 14 years of experience in systematic literature reviews and evidence synthesis in the pharmaceutical, biotech or consulting setting OR, Diploma in Health Economics, Public Health, Epidemiology, Pharmacy, life sciences or related field and 14 to 18 years of experience in systematic literature reviews and evidence synthesis in the pharmaceutical, biotech or consulting setting 3+ years of experience in team management capacity. Skills & Competencies: Exceptional leadership, mentoring, and project management skills. Excellent English oral and written communication, with ability to tailor content to different key partners; past medical writing experience is a plus Advanced proficiency with systematic review tools and citation databases (e.g., PubMed, EMBASE). Skilled in Microsoft Office (Word, PowerPoint, Excel); experience with EndNote or other reference tools preferred. High attention to detail, quality assurance, and evidence integrity. Innovative use of artificial intelligence to boost efficiency Organizational Behaviors: Solution-oriented with a continuous improvement attitude. Strong interpersonal and customer engagement capabilities. Comfortable working in a distributed team across time zones and cultures.

Monitor Field Force activity & sales Digitally Analyze statements & reporting the Mgt Support FF to achieve targets Monitor & Plan-trade schemes & incentives for Field force-dispatch of Stocks & Sales promotion material - gifts-brochures-posters. Required Candidate profile Exp. as ASM in Pharma - preferred. Willing to work @ Head Office Know reporting systems, man mgt, data analysis, planning & computer skills Must know English, Telugu, Oriya, Hindi. Call - 8871829882