3740 Pharma Jobs - Page 4

Primary Function/Primary Goals/Objective Ensure Food Safety Plan is implemented as per Abbotts Internal Policies & External Requirements, (such as FSSC22000 & Extenal Regulatory Bodies). Changes in Products, Production Processes, Equipments, Facilities etc are evaluated from Food Safety Risk Assessment with Mitigation Plans till Execution. Provide oversight to Plant GMP, Cleaning & Sanitation, Validation & CAPA Activities linked with Food Safety Support cascade of Global Food Safety Initiatives at Shop Floor Level. This list of responsibilities may change depending on plant needs and employees are expected to be adaptable and flexible where this need arises. Major Responsibilities: The role of Food Safety Engineer is part of the sites success and compliance by: Review & Improve Site Food Safety Plan through End to End Implementation of HACCP Principles into daily ways of working Promote Food Safety Culture & Vital Behaviours. Use Existing Databases to Track & Trend Data Points from Multiple Workstream to derive meaningful inferences & future improvement projects for Food Safety Improvements Lead/ Support Food Safety Risk Assessment with Mitigation Proposals linked with Change Management Cycle of RM/PM, Product, Process, Equipment, Facilities & Capital Projects. Lead/ Support Food Safety Event Investigation & Implementation of linked CAPAs with focus on systems & still remain reliable during manual operation. Participate in Abbotts Validation Review Board Meeting as well as CAPA Review Board Meetings for Proactive & Reactive Food Safety Risk Management. Active contribution to implementation of Global Food Safety Initiatives Provide oversight to Sites Cleaning, Sanitation & Hygiene Management Program Active coordination between Production, QA & Engineering Function for effective implementation of GMP, EMP & Sanitation Management Provide Periodic Refresher Trainings to Site Staff & Cascade Learnings from Global Food Safety Events from time to time. Liase with Global Subject Matter Experts from time to time to align improvement initiatives. Support Internal & External Food Safety Audits as per assigned responsibilities. Systematic Documentation linked with Quality System Compliances Provide Food Safety related Inputs to Leadership through Management Reviews/ other defined Mechanisms. Education: Minimum Bachelors Degree in Food Technology/ Daity Technology/ Food Engineering/ Microbiology/ Pharma with relavant experience in Plant Quality/ Food Safety/ GMP/ Hygiene & Sanitation. Experience of 7 to 10 years in Dairy/ Food/ Nutritional Powder Manufacturing Facility with emphasis on Infant Powder is preferred. Background Understanding and application of HACCP Principles with in depth understanding of Physical, Chemical & Microbiological Hazards with focus on food borne pathogen knowledge. Cleaning & Sanitation principles including Mode of Actions of chemicals Integrated Pest Control & Management Critical & Strategic thinking in order to go in depth understanding of Site Operations and related complex issues and provide the best feasible solutions at all levels. Communication, Collaboration & Influencing Skills Interpersonal skills in order to have healthy relationship with colleagues working in different functions at site Continuous Improvement Mindset Project Management Skills. Accountability/Scope: Keep Sites Food Safety Management System Live & Breathing with Continuous Improvement Food Safety Risks are proactively identified & appropriately mitigated. Learnings are built effectively in system to avoid repeat incidents. JOB FAMILY: Operations Quality DIVISION: ANSC Nutrition Supply Chain LOCATION: India > Jhagadia : Operation Support TRAVEL: Yes, 25 % of the Time t SIGNIFICANT WORK ACTIVITIES: Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)

Annalect is looking for Art Direction - Senior Designer to join our dynamic team and embark on a rewarding career journey Oversee all design projects, from conception to deliveryReview junior designers work to ensure high qualityGenerate ideas to portray concepts and advertise products/servicesIncrease user friendliness in digital productsMaintain brand consistency throughout all our marketing projectsLiaise with marketing and design teams to ensure deadlines are met

Spectrum Pharmatech Consultants Pvt. Ltd. is looking for Project - Officer to join our dynamic team and embark on a rewarding career journey Collaborate with cross-functional teams to achieve strategic outcomes Apply subject expertise to support operations, planning, and decision-making Utilize tools, analytics, or platforms relevant to the job domain Ensure compliance with policies while improving efficiency and outcomes

Spectrum Pharmatech Consultants Pvt. Ltd. is looking for Process-Designer to join our dynamic team and embark on a rewarding career journey Conceptualize and Create Designs:Develop creative and innovative design concepts for various projects Produce high-quality visual designs from concept to execution, including those for desktop, web, and mobile devices Collaborate with Cross-Functional Teams:Work closely with cross-functional teams, including product managers, developers, and marketing teams, to ensure design concepts align with project goals and objectives User Interface (UI) and User Experience (UX) Design:Design and deliver wireframes, user journeys, and mockups optimized for a wide range of devices and interfaces Conduct user research and evaluate user feedback to enhance the user experience Brand Consistency:Ensure consistency of brand and creative across digital and print materials Stay Updated on Design Trends:Stay up-to-date with industry trends and incorporate the latest design technologies and tools into daily work Iterative Design:Iterate on designs based on feedback from team members and stakeholders Qualifications:Bachelor's degree in Design, Fine Arts, or related field Proven experience as a designer, with a strong portfolio showcasing a variety of design projects Proficient in design software such as Adobe Creative Suite Strong understanding of UI/UX principles and best practices Excellent communication and collaboration skills Ability to work on multiple projects simultaneously and meet deadlines

Electrical-Executive Qualification: BE in Electrical Engineering Experience: 7-8 years in pharma consulting (only) Job Description - Experience in maintenance will not be considered Experience in design of ELV systems like fire alarm system, access control system, CCTV systems Calculations for equipment/components sizing such as transformer, generator back up, UPS, Cables, Cable Tray, Switchgear, etc Prepare technical specifications, data sheets, BOQ, and construction drawings Knowledge of AutoCAD & Revit Software is mandatory Location - Thane, MS

HVAC-Designer Qualification: ITI Diploma in Mechanical drafting OR Engineering Experience: 4-8 years in pharma consulting (only) Job Description - Prepare/Review Design Drawings as project deliverables: Like Air Flow Diagrams, RCP, Ducting Layouts Coordination with other departments Good hands-on experience in AutoCAD & Conversant with Revit Software is mandatory Location - Thane, MS

Electrical-Officer Qualification: BE - Electrical Experience: 4-5 years in pharma consulting (only) Job Description - Calculations for equipment/components sizing such as transformer, generator back up, UPS, Cables, Cable Tray, Switchgear, etc Experience in design of ELV systems like fire alarm system, access control system, CCTV systems Prepare technical specifications, data sheets, BOQ, and construction drawings Good hands-on experience in AutoCAD & Conversant with Revit Software is mandatory Location - Thane, MS

/h4> Academics & Experience: B Pharmacy or B Sc 1-5 Years of sales & marketing experience in a pharma or OTC products company. Candidate should have excellent communication skills both written and verbal in English. Should be a go-getter and achiever both in academics and professional career. Willingness to work hard and high task achievement orientation.

Premier Research is looking for a Associate Data Manager - FS (4 month fixed-term contract) to join our Functional Services Provider (FSP) team. You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success. We are Built for You. We are here to help you grow, to give you the skills and opportunities to excel at work with the flexibility and balance your life requires. We are Built by You. Your ideas influence the way we work, and your voice matters here. We are Built with You. As an essential part of our team, you help us deliver the medical innovation that patients are desperate for. Together, we are Built for Biotech . Join us and build your future here. What we are searching for: Assists in preparing clean databases by performing a review of clinical trial data through the CDMS or external data listings to ensure all captured data follows the rules outlined by the protocol and Data Management Plan Provide input to and review of Data Management Plans in support of clinical study deliverables Generates queries to appropriate internal or external personnel (e.g. - investigational sites, vendors, Clinical Research Associates, and client representatives) to resolve problematic data identified during every aspect of the data management process Reviews responses to queries for appropriateness, resolves any discrepancies, and modifies the database accordingly Supports the development of CRFs and edit check specifications per protocol and participates in user acceptance testing of CRFs and associated edit check specifications as required Assists in the user acceptance testing for study-specific data listings ensuring data output adheres with requirements Prepares and maintains documentation related to CRF, edit check, and data listing testing including initial testing and follow-up testing to ensure that the changes have been made, as required What we are searching for: Bachelor degree, or international equivalent from an accredited institution, preferably in a technical, clinical, or health-related field], or equivalent combination of education, training and experience 3 to 5 years of practical experience using commercial clinical data management systems and/or EDC products (eg - Oracle RDC / Inform, Medidata Rave, DataLabs, etc). Alternately, must have proven experience in all primary job functions. Demonstrates excellent English verbal and written communication skills Excellent computer skills in a Microsoft Windows environment including proficiency in the Microsoft Office Suite of tools (eg - Outlook, Work, Excel, etc) Proven ability to drive a successful customer experience through positive customer interactions, provision of quality and timely deliverables, and task ownership Strong analytical and organization skills, able to work independently and manage multiple projects simultaneously in a fast-paced environment with changing priorities

Job Title: Manager-2/Manager-1 Job Grade: G11A/G10 Function: Global Business Development Sub-function: IP Litigation Manager s Job Title: Sr. General Manager Skip Level Manager s Title: Function Head Title: Sr. Vice-President Location: Baroda Areas Of Responsibility At Sun Pharma, we commit to helping you Create your own sunshine by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you ll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each other s journeys. Areas Of Responsibility: Management of the branded portfolio from IP perspective Life Cycle management of branded portfolio from IP perspective Preparation of landscape Preparation of FTO and infringement analysis report Identifying and tracking competition Determining LoE (earliest generic entry) and means to extend it Monitoring applicable regulatory exclusivities Patentability evaluation, patent filing and prosecution Life Cycle management of NCE portfolio Support and Preparation for activities related with enforcement of IP Search and analysis- in NCE, formulation based technologies, Medical Devices related Inventions IP due diligence for technologies and products for in-licensing IP due diligence to support merger and acquisitions IP support for out-licensing projects Agreement review including CDA, IITs, MSA, MTA etc. Performing validity analysis of blocking patents Identifying new opportunities for in-licensing Travel Estimate Up to % Job Scope Internal Interactions (within the organization) With all stake holders External Interactions (outside the organization) With attorneys globally Geographical Scope Global Financial Accountability (cost/revenue with exclusive authority) Job Requirements Educational Qualification M.Pharm (P ceutical chemistry)/Ph.D in Pharmacy Specific Certification Certification on patent law- preferred Skills Experience on handling: NCE portfolio Patent drafting and Prosecution Experience 8-12 years Your Success Matters to Us At Sun Pharma, your success and well-being are our top priorities! We provide robust benefits and opportunities to foster personal and professional growth. Join us at Sun Pharma, where every day is an opportunity to grow, collaborate, and make a lasting impact. Let s create a brighter future together!

For the past 20 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the complete product lifecycle. With deep domain expertise in regulatory sciences, clinical research solutions, quality & compliance, pharmacovigilance, medical information, and R&D technology, ProPharma offers an end-to-end suite of fully customizable consulting solutions that de-risk and accelerate our partners most high-profile drug and device programs. Job Description The Medical Information Admin Assistant provides comprehensive administrative support to the Medical Information (MI) Enquiry Handling teams and Senior Management in an accurate and efficient manner. Responsibilities General administrative duties as delegated by management. Answering the main telephone line of the Company in a professional manner and transferring calls as appropriate. On an ad-hoc basis providing reception cover which includes meeting, greeting, and signing in all visitors to the ProPharma office in a friendly, courteous, and professional manner. Supporting the filing clerks, including opening the daily mail received into the company, franking, and posting the mail, filing, archiving and checking stationery stocks. Effectively perform in at least three task areas. Quality Assurance Maintaining a good level of quality in all aspects of the job. Complying with the procedures documented in the Company Standard Operating Procedures (SOPs) and Working Instructions (WIs). General Having a solid working knowledge of, and complying with, the Standard Operating Procedures of ProPharma Working in a professional manner at all times, with clients, customers, team members and management. Complying with the Company s Health and Safety Policies. Ensuring the Confidentiality Statement within the Contract of Employment is always adhered to in respect of the data and property of ProPharma, its clients and employees of the business. Ensuring that any confidential information or personal data related to ProPharma and its clients is managed in accordance with Data Privacy regulations as described in ProPharma SOPs. Other duties as assigned. Necessary Skills and Abilities: Able to work within a team in a professional manner. Sound written and oral communication skills. Good accuracy and attention to detail skills. Solid level of productivity on all tasks. Sound organizational and prioritizing skills showing an effective workload management system. Able to understand and follow processes. Pleasant and professional telephone manner. Computer literacy (MS Office). ***ProPharma Group does not accept unsolicited resumes from recruiters/third parties. Please, no phone calls or emails to anyone regarding this posting.***

Operations Manager Position Summary: Manage operations part for the client delivery team and to ensure all operations are met within agreed timelines with quality. Under the guidance of Director Operations perform operations support activities including Employee Onboarding, Training Coordination, Performance appraisal, termination documentation/communication, bench management, immigration, liaise with finance/legal/HR/Immigration to resolve queries/issues, support Engagement Managers with invoice data or any other associate data under minimal supervision. With support from Director Operations and Engagement Managers manage metrics data generated by deliverable teams and are met to expected quality and timelines. Mentor/develop employees under the guidance of AD/Dir or designee. Lead/support data collection activity to help with governance meetings (ex: metrics data to be presented at governance meetings). Support to improve engagement levels as needed under the Guidance of AD / Dir Operations Mandatory Experience/Skills/Knowledge Requirements To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions; 10-12 years appropriate experience in similar role; A minimum of 5 years of management/leadership experience; Appropriate understanding of at least one hiring systems, employee verification process & Operations Management systems for managing employees timesheet, invoice & billing etc.,, Prior experience with successfully leading project team(s); Ability to liaise successfully with internal & external stakeholders, including excellent written and verbal communication skills; Ability and willingness to travel as required, up to 10%; Education: Bachelors/Masters in any discipline (Preferably, life sciences education) With relevant experience in Pharma and drug development /operations management in Pharma/CRO industry. Job Function/Responsibilities: Recognize, demonstrate and observe Cytel values which center on our commitment to People, Clients and Performance. Recognize the importance of and create a culture of process improvement with a focus on streamlining current processes adding value to Cytel business and meeting client needs. Travel both domestic and/or international is required. Read, understand and adhere to all assigned Cytel SOPs and working procedures (or sponsor as appropriate). Identify and organize the training needs as appropriate in coordination with Engagement Managers or designee. Ensure completion of all assigned training courses, ensuring that mandatory courses are completed before designated date and that the required system specific training has been completed for current studies. Perform interim /annual performance appraisal of assigned team members and identify gaps and propose development plans in consultation with Engagement Managers or designee. Identify gaps and suggest process improvements (internal/external) on an ongoing basis. Responsible for administrative activities and perform other general duties as required to support the company. Liaise with the AD/Dir and Sr.Leadership team in order to ensure that overall project objectives are met in an efficient manner. Provide input to the development of new systems and processes, as required. Under the guidance of Director Operations/EMs, ensure adequate processes are put in place in response to deviations in data quality, timelines and/or budget. Provide regular feedback to the delivery team members on their performance and initiate follow up review where required (work with Group TA heads on performance concerns, mitigations plans, and expected improvement; awarding/sending accolades with appropriate follow-ups and confirmation).

Shall be able to prepare schematics for process, utility and gas generation and distribution systems. Preparation of Isometric drawings, Construction drawings and sections. BOQ/MTO estimation. Good Experience in Auto Cad Plant 3D/ P&ID.

Job title: (Senior) Manager, GOE LCP Digital Manufacturing and Process Control Service Group/Unit : Engineering / LCP Job location: Mumbai, India The position reports to Director GOE LCP Process and Controls and the incumbent shall lead the design and execution of Large Capital Projects in the field of Digital Manufacturing, Process Control and Electrical Engineering . This role focuses on implementing and servicing new production lines and greenfield factory developments. Responsibilities also include developing and maintaining comprehensive project plans and schedules while sharing accountability for project outcomes. The Large Capital Project (LCP) organization for dsm-firmenich in India acts as a key support function for all business units. As the companys reference group, LCP is responsible for managing and delivering the portfolio of large capital projects, ensuring alignment with strategic objectives and operational excellence. At dsm-firmenich, being a force for good is not optional. Diversity, Equity & Inclusion is a shared responsibility woven into our daily work, benefiting to our People, Customers & Communities and driving business value. Equal access to opportunities is a given, belonging is a shared feeling, authenticity is celebrated. Your key responsibilities : Digital Manufacturing Strategy & Integration Support Business Units in defining and aligning Digital Manufacturing scope across stakeholders, ensuring D&T integration in LCP projects with proper controls for on-time, budget-compliant, and quality delivery. Project & Process Standardization Drive the standardization of LCP Work Processes to streamline project execution; coordinate the design and rollout of MES, LIMS, and other manufacturing data platforms. Process Control Implementation Develop and implement Process Control strategies across all LCP phases; guide engineering teams on Automation, Electrical, and Instrumentation design and construction. Operational Support & Optimization Lead commissioning, validation, and start-up activities with cross-functional teams; provide technical expertise in troubleshooting and optimizing DCS, PLC, and instrumentation systems. Compliance, Safety & Innovation Ensure adherence to safety standards (e.g., Process Safety, OBRA); challenge conventional methods by applying best practices to enhance efficiency, safety, and compliance across operations. Leadership, Governance & Cybersecurity Manage cross-country projects, stakeholder relations, and contractual partnerships; oversee budgets, maintain strong project controls, strengthen cybersecurity, and hold authority to stop unsafe work practices. You Bring: Technical Leadership & Stakeholder Collaboration Strong leadership skills to align cross-functional teams, vendors, and stakeholders; proven ability to navigate complex, multi-disciplinary environments across Automation, Electrical, Instrumentation, D&T, and Operations. Global & Cultural Agility Adept at communicating in diverse, multicultural settings with both technical and non-technical audiences; brings cultural intelligence and adaptability to collaborate across regions. Travel within India and globally is essential. Analytical & Decision-Making Excellence Demonstrates sharp analytical thinking, problem-solving, and risk management in high-impact, fast-paced engineering environments with multiple competing priorities. Advanced Education & Technical Expertise Holds a Bachelor s or higher degree in Automation, Electrical, or Mechatronics; deep expertise in Digital Manufacturing and Process Control, with hands-on experience in PLCs, HMI, SCADA (Allen Bradley, Rockwell, Siemens), DCS (Emerson, Siemens, ABB), and data platforms like OSI PI. IT-OT Integration & Cybersecurity Knowledge Solid grasp of networking protocols, system architecture, and OT cybersecurity, including patch management, disaster recovery, and vulnerability assessments; understands the critical interface between IT and OT systems. Extensive Industry & Project Experience Brings over 10 years of experience leading large-scale Digital Manufacturing and Automation projects (> $10M) in industries like food, fine chemicals, pharma, or oil & gas; proven ability to manage full project life cycles and ensure regulatory compliance (ATEX, OSHA, GMP, HAZOP). We bring: A team of diverse employees who aren t afraid to think outside of the box. A truly global and collaborative team that cares about the experience of our employees. The encouragement you need to develop and achieve personal growth. A role that is crucial on projects and allows you to build your brand. A caring and supportive environment where you re empowered to grow and share your ideas. The application process. Interested in this position? Please apply on-line by uploading your resume in English via our career portal. For . We aim to build a workplace where opportunity really is equal, so everyone can thrive. We do not discriminate; theres a place for everyone at dsm-firmenich. Dsm-firmenich is an Equal Opportunity and Affirmative Action Employer. dsm-firmenich people are as diverse as our customers. For us that includes a commitment to ensuring equal employment opportunities for all job applicants and employees. Employment decisions are based upon job-related reasons regardless of an applicants race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, marital status, genetic information, protected veteran status, or any other status protected by law. We are committed to providing reasonable support for disabled applicants in our recruiting process. Should you need assistance, and are comfortable to share this, please let us know. About dsm-firmenich As innovators in nutrition, health, and beauty, dsm-firmenich reinvents, manufactures, and combines vital nutrients, flavors, and fragrances for the worlds growing population to thrive. With our comprehensive range of solutions, with natural and renewable ingredients and renowned science and technology capabilities, we work to create what is essential for life, desirable for consumers, and more sustainable for the planet dsm-firmenich is a Swiss Dutch company, listed on the Euronext Amsterdam, with operations in almost 60 countries and revenues of more than 12 billion. With a diverse, worldwide team of nearly 30,000 employees, we bring progress to life every day, everywhere, for billions of people

Interview for Production Dept on 02-08 in Bharuch for API Pharma Company in Dahej Qualification: BE / Diploma Chemical / BSC / MSC Chemistry / ITI AOCP Experience: 3 to 13 Years CTC: Up to 8 LPA No Charges Free Jobs Share with Your Friends!!! Required Candidate profile Send CV on sdpbharuch@gmail.com with Subject: Production Dahej & Call on 760033423 Interview Venue: SDP HR SOLUTION, Sixth Floor, 611, Golden Square, Beside DMART, Near ABC Circle, Bholav, Bharuch

Job Title: Programming Intern - Pharmaceutical Integration Location: Chennai, India Job Description: We are seeking a motivated and talented Programming Intern to join our dynamic team at Pfizer, IITMRP site, Chennai. The ideal candidate will have strong programming skills, particularly in Python, and will assist in data integration across chemistry, analytical, and engineering processes to enhance our research and development capabilities. Key Responsibilities: Programming and Scripting: Develop and maintain scripts and software tools using Python and other programming languages to automate and streamline laboratory and engineering workflows. Data Integration: Collaborate with chemists, analysts, and engineers to integrate data from various sources, ensuring seamless data flow and accessibility across departments. Software Development: Assist in the development of custom software solutions to support analytical and engineering tasks, including data analysis, visualization, and reporting. Database Management: Support the management and maintenance of databases, ensuring data integrity and security. Research Support: Provide programming support for research projects, including the development of algorithms and models to analyze experimental data. Documentation: Maintain comprehensive documentation of code, processes, and workflows to ensure reproducibility and knowledge sharing. Collaboration: Work closely with cross-functional teams to understand their needs and provide technical solutions that enhance productivity and efficiency. Qualifications: Educational Background: Currently pursuing or recently completed a degree in Computer Science, Chemical Engineering, Chemistry, or a related field. Programming Skills: Proficiency in Python is essential. Knowledge of other programming languages such as R, Java, or C++ is a plus. Analytical Skills: Strong analytical and problem-solving skills with the ability to interpret complex data sets. Technical Knowledge: Basic understanding of chemistry and engineering principles is preferred. Communication Skills: Excellent verbal and written communication skills to effectively collaborate with multidisciplinary teams. Attention to Detail: High level of accuracy and attention to detail in all tasks. Team Player: Ability to work independently as well as part of a team in a fast-paced environment. Benefits: Gain hands-on experience in a leading pharmaceutical company like Pfizer. Work on cutting-edge projects that integrate chemistry, analytical, and engineering disciplines. Opportunity to learn from experienced professionals and expand your skill set. Competitive stipend and potential for future employment opportunities. Work Location Assignment: On Premise Research and Development

Greetings from CorroHealth ! We are Hiring Paramedical Graduates! We are pleased to invite you for a direct walk-in interview. If you are enthusiastic, eager to learn, and ready to kickstart your career, we would love to meet you! Walk-In Details: Time: 9am to 12pm Interview Venue: Venue - Kochi CorroHealth 4th Floor, Double Tree Properties, Opposite Ernakulan Medical Center, Eranakulam, Chakkaraparambu, Palarivattom, Ernakulam, Kerala 682025 Eligibility Criteria: Qualification: B Pharm / M Pharm / PharmD / Biotechnology / Microbiology only Year of Passing: 2024 / 2025 Percentage: Min 60% in all academic year (10th, 12th, UG & PG) Documents to Carry: * Updated Resume * Government-issued ID proof * Passport-size photograph Note: Only direct walk-in. Please Call or WhatsApp 9043979492 for registration or Mention Sushil on top of your Resume

Role Implant / RPO Job Location – Matoda Ahmedabad Client Industry – Pharma (Non IT Hiring) RESPONSIBILITIES: 1. Managing stakeholders (Client Hiring Managers, Back-end Delivery team, candidate management, Team Management, etc.) 2. Validating manpower requisition in consultation with line and business HR. 3. Working closely with the client HR team and Hiring Managers to understand the requirements and then cascading to the back-end delivery team. 4. Maximizing the mandate & working closely with the Head-Ops, so as to meet or exceed client expectations. DESIRED CANDIDATE PROFILE: 1 .Candidate should have experience in Recruitment 2. Should have effective Convincing and negotiation skills to impress and attract top talent. 3. Developing & maintaining relations with Client Hiring Managers, Business Leaders and Heads. 4. Recruitment Life cycle, Stake holder Management, Team Management with cross-functional teams. 5. Understanding the requirements and then cascading the same to the back-end delivery team. 6. Energetic, accomplished and creative personnel with great recruitment and management skills.

Job Opportunity: Medical Coder Medical Coding is the process of converting Verbal Descriptions into numeric or alpha numeric by using ICD 10-CM, CPT && HCPCS. As per HIPAA rules healthcare providers need efficient Medical Coders. Qualification & Specifications : MBBS, BDS, BHMS, BAMS, BSMS, PHARMACY B.Sc/M.Sc (Life Sciences / Biology / Bio Chemistry / Micro Biology / Nursing / Bio Technology), B.P.T, B.E BIOMEDICAL, B.Tech (Biotechnology/Bio Chemistry). 2020-2025 passed out Skills Required: * Candidates should have Good Communication & Analytical Skills and should be Good at Medical Terminology (Physiology & Anatomy). Role: To review US medical records Initial file review for identifying merits Subjective review and analysis to identify instances of negligence, factors contributing to it To review surgical procedures, pre and post-surgical care, nursing home negligence To prepare medical submissions To prepare the medical malpractice case Regards Contact: HR Anu: + 91 9500408540

You will be working as an Associate Consultant in Pharma & Commercial Due Diligence. It is essential to have industry experience in Commercial Due Diligence/Deal Advisory Consulting for Pharma/Life Sciences on a global scale. The job location can be in Mumbai, Bangalore, Delhi, Noida, or Gurgaon. In this role, you will be part of IQVIA's Financial Institutions Consulting (FIC) team, where you will be advising investors such as private equity, venture capital, hedge funds, etc. on biopharma and life sciences investments. Your responsibilities will include conducting commercial due diligence, asset and target screening, portfolio company growth strategy, and exit/divestment strategy. As an Associate Consultant, your main tasks will involve managing projects related to due diligence (buy- and sell-side), asset/portfolio/company valuation, asset screening, and growth strategy. You will utilize your consulting and transaction advisory experience, along with IQVIA's information and expertise, to address client/business questions effectively. Your role will also require you to diagnose complex strategic issues/diligence questions, structure project approaches, manage project teams, and serve as the primary contact with clients during project delivery. Additionally, you will contribute to the overall capabilities of the FIC team by developing intellectual property, marketing materials, training, recruitment, and supporting business development activities. To qualify for this position, you must have a Master's Degree and 3 to 5 years of relevant experience in consulting, pharmaceutical, and/or healthcare industry. You should have a proven track record in teamwork, leadership, and be willing to travel as needed.,

As a Sales Executive with 2 years of experience in the pharmaceutical industry, you will be responsible for driving sales and business development for our pharmaceutical company located in Chandigarh, Chandigarh. Your role will involve generating leads, meeting sales targets, and contributing to the overall growth of the business. This is a full-time, permanent position that requires a Bachelor's degree as well as 2 years of experience in pharmaceutical sales, business development, lead generation, and overall sales experience. Fluency in English is a requirement for this role. In addition to a competitive compensation package that includes performance bonuses and yearly bonuses, we offer benefits such as cell phone reimbursement, health insurance, leave encashment, and Provident Fund contributions. The work schedule for this position is a day shift, and the work location is in person. If you are a motivated and results-driven individual with a passion for sales in the pharmaceutical industry, we invite you to apply for this exciting opportunity to join our team.,

As a Horeca Sales Manager at Prestige Pursuits Pvt. Ltd., a Channel Partner of Procter & Gamble (P&G) Brands (Braun Gillette/ Olay / Whisper etc.), you will play a crucial role in driving sales and marketing activities in the Ghaziabad/ Delhi/ Noida region. Your responsibilities will include maintaining strong relationships with clients, understanding the HORECA business model, and achieving sales targets through effective planning and execution. You will be required to conduct 5-6 client visits daily to corporate companies for sales meetings, focusing on cross-selling, upselling, and range expansion. Developing an area coverage plan, planning target account-wise share, and ensuring profitability in the HORECA segment will be key aspects of your role. Additionally, you will be responsible for interacting with various business houses and corporates, presenting products, and closing deals in coordination with internal teams. To succeed in this role, you must have proven experience in Pharma/FMCG as a B2B Sales Manager, with a strong sales track record and proficiency in computer skills. Excellent communication, negotiation, and time management skills are essential, along with the ability to build rapport and create awareness of products and brands in the market. A graduate/postgraduate degree in Marketing is required, and the work timings are from 9:00 AM to 6:00 PM, with a mix of work from home and field activities. The salary for this position is negotiable based on your interview performance and experience. Both male and female candidates are encouraged to apply for this full-time job opportunity. If you are ready to take on this challenging yet rewarding role, please contact Human Resources at 8700144617 to learn more about the application process.,

As the Director of Regulatory Research & Intelligence at Kamet Consulting Group, you will be responsible for leading and developing a team of research consultants in the life sciences and healthcare technology industry. Your role will involve overseeing regulatory intelligence, compliance support, and advisory services for clients in the pharmaceutical and medical device sectors. You will be the key authority for regulatory research activities in India, ensuring delivery excellence, quality control, and strategic insights. Your core responsibilities will include building and mentoring a team of research consultants, setting performance targets, and fostering their professional development. You will also be responsible for ensuring that all research, analysis, and regulatory intelligence meets global quality and compliance standards. Additionally, you will define and evolve the research agenda in alignment with regulatory trends and client priorities, oversee project delivery, and communicate complex regulatory insights to executive audiences. To qualify for this role, you should have an advanced degree in Pharmacy, Life Sciences, Regulatory Affairs, or a related field, with a preference for a PhD or MBA. You should have at least 10 years of experience in regulatory affairs, regulatory intelligence, or compliance within the pharma/medical devices industry, including 5 years in consulting and team management roles. Strong leadership skills, expert knowledge of global and Indian regulatory frameworks, exceptional communication abilities, project management experience, and an entrepreneurial mindset are essential for this position. Desired traits for the role include being well-read on regulatory and scientific literature, culturally adept in global teams, and having high ethical standards and a passion for quality in research and client service. Kamet Consulting Group offers a collaborative and innovative work environment, competitive compensation and benefits package, flexible working arrangements, and growth opportunities for all qualified applicants. Join us to contribute to meaningful technology in the life sciences domain and be part of a team committed to innovation.,

As an experienced professional with 10 to 15 years of experience, you will be responsible for various key aspects including Regulatory Affairs, Artwork Management, Supply Chain in the pharmaceutical industry, and Lean Business Process Management. This role requires you to work the 2pm to 11pm shift and offers a competitive salary of 31.5 Lakhs per annum. Your expertise in the mentioned areas will be crucial in ensuring the efficiency and compliance of operations within the organization.,

ZS is a place where passion changes lives. As a management consulting and technology firm focused on improving life and how we live it, our most valuable asset is our people. Here you'll work side-by-side with a powerful collective of thinkers and experts shaping life-changing solutions for patients, caregivers, and consumers worldwide. ZSers drive impact by bringing a client-first mentality to each and every engagement. We partner collaboratively with our clients to develop custom solutions and technology products that create value and deliver company results across critical areas of their business. Bring your curiosity for learning, bold ideas, courage, and passion to drive life-changing impact to ZS. Our most valuable asset is our people. At ZS, we honor the visible and invisible elements of our identities, personal experiences, and belief systems - the ones that comprise us as individuals, shape who we are, and make us unique. We believe your personal interests, identities, and desire to learn are part of your success here. Learn more about our diversity, equity, and inclusion efforts and the networks ZS supports to assist our ZSers in cultivating community spaces, obtaining the resources they need to thrive, and sharing the messages they are passionate about. **What you'll do:** We are looking for experienced Knowledge Graph developers who have the following set of technical skillsets and experience. Undertake complete ownership in accomplishing activities and assigned responsibilities across all phases of the project lifecycle to solve business problems across one or more client engagements. Apply appropriate development methodologies (e.g., agile, waterfall) and best practices (e.g., mid-development client reviews, embedded QA procedures, unit testing) to ensure successful and timely completion of assignments. Collaborate with other team members to leverage expertise and ensure seamless transitions; Exhibit flexibility in undertaking new and challenging problems and demonstrate excellent task management. Assist in creating project outputs such as business case development, solution vision and design, user requirements, prototypes, and technical architecture (if needed), test cases, and operations management. Bring transparency in driving assigned tasks to completion and report accurate status. Bring a Consulting mindset in problem-solving, innovation by leveraging technical and business knowledge/expertise and collaborate across other teams. Assist senior team members, delivery leads in project management responsibilities. Build complex solutions using Programming languages, ETL service platform, etc. **What you'll bring:** - Bachelor's or master's degree in computer science, Engineering, or a related field. - 4+ years of professional experience in Knowledge Graph development in Neo4j or AWS Neptune or Anzo knowledge graph Database. - 3+ years of experience in RDF ontologies, Data modeling & ontology development. - Strong expertise in python, pyspark, SQL. - Strong ability to identify data anomalies, design data validation rules, and perform data cleanup to ensure high-quality data. - Project management and task planning experience, ensuring smooth execution of deliverables and timelines. - Strong communication and interpersonal skills to collaborate with both technical and non-technical teams. - Experience with automation testing. - Performance Optimization: Knowledge of techniques to optimize knowledge graph operations like data inserts. - Data Modeling: Proficiency in designing effective data models within Knowledge Graph, including relationships between tables and optimizing data for reporting. - Motivation and willingness to learn new tools and technologies as per the team's requirements. **Additional Skills:** - Strong communication skills, both verbal and written, with the ability to structure thoughts logically during discussions and presentations. - Experience in pharma or life sciences data: Familiarity with pharmaceutical datasets, including product, patient, or healthcare provider data, is a plus. - Experience in manufacturing data is a plus. - Capability to simplify complex concepts into easily understandable frameworks and presentations. - Proficiency in working within a virtual global team environment, contributing to the timely delivery of multiple projects. - Travel to other offices as required to collaborate with clients and internal project teams. **Perks & Benefits:** ZS offers a comprehensive total rewards package including health and well-being, financial planning, annual leave, personal growth, and professional development. Our robust skills development programs, multiple career progression options, and internal mobility paths and collaborative culture empower you to thrive as an individual and global team member. We are committed to giving our employees a flexible and connected way of working. A flexible and connected ZS allows us to combine work from home and on-site presence at clients/ZS offices for the majority of our week. The magic of ZS culture and innovation thrives in both planned and spontaneous face-to-face connections. **Travel:** Travel is a requirement at ZS for client-facing ZSers; business needs of your project and client are the priority. While some projects may be local, all client-facing ZSers should be prepared to travel as needed. Travel provides opportunities to strengthen client relationships, gain diverse experiences, and enhance professional growth by working in different environments and cultures. **Considering applying ** At ZS, we're building a diverse and inclusive company where people bring their passions to inspire life-changing impact and deliver better outcomes for all. We are most interested in finding the best candidate for the job and recognize the value that candidates with all backgrounds, including non-traditional ones, bring. If you are interested in joining us, we encourage you to apply even if you don't meet 100% of the requirements listed above. ZS is an equal opportunity employer and is committed to providing equal employment and advancement opportunities without regard to any class protected by applicable law. **To Complete Your Application:** Candidates must possess or be able to obtain work authorization for their intended country of employment. An online application, including a full set of transcripts (official or unofficial), is required to be considered. NO AGENCY CALLS, PLEASE. Find Out More At: www.zs.com,