1094 Pharmaceutical Jobs - Page 41

Fresher Hiring 2021 - 2024 Passouts only - All India Qualification - B.Pharm, M.Pharm, B.SC, M.SC, Life Sciences Graduates & Post Graduates Medical - BDS, BHMS, BAMS, MBBS Role & responsibilities Perform data reconciliation between different data sources and study documents to ensure data integrity and consistency across datasets. Generate data queries to address discrepancies, inconsistencies, and missing data identified during data review, ensuring timely resolution and documentation of data queries Communicate data queries to investigative sites, data managers, and study personnel, following up on query responses and resolving discrepancies in collaboration with relevant stakeholders Identify deviations from protocol-specified procedures, eligibility criteria, and data collection guidelines, escalating issues to appropriate personnel for resolution Perform quality checks and data validation procedures to ensure accuracy, consistency, and reliability of clinical trial data, adhering to data management standards and industry best practices Assist in the development and implementation of data validation plans, data review guidelines, and quality control procedures to maintain high standards of data quality and integrity. Assist in a variety of specialties including but not limited to primary care, orthopedics, rheumatology, etc. Updates patient history, physical exam, and other pertinent health information in the document as required. Complies with Compliance standards of the Organization as laid by HIPAA. Performs other duties and tasks to improve provider productivity and workflow as assigned by supervisors. Assist documenting the patients, electronic health record (EHR). Fresher Hiring - Pharma / Life Sciences / Medical Qualification - B.Pharm, M.Pharm, B.SC, M.SC, Life Sciences Graduates & Post Graduates Medical - BDS, BHMS, BAMS, MBBS Location - All India - Delhi, Mumbai, Pune, Bangalore, Kochi, Chennai, Hyderabad, Ahmedabad, Bhopal, Indore, Kolkata, Chandigarh

Role & responsibilities I. Setting up International Business set-up at Tirupati Group. II. Generate new business from International clients in P2P / Contract manufacturing model from ROW Countries. Explore markets with different business Strategies, Negotiate Commercial business Terms & Executes agreements and post deal management. III. To handle and coordinate with existing clients and get new products from them. IV. Find out right business partner (Globally) for right products & registration process, To ensure coordination between clients & internal department if need and close the enquiry with proper actions like offer /samples/data etc. V. To work on a growth strategy focusing customer satisfaction and financial gains. VI. To provide full MIS to Management on Queries, Closing Deeds and monthly accomplishment based on product category and production line with proper analysis. VII. To act as the escalation point for the team. VIII. To identify the bottleneck in timely execution of tasks and eliminating them. Manage related operational activities for the region to ensure on-time supply of products IX. To coordinate with SCM on existing and prospective business orders. Shall have regular review with HODs to sort out the pending issues. X. To arrange business meetings and to promote company's product / services addressing clients objectives. XI. Manage a team of sales & marketing employees and helping them grow the business. XII. Conducts search and evaluation of collaboration and out-licensing opportunities with large pharmaceutical companies conduct market mapping, generating enquiries & check for technical compatibilities between products and requirements. Preferred candidate profile: - 8+ Years of experience in International Business Development. Contract Pharma manufacturing experience would be preferred. - Proficient with use of the Internet, MS outlook, MS office - including word, excel and PowerPoint. - Project management & data interpretation skills. - Ability to make & deliver process training sessions. - Expert in making and giving out articulate presentations with audio/video inputs in PPT. - Exposure to Pharma/Nutra/Sports Nutrition/Ayurveda Segments.

We are hiring for a leading Pharma formulation Group. Oversee 7 pharma plants across India. Responsible for Operations Management , Regulatory Compliance & QA Supply Chain, Process Improvement & Cost Optimization Budgeting & Financial Planning etc Required Candidate profile 20+ years in pharma formulation manufacturing, including 5+ years in leadership Strong leadership, decision-making & problem-solving skills. Experience in handling large-scale manufacturing plants

This is a full-time on-site role for a Manager of Project Management at Energon Labs in Hyderabad. The Manager will oversee day-to-day project management tasks related to analytical testing services and coordinate with various teams within the lab. Required Candidate profile Lead cross-functional project teams in the development and implementation of pharmaceutical projects, including drug development, Develop project plans, timelines, track progress.

Recruiter Details Mohaneswara Reddy https://www.linkedin.com/in/mohaneswarareddy Role & responsibilities 1. Ensure compliance of applicable legal & statutory requirements related to Environment, Occupational Health and Safety Management system. 2. Liaising with Directorate of Industrial Safety & Health (DISH) office, PECO, Fire department, District supply officer, MPCB, CPCB need basis for legal requirements. 3. Ensure effective implementation of Environment, Occupational Health and Safety Management system. 4. Ensuring initiation, planning & support for trainings, examine the effective of training. 5. To advise concerned department heads for implementation of Environment Health and Safety policy. 6. Finalising EHS goals/ objectives and EHS programme. 7. Ensure Effluent treatment plants smooth operation & its compliance as per MPCB/CPCB norms. 8. Support to unit for trouble shooting operations. 9. Ensure types of audits compliance & CAPA implementation for site. 10. Ensuring compliance of Corporates Environment, Occupational Health and Safety initiatives at site. 11. Ensure and participate in EHS incident investigation to prevent recurrence in future. 12. Ensure Process Safety hazard assessment and its compliance. 13. To operate the Cipla- Quality Management system based on the roles and rights provided in the application. 15. To promote setting up of Safety committees and act as adviser to such committees. 16. Ensure emergency preparedness across Site to reduce impact of Incidences to human and property. 17. Build competencies and guide in professional building to create a future ready team. 18. Ensure Safety promotional activities conducted to enhance safety awareness by conducted Safety Campaigns on regular basis as per need of the organization, National Safety Week Celebrations, National Fire service Day, environment week etc. 19. Ensure reliability of data, either paper or electronic, with an intention to integrity of GXP data. 20. Ensuring strict adherence to Environment, Health and safety rules and procedures 21. To operate various software like Cipla- Quality Management System (QMS), SAP, Document Management system (Cip Dox), MYSETU, LMS, etc. based on the roles and rights provided in the application. 22. Any other Job allocated by the senior Management. Preferred candidate profile B.Tech Chemical / M.Tech Chemical /M.Tech Environmental / M.sc Environmental degree with 10+ years of experience in EHS

To understand, communicate and prepare a system to meet the desired production of each product as per the plan agreed by SCM team. To manufacture all products of high quality by complying with CGMP and safety systems at Udaipur Plants. Required Candidate profile Sound good knowledge of Sterile API.

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Our multidisciplinary Modelling and Simulation experts design and implement health economic models that describe complex medical processes to understand and evaluate the implications of clinical trials; demonstrate the value of interventions beyond efficacy, and assess benefits, risks, and the economic consequences associated with healthcare interventions. Our team conducts cost-effectiveness analyses of healthcare interventions and have experience conceptualizing and implementing simulation models (e.g., discrete event simulation) and other decision-analytic models (e.g., decision trees, Markov, individual state-transition, survival partition). Research Scientist Independent project lead & principal investigator of projects responsible for overseeing all aspects of project delivery; delegates project management tasks to mid-level and junior staff. Conceptualization, design and implementation of health economic models to conduct cost-effectiveness and budget impact analyses of healthcare interventions. Scientific responsibility for project completion; responsible for strategic consultation and for use of best methods to address research needs. Oversees and participates in a large project portfolio. Innovates scientifically and produces output of high scientific quality. Assumes significant responsibility for sales targets and building client relationships. Essential Duties and Responsibilities (other duties may be assigned): Scientifically responsible person for design and implementation of selected studies or models; conceptualize advanced model design and advanced study protocols and statistical analysis plans. Lead interactions with clients in the pharmaceutical and medical device industries, develops and maintains client relationships. Bring in proposal leads, manages proposal writing process and closes sales Review and finalize project deliverables and ensure study findings are valid and reliable. As project lead/principal investigator: project budget, deliverable and project timeline responsibility; identify scope expansion and need for amendments. Serve as advisor or mentor to other principal investigators or team members. Direct other "non-billable" activities (e.g. design conceptual approaches for proposals, supervise junior staff, identify and pursue business opportunities within Evidera and bring in new projects). Education, Professional Skills & Experience: PhD, Masters or Bachelors degree in Operations Research, Mathematics, Economics, Engineering, Biostatistics or related field with at least 7 to 10 years of directly relevant work experience in similar industry or consulting environment. Proven record in business development, as well as discussion of new opportunities with existing clients Required: Advanced Microsoft Excel modelling skills. Proficiency in Microsoft Word, and Microsoft PowerPoint. Broad experience in health economics and development of models suitable for submission to Health Technology Assessment groups or to support other reimbursement decisions Advanced level understanding of relevant methodology and statistics Extensive knowledge of practical research implementation Personal Skills & Competencies: Ability to communicate effectively with clients, project teams and senior managers Demonstrated ability to lead global cross-functional project teams to deliver projects across many therapeutic areas in a fast-paced, matrixed environment Excellent organizational and leadership skills Excels in handling staff growth and synergy, as well as client relations Competent in written and spoken English. Line manager: Experience in a line manager position, hiring, on-boarding, coaching, supporting staff development and project staffing plans Travel (international) is expected

Discover Impactful Work: Establish and build long term relationship with the Key Accounts of Thermo Fisher Scientific for the territory with Implementation of balanced action plans to expand the business opportunities across Chemicals, consumables, and Equipment business units in Laboratory solutions. Develop and implement an account plan to grow the revenues at the account above market average. Deliver on bookings and revenues on the Annual Sales Plan in line with Sales budget defined. Be accountable for the commercial performance and growth in share of wallet of the designated account with product mix performance and innovative solutions. A day in the Life: Provide quarterly and monthly prospect pipeline and revenue forecast across all business units. Take a hands-on approach, and act as partner concern point for all customer and system issues. Collaborate with matrix teams to develop joint initiatives and provide appropriate customer support in order to improve customer allegiance score. Increase brand awareness about Thermo Fisher Scientific products within the account by facilitating and driving customer engagement events. Build strong communication with the service and operation teams that support the account to establish high count of promoters. Keep abreast on market and customer research to provide knowledge about addressable potential. Mapping and reporting of direct and indirect sales in the account. Education Postgraduate preferably in Science / MBA or Management qualification with Bachelors degree in science Experience 10 to 15 years experience in sales / Key account Management Earlier experience in handling major Pharmaceutical and Bio Pharmaceutical key accounts In depth knowledge of Pharmaceutical /Bio Pharmaceutical workflows Experience of managing key relationships and execution of contracts. Strong communication, presentation, and negotiation skills. Knowledge, Skills, Abilities Strong analytical skills and problem-solving skills Is a self-starter and drives actions with passion and serves as a consultant to the target accounts. Implement Account specific strategy plans. Has very strong convincing and influencing skills.

Qualifications & Skills: Bachelors degree in Pharmacy, Life Sciences, or a related field (Master’s degree preferred). Minimum 8-12 years of experience in quality management systems, production quality assurance, or training roles within the pharmaceutical industry. Strong understanding of GMP, GDP, and regulatory requirements. Experience in developing and delivering training programs in a regulated environment. Strong project management, organizational, and leadership skills. Excellent communication skills and ability to interact with all levels of the organization. QMS Implementation and Maintenance : Manage the development, implementation, and maintenance of the Quality Management System (QMS) within the production department to ensure compliance with GMP, regulatory guidelines, and internal company standards. Ensure that the QMS is aligned with regulatory bodies’ expectations (e.g., FDA, EMA, etc.) and industry best practices. Oversee the creation and periodic review of production-related documents, including SOPs, batch records, and work instructions, ensuring they are up-to-date and compliant. Quality Assurance and Compliance : Monitor and audit production processes to ensure compliance with the QMS and regulatory requirements. Identify gaps or areas of non-compliance and implement corrective and preventive actions (CAPA). Conduct internal and external audits, ensuring that all required documentation, records, and processes are in place and effective. Assist in regulatory inspections and support the production team in addressing audit findings. Training and Development : Develop and implement a comprehensive training program for production personnel on topics such as GMP, SOPs, QMS requirements, and other regulatory standards. Design and deliver training sessions, workshops, and refresher courses to ensure all team members are continuously updated on best practices and compliance requirements. Assess training needs and evaluate the effectiveness of training programs. Maintain training records and ensure that all employees have received the necessary training to perform their roles in compliance with quality standards. Continuous Improvement : Drive continuous improvement initiatives in the production department, working closely with cross-functional teams to identify areas for efficiency gains and enhanced compliance. Implement best practices for quality management and training to improve overall product quality and reduce errors or deviations. Act as a change agent to promote a culture of quality within the production team. Documentation and Reporting : Maintain accurate and up-to-date documentation for all QMS-related activities, including training logs, audit reports, and CAPA records. Prepare regular reports for senior management on the status of quality systems, training progress, audit outcomes, and any non-compliance issues. Review and approve training materials, documents, and training evaluations. Collaboration with Cross-Functional Teams : Work closely with other departments (e.g., Quality Control, Regulatory Affairs, Production, and R&D) to ensure that quality management systems are integrated into all aspects of production. Support production teams in troubleshooting quality issues and implementing solutions. Risk Management : Assess potential risks related to production processes and quality management systems. Develop and implement strategies to mitigate risks to product quality, ensuring patient safety and regulatory compliance.

Review material shortage/excess Managing outgoing material maintain 100% FIFO delivery challans, Invoices, looking after waybills daily truck availability check Packaging and Labeling Products Contacting transport companies and coordinating dispatch

Work Location: Ahmedabad, Hyderabad | Years of experience: 8+years | Entity: India Business | Level :Manager In an era of market disruption, the Accenture consumer goods industry helps businesses digitize, transform and reach the always-connected consumer. Do you recognize and understand the impact that digital and technology have on industries? Are you passionate about shaping unique strategies that allow businesses to succeed and lead? Do you lead by example? Key responsibilities Drive client value creation Understand the client's business, priorities and leadership agenda Co-create with the client, articulate transformation and drive innovation agenda for the client Align the right teams or capabilities to enable (sell and deliver) successful transformation/innovation agenda Build long-standing, trust-based relationships Establish self as a trusted advisor with the client C-suite through an in-depth understanding of the client as well as industry Build networks at Accenture to be able to bring the best of Accenture to the client Grow the business/account Drive sales, account mining/ hunting, revenue generation/ with P&L accountability and responsible for account financials/key commercial processes (MMS/MMP, MME, MMB) for the account Help originate deals based on defined commercial pathways; drive innovative deal construct and solutioning to grow business Delivery ownership and excellence Professional qualifications Rich experience in the Consumer Product and Goods, Life Sciences/ Pharma or Automotive industry with in-depth industry expertise including the industry/ digital/ technology trends Demonstrate sustained client relations management experience at a C-suite level or operated at a senior management level in the industry role Experience of 8-12 years in consulting and account management experience; domestic consulting experience preferred Experience of working in a consulting firm will be preferred Experience of working with C-level executives at the client organization Qualification Educational qualifications Master's degree in business administration (MBA) or post graduate degree in management (PGDM) from premier institutes preferred What's in-store for you? Learn and grow continuously: Build new skills, grow existing skills, develop new areas of expertise within functional, technical or industry areas of the business with Accenture's unmatched 24/7 expert-curated learning boards, webinars and classroom-style training programs Innovate: Get access to resources that will allow you to leverage the latest technologies and bring innovation to life with the world's most recognizable companies Thrive and advance: Grow your career as far as your ambitions take you. Truly human: Bring your whole self to a company that aims to be the most diverse in the world and delivers real-time performance feedback based on your strengths, not stats Case Studies

Skill required: Marketing Operations - Medical Affairs Designation: Copywriting Senior Analyst Qualifications: MBBS/Master of Pharmacy/MD Years of Experience: 5 to 8 years What would you do? Help balance increased marketing complexity and diminishing marketing resources. Drive marketing performance with deep functional and technical expertise, while accelerating time-to-market and operating efficiencies at scale through Data and Technology, Next Generation Content Services, Digital Marketing Services & Customer Engagement and Media Growth Services.Role requires Digital Marketing Ads & Promotion creation/designIn Medical Affairs, you will have to design, develop and deliver business solutions related to the medical affairs group of pharmaceutical companies, including thought leadership development, medical publications, education and information, medical grants, advisory boards and advocacy, regulatory review and approval of pharmaceutical drugs and perform publishing and quality control tasks on submission components. What are we looking for? Clinical & Regulatory Writing Life Sciences Regulatory Operations Life Sciences Regulatory Affairs Medical Review Medical Affairs Written and verbal communication Strong analytical skills Results orientation Experience in research and development Collaboration and interpersonal skills Roles and Responsibilities: In this role you are required to do analysis and solving of increasingly complex problems Your day to day interactions are with peers within Accenture You are likely to have some interaction with clients and/or Accenture management You will be given minimal instruction on daily work/tasks and a moderate level of instruction on new assignments Decisions that are made by you impact your own work and may impact the work of others In this role you would be an individual contributor and/or oversee a small work effort and/or team Please note that this role may require you to work in rotational shifts Qualification MBBS,Master of Pharmacy,MD

Graduate / BPharma / MPharma / BDS / Preferably MBA from reputed college. Should additionally possess sound technical knowledge of MS Office, Creation of Power Points Presentation, Google Search etc and ability to coordinate with stake holders & team members. Strong Business acumen and Communication skills. We are looking for passionate and energetic individuals who believe in the power of digital technologies to improve healthcare. Role Description : Work closely with existing business partners and marketers from Pharmaceutical Industry & built new partners Healthcare Industry clients. Building project plans and proposals with thorough research. Ability to build a strong rapport with the clients/ Pharma Marketers. Support projects involving discussion with Pharma Industry Marketing teams, interacting with internal operations and video production teams. Stay Current with Medical Updates and Advancements. Establish MediSage as Partner for their brand growth by supporting their marketing endeavors and introducing them to new channels. Be responsible for achieving Revenue targets on quarterly and yearly basis. Why us Best-in-Industry Pay A steep learning curve and growth trajectory based on individual performance. We offer a positive environment where growth is encouraged and supported by experienced leaders. Our collaborative approach provides plenty of opportunities to work as a team. So if you are looking for career growth where your work makes an impact then you are the right fit for MediSage.

ASTER DM HEALTHCARE LIMITED is looking for Senior Pharmacist Pharmacy 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.

Tablets India Ltd. is looking for Marketing Executive (Medical Representative) to join our dynamic team and embark on a rewarding career journey. Researching and brainstorming each stage of the project. Delegating assignments to members of the graphics and advertising departments, as needed. Supervising employees' work, providing direction and clarification, as needed. Ensuring adherence to clients' specifications. Coordinating efforts to ensure that campaigns are completed. Adhering to time and financial restrictions. Tracking changes in consumer engagement following the roll-out of each marketing campaign. Compiling reports detailing the effects exerted by each campaign, and sharing these with clients.

Tablets India Ltd. is looking for Marketing Executive (Medical Representative) to join our dynamic team and embark on a rewarding career journey. Researching and brainstorming each stage of the project. Delegating assignments to members of the graphics and advertising departments, as needed. Supervising employees' work, providing direction and clarification, as needed. Ensuring adherence to clients' specifications. Coordinating efforts to ensure that campaigns are completed. Adhering to time and financial restrictions. Tracking changes in consumer engagement following the roll-out of each marketing campaign. Compiling reports detailing the effects exerted by each campaign, and sharing these with clients.

Background Position Description: Company Representative - India Operations A prominent natural health company in the USA seeks to expand its operations in India. The company has established a partnership with a Bangalore-based manufacturer in Karnataka, southern India, to produce ingredients for health supplements. Initially, these ingredients will be shipped to the USA for bottling and final packaging. Following successful implementation, company intends to establish complete manufacturing, encapsulation, bottling, packaging, and distribution operations in India, with potential market expansion into Southeast Asia. Roles and Responsibilities: A Representative for a Health Supplement Company managing relationships with ingredient manufacturers would have the following roles and responsibilities: Relationship Management - Develop and maintain strong relationships with ingredient manufacturers. - Serve as the primary point of contact for issue resolution, and ongoing communication. - Conduct regular meetings (in-person and virtual) and in-person to ensure alignment with company goals and objectives. Supplier Evaluation - Conduct due diligence on supplier capabilities, certifications, and compliance standards. - Coordinate negotiations for pricing, contracts, and supply agreements to optimize costs and quality. Quality Assurance & Compliance - Verify that ingredients meet regulatory requirements (e.g., FDA, GMP, NSF, organic, non-GMO). - Collaborate with quality control teams to monitor specifications, safety, and consistency. - Address quality or compliance issues with manufacturers proactively. Supply Chain & Logistics Oversight - Monitor supply chain performance to ensure timely ingredient delivery. - Coordinate with procurement and production teams to prevent shortages or overstocking. - Implement risk management strategies for supply disruptions. Cost & Budget Management - In conjunction with the US team, analyze cost structures and identify opportunities for cost savings without compromising quality. - In conjunction with the US team, develop budget forecasts for ingredient procurement and supplier expenses. Market & Industry Research - Stay informed about industry trends, new ingredient innovations, and regulatory changes. - Evaluate alternative ingredients or suppliers that align with product development goals. Cross-Functional Collaboration - Partner with legal and compliance teams to manage supplier agreements and regulatory documentation. Executive Reporting and Issue Resolution - Provide a weekly status report on accomplishments, metrics, risks, and bottlenecks. - Escalate manufacturing delays, quality concerns, or regulatory issues in a timely manner, providing options for resolutions. - Develop strategies for continuous improvement in supplier performance and ingredient quality. Basic Qualifications (Required) Education - Bachelors degree in supply chain management, Business, Food Science, Nutrition, Chemistry, or a related field. Experience: - Minimum 3-5 years of experience in supplier management, procurement, or sourcing within the food, nutraceutical, or pharmaceutical industry. - Demonstrated experience in vendor negotiations and contract management. Knowledge & Skills: - Strong communication and relationship management skills. - Basic knowledge of ingredient sourcing, quality control, and supply chain logistics. - Proficiency in Microsoft [ Office Suite (Excel, Word, PowerPoint). - Good situational awareness to identify issues, communicate, and escalate. - Understanding of FDA, GMP, NSF, and other regulatory standards for dietary supplements. - Ability to analyze supplier data, cost structures, and industry trends. 4. Other Requirements: - Willingness to travel for supplier audits, trade shows, and industry events. - Problem-solving skills and the ability to manage multiple suppliers and projects simultaneously. - Work during united states hours, as and when required. - Be flexible and interested in taking additional responsibilities to establish and expand company operations in India. Preferred Qualifications (Ideal Candidate Profile) Advanced Education: Masters degree in business (MBA), Food Science, or Supply Chain Management. Industry Experience: - 5+ years of experience in health supplements, functional foods, or nutraceuticals. - Previous experience working with international suppliers. Technical Expertise: - Familiarity with organic, non-GMO, and sustainable sourcing practices. - Experience with quality assurance audits and supplier risk management. - Certification in Supply Chain Management (APICS, CSCP, CPSM) or Quality Management (HACCP, SQF, Six Sigma). Additional Skills: - Ability to work cross-functionally with R&D, Marketing, and Regulatory teams. - Experience using AI-driven procurement tools or supplier relationship management platforms. - Strong negotiation skills with a proven track record of cost savings and supplier performance improvements.

Skill required: Pharmacovigilance Operations - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services Associate Qualifications: Any Graduation Years of Experience: 1 to 3 years Language - Ability: Japanese - Elementary What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world's leading biopharma companies bring their vision to life - enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.Management of the Affiliate Mailbox, reconciliation of reports per process, and performance of all written follow-up attempts to include both Serious and Non-serious cases.In this role, you will be expected to create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database as per client guidelines and applicable global regulatory requirements. What are we looking for? Agility for quick learning Collaboration and interpersonal skills Commitment to quality Ability to perform under pressure Prioritization of workload Roles and Responsibilities: In this role you are required to solve routine problems, largely through precedent and referral to general guidelines Your expected interactions are within your own team and direct supervisor You will be provided detailed to moderate level of instruction on daily work tasks and detailed instruction on new assignments The decisions that you make would impact your own work You will be an individual contributor as a part of a team, with a predetermined, focused scope of work Please note that this role may require you to work in rotational shifts Qualifications Any Graduation

Skill required: Clinical Data Services - Clinical Database Programming Designation: Clinical Data Svs Sr Analyst Qualifications: BE/BTech/MCA Years of Experience: 5 to 8 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, Clinical Automation, helping the world's leading biopharma companies bring their vision to life - enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.The Clinical Automation Team focuses on the development and implementation of innovative concepts and application for out clients across different accounts in Operations. The team is responsible for designing and implementing highly interactive, scalable web apps and prototypes at Enterprise level. The team is responsible for collaborate with frontend and backend developers to define API requirements and Ensure API security and authentication mechanisms are robust.You will be expected to develop and implement complex APIs based on requirements using different tools/techs such as .Net, Java, PL/SQL, C# or any other applicable systems. What are we looking for? Adaptable and flexible Ability to perform under pressure Problem-solving skills Agility for quick learning Ability to work well in a team Bachelor's degree in computer science, Information Technology, Engineering or any computer related discipline. Work experience of at least 3 years in relevant industries (Financial Services, Network, Utilities, Health Care, Marketing, Pharma, Retail etc.). Work experience of at least 4 years in designing, coding, APIs, testing, debugging, documenting, and implementing enhancements and fix solutions. Work experience in Implementing APIs based architecture frameworks. Aptitude to learn, think creativity to solve real world business problems, and work in a global collaborative team environment. Proficient verbal and written communication skills in English. Roles and Responsibilities: Work as a technical lead to architect and develop innovative concepts and applications for our clients across different accounts in Operations. Design and implement highly interactive, scalable web apps and prototypes at Enterprise level. Build and modify high-performance APIs and Monitor API performance and troubleshoot issues promptly. Implement APIs based on architecture frameworks and guidelines. Work with DevOps engineers to integrate new code into existing continuous integration (CI) and continuous delivery/deployment (CD) pipelines. Able to lead Automation initiatives within his account. Work closely with the team and client to understand requirements and guiding them to deliver the most effective solution. Participate in the development of automation solutions, from prototyping new functionality and technologies to integrating them in our overall products and offerings, thus developing expertise and skills in this domain. Collaborate with frontend and backend developers to define API requirements and Ensure API security and authentication mechanisms are robust. You should be able to pilot and deploy automation solutions at scale. Partner with the testing team to ensure applications/components are fully functional. Oversee and fix any defects or performance problems discovered in testing. Participating in analyses of requirements as well as functional design whenever necessary. Be involved in the design of the solution. Performing design, coding, application maintenance and testing activities. Take ownership of the successful implementation of the solution. Interact with the end client as required to ensure the solution is implemented as per requirements. Deliver code to time and quality expectations. Fully unit test developed solutions. Qualifications BE,BTech,MCA

3-5 years of exp in supplier management, procurement, or sourcing within the food, nutraceutical, or pharma industry. Demonstrated exp in vendor and contract management .5+ years of exp in health supplements, functional foods, or nutraceuticals.

Skill required: Pharmacovigilance Services - Pharmacovigilance & Drug Safety Surveillance Designation: Pharmacovigilance Services New Associate Qualifications: Bachelor of Pharmacy Years of Experience: 0 to 1 years Language - Ability: English - Advanced What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world's leading biopharma companies bring their vision to life - enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.Management of the Affiliate Mailbox, reconciliation of reports per process, and performance of all written follow-up attempts to include both Serious and Non-serious cases.In this role, you will be expected to create and manage case identification, data entry, MedDRA coding, case processing, submission, and follow-ups for ICSRs in the safety database as per client guidelines and applicable global regulatory requirements. What are we looking for? In this role you are required to solve routine problems, largely through precedent and referral to general guidelines Your primary interaction is within your own team and your direct supervisor In this role you will be given detailed instructions on all tasks The decisions that you make impact your own work and are closely supervised You will be an individual contributor as a part of a team with a predetermined, narrow scope of work Please note that this role may require you to work in rotational shifts Roles and Responsibilities: In this role you are required to solve routine problems, largely through precedent and referral to general guidelines Your primary interaction is within your own team and your direct supervisor In this role you will be given detailed instructions on all tasks The decisions that you make impact your own work and are closely supervised You will be an individual contributor as a part of a team with a predetermined, narrow scope of work Please note that this role may require you to work in rotational shifts Qualifications Bachelor of Pharmacy

Skill required: Clinical Data Services - Clinical Data Management Designation: Clinical Data Svs Specialist Qualifications: Bachelor of Pharmacy Years of Experience: 7 to 11 years What would you do? You will be aligned with our Life Sciences R&D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance & Regulatory, helping the world's leading biopharma companies bring their vision to life - enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience.The Clinical Data Management team focuses on the collection, integration, and availability of data at appropriate quality and cost. The team is responsible for performing data management activities including discrepancy review, query generation, and resolution. The team is also responsible for creating CRF Completion Guidelines (CCG) and SAE reconciliation guidelines. They help identify and raise protocol deviations in the database, perform edit check validation by creating test cases, write test scripts, and carry out database validation (UAT) against the specified CRF/ECRF. The team also managing clinical data management projects.The Clinical Data Management team focuses on the collection, integration, and availability of data at appropriate quality and cost. The team is responsible for performing data management activities including discrepancy review, query generation, and resolution. The team is also responsible for creating CRF Completion Guidelines (CCG) and SAE reconciliation guidelines. The role may require you to identify and raise protocol deviations in the database, perform edit check validation by creating test cases, write test scripts, and carry out database validation (UAT) against the specified CRF/ECRF. The role may also need expertise in managing clinical data management projects. What are we looking for? Adaptable and flexible Ability to perform under pressure Problem-solving skills Roles and Responsibilities: Overall experience of 4+ years in Clinical review and reporting programming, business analytics and/or clinical trial setup, gained in the pharmaceutical industry, CRO or Life Science related industry preferred. o Participate in the lifecycle of producing key data and/or reports in support of data review reporting development including evaluation of requirements, design specifications, interface to programmers, report programming, coordinate validation and rollout activities along with providing quantitative analytical support. o Provide understandable and actionable reports on clinical data and monitoring of clinical data for key stakeholders. o Facilitate interaction with end user on creating specifications and working with programmers or performing the programming activities for successful delivery. o Program reports of various complexity from documented requirements, within the clinical reporting systems using SQL, PL/SQL, SAS, and JReview etc. preferred. o Good analytical and communication skills. Qualifications Bachelor of Pharmacy

ROLE: Senior Consultant - Healthcare LOCATION: Gurgaon (Preferred) OR Mumbai EXPERIENCE: 3- 6 years of healthcare consulting experience Job Description We are seeking a highly skilled and experienced person to join as a Senior Consultant in Healthcare domain. In this role, the candidate will be involved in executing consulting assignments, providing expert guidance and strategic insights to clients in healthcare domain. The candidate will utilize his/ her extensive knowledge of Indian healthcare market, provider, payer and life sciences ecosystem and market trends, and public health policy to develop and implement innovative solutions for clients. Responsibilities: Work independently / in a team on consulting assignments; manage projects from scoping to delivery including assignment quality, timelines, client management, client satisfaction / relationship, etc. Engage with private and public sector clients including but not limited to hospitals, diagnostics, payers, government agencies, pharmaceuticals, medical devices, investors/ private equity players/investment banks, financial institutions, and multilateral agencies. Strategic advisory: Develop tailored strategies and roadmaps for clients in healthcare and life sciences domain. Develop/ conduct go-to-market strategies, business analysis and planning, feasibility studies, impact assessment studies, performance improvement of operations, cost optimization, vendor and shared services setup evaluation. Conduct market research, analyze industry trends, and stay updated on policy developments to provide clients with informed recommendations. Bid and transaction advisory Analyze bid opportunities, including requests for proposals (RFPs), tenders, and competitive bidding processes. Develop bid proposals, ensuring compliance with technical specifications, commercial requirements, and contractual terms. Due Diligence and project valuation : Conduct detailed commercial and financial due diligence of assets/ portfolios and develop robust financial models to evaluate healthcare projects. Stakeholder engagement : Collaborate with government agencies, industry associations, and other key stakeholders to foster strategic partnerships and drive collaborative initiatives in healthcare and life sciences domain. Support in business development outreach and related activities. Thought leadership : Stay abreast of industry advancements and technological innovations in healthcare and life sciences domain. Contribute to the development of thought leadership content, whitepapers, and industry reports to showcase expertise. Qualifications: MBA/ Master's degree in healthcare, or a related field. Prior consulting experience in healthcare is a must. Strong knowledge of Indian economic and healthcare and life sciences ecosystem. Excellent communication and presentation skills, with the ability to convey complex concepts to both technical and non-technical stakeholders. Demonstrated ability to work independently and effectively in a team environment as well as manage multiple stakeholders. Ability to travel for work whenever required both from execution as well as business development perspective. Be a strong role model, mentor and coach.

Job Summary The incumbent will be responsible for supporting the successful transfer of pharmaceutical processes and technologies from the R&D phase to the manufacturing phase. This position will involve working closely with cross-functional teams, including R&D, Quality, Regulatory, and Manufacturing, to ensure smooth and timely implementation of processes at scale. The ideal candidate will have a strong technical background in pharmaceutical development, process optimization, and excellent problem-solving skills. Key Responsibilities Tech Transfer Coordination : Assist in managing the transfer of drug formulations, processes, and technologies from R&D to manufacturing. Ensure the seamless scaling of processes from laboratory to commercial production, maintaining quality and regulatory compliance. Support process development teams during the transfer phase and troubleshoot technical challenges as needed. Documentation and Compliance : Prepare and review the necessary documentation for tech transfer, including SOPs (Standard Operating Procedures), protocols, and reports. Ensure all documentation meets regulatory requirements and follows company standards. Support the creation of risk assessments and control strategies for the transferred processes. Cross-Functional Collaboration : Work closely with R&D, Manufacturing, and Quality Assurance teams to gather necessary data and insights for tech transfer. Coordinate between multiple departments to address any issues arising during the tech transfer process. Facilitate smooth communication across teams to ensure timelines are met and quality standards are upheld. Process Optimization & Problem-Solving : Identify potential improvements in transfer processes to enhance efficiency, reduce costs, and minimize risk. Investigate and resolve any challenges encountered during scale-up activities, ensuring the process works as intended at large-scale manufacturing. Conduct troubleshooting and provide technical support for any issues during tech transfer execution. Training and Support : Assist in training manufacturing personnel on new processes or technologies during tech transfer. Support the development of training materials and presentations to ensure smooth adoption of transferred processes. Project Management : Support the management of project timelines, deliverables, and milestones. Monitor progress and provide regular status updates to senior management and stakeholders. Track the progress of ongoing tech transfer projects and ensure adherence to established timelines and quality standards. Key Requirements: Educational Qualifications : Masters degree in Pharmaceutical Sciences, Chemical Engineering, Biotechnology, or a related field. Experience : 8-12 years of experience in pharmaceutical R&D, process development, or tech transfer, ideally in a GMP (Good Manufacturing Practices) environment. Prior experience with technology transfer in a regulated industry (preferably in pharmaceuticals or biopharmaceuticals). Technical Skills : Strong understanding of pharmaceutical development processes, including formulation, manufacturing, and scaling up. Experience with equipment, process technologies, and techniques used in the production of pharmaceutical products. Knowledge of regulatory requirements, including FDA, EMA, and ICH guidelines. Soft Skills : Strong communication and interpersonal skills, with the ability to collaborate effectively across departments. Detail-oriented with excellent organizational and documentation skills. Ability to work in a fast-paced environment and manage multiple projects simultaneously. Other : Proficiency in Microsoft Office Suite (Excel, PowerPoint, Word). Familiarity with process modeling and data analysis tools is a plus. Knowledge of project management tools and techniques is a plus.

Salary : Upto 15 LPA + Huge Incentives + Travel Allowance Sales, strategy and market expansion - skin care and derma, doctor sales, building strong relationships with dermatologists and healthcare professionals. Required Candidate profile . Proven experience as a Medical Representative or similar role in the healthcare industry. Perks and benefits . Incentives + Travel Allowance + Insurance