7291 Pharma Jobs - Page 49

The Associate III, with minimal to no guidance, prepares, reviews and submits high quality regulatory submissions to the FDA within company timelines and in accordance with regulatory guidelines. The Associate III will be responsible for independently evaluating change controls (intended for post approval changes), will ensure the CC is complete and accurate and in the absence of any comments will progress the CC accordingly. In addition, he/she will monitor any/all Regulatory or team databases and trackers and will proactively and accurately update them when changes are required. Annual Reports, supplements, post approval submissions and assisting management with the training of regulatory ...

Monthly review of Health Canada brand safety updates. Align updates with internal product lists and communicate relevant changes to cross-functional teams. Strategize and implement changes impacting multiple product documents. Track and retrieve the latest innovator PMs from the Health Canada Drug Product Database. Create and update Teva PMs by referencing Canadian innovator products. Use tools like TVT for document comparison, ensuring compliance with HC master templates. Perform thorough QC, editing, formatting, and coordinating the review and approval processes. Collaborate with French translators for bilingual PMs. Coordinate with artwork team the creation of packaging components (Insert...

MAIN PURPOSE OF ROLE Summarize the main purpose of the role. Conduct market research and feasibility studies to analyze the viability of alternative business development opportunities. MAIN RESPONSIBILITIES Collect, compile, verify, and analyze financial, competitive, sales, marketing, and other information about potential business partners, new markets, products and services, or other business opportunities so that senior management has accurate and timely information for making strategic and operational decisions. Prepare documents and materials (for example, reports, presentations, information packages) for meetings and negotiations with potential clients and business partners so that the...

MAIN PURPOSE OF ROLE Conduct market research and feasibility studies to analyze the viability of alternative business development opportunities. MAIN RESPONSIBILITIES Collect, compile, verify, and analyze financial, competitive, sales, marketing, and other information about potential business partners, new markets, products and services, or other business opportunities so that senior management has accurate and timely information for making strategic and operational decisions. Prepare documents and materials (for example, reports, presentations, information packages) for meetings and negotiations with potential clients and business partners so that the information provided is accurate and ap...

The Director, Platform Operations, will oversee the day-to-day operations of our platforms and business applications. The ideal candidate will have a strong background in platform management, management of business applications with excellent leadership skills, and a passion for optimizing performance and ensuring reliability. About the Role Key Responsibilities: Lead and manage the platform operations and applications operations team, providing guidance, mentorship, and support. Oversee the monitoring, maintenance, and optimization of platform(s) and applications performance to ensure high availability and reliability. Develop and implement operational plans, policies, and procedures to enh...

The candidate in this role will be expected to work with colleagues located in Hyderabad, Mexico, Ireland and the US, and work as per the shift-time aligned to US teams working hours. The GD-C is a part of Creative team under CAST and must demonstrate strong collaboration with colleagues across all Novartis sites, work in a high-volume work environment, maintain the highest quality standards, and live Novartis values and behaviors every day. Key Responsibilities: Design and produce medical contents generated by Content Team into aesthetically pleasing creative communication (Asset) as per the Brand / Design Guidelines. If an asset already exists, then GD-C will make updates to those as requi...

This role involves working in the Digital Commerce Platforms group to develop and implement enterprise initiatives and technical projects for Fisher Scientific and Thermo Fisher Scientific ecommerce websites. As a senior software engineer, you will be responsible for: Designing, developing, testing, and deploying applications, participating in architecture and code reviews, helping to prioritize features and bug fixes, working collaboratively with cross-functional teams at Thermofisher, leading in the pursuit and delivery of the best possible product. Job Functions: Define and develop verifiable requirements and software designs. Develop technical documentation for software architecture, des...

The Associate Director, Medical Information is accountable for high-quality medical information documents and responses for assigned assets/disease areas aligned to Therapeutic Areas (TAs). These assets will shape practitioner understanding of Novartis products and support clinical practice. The remit of accountabilities extends to the execution of medical information processes, content and systems, adhering to internal compliance and regulatory requirements. This role must strive to implement industry-leading practices and adopt new technologies in line with emerging medical information standards. Critical to success will be developing productive partnerships with enterprise stakeholders (B...

As Associate Director Integrated Evidence Excellence, you ll champion best practices across global teams, driving innovation in both interventional and non-interventional studies. You ll lead capability development, foster cross-functional collaboration, and elevate the visibility of evidence generation ensuring Novartis remains at the forefront of scientific rigor and stakeholder value. This is your opportunity to influence global standards, empower teams, and make a meaningful difference in patient outcomes. About the Role Key Responsibilities Drive development of capabilities for integrated evidence generation across global functions and key countries Identify and scale high-impact countr...

Execute sales and consistently achieve defined targets for semi-finished formulations (pellets, granules, ready-to-compress blends, pre-mixes, etc.). Develop and implement sales strategies to expand business in semi-formulations across domestic and international markets. Identify, engage, and secure new B2B opportunities with formulation manufacturers, CDMOs, nutraceutical companies, and contract partners. Build and maintain long-term business relationships with key clients, stakeholders, and channel partners. Collaborate with cross-functional teams (R&D, production, supply chain, regulatory) to ensure smooth delivery and customer satisfaction. Provide market intelligence and feedback to dri...

Bachelors degree in engineering / science. 3+ years of experience/ exposure to Computerized System Validation (CSV), US FDA 21 CFR Part 11, EU Annex 11 and GAMP 5. Experience with the implementation of Quality Management systems (Track wise/ Master control / ETQ/ CEBOS) Should be able to Develop validation documentation for pharmaceutical equipment, facilities and computerized systems used in GLP, GMP and GCP environments. Should be able to create project Deliverables which will encompass validation plans, specifications, test protocols and standard operation procedures Good communication and technical writing skills are a must. Should be able to work Independently. Should be Flexible to han...

Civil & Structural Engineering experience in the Industrial domains such as Oil & Gas or Petrochemical Industry or Power Plants or Food & Beverages/ Pharma/ Semi-Conductor plant or other Industrial projects is preferred with a varied range of project execution. Demonstrated ability towards load calculation, structural analysis, sizing, design, and report preparation. Strong FEED and detailed design experience in steel & concrete structures, different foundation systems. Working knowledge on typical American codes such as IBC, ASCE, AISC and ACI Sound knowledge of structural calculation software such as STAAD, RISA3D, RISA FOUNDATION, RISA CONNECTION, LPILE etc. Structural Calculation Experie...

Position requires a Structural Engineer with 5 to 15 years of experience with thorough knowledge of Civil & Structural design and Engineering techniques Responsible to perform Structural calculations independently, lead projects & deliver good quality reports and drawings Responsible to plan & conduct independent work requiring judgement in evaluation, selection, application and compliance to codes, standards, specifications, and criteria Devise new approaches to structural engineering problems and arrive workable solutions within budgeted hours and resources Through professional communication skills, should be able to work with other engineering disciplines, sometimes across multiple office...

Serve as the primary contact for customers for product onboarding, training, and support. Understand customer needs and provide consultative solutions using SANeForce products. Handle customer queries and complaints promptly and professionally. Monitor customer health and engagement metrics to drive product adoption and retention. Work cross-functionally with internal teams (Product, Tech, Sales) to ensure customer success. Gather customer feedback and share insights for product and process improvements. Maintain up-to-date knowledge of product offerings and industry trends. Requirements: Bachelor s degree in any discipline. 1 2 years of experience in a customer-facing role, preferably in a ...

Design engaging, user-friendly interfaces for web and mobile applications. Create wireframes, prototypes, and high-fidelity mockups that communicate design concepts effectively. Collaborate with product managers, developers, and stakeholders to define and deliver intuitive user experiences. Conduct user research and usability testing to gather feedback and improve designs. Maintain consistency in visual elements and branding across all products. Stay up-to-date with UI/UX trends, tools, and best practices. Requirements: 1-2 years of experience in UI/UX design for web or mobile platforms. Proficiency in Figma and/or Adobe XD (experience with other design tools is a plus). Strong understanding...

Gather and document business requirements through client interactions, workshops, and research. Analyze existing business processes and recommend technology-driven improvements. Collaborate with cross-functional teams including development, testing, and implementation to ensure accurate solution delivery. Prepare functional specifications, workflows, and user documentation. Participate in product demonstrations and client training sessions. Assist in project planning, monitoring progress, and ensuring timelines are met. Support quality assurance processes by validating solutions against requirements. Required Skills & Qualifications Bachelor s degree in engineering, Computer Science, Busines...

Preparation of registration strategy for Brazil submission Adequate understanding on respective authority guidance and filing of new product and post approval changes Review of documents related to product registration and dossier submission leading to faster approval Prepare response to deficiency letter received from Anvisa, Brazil Maintain life-cycle (PCH) / post approval changes for drug product registration dossiers including timely circulation of approval information Provide regulatory support to cross functional department Adequate assessment of change control as per regulatory guidance Prepare and submit scientific advice to Anvisa, Brazil

Responsible for Cleaning and Operation of equipment and respective area as per SOP. Responsible for capsulation activities machine wise and area wise. Responsible for setting of capsulation machine with minimum Non-recoverable recovery. Responsible for online In-process checking of Weight of 20 caps, individual wt. variation, Locking length, individual weight of caps, disintegration time and other critical check points of the filled capsule. On line weighing and online process checking of capsules and transferring of container to respective quarantine area along with documentation. Precaution to be taken and follow the safety in manufacturing area. Responsible for execution of the day to day...

Review of R&D documents such as stability data, Analytical reports, Method verification reports, Method validation protocols & reports, analytical data of pilot bio batches/DQ batches and Product development data for its adequacy, accuracy and completeness as per regulatory and business requirement in order to achieve robust method development and to decrease method failure at site. Review of QMS documents like Lab Events/Deviations/Change control/CAPA and associated investigation reports prior to Technology Transfer. Support and participate in failure investigations and resolution of root causes for issues related to systems and products developed within Sun Pharmaceutical Industries Limite...

To perform Service interventions in line with product requirements in an efficient manner with an objective of achieving VTS growth targets & customer satisfaction within VTS structure & guidelines. Service Operations - - Receive the weekly preventive maintenance and daily breakdown schedule from the service planner. Check with the service planner and sales engineer for spare parts availability at site. Complete the service at customer site. - Understand the service procedure from the technical support team in case of a complex procedure. - Create the service report post job. Supporting multi brand products by maintaining respective brand dignity. In order to complete service interventions a...

Responsible for analyzing and processing of Medicaid Invoices received from US States as claims Calculate, validate and process all assigned Medicaid and State Program rebates within legislative timeline and maintain the SLA to avoid late fee or interest Identify root cause of issues with state invoice discrepancies and recommend corrective action to eliminate future occurrences Ensure customer disputes, if any, are resolved with customers in a timely manner. Prepare reports required for like ROSI/PQAs submission to states Provide support for ad hoc requests and audit documentation/queries Promptly respond to state queries, providing necessary information and supporting documents. Participat...

Achievement of set targets. Maintaining set call Average/coverage. Complete use of allotted resources. Increasing prescriber base Focus on target customers. Maintaining call average and customer coverage Increasing PCPM. Timely reporting. Ensuring ROI Relationships around the role Reporting to (Business) Regional Sales Manager / Sr. Regional Sales Manager Key External Stakeholder(s) Doctors, Stockiest, Retailers, CFA staff, Fellow professionals, institutional administrators Key Internal Stakeholder(s) RSM, ZSM, BDM, NSM / SM, PMT, HR & Sales Admin Competencies critical for the role Scientific/ Technical Competencies Proficiency level Convincing ability Presentation Selling Communication Beha...

The incumbent will be responsible for driving business growth in assigned territory for Oncology franchise, maintaining effective customer relations, mapping territory potential, cascading science behind brands with benefits of brands and collaborating with Health Care Practitioners. Job Responsibilities: Market Development Maps potential of territory bringing in insights from market trends, referral pathway bottlenecks, competitors activities and unmet needs from a patient and care-giver perspective Profiles, assesses potential, prepares target list and enlists new doctors as per business requirement. Helps build stakeholder maps including HCPs, local patient advocacy groups, influencers et...

We are recruiting for a Manager Market Access based in Mumbai . The Manager- Market Access will be part of the Market Access Team of J&J India and will be responsible for leading the identification, development, and communication of the Value proposition for J&J Innovative Medicine (IM) portfolio across key payers, decision makers and other stakeholders across India. In addition, the individual will be also driving value beyond convention clinical science by developing innovative health economic models as well as identifying potential partnership opportunities to maximize access. Key Responsibilities: Patient Access & Support Program (50%) Design and oversee patient support initiatives to im...

The Software Product Engineering (SPE) organization is actively looking for a Senior Quality Engineer with strong hands-on experience in AI platform testing, chatbot testing, AI model validation, agents testing, AI test automation, and API testing. This is a highly specialized role focused on validating complex AI and ML systems and ensuring scalable, safe, and effective deployment of AI-based solutions. UI automation experience using tools like Selenium, Cypress, or Playwright is desirable as a secondary skill. What You ll Be Doing: You will drive quality engineering initiatives specifically focused on AI-powered platforms and solutions, including LLMs, chatbots, AI agents, and intelligent ...