37 Pharmaceutical Industry Jobs - Page 2

As a science graduate, preferably with an MBA, and possessing a minimum of 6 to 8 years of marketing and hard-core sales experience in the pharmaceutical industry, you will play a crucial role in our company based in Bangalore or Chennai. Your strong conceptual skills, analytical abilities, and creative outlook will be essential assets in this position. In this role, you will be responsible for leading a team of representatives and managers, as well as implementing the company's marketing plans and strategies to achieve business objectives within the assigned zone. Your expertise and leadership will be instrumental in driving the team towards success. We offer an attractive remuneration package along with incentives to recognize and reward your contributions. If you are ready to take on this exciting challenge and be part of our dynamic team, please email your resume to: torrel.hr@gmail.com / torrel_sna@yahoo.co.in / torrel_hr@yahoo.co.in. Join us in shaping the future of the pharmaceutical industry and making a positive impact on healthcare.,

As a CRM Business Analyst at QuadricIT, you will play a crucial role in gathering and analyzing business requirements, configuring CRM systems, and providing end-user support in the pharmaceutical industry. Your primary focus will be on Viva CRM, ensuring that system configurations meet business needs and driving operational excellence. With over 8 years of experience, you will work offshore during UK business hours, collaborating with cross-functional teams and engaging with stakeholders to drive successful CRM implementations. Your responsibilities will include gathering and documenting CRM-related business requirements, supporting Viva CRM implementations for pharma clients, and serving as a liaison between technical teams and business stakeholders. You will lead user acceptance testing, training sessions, and provide post-implementation support. Your strong understanding of CRM processes, excellent communication skills, and attention to detail will be essential in this client-facing role. To excel in this position, you must have 8+ years of experience as a CRM Business Analyst, with hands-on experience in Viva CRM and a solid background in the pharmaceutical industry. Your ability to work independently offshore during UK hours, along with your familiarity with compliance requirements in the pharma sector, will be key to your success. Additionally, experience with documentation tools, business process modeling, and testing will be advantageous. Preferred qualifications for this role include Viva CRM certification or proven hands-on experience, previous involvement in pharma CRM rollouts or upgrades, and knowledge of compliance requirements in life sciences. Familiarity with Agile or hybrid delivery methodologies will also be beneficial as you identify opportunities for process improvement and system optimization. If you are a detail-oriented and proactive CRM Business Analyst with a passion for driving operational efficiency and compliance in the pharmaceutical industry, we invite you to join our team at QuadricIT and contribute to the success of our clients through innovative technology solutions.,

You are a highly experienced and motivated Subject Matter Expert (SME) for Veeva Vault QMS, responsible for leading the deployment and optimization of Quality Management System processes. Your deep domain expertise in QMS processes within the life sciences or pharmaceutical industry will be crucial in driving compliance, efficiency, and user adoption through effective system design and implementation. Your key responsibilities include serving as the SME for Veeva Vault QMS, leading deployment, configuration, and optimization efforts. You will analyze existing QMS processes and workflows, identify gaps, inefficiencies, and areas for improvement, and work closely with stakeholders, business users, and functional SMEs to gather requirements. Your role involves designing, implementing, and refining user-friendly QMS processes and workflows aligned with global regulatory requirements such as 21 CFR Part 11, GxP, and ISO standards. You will also support validation and testing of QMS functionalities, ensuring documentation compliance, provide training and ongoing support, and collaborate cross-functionally with various teams. To excel in this role, you should have a minimum of 8 years of experience in the QMS domain within pharma/biotech/life sciences, with proven expertise in leading or acting as an SME for Veeva Vault QMS deployment. Your deep understanding of Quality Management processes like CAPA, Change Control, Audit Management, and Deviations is essential, along with strong knowledge of industry regulations and compliance frameworks such as GxP, 21 CFR Part 11, and ISO standards. Excellent communication, stakeholder engagement, problem-solving skills, and experience in driving process design and change management initiatives are key requirements. Preferred qualifications include Veeva Vault QMS certification, a background in Quality Assurance or Regulatory Operations, and experience in global delivery models involving onsite-offshore collaboration. Your role as a liaison between business and technical teams will ensure seamless integration and solution delivery, making you a vital asset in the optimization of QMS processes.,

As an Accounts Manager (Field Sales Ophthalmology) at Amneal, your primary responsibility will be to manage and cultivate relationships with ophthalmology clients. You will play a crucial role in achieving sales targets and expanding the customer base. Your day-to-day tasks will include developing and executing sales strategies, conducting market research, attending industry events, and collaborating with the marketing and product teams to ensure customer satisfaction and product optimization. To excel in this role, you should possess strong sales and account management skills within the ophthalmology sector. Your ability to build and nurture relationships, coupled with a proven track record of meeting sales targets and expanding customer bases, will be essential. Excellent verbal and written communication skills are a must, along with strong organizational and time-management abilities. Being able to work both independently and as part of a team is crucial for success in this role. A bachelor's degree in Science/Business Administration, Marketing, or a related field is required. Any experience in the pharmaceutical industry would be considered a plus. Join us at Amneal, a purpose-driven pharmaceutical company dedicated to making healthy living possible through our innovative products and dedicated team of employees.,

In this vital role, you will be responsible for developing and leading a highly talented team focused on delivering high-end and innovative technologies in the biotechnology industry. The ideal candidate should possess a consistent record of leadership in technology-driven environments, utilizing the 3DEXPERIENCE Cloud platform. Collaboration with cross-functional and global teams is essential to ensure seamless integration and operational excellence. You will need a strong background in the end-to-end software development lifecycle, be a Scaled Agile practitioner, and have experience in leadership and transformation. As a leader in this role, you will maintain strategic relationships and effective communication with the leadership team regarding IS services and service roadmaps. Leading and managing large, diverse teams within a matrixed organization will be a key responsibility. Collaboration with geographically dispersed teams, fostering a culture of collaboration, innovation, and continuous improvement, and developing talent within the Amgen Technology team in India are crucial aspects of this position. Understanding the decision-making process, workflows, and the business and information needs of partners and collaborators will be necessary. You will contribute to defining business outcomes, requirements, technology solutions, and services, as well as improving activities through "test & learn" approaches. Collaborating with Product Owners, Service Owners, and delivery teams to ensure commitments are met, communicating key performance metrics, and ensuring compliance with quality and regulatory requirements are key responsibilities. The basic qualifications for this role include a Doctorate degree, Master's degree, or Bachelor's degree with 12 to 17 years of experience in Business, Engineering, IT, or a related field. Preferred qualifications include experience in PLM roadmap implementation using the 3DEXPERIENCE platform, GMP applications, PLM integration with enterprise systems, and people management skills. Must-have skills entail strong technical and functional experience in solutioning GMP applications, hands-on experience with PLM solutions, integration with enterprise systems, and experience in leading matrixed teams. Good-to-have skills include leadership experience in pharmaceutical or technology organizations, configuring and customizing solutions, data migration to 3DEXPERIENCE platforms, and software development lifecycle experience. Professional certifications in Scaled Agile Framework (SAFe) for Teams are preferred. Soft skills required for this role include excellent leadership, team management, collaboration, communication, initiative, self-motivation, and the ability to manage multiple priorities effectively. At Amgen, we offer competitive benefits, a collaborative culture, and comprehensive Total Rewards Plans aligned with industry standards. Join us now and make a significant impact with the Amgen team. Apply at careers.amgen.com.,

We are looking for a meticulous and proactive Production Planning Inventory Control (PPIC) professional to join our team in Ahmedabad (Mahemdavad). You should have at least 2 years of experience in production planning and inventory control within the pharmaceutical industry. Your role will be crucial in ensuring smooth production operations, maintaining optimal inventory levels, and ensuring timely product delivery. Your responsibilities will include developing and managing detailed production schedules, optimizing resource utilization, and minimizing downtime. You will also be responsible for monitoring and maintaining optimal inventory levels of raw materials, work-in-progress, and finished goods. Collaborating with production, procurement, and quality assurance teams to ensure alignment of production schedules with material availability and quality standards is also a key aspect of the role. You will need to analyze sales forecasts and historical data to predict production requirements, adjust planning accordingly, and coordinate with suppliers and vendors to ensure timely delivery of raw materials and components required for production. Additionally, tracking production performance, inventory levels, and material usage, providing regular reports and insights to management, and identifying and implementing process improvements will be part of your responsibilities. Ensuring compliance with regulatory standards and company policies, particularly in the pharmaceutical sector, and maintaining accurate records of production schedules, inventory levels, and related documentation for audit and review purposes are also essential. Key Requirements: Educational Background: - Bachelor's degree in Science (B.Sc) or Pharmacy - Minimum of 2 years of experience in production planning and inventory control, preferably in the pharmaceutical industry Technical Skills: - Proficiency in inventory management and production planning software (e.g., SAP, ERP systems) - Strong analytical skills with the ability to forecast demand and plan production accordingly - Knowledge of supply chain management, procurement processes, and vendor management Soft Skills: - Excellent organizational and time management skills - Strong communication and interpersonal skills to work effectively with cross-functional teams - Detail-oriented with a proactive approach to problem-solving Location: You must be based in or willing to work in Ahmedabad. We offer a competitive salary with performance-based incentives, an opportunity to work in a reputable pharmaceutical company, health insurance, and other employee benefits, as well as professional development and growth opportunities.,

Zoetis, Inc. is the world's largest producer of medicine and vaccinations for pets and livestock. Join the Zoetis Tech & Digital (ZTD) Global ERP organization at Zoetis India Capability Center (ZICC) in Hyderabad, where innovation meets excellence. As part of a leading animal healthcare company, ZICC is dedicated to driving transformative advancements and applying technology to solve complex problems. The mission is to ensure sustainable growth and maintain a competitive edge for Zoetis globally by leveraging exceptional talent in India. As a member of ZICC, you will collaborate with colleagues worldwide, embodying the spirit of One Zoetis. Together, seamless integration and collaboration are fostered to create an environment where your contributions can have a real impact. Join us on the journey to pioneer innovation and drive the future of animal healthcare. The role entails responsibility for SAP Plant Maintenance module, Production Planning, Manufacturing, Lab Information Management System ERP system solutions at Zoetis. It requires strong experience with SAP Quality Management. Responsibilities: - Act as an SAP Solution Architect / Functional Designer - Deliver SAP Solutions aligned with business requirements and best practices - Gather requirements and estimate for SAP Project requests - Analyze to identify potential impacts for project/enhancement requests - Design, configure, and test SAP PP-PM and QM solutions - Integrate QM interfaces with third-party applications - Work with peers and business representatives to determine business process and solution design - Collaborate with other SAP functions to ensure process integration and consistency - Train others for quick onboarding and productivity - Manage colleagues and/or contractors reporting to this position - Provide support for global and regional systems and services - Ensure audit, SOX, and other compliance requirements - Identify and initiate process improvements - Monitor process compliance and performance metrics Position Responsibilities: - Act as a bridge between Business and technical teams - Work closely with stakeholders to deliver robust and compliant SAP Manufacturing solutions - Responsible for meeting KPI targets, continuous improvement, and automation - Serve as a Technical Subject Matter Expert for SAP Manufacturing Plant Maintenance Education and Experience: - Bachelor's degree in engineering, Computer Science, Manufacturing, Supply Chain, or related field. Master's degree preferred - 8+ years of SAP delivery & configuration experience with multiple full life cycle implementations - Functional/Technical proficiency with at least 3 full lifecycle SAP implementations - Experience in pharmaceutical/life science business and knowledge of GxP is a plus - S4/Hana Experience for Manufacturing and Quality Solutions preferred - Ability to work independently and coordinate multiple priorities in a collaborative environment Technical Skills Requirements: - Experience with configuration of SAP S4 HANA, ECC 6.0, MM IM WM - Detailed knowledge of SAP Plant Maintenance, Transactional activities, Maintenance notifications, orders, Preventive Maintenance, Calibration, etc. - Extensive experience in interface with external systems, data transfers, and reporting - Ability to configure master data, work orders, maintenance plans, etc. - Proficient in testing, development, enhancement, UAT, and user training Physical Position Requirements: This role is based in Hyderabad, India, with occasional weekend work and travel requirements based on project demands. Regular hours are from 3:00 AM to 12:00 PM EST. Join Zoetis, a Fortune 500 company, and world leader in animal health, to advance care for animals and humankind. Embrace a culture of inclusion and diversity, where each colleague can thrive and make a positive impact.,

As an Assistant Professor, you will be required to meet the following qualifications and responsibilities: Essential: - Hold a Ph.D. with a minimum of 55% in a Masters Degree in Business Management / Administration / in a relevant discipline. - Demonstrate a consistently good academic record with a First Class (or an equivalent grade) in Masters Degree in Business Management / Administration / in a related management discipline or first class in a two-year full-time PGDM program from an institute accredited by the AICTE / UGC. - Possess a minimum of two years of teaching experience, excluding the time spent on obtaining the research degree. Candidates with teaching experience will be preferred. - Have at least 2 SCI Publications in refereed journals. Desirable: - Show expertise in teaching, research, industrial, and/or professional experience within a reputable organization. - Present papers at conferences, publish research papers, books, or technical reports in referred journals, and have patents filed or obtained. Alternatively, if you are from the industry, the following requirements will be considered essential: Essential: - Maintain a consistently good academic record with a First Class (or equivalent) in Masters Degree in Business Management / Administration / in a related management discipline or first class in a two-year full-time PGDM program from an institute accredited by the AICTE / UGC. - Have a minimum of ten years of professional work experience at the managerial level in the field of Supply Chain/ Production/ Quality Management/ Consulting/ Project Management/ Analytics in the Pharmaceutical or healthcare industry.,

As a Global Category Buyer for Asian Raw Materials at Sanofi, you will be an integral part of the team that is dedicated to improving the lives of patients worldwide through groundbreaking medicines and vaccines. Sanofi, a leading global healthcare company, is committed to driving innovation and making a positive impact on the communities it serves. With a strong focus on research and development, Sanofi operates in 90 countries and employs 91,000 individuals worldwide. In this role, you will be responsible for developing and executing strategic sourcing strategies for raw materials, contributing significantly to the manufacturing and supply chain excellence of the company. With a robust pipeline of products in the pharmaceutical industry, you will lead innovation and collaboration with strategic partners to ensure a secure supply chain, market agility, cost-effectiveness, and manufacturability for both commercial and pre-launch activities. Your main responsibilities will include negotiating globally to deliver savings, conducting Global Business Reviews with strategic partners, developing innovative sub-category strategies in the Asia-Pacific region, and identifying potential suppliers in various subcategories. Additionally, you will leverage artificial intelligence in sourcing, ensure procurement technical excellence at a global level, and directly impact company revenue and product launches across different modalities. To excel in this role, you should have experience in strategic sourcing, negotiation, and supplier management for raw materials in the pharmaceutical or biotechnology industry. You should possess global sourcing experience, strong negotiation skills, and a deep understanding of raw materials procurement value chains. Excellent communication, presentation, and organizational skills are essential, along with the ability to manage complex business situations in a multicultural environment. A minimum university degree from an accredited institution is required, along with proficiency in English. Knowledge of French is a plus. By joining Sanofi, you will have the opportunity to contribute to groundbreaking scientific advancements, work with a forward-thinking team, and be part of a company that is committed to progress and excellence. Come be a part of our team as we pursue progress and discover extraordinary together. Join us in making miracles happen and driving positive change in the world of healthcare.,

We are seeking a meticulous and experienced Executive/Sr. Executive to spearhead chromatographic analysis and data review at Synnat Pharma Private Limited, a rapidly growing API manufacturer. In this pivotal role, you will be responsible for ensuring the accuracy, reliability, and compliance of analytical data generated within our QC laboratory. Your expertise will be crucial in adhering to stringent regulatory standards, including ICH guidelines and pharmacopeial requirements, while contributing to the overall quality and integrity of our pharmaceutical products. The ideal candidate will possess a strong understanding of HPLC and GC systems, coupled with proficiency in Empower CDS and a deep commitment to data integrity and GLP/GMP principles. This role demands a proactive individual capable of troubleshooting analytical issues, leading OOS/OOT investigations, and implementing effective CAPA measures. You will collaborate closely with cross-functional teams to maintain a robust Laboratory QMS and ensure seamless method of transfer and validation processes. If you are passionate about pharmaceutical sciences and dedicated to maintaining the highest standards of quality in API manufacturing, we encourage you to apply. Job Details: Industry: Active Pharmaceutical Ingredient (API) Manufacturing Department: Quality Control Role: Executive/Sr. Executive Location: Visakhapatnam Compensation: 4,00,000 to 8,00,000 INR per annum Experience: 4-7 years Qualification: Bachelor's or Master's degree Chemistry, or a related field Employment Type: Full-time Responsibilities: Chromatographic Analysis and Data Review Perform chromatographic analysis of raw materials, in-process samples, and finished products using HPLC and GC techniques, ensuring compliance with established test procedures and pharmacopeial requirements. Review chromatographic data generated by other analysts for accuracy, completeness, and compliance with data integrity and GDP. Troubleshoot HPLC and GC systems, resolving issues to ensure reliable instrument performance. Participate in method validation and transfer activities in line with regulatory expectations. Analyze stability samples and maintain data integrity in accordance with ICH guidelines. Prepare reports summarizing analytical results and findings. Quality Control and Compliance Implement and maintain a robust Laboratory QMS as per GLP, GMP, and internal quality standards. Lead OOS and OOT investigations and implement corrective actions to prevent recurrence. Manage and document CAPA activities effectively. Ensure data integrity through robust controls and secure data handling practices. Participate in audits and address regulatory observations. Maintain accurate documentation as per GDP guidelines. Laboratory Operations and Maintenance Oversee calibration and maintenance of HPLC and GC systems. Manage lab supplies and ensure proper storage and inventory control. Maintain a clean and compliant lab environment. Train junior staff in instrumentation, methods, and data practices. Develop SOPs and contribute to continuous improvement of test procedures. Support cross-functional teams in resolving quality-related issues. Stakeholder Management and Reporting Collaborate with R&D, production, and regulatory affairs teams. Communicate analytical findings effectively for decision-making. Prepare periodic reports for management summarizing QC trends. Participate in regulatory inspections and audits. Coordinate with external vendors for analytical services. Represent the QC department in internal/external meetings. General Expectations and Past Experiences: Possess a Bachelor's or Masters degree in Pharmaceutical Sciences, Chemistry, or a related field. Have 4-7 years of experience in a pharmaceutical QC lab, preferably API-focused. Demonstrate expertise in HPLC and GC, including troubleshooting and method validation. Exhibit a strong understanding of GMP, GLP, ICH, and pharmacopeial compliance. Proficiency in Empower CDS is essential. Strong skills in data review, OOS/OOT handling, CAPA, and documentation. Excellent team collaboration, problem-solving, and communication abilities.

Role & responsibilities Key Responsibilities: The role of our ideal candidate will include but not limited to Design and Development : Participate in designing software solutions and contribute significantly to the development of new features and functionalities. Code Quality : Ensure code quality through best practices, including writing clean, efficient, and maintainable code. Code Reviews : Conduct and participate in code reviews to maintain high code standards and provide constructive feedback to peers. Mentoring : Provide guidance and mentorship to junior engineers, helping them improve their technical skills and understanding of projects. Problem Solving : Analyse and resolve complex technical issues and assist the team in troubleshooting problems effectively. Testing and Debugging : Implement automation testing strategies, including unit and integration tests, and actively participate in debugging and performance optimization. Collaboration : Collaborate with cross-functional teams, including product, design, and QA, to ensure alignment and successful project delivery. Documentation : Maintain up-to-date documentation for software designs, processes, and codebases to ensure knowledge sharing and project continuity. Project Planning : Contribute to project planning and estimation efforts. Continuous Learning : Stay updated with new technologies, tools, and industry trends to bring innovative solutions to the team. Technical Leadership : Take ownership of components or modules of the software, driving their successful execution from design to deployment. Communication : Clearly communicate technical concepts and project statuses to stakeholders, including non-technical team members. Mandatory Skills Advanced Python Programming : Proficiency in Python, including advanced features such as decorators, generators, context managers, and multithreading/multiprocessing. Proficiency in dependency management in tools such as Pipenv, Poetry or Conda. Front-end Python Experience: Strong understanding of front-end Python frameworks such as Flask and Django. Strong understanding of SPA frameworks like React or Angular. AWS Proficiency : Strong understanding of core AWS services like EC2, S3, VPC, RDS, IAM, and Lambda. Boto3 and AWS SDKs : Expertise in using Boto3 to automate AWS service interactions and deployments. DevOps and CI/CD : Familiarity with DevOps practices and tools such as Jenkins or GitHub Actions to automate deployment processes. Containerisation : Experience with Docker and container orchestration tools such as Kubernetes or AWS ECS/EKS. Networking and Security : Awareness of AWS security best practices, including access management with IAM roles and policies. Experience of securing web applications with SSO and token-based authentication. Database Management : Experience with relational and NoSQL databases. API Development : Experience designing, building, and maintaining RESTful APIs. Problem Solving and Debugging : Strong analytical skills to solve complex problems and troubleshoot efficiently. Version Control and Collaboration : Proficiency with Git and collaborative development practices, including branching and merging strategies. Test-Driven Development: Experience of writing unit and integration tests with tools such as Pytest. Experience of writing front-end unit tests with tools such as Jest. Clean Coding: Strong skills in writing clean and maintainable code. Agile methodologies: Experience of working with Agile methodologies, such as Scrum or Kanban. Preferred Skills Experience in the scientific or pharmaceutical industry Understanding of the fundamentals of science and experience in the pharmaceutical sector Advanced end-to-end testing: Experience of testing methods such as shift-left testing and BDD . Serverless Architecture : Knowledge of building and managing serverless applications using components such as AWS Glue and AWS Batch. Microservices Architecture : Familiarity with designing and implementing a distributed architecture, particularly within AWS environments. Infrastructure as Code (IaC) : Proficiency with CloudFormation, CDK or Terraform for managing cloud infrastructure. Advanced Security : Experience with security mechanisms such as SSO and OAuth2. Data Engineering : Skills in data processing and storage using tools such as DBT and Snowflake. Performance Optimization : Ability to analyse and improve application performance including cost optimization strategies on AWS. Soft Skills and Leadership : Strong interpersonal and leadership skills to lead teams or manage cross functional projects. Certification : AWS Certifications as recognition of expertise. Educational Requirements Bachelors or master’s degree in computer science or an IT-related discipline with at least 6 years of experience in the IT industry.

Perform comprehensive data management tasks, Validation, Data transfers and quality control procedures. Provide Clinical Data Management team with technical expertise. Perform tasks as communicated by TL/LDM Create/review the Data Management Plans Required Candidate profile Graduate/Postgraduate in Computer Science/Computer Application/Physics/Math/Life Sciences/Pharmacy 2-8 years of experience in Statistical (SAS) programming International BPO experience is mandatory