87 Pharmaceutical Industry Jobs - Page 3

As a CSV (Computer System Validation) Sales Engineer at Instrumentation and Control Solutions (ICS) in Hyderabad, you will play a crucial role in engaging with clients to understand their CSV requirements and recommending appropriate solutions based on their needs. You will provide technical guidance on validation strategies and industry regulations such as FDA and EMA. Conducting product presentations, demos, and workshops to showcase the value of our solutions will be a key aspect of your role. Your responsibilities will also include developing sales strategies to achieve revenue targets, expanding the client base, and collaborating with teams to design tailored solutions and enhance produ...

As a leading multinational pharmaceutical company, Dr. Reddys Laboratories Ltd. is committed to accelerating access to affordable and innovative medicines to improve global health. Established in 1984, our company has grown to have a significant presence in 66 countries, with a workforce of over 24,000 employees who share the collective purpose of advancing healthcare solutions. With a foundation built on deep science, progressive people practices, and robust corporate governance, we have consistently championed access, affordability, and innovation in the pharmaceutical industry. As the landscape of healthcare evolves, we are poised to strengthen our core operations and embrace new opportun...

The Regulatory Affairs - International Business role at Nexaa VRA Lifescience Pvt Ltd is a full-time position based in Dehradun. As a Regulatory Affairs professional, you will play a crucial role in ensuring compliance with international regulatory agencies. Your responsibilities will include preparing and submitting regulatory documents, staying updated on regulations and guidelines, liaising with international business partners, and providing guidance on regulatory requirements and strategies. You will be actively involved in managing regulatory submissions, reviewing product labels and marketing materials, and collaborating with various teams to ensure adherence to regulatory standards. T...

The Marketing Manager at JRC & Lamrin Labs is a full-time on-site role based in Vadodara. You will be responsible for planning, developing, and executing marketing strategies for both domestic and international markets. Your daily tasks will include conducting market research, creating marketing campaigns, collaborating with sales teams, managing budgets, analyzing performance metrics, and ensuring compliance with regulatory standards. Additionally, you will need to maintain regular communication with stakeholders and clients to achieve marketing objectives. To excel in this role, you should possess proven experience in devising marketing strategies and organizing marketing campaigns. Strong...

As a tele marketer in this role, you are expected to utilize your experience and expertise in the pharmaceutical industry or from working in a pharmaceutical company. Having knowledge of PCD Companies will be considered a bonus. The salary for deserving candidates is negotiable, reflecting the value you bring to the role. This is a full-time, permanent position with benefits including cell phone reimbursement and paid time off. The work schedule is during the day shift, and there is potential for a performance bonus based on your results. The ideal candidate will have a total of 2 years of work experience, with at least 2 years in telemarketing and 1 year in pharmaceutical sales. Being able ...

Dr. Reddys Laboratories Ltd. is a leading multinational pharmaceutical company with a global presence and a workforce of over 24,000 employees. Each member of our team is dedicated to accelerating access to affordable and innovative medicines because Good Health Can't Wait. Founded in 1984 with a modest investment and 20 employees, we have since expanded our research and development centres, manufacturing facilities, and commercial presence to 66 countries. For almost four decades, we have been committed to providing access, affordability, and innovation rooted in deep scientific knowledge, progressive people practices, and strong corporate governance. As the pharmaceutical industry continue...

As a Scientific Content Writer at our company, your primary responsibility will be to prepare and create high-quality scientific content in compliance with industry standards and company SOPs. You will curate scientific information with precision, ensuring proper formatting and clarity to accurately represent scientific and clinical data while maintaining originality in writing. It will be essential for you to stay informed about industry trends, regulatory changes, guideline updates, and recent medical literature to enhance content quality and include clinically relevant information. Managing timelines and deliverables efficiently will be crucial to uphold the quality of content without com...

You should have a minimum of 5 years of experience in MRs/sales/marketing roles within Pharma companies. A background in Pharmacy/Science (B. Pharm/B.Sc.) along with a master's degree in management (MBA) or Marketing is preferred, with additional experience in a similar role. Fluency in English is also preferred. As a part of the team reporting to the Sr. Associate Director BD, you will be responsible for identifying potential clients, conducting research on clients" therapy-wise business needs, and developing relationships with new and existing clients. You will collaborate with internal teams to create proposals, negotiate contract terms, and stay updated on industry news and competition. ...

About the Company: Pharmintech Turnkey Solutions Pvt. Ltd. is a technology-driven, information-focused organization dedicated to delivering the highest quality cleanroom solutions at competitive prices. Our strategic vision is to continuously introduce advanced technologies in the cleanroom industry and ensure timely delivery of innovative solutions. We specialize in manufacturing and supplying pharmaceutical cleanroom projects, offering turnkey solutions to contractors across Mumbai, India, and globally, adhering to the latest international standards. Our commitment to excellence and quality drives us to deliver defect-free and reliable products that are in high demand across Pharmaceutical...

As a Regulatory Specialist at Divit Nutraceuticals Pvt. Ltd., you will play a crucial role in ensuring regulatory compliance and upholding the company's commitment to producing high-quality nutrition-based products. Your responsibilities will include interpreting and implementing regulatory requirements, analyzing data with precision, effectively communicating regulatory information, and overseeing regulatory affairs operations. To excel in this role, you should possess a strong understanding of regulatory compliance and requirements, demonstrating proficiency in analytical skills to evaluate complex data sets. Your ability to communicate regulatory updates clearly and concisely will be esse...

Are you a person with innovative thinking and a proactive attitude Do you have a continuous improvement and process delivery mindset If so, we have an exciting opportunity for you to join the Global Business Service (GBS) Finance team at Novo Nordisk. Take the next step in your career and apply today for a life-changing opportunity. You will be joining the Global Finance GBS Bangalore team, which was established in 2007. Our team is responsible for supporting Accounting, Finance & Procurement, Financial Planning & Analysis (FP&A) for Headquarters, North America, International Operations (IO), Product Supply & GBS Bangalore. Our main purpose is to provide superior service to our stakeholders ...

The U.S. Pharmacopeial Convention (USP) is an independent scientific organization collaborating with global health and science authorities to develop quality standards for medicines, dietary supplements, and food ingredients. With a core value of Passion for Quality, USP aims to strengthen the supply of safe, quality medicines and supplements worldwide through the dedication of its more than 1,300 professionals across twenty global locations. At USP, inclusivity is valued, with a focus on creating a culture that offers meaningful opportunities for mentorship and professional growth. Emphasizing Diversity, Equity, Inclusion, and Belonging, USP strives to build a world where quality in health ...

As an Area Sales Manager at Biotics Lab, you will be responsible for leading the sales team and driving growth in the assigned territories. Your role will involve developing and implementing regional business strategies to achieve revenue targets. You will lead, guide, and monitor the field sales team to ensure the execution of sales strategies in alignment with company goals. Coordination with ABMs, RBMs, and the Head Office will be essential to ensure consistency in field activities. Your responsibilities will include designing and overseeing call plans for each territory, tracking and analyzing territory performance and market trends, and adjusting tactics accordingly. You will be in char...

As an experienced professional in the pharmaceutical industry, you will be responsible for ensuring the pharmaceutical, medical, and regulatory accuracy of English product information for European procedures. In this role, you will work with innovative, biosimilar, and generic products, contributing to regulatory compliance and addressing internal and authority-related inquiries. Your day-to-day activities will involve creating and updating compliant English product information for EU procedures, strategic planning for changes affecting multiple product documents, evaluating and approving change requests, and coordinating submissions with EU regulatory units. Additionally, you will collabora...

As an M Pharm professional with experience in the Pharmaceutical Industry, particularly in the Quality Assurance Department, you will play a crucial role in ensuring the quality and compliance of products and processes. Your expertise in this field will be instrumental in upholding industry standards and regulatory requirements. Ideally, you should have a strong background in Quality Assurance practices within the pharmaceutical sector. Experience in Computer System Validation would be an added advantage, as it demonstrates your familiarity with ensuring the accuracy and reliability of computer systems used in pharmaceutical processes. Your attention to detail, analytical skills, and knowled...

The Senior Document Management Associate (SDMA) will provide support for Trial Master File (TMF) activities to the clinical teams for all assigned projects. This role will be responsible for working with study teams, both internal and external, to manage both paper and electronic Trial Master Files (TMF), according to project requirements, ICH GCP guidelines, local/global regulatory requirements and Novotech/Client SOPs. The SDMA will also be responsible for performing comprehensive QC reviews. Minimum Qualifications & Experience: - At least more than 2 years of experience in a clinical research organization or equivalent role. - Practical experience in handling Trial Master File activities ...

As a Senior Sales Manager / Sales Manager / Assistant Manager / Sr. Sales Executive in Pharma Filtration, you will play a crucial role in driving B2B/OEM sales of validated filtration products to pharmaceutical API/formulation and biotech plants. You will be responsible for managing and growing key pharma/biotech accounts by offering consultative, solution-driven filtration systems. Your expertise will be instrumental in identifying and converting new business opportunities across API, formulation, sterile injectables, and biotech segments. Your key responsibilities will include engaging with decision-makers such as Plant Heads, QA/Validation Teams, Utility Heads, and Engineering Managers. Y...

AstraZeneca is a global, science-led, patient-focused biopharmaceutical company dedicated to the discovery, development, and commercialization of prescription medicines for some of the world's most serious diseases. Beyond being one of the world's leading pharmaceutical companies, we strive to make a difference in medicine, patients, and society. Our inclusive culture values diversity, collaboration, and lifelong learning, empowering individuals to push the boundaries of science and unleash their entrepreneurial spirit. In this role, you will act as a country or regional expert supporting the Medical Affairs function and project teams within your area of expertise. You will serve as the seni...

Illumina is a leading developer, manufacturer, and marketer of life science tools and integrated systems dedicated to making genomics useful for all. Our integrated Indian global hub in Bengaluru, Illumina India Biotechnology Private Limited, is focused on technology activities that will help usher in the next wave of innovation in healthcare and medical research. If you are eager to work on challenging projects that use cutting-edge technology to transform the future of healthcare, this is your chance to join a truly remarkable team. We are currently seeking an EHS Specialist to join our talented team in Bangalore. In this role, you will support the Global EHS strategy for compliance and ri...

Are you an experienced project manager with a passion for driving change and delivering results Are you ready to take on a challenging role in a global pharmaceutical company We are looking for a Global Associate Project Lead to join our team at Novo Nordisk. If you have excellent communication and collaboration skills, and a strong background in project management, then read on and apply today for a life-changing career. The Global Associate Project Lead at Novo Nordisk will work closely with the Global Project Lead under the guidance of the Manager Global Insulin Marketing, Diabetes Therapy Areas. In this role, you will be responsible for driving and supporting the overall strategic planni...

You will be responsible for the site Master Data processes to ensure accurate and timely creation and maintenance of master data in the ERP System, aligning with local and global requirements. As the Material Planner, your role involves driving the tactical purchasing process for all materials to ensure materials availability and execution plan feasibility in accordance with Site inventory policy. Your primary responsibilities will include focusing on accurate and timely preparation and maintenance of master data in the SAP ERP system, aligning with Supply chain operational activities in compliance with GxP & Regulatory requirements, internal regulations, Good Practices, and business objecti...

ZS is a place where passion changes lives. As a management consulting and technology firm focused on improving life and how we live it, our most valuable asset is our people. Here you'll work side-by-side with a powerful collective of thinkers and experts shaping life-changing solutions for patients, caregivers, and consumers, worldwide. ZSers drive impact by bringing a client-first mentality to each and every engagement. We partner collaboratively with our clients to develop custom solutions and technology products that create value and deliver company results across critical areas of their business. Bring your curiosity for learning; bold ideas; courage and passion to drive life-changing i...

As a Senior Executive in Business Development within the pharmaceutical sector, you will be responsible for driving strategic growth initiatives and expanding market presence. You should possess a strong educational background, either as a commerce graduate with an MBA in Marketing or a BPharm/MPharm with expertise in international regulatory affairs and the ability to prepare CTD Format Dossiers effectively. Ideal candidates for this role should have a minimum of 4-5 years of hands-on experience in the pharmaceutical industry, with a preference for candidates with a background in international marketing. This experience will enable you to navigate the complexities of global markets and deve...

As a key resource within the Audit Management Office (AMO), you will ensure effective coordination and management of audits and inspections involving Data, Digital & IT (DD&IT) systems and processes. This includes supporting GxP audits (e.g., GMP, GCP) and regulatory inspections by authorities such as FDA, EMA, MHRA, and Swissmedic. Your role as an associate will involve acting as a liaison, ensuring that relevant DD&IT subject matter experts address audit queries and deliver required documentation in a timely and accurate manner. Additionally, you will be responsible for monitoring audit findings, overseeing remediations, and driving continuous improvement in audit readiness. Govern process...

We are a technology-led healthcare solutions provider driven by our purpose to enable healthcare organizations to be future-ready. At Indegene, we offer accelerated global growth opportunities for bold, industrious, and nimble individuals, providing a unique career experience that celebrates entrepreneurship and is guided by passion, innovation, collaboration, and empathy. To explore exciting opportunities at the convergence of healthcare and technology, visit www.careers.indegene.com. Looking to jump-start your career At Indegene, we understand the significance of the first few years of your professional journey, which lay the foundation for your entire career. We promise a differentiated c...