87 Pharmaceutical Industry Jobs

Oversee complete Production & Manufacturing operations at the Pharmaceutical Formulation Unit Ensure smooth execution of batch manufacturing for OSD (Tablets, Capsules, Dry Syrups) Ensure compliance with FDA regulations and GMP guidelines Monitor production efficiency, process optimization & manpower management Coordinate with QA, QC, and Regulatory teams for smooth operations Handle regulatory audits, validation, and documentation processes OSD Manufacturing Tablets, Capsules, Dry Syrups FDA Approval & Regulatory Compliance (WHO-GMP, Schedule M preferred) Production Planning & Process Optimization Team Leadership & Manpower Management

Role Overview: As a Senior HR Executive, you will be responsible for recruitment activities with a focus on the pharmaceutical industry. Your role will involve sourcing and onboarding candidates while ensuring compliance with company policies and procedures. The position is based at a prime location near Reliance Jio Garden in BKC, Bandra East, Mumbai. Key Responsibilities: - Source and attract candidates through various channels for recruitment in the pharmaceutical industry - Conduct interviews, assess applicants, and make recommendations to hiring managers - Coordinate with departments to ensure smooth onboarding processes - Maintain and update recruitment records and reports - Stay updat...

As a Global Associate Project Lead at Novo Nordisk, you will work closely with the Global Project Lead under the guidance of the Manager Global Insulin Marketing, Diabetes Therapy Areas. Your main responsibilities will include: - Driving and supporting the overall strategic planning, preparation, and execution of the roll-out plan for Portfolio Consolidation Excellence Framework. - Ensuring strong execution of portfolio consolidation decisions and collaborating with stakeholders across the organization to ensure broad alignment and navigate efficiently. - Spearheading training initiatives and ensuring effective dissemination of knowledge through strategic planning, execution of "Train the Tr...

Role Overview: As the Godown Incharge at Kroyf Lab & Co., you will be responsible for managing all aspects of the pharmaceutical warehouse operations. This includes overseeing the receipt, storage, and dispatch of pharmaceutical products to ensure smooth supply chain operations. Key Responsibilities: - Maintain accurate inventory records and conduct regular stock checks. - Ensure warehouse cleanliness to uphold quality standards. - Coordinate with procurement, sales, and logistics teams for efficient operations. - Manage documentation related to inventory, shipments, and audit compliance. - Lead and train warehouse personnel, assign duties, and monitor performance to ensure operational effic...

As a Project Quality Manager at Shree Biocare Solutions Pvt. Ltd., you will play a crucial role in ensuring the quality and compliance of all projects with ASME standards and regulatory requirements. Your responsibilities will include: - Developing and implementing quality control processes to uphold high standards - Conducting ASME audits and managing documentation effectively - Coordinating with cross-functional teams to address and resolve quality issues - Ensuring project timelines are met while maintaining customer satisfaction To excel in this role, you should have the following qualifications: - Experience in Quality Control and Quality Assurance processes in accordance with ASME - St...

Role Overview: At Unijules Life Sciences Ltd., we believe in the immense potential for growth and innovation in the pharmaceutical industry. As new technologies continue to emerge, we understand the importance of expertise and skill to stay ahead in this rapidly evolving field. We provide a learning platform for individuals who are energetic, enthusiastic, and dedicated to learning and excelling in their careers. If you are committed to growth, development, sincerity, and quality, we welcome you to join the Unijules Pariwar family. Key Responsibilities: - Conduct audits in the pharmaceutical manufacturing plant, preferably specializing in Liquid/Solid dosage. - Implement cGMP system to ensur...

Role Overview: You will be responsible for overseeing the herbal extraction and processing operations at the Hassan facility of a leading manufacturer of premium herbal extracts. As a Production Supervisor, you will play a crucial role in ensuring compliance with GMP, safety protocols, and quality standards while supervising daily production activities, coordinating workflow, and troubleshooting production issues. Key Responsibilities: - Supervise daily production activities and coordinate workflow - Ensure compliance with GMP, safety protocols, and quality standards - Monitor equipment performance and coordinate maintenance activities - Train and mentor production staff on procedures and be...

As a Senior Business Development Manager for the Active Pharmaceutical Ingredient (API) division, your role will be crucial in driving business growth, expanding the API portfolio, and fostering key relationships in the pharmaceutical industry. You will play a significant part in identifying market opportunities, developing new partnerships, and contributing to the company's strategic vision. **Key Responsibilities:** - **Business Development & Strategy:** - Identify and evaluate new business opportunities in the API sector. - Develop and implement strategic initiatives to expand the company's API portfolio and market share. - Establish and maintain relationships with key customers, partners...

As a Senior HR Executive, your role will involve overseeing human resources activities within the pharmaceutical industry. Your key responsibilities will include: - Having a minimum of 5 years of relevant experience, with at least 3 years specifically in the pharmaceutical industry, focusing primarily on recruitment. - Sourcing and attracting early joiners, with a maximum notice period of 30 days. - Working full-time on a permanent basis, requiring in-person presence at the office located near Reliance Jio Garden, BKC, Bandra East, Mumbai. Qualifications required for this role include: - Any graduate degree. - Master's degree in Human Resource. - Any post-graduation. Please note that only ma...

URGENT HIRING !!! location's : Canada , Australia , New Zealand , UK, Germany , Singapore ( Not In India ) Benefits : Medical Insurances , Travel allowances , Flight Tickets , Meals , etc For more information call or whatsapp +91 9220850077 Key Responsibilities: Coordinate and oversee the day-to-day operations of the pharmacy store Lead, coach, mentor and develop your team to deliver high performance Oversee the procurement and supply of medicines Administer immunisations and vaccines to patients Monitor and ensure customers are prescribed the correct medicines Develop strong relationships with customers, GPs and other health professionals Ownership and delivery of financial targets for the ...

As a leading multinational pharmaceutical company, Dr. Reddys Laboratories Ltd. is committed to accelerating access to affordable and innovative medicines to improve global healthcare. With over 24,000 employees worldwide, we have established a strong presence in 66 countries since our inception in 1984. Our core values of access, affordability, and innovation are deeply rooted in science, progressive practices, and corporate governance. Embracing the evolving pharmaceutical landscape, we strive to strengthen our foundation and embrace future opportunities. We aim to be purpose-driven, future-ready, and sustainable, reaching over 1.5 billion patients by 2030. Sustainability is at the heart o...

As a member of the Biocon Biologics team, you will play a crucial role in ensuring the integrity and compliance of our operations. Your primary responsibility will be to conduct commercial, corporate, financial, and compliance audits, taking charge of the planning, fieldwork, and reporting phases of the audit process. You will also be tasked with managing and coordinating outsource/co-source audits with external firms to guarantee a comprehensive audit plan and delivery of all necessary documentation and reports. Your expertise in reviewing and evaluating internal controls, ensuring compliance with regulations and policies, and advising management on risk and control matters will be invaluab...

As a US Pharma Recruiter based in Mohali, your primary responsibility will be to attract top talent for our US-based pharmaceutical clients. You should possess a deep understanding of the US pharmaceutical industry, excellent communication skills, and the ability to thrive in a dynamic work environment. Your key duties will include sourcing and recruiting pharmaceutical professionals, nurturing relationships with clients and candidates, conducting interviews and assessments, overseeing the recruitment process end-to-end, meeting recruitment targets, and staying informed about industry trends in the US pharmaceutical market. To excel in this role, you should have at least 2 years of recruitme...

As a leading multinational pharmaceutical company, Dr. Reddys Laboratories Ltd. is committed to accelerating access to affordable and innovative medicines. With over 24,000 employees worldwide, our collective purpose is driven by the belief that Good Health Cant Wait. Since our inception in 1984, we have expanded our presence to 66 countries, encompassing research and development centers, manufacturing facilities, and commercial operations. For nearly four decades, we have championed access, affordability, and innovation through a foundation of deep scientific expertise, progressive people practices, and robust corporate governance. As the pharmaceutical industry experiences transformation, ...

You are a dedicated Quality Assurance Officer joining a team in Halol. Your experience in the chemical or pharmaceutical industry will be crucial as you ensure compliance with quality standards, implement QA protocols, and maintain regulatory documentation. Your role will involve overseeing quality assurance processes in production to uphold high standards, ensuring compliance with industry regulations and company policies, and updating quality documentation, reports, and audits. Collaborating with cross-functional teams to enhance quality standards will be essential, along with assisting in audits and regulatory inspections. You will be responsible for documenting and reporting product or s...

The U.S. Pharmacopeial Convention (USP) is an independent scientific organization dedicated to 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 strives to strengthen the supply of safe, quality medicines and supplements worldwide through the efforts of over 1,300 professionals across twenty global locations. At USP, inclusivity is highly valued, and the organization is committed to fostering a culture that offers meaningful opportunities for mentorship and professional growth. Emphasizing Diversity, Equity, Inclusion, and Belonging, USP aims to create a...

As a Portfolio Associate reporting to the Senior VP, your primary responsibility will be to conduct daily information collection and analysis. You will then provide meaningful market insights to Marketing, Business Development, and Commercial Operations teams. It is crucial to compile daily reports with information on New Drugs Approvals, T3 status changes, drug shortages, NOCs, and supplements approved in North America, among other key data points. Additionally, you will be managing databases of injectable drug approvals, CMO/CDMO details, and under-review submissions. Your role will involve presenting findings to senior management, highlighting new product approvals, and assessing risks to...

We are seeking an experienced and detail-oriented Medical Reviewer to join our team. The role involves reviewing, analyzing, and ensuring accuracy, consistency, and compliance of medical and scientific content in alignment with regulatory, clinical, and organizational standards. Key Responsibilities Review medical, clinical, and regulatory documents for scientific accuracy, clarity, grammar, and compliance. Ensure consistency of terminology, data, and style across all documents. Validate clinical and safety data in reports and submissions against source documents. Collaborate with cross-functional teams including medical writers, clinical research, and regulatory affairs. Provide feedback an...

As a member of Havas Life, you will be responsible for providing scientific and technical information to various stakeholders, including physicians, research staff, and sales and marketing personnel. Your role will involve presenting scientific findings, offering strategic recommendations, and contributing to the planning, development, and delivery of medical communications programs. In terms of business management, you will lead and supervise the development of scientific, medico-marketing, and strategic content for brands. Collaboration with creative and copy teams is essential to ensure the production of professional content. You will work closely with other departments such as PR, Manage...

You are a driven, resourceful, and remarkably smart individual. As an R&D Analyst at Syneos Health Consulting, you will be responsible for conducting secondary research to create high-quality project materials and customer deliverables. Within the R&D Advisory Group, your role will focus on enhancing the efficiency and effectiveness of life science R&D organizations and operations across various areas such as research, clinical, regulatory, quality, and pharmacovigilance. Your key responsibilities will include helping organizations navigate through changes, fostering positive relationships with customers and internal teams, creating project deliverables, identifying challenges and opportunit...

You will be joining the Infotech department as an HO Executive based in Ahmedabad. The ideal candidate should possess a BE/BTech/MCA in IT/Computer/Graduate degree along with SAP Certification, which is considered an added advantage. Your primary responsibility will be to demonstrate expertise in SAP PPQM with a background in global rollout projects and experience in cross-module integration within the pharmaceutical industry. You should have a strong skill set in configuration, testing, documentation, and providing end-user support. If you meet the above qualifications and are looking to showcase your skills in SAP PPQM within the pharmaceutical sector, this position could be an excellent f...

As a global engineering, management, and development consultancy committed to delivering impactful work that shapes the future, Mott MacDonald is seeking a skilled professional to join our team. With over 20,000 experts working across more than 50 countries, we take pride in being part of an ever-changing global industry that delivers transformative work defining our future. At Mott MacDonald, our people power our performance, and as an employee-owned business, we invest in creating a safe, valued, and empowered space for all employees, providing the right tools and support for success. We offer a dynamic environment where you can pursue excellence in your specialism or explore flexible role...

Education :- Diploma/BE in Mechanical Experience: - Fresher Salary: - As per candidates Location:- Dabhel, Daman Industry:- Pharmaceutical Company Gender : - Female candidates preferred Only Interested candidate are invited call on +91 9662780300

In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices. Piramal Group is committed to providing equal employment opportunities. Employment decisions are based on merit considering qualifications, skills, performance, and achievements. The company ensures that all applicants and employees receive equal opportunities in various personnel matters, including recruitment, selection, training, placement, promotion, demotion, compensation and benefits, transfers, terminations, and working conditions. Reas...

As a Labeling Specialist in the Pharmaceutical Industry, you will be responsible for developing US labeling documents to align with company goals and submission requirements for assigned ANDAs and/or 505(b)(2)s. Your role will involve ensuring that labeling meets all legal and regulatory requirements through QC, proofing, editing, and formatting of documents. You will coordinate the review and approval of final submission documents with all relevant departments. Your expertise will be crucial in developing labeling content that requires carve-outs due to protected language associated with patents/exclusivities. Serving as a Subject Matter Expert (SME) in SPL/drug listing, you will provide gu...