105 Pharmaceutical Manufacturing Jobs - Page 2

Role & responsibilities : Partner with business leadership to understand the business requirement and try to fulfil or suggest improvement plan. Responsible for meeting production schedules with efficient and optimized use of resources and machine time. Managing multiple priorities in a fast paced manufacturing environment. Budget preparation and adherence with approved budget. Interfaces with supply chain to develop mid-and long range master production schedules. Plan, organize, and control the production process to ensure the efficient and timely manufacturing of products. Monitor production schedules and adjust as necessary to meet demand and maintain inventory levels. Ensure adherence to...

We are looking for an experienced Quality Assurance Manager to lead and oversee QA activities at our API manufacturing facility.

Roles and Responsibilities Source packaging materials from vendors, negotiate prices, and manage vendor relationships. Coordinate with internal stakeholders to understand procurement requirements and ensure timely delivery of materials. Conduct market research to identify potential suppliers and evaluate their capabilities. Develop and maintain a database of approved vendors for easy reference. Ensure compliance with regulatory requirements related to pharmaceutical manufacturing. Desired Candidate Profile 3-6 years of experience in procurement or supply chain management (SCM) operations in the pharmaceutical industry. Strong knowledge of packaging material sourcing, procurement processes, a...

As a Production Planner (PPIC) at Amneal Pharmaceuticals in Ahmedabad, your key responsibility will be to develop and maintain detailed production plans based on sales forecasts, inventory levels, and customer orders. You will coordinate with procurement, quality assurance, warehouse, and manufacturing teams to ensure alignment of production plans. Monitoring production progress, adjusting schedules to avoid delays, and ensuring timely product delivery will be crucial aspects of your role. Your qualifications should include 4-8 years of experience in production planning within pharmaceutical manufacturing (formulations) along with a degree in B.Pharm, M.Pharm, M.Sc, or MBA. Familiarity with ...

Greetings!! We are looking for Assistant Manager (Process Support) - Business Development & Licensing (Andheri, Mumbai) Role & responsibilities Work closely with the business development team to understand customer requirements and translate them into feasible manufacturing plans. Coordinate with various departments (e.g., R&D, quality control, production, and regulatory affairs) to ensure alignment in evaluating process optimization. Support the creation of timelines and execution plans for potential manufacturing projects. Continuously assess and identify opportunities for process optimization to reduce manufacturing costs. Ensure all potential risks are identified and managed, particularl...

Role Description: The Senior Manager Quality Compliance External Affairs will enhance quality, compliance, and regulatory flexibility by providing leadership and support of external activities impacting Amgens Operations function with link to Regulatory Affairs-CMC, with a regional focus on Japan & Asia Pacific (JAPAC) This role will shape, coordinate and provide input in the development of policy, regulatory requirements, and expectations consistent with Amgens position and priorities on GMP/GDP primarily in JAPAC and regarding related international organizations (e-g , APEC, ICH, Pharmacopoeias, PIC/S, WHO) in support for GCP, GLP, GPvP compliance, as requested The senior manager will expl...

Job Summary: The MES Lifecycle Manager drives the strategic planning and execution of MES installations, updates and migrations across Sanofi's industrial network and the lifecycle planning in alignment with the Product Owner Vision & product Roadmap. This role provides technical and strategic leadership in developing and implementing long-term strategies to optimize MES performance, reduce obsolescence, and align MES capabilities with Sanofi's digital transformation goals. Main Responsibilities: Strategic MES Lifecycle Management: Develop and execute a comprehensive MES lifecycle planning/ strategy aligned with Sanofi's digital transformation objectives, Product Owner Vision & product Roadm...

About the Job Job Summary The MES Reliability Engineer ensures the stability and performance of Manufacturing Execution Systems (MES) to maximize operational value. This role serves as a bridge between development and operations teams, taking a proactive approach to prevent downtime, optimize system performance, and ensure the reliable operation of manufacturing systems that are critical to production. Main Responsibilities Incident Management and Resolution Anticipate, Prevent and Lead incident response efforts to swiftly resolve MES service disruptions, minimizing impact on manufacturing operations Conduct thorough analyses of system failures and implement preventive measures to avoid futu...

Job Description Summary This role is responsible for the coordination between various stakeholders of the project and preparing management information reports. This includes working closely with the project head and other team members of the project. Must have experience in working for Healthcare/Pharmaceutical Manufacturing project Job Description About the Role: Prepare various reports including daily, weekly, monthly project reports. Provide administrative support to project managers, including scheduling meetings, preparing presentations, preparing agendas, and taking minutes. Assist project managers in planning and executing construction projects. Assist in the coordination of permits, ...

Role Overview: You will be joining Sohan Healthcare Pvt. Ltd., a renowned fully integrated pharmaceutical company specializing in Active Pharmaceuticals Ingredients, Semi-Finished Formulations, and Pharmaceutical formulations development & manufacturing. Our facilities are equipped with state-of-the-art technology and adhere to world-class manufacturing standards. Key Responsibilities: - Development, manufacturing, and supply of API - Manufacturing of semi-finished formulations such as pellets and Directly Compressible Granules - Development of finished formulations for global markets - Recognized as one of the largest manufacturers of METFORMIN API for esteemed global clientele Qualificatio...

Job Title: Office Professionals (4 Positions) Location 1: Vadsar Kalali Ring Road, Vadodara Location 2: Kheda Industrial & Logistics Park, Kheda Office Time: 09.30 am to 06:00 pm Job Type: Full-time Nourish Pharmaceutical Pvt Ltd is a leading manufacturer of finish dosage formulations, including tablets, capsules, and oral liquids. We are seeking skilled professionals to join our corporate office team. Positions: 1. Purchase Officer 2 (Pharmaceutical Manufacturing) 2. Product Packing Material Designer (Pharmaceutical Manufacturing) 3. Business Development Executive How to Apply: If you're a motivated and skilled professional looking to join a dynamic team, please submit your resume to info@n...

Role Overview: As a Team Member in IPQA for Injectables/OSD, you will be a skilled professional with over 5 years of experience in real-time monitoring of manufacturing and packaging processes. Your responsibilities will include line clearance, in-process checks, and reviewing Batch Manufacturing Records (BMR) and Batch Packing Records (BPR) to ensure compliance with GMP and regulatory standards. You will also be involved in deviation handling, documentation, and providing audit support for injectable and oral solid dosage forms. Key Responsibilities: - Real-time monitoring of manufacturing and packaging processes - Conducting line clearance and in-process checks - Reviewing Batch Manufactur...

YASH Technologies is a leading technology integrator specializing in helping clients reimagine operating models, enhance competitiveness, optimize costs, foster exceptional stakeholder experiences, and drive business transformation. At YASH, were a cluster of the brightest stars working with cutting-edge technologies. Our purpose is anchored in a single truth bringing real positive changes in an increasingly virtual world and it drives us beyond generational gaps and disruptions of the future. We are looking forward to hireAspenTech MES Professionals in the following areas : Job Description: Job Title: MES Aspen Application Expert Requirement: Bachelors degree Science or Engineering related ...

1 Responsible for Receipt of Raw, Packing & Miscellaneous Materials as per cGMP norms. 2 Responsible for Preparation of GRN on time and same to be entered in LIMS system. 3 Responsible for all time readiness for inspections by continuous monitoring of cGMP & regulatory norms. 4 Responsible & ensure online documentation related to warehouse. 5 Responsible for preparing shortage of packing materials as per RFC. 6 Responsible for initiation of Packing materials PRs as per shortages & co-ordination with Purchase team for delivery. 7 Responsible for preparation of STO / PO for internal units transfer materials. 8 Ensure that, the proper review of deviation, change request documentation, risk asse...

Key Responsibilities: Operate and maintain production and processing equipment related to chemical manufacturing Monitor production processes to ensure compliance with quality and safety standards Troubleshoot and resolve minor equipment issues to minimize downtime Maintain proper documentation of production activities and equipment maintenance Follow safety protocols and standard operating procedures at all times Collaborate with the production team to achieve daily manufacturing targets Eligibility Criteria: Any Graduate with ITI AOCP certification 1 to 3 years of experience in pharmaceutical manufacturing Knowledge of chemical production and processing in a plant environment Ability to op...

Key Responsibilities: Operate and maintain production and processing equipment related to chemical manufacturing Monitor production processes to ensure compliance with quality and safety standards Troubleshoot and resolve minor equipment issues to minimize downtime Maintain proper documentation of production activities and equipment maintenance Follow safety protocols and standard operating procedures at all times Collaborate with the production team to achieve daily manufacturing targets Eligibility Criteria: Any Graduate with ITI AOCP certification 1 to 3 years of experience in pharmaceutical manufacturing Knowledge of chemical production and processing in a plant environment Ability to op...

Walk-in at Matoda We are hiring multiple positions for our manufacturing facility at Matoda as mentioned below. Please find our current job requirements and venue details mentioned. If any of the requirements match your current job profile, kindly walk in with your latest resume. Role & responsibilities Injectable Manufacturing (Executive/Senior Officer / Officer) Experience - 02 to 08 Years Qualification - B. Pharmacy/ M Pharmacy / Msc / Bsc / Engineering - (Instrumentation / Process Equipment Maintenance) (Senior Executive / Executive / Senior Officer) Experience - 03 to 10 Years Qualification BE / B Tech QUALITY ASSURANCE IPQA (injectable) / QMS / Documentation (Officer / Senior Officer /...

Post- Manager - Supply Chain Location Pune Hadapsar , Magarpatta Experience - 08-10 yrs Skills - pharmaceutical supply chain management. Strong understanding of GMP, GDP Education - Bachelor's/Master's degree in Supply Chain Management, Business Administration Job Overview : The Supply Chain Manager oversees and manages the end-to-end supply chain operations, ensuring the timely delivery of pharmaceutical products while maintaining quality, compliance, cost efficiency, and customer satisfaction. JD Develop and implement supply chain strategies Manage warehousing, inventory management, and distribution activities. Ensure compliance with industry regulations and quality standards. Collaborate ...

Role Overview: As a Production Chemist at our manufacturing team, your primary responsibility will be to focus on the production of solvents and specialty chemicals while ensuring compliance with safety, quality, and operational standards. You will be expected to execute daily production activities, handle manufacturing processes, maintain quality standards, and coordinate with various departments to ensure smooth production flow. Key Responsibilities: - Execute daily production activities as per the production plan and SOPs. - Handle and monitor the manufacturing processes for solvents & specialty chemicals. - Ensure adherence to quality standards, safety protocols, and regulatory guideline...

To operate and monitor granulation equipment and processes in compliance with cGMP, SOPs, and safety standards, ensuring consistent production of high-quality pharmaceutical granules for tablet or capsule formulation. Key Responsibilities: Operate granulation equipment such as high-shear mixers, fluid bed dryers, oscillating mills, and blenders. Weigh, dispense, and mix raw materials as per batch manufacturing records (BMR). Monitor granulation parameters and adjust settings to maintain product quality. Perform in-process checks (e.g., moisture content, granule size) and document results accurately. Clean and maintain equipment and work areas as per SOPs. Execute machine changeovers and line...

Location: Bangalore,IND Unique Opportunity As a Field Service Engineer Lead er , you will play an integral role in supporting the first private semiconductor FAB in India and in building the semiconductor ecosystem within the country. This position offers the prospect of advancing your career alongside the industry while establishing a high-performing team from the ground up. To learn more about life as a Field Service Engineer, visit the Field Service Engineer page. Responsibilities Building the OrganizationResponsible for creating the Field Service Organization, which includes hiring, onboarding, and upskilling talent to meet business requirements. LeadershipProvides direction, coaching, a...

Officer - Quality Control: Qualification - M.Sc / B. Pharm / M.Pharm Experience - 03-05 years experience in pharmaceutical manufacturing machine maintenance Job Responsibility - 1. Sampling and Testing of raw material . 2. Testing of Finished product & semi finished products 3. Knowledge of HPLC/ GC Empower software 4. Knowledge of Operation of instruments like Dissolution/ FTIR / HPLC / GC / Polarimeter 5. Knowledge about basic QMS in QC like Incidence / OOS etc. 6. Handling of Instrument related software. 7. Awareness about instrument calibration.

Officer Sr. Officer - Engineering: Qualification - B. E (Mechanical/ Electrical) Experience - 03-06 years experience in pharmaceutical manufacturing machine maintenance Job Responsibility - 1. E xperience in maintenanceof semisolids (Ointment/ cream / gel manufacturing machines, Metal andlaminated tube filling machines) oral liquid manufacturing (mfg. Tanks withbottom entry agitators, volumetric filling machine, ROPP Cap sealing machine). 2. Should be able to draw & edit 2 D drawings with AutoCAD. 3. Mechanicalseal handling, assembly, dismantling and troubleshooting 4. Should haveknowledge about CLIT 5S and Kaizen 5. Maintaindocumentation related to ISO - EMS and OHS standards 6. GMPdocument...

About The Role Project Role : Software Development Lead Project Role Description : Develop and configure software systems either end-to-end or for a specific stage of product lifecycle. Apply knowledge of technologies, applications, methodologies, processes and tools to support a client, project or entity. Must have skills : Manufacturing Engineering MES Good to have skills : NA Minimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a Pharmasuite MES Architect, you will be responsible for designing, developing template based MES recipes in Rockwell FactoryTalk PharmaSuite (FTPS) to support pharmaceutical manufacturing processes. You w...

About The Role Project Role : Software Development Engineer Project Role Description : Analyze, design, code and test multiple components of application code across one or more clients. Perform maintenance, enhancements and/or development work. Must have skills : Manufacturing Engineering MES Good to have skills : NA Minimum 7.5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a Pharmasuite MES Architect, you will be responsible for designing, developing template based MES recipes in Rockwell FactoryTalk PharmaSuite (FTPS) to support pharmaceutical manufacturing processes. You will collaborate with cross-functional teams to ensure efficie...