105 Pharmaceutical Manufacturing Jobs - Page 3

About The Role Project Role : Custom Software Engineer Project Role Description : Develop custom software solutions to design, code, and enhance components across systems or applications. Use modern frameworks and agile practices to deliver scalable, high-performing solutions tailored to specific business needs. Must have skills : Manufacturing Engineering MES, communication skills verbal and written, microsoft excel Good to have skills : NA Minimum 3 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...

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, communication skills verbal and written, microsoft excel 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...

The Manufacturing QA Specialist in the Pharma Solutions division at Lexington plays a crucial role in ensuring compliance with regulations and standard operating procedures. You will be responsible for overseeing quality activities throughout the manufacturing, testing, warehousing, and distribution of pharmaceutical drug products. Reporting to the QA Supervisor, you will review batch records, protocols, and documentation, collaborate with departments to address issues, and conduct on-the-floor activities like line clearances and product inspections. Your role will also involve providing QA oversight, troubleshooting GMP issues, and offering leadership on projects that interact with other de...

You are an experienced project management professional with a proven ability to lead complex, cross-functional projects in a dynamic environment. Your expertise lies in managing projects that ensure the timely execution of R&D, clinical trials, and product launches. Your strategic oversight, strong collaboration across departments, and ability to deliver results in a fast-paced environment are key drivers of success. You will oversee the entire lifecycle of projects, from initiation through launch, ensuring alignment with business goals. Leading cross-functional teams, coordinating with R&D, manufacturing, regulatory, clinical, and BD teams to drive project milestones. Ensure clinical trials...

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 : NAMinimum 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 collaborat...

The ideal candidate should have a minimum of 3-4 years of experience in production planning within a cosmetic/pharmaceutical manufacturing plant. It is essential to have a working knowledge of processes and systems of a GMP certified manufacturing plant. This is a full-time and permanent job opportunity with a day shift schedule. The preferred candidate should have a total of 3 years of work experience. The work location will be in person.,

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 & Visual Inspection & Packing Aseptic operations/ QMS / SKID / Multi-vessel / SVP / Visual Inspection / Packing / VI (Senior Officer / Officer / Associate) Experience - 02 to 07 Years Qualification - B. Pharmacy/ M Pharmacy / Msc /Bsc / Diploma / ITI Engineering (Instrumentation / Process Equipment Maintenance) (Senior Executive / Executive / Senior Officer) Experienc...

You will be working as a Maintenance Engineer at Meha Pharma Private Limited, a renowned manufacturer of various salts of aluminum, calcium, iron, magnesium, silica, and simethicones. The company takes pride in producing all antacid actives under one roof, ensuring top-notch quality and efficiency in their pharmaceutical products. Your primary responsibility in this full-time on-site role will be to oversee the maintenance activities at the pharmaceutical manufacturing facility. This includes conducting regular maintenance tasks, troubleshooting equipment issues, coordinating repairs, and ensuring the seamless operation of all machinery and systems within the facility. To excel in this role,...

You will be joining a dynamic and purpose-driven manufacturing team focused on delivering high-quality oral solid dosage forms (tablets and capsules) to various markets in Africa. Your role will be crucial in maintaining product quality, operational excellence, and regulatory compliance, ultimately contributing to the goal of enhancing access to essential medicines across the continent. Your responsibilities will include managing daily production activities for tablets and capsules, ensuring compliance with cGMP standards and production targets. Leading and guiding the production team to promote efficiency, training, and adherence to SOPs will also be a key part of your role. Additionally, y...

As a MES Consultant or Recipe Author, you should have experience in Rockwell PharmaSuite MES and a solid understanding of pharmaceutical manufacturing processes, particularly in solid oral dose and packaging. Your skills should encompass EBR design and configuration, validation documentation, and ensuring GMP compliance. Proficiency in tools such as Microsoft Visio, Rockwell PharmaSuite, and any legacy EBR tools like P2C2 and PMX is essential for this role. Having experience in working with Italian clients would be a bonus, especially if you possess Italian language proficiency. The preferred start date for this position is July 1, 2025. The job locations available for this role are in India...

As a Biomedical & Industrial Manufacturing Intern at Raja Industries in Thoothukudi, Tamil Nadu, India, you will have the opportunity to work at the intersection of biomedical materials, pharmaceutical packaging, and industrial fabrication. Raja Industries, an engineering and advanced manufacturing company, specializes in precision fabrication, structural engineering, and industrial solutions. With a legacy spanning various sectors including thermal power plant infrastructure, aerospace structures, and medical-grade manufacturing, the company is now expanding into biomedical and pharmaceutical engineering. Your role will involve gaining hands-on experience in medical-grade material selection...

As an individual working with the Site Investigations team member (Microbiology) at Dr. Reddys Laboratories Ltd., your primary responsibility is to ensure effective investigations and root cause analysis for microbiology-related deviations, Out of Specification (OOS), and Out of Trend (OOT) results. Your role involves driving these investigations towards closure in a timely manner with adequacy. Key Responsibilities: - Performing root cause analysis for microbiology-related deviations, OOS, and OOT results, including Bioburden, Sterility, and Bacterial Endotoxins Test (BET). - Collaborating with cross-functional teams to ensure timely and adequate closure of investigations. - Conducting tren...

The Technical Executive role requires a minimum of 7 to 10 years of hands-on experience in operating blister packaging machines within the pharmaceutical industry. The preferred location for this position is Bangalore. Key requirements for this role include strong operational expertise in blister packaging machines, sound knowledge of cGMP and GPP manufacturing practices, and a stable track record in pharmaceutical manufacturing setups. Candidates with the ability to join sooner than a 90-day notice period will be given preference. Candidates with solid backgrounds in pharmaceutical production will be prioritized for this role. Coordination within the recruitment team is essential for stream...

The incumbent will be responsible for calibration activities related to injectable plant. You will lead and perform complex calibration tasks to ensure compliance with GMP and ISO standards. This will involve coordinating with OEM vendors and the engineering team to execute qualification, calibration, and requalification activities for QC equipment. Additionally, you will provide support for the installation and maintenance of pharmaceutical manufacturing and laboratory equipment. It is crucial to record data and results in accordance with Good Manufacturing Practices (GMPs) and ISO quality standards. Maintaining up-to-date calibration documentation and certificates will also be part of your...

Officer Production, Vapi, Gujarat Responsibilities: Equipment cleaning as per ECR/SOPs Ensure cGMP compliance Execute batch charging (BMR/BPR) Maintain records Complete BMR/BPR/ECR documentation Apply at talent@hireindians.com or call 8882212459. Required Candidate profile Qualifications & Skills: * B.Sc. / M.Sc. in Chemistry (Analytical/Organic/Industrial) or B. Pharma. * 1–4 years of experience in pharmaceutical formulation/API manufacturing.

As a Process Equipment Systems Engineer in the pharmaceutical manufacturing industry, your primary responsibility will be to design and specify process equipment systems for manufacturing plants. This involves ensuring that the equipment aligns with project goals and meets regulatory standards such as GMP, FDA, and EMA. You will need to select appropriate equipment based on factors like material compatibility, process requirements, automation, and cost-effectiveness. Your role will also involve developing equipment specifications, datasheets, and technical documentation for procurement and installation purposes. It is essential to have hands-on experience in installing isolator-based filling...

As a Senior Production Manager at Illusion Dental Laboratory and Laxmi Dental in Mumbai, Maharashtra, you will be responsible for leading our production operations and ensuring excellence in manufacturing processes at our facility. You will play a crucial role in overseeing production planning, operations management, quality control, process improvement, team leadership, reporting, and budgeting. Your key responsibilities will include developing and managing effective production schedules, monitoring and adjusting schedules to meet production goals, determining material and equipment resources, and enforcing standard operating procedures and safety standards. You will also be responsible for...

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 & Visual Inspection & Packing Aseptic operations/ QMS / SKID / Multi-vessel / SVP / Visual Inspection / Packing / VI (Senior Officer / Officer / Associate) Experience - 02 to 07 Years Qualification - B. Pharmacy/ M Pharmacy / Msc /Bsc / Diploma / ITI Engineering (Instrumentation / Process Equipment Maintenance) (Senior Executive / Executive / Senior Officer) Experienc...

We are looking for a meticulous and proactive Assistant Manager - Utilities to champion the operation and maintenance of critical utility systems at Synnat Pharma. This role is pivotal in ensuring the seamless functioning of essential infrastructure, including boilers, cooling towers, refrigeration systems, AHUs, water treatment (RO/DM), and compressed air/nitrogen systems. As the Assistant Manager, you will blend hands-on site responsibilities with strategic office-based tasks, such as data capture and engineering calculations, to drive efficiency enhancement. The ideal candidate will possess a strong understanding of pharmaceutical manufacturing, API production, and regulatory compliance, ...

We are looking for QA Manager / QA Executive to join our dynamic team and embark on a rewarding career journey You will also be responsible for identifying and resolving quality-related issues and ensuring that the company's products and services meet the requirements of customers Conduct regular quality audits to identify and resolve quality-related issues Develop and maintain quality metrics to track performance and identify areas for improvement Manage the documentation process for quality assurance procedures, including the creation and maintenance of standard operating procedures (SOPs).

Roles and Responsibilities: Supervise and manage daily manufacturing operations in accordance with pharmaceutical production standards, including GMP and SOP compliance. Collaborate with the maintenance team to improve the reliability and efficiency of production machinery. Ensure safe operation of all equipment and enforce safety protocols within the production area. Monitor and support mechanical aspects of pharmaceutical production processes and machinery. Identify and address any mechanical issues impacting production performance. Qualifications: Educational Background: B.E./B.Tech in Mechanical Engineering (Production specialization preferred) Experience: 24 years of experience as a Pro...

The Production Planner is responsible for developing and managing efficient production schedules to meet demand forecasts, optimize resource utilization, ensure compliance with GMP and regulatory standards, and minimize downtime in a pharmaceutical manufacturing environment. Key Responsibilities: - Develop and maintain detailed production plans based on sales forecasts, inventory levels, and customer orders. - Coordinate with procurement, quality assurance, warehouse, and manufacturing teams to align production plans. - Monitor production progress and adjust schedules as necessary to avoid delays and ensure timely product delivery. - Ensure planning aligns with cGMP, regulatory requirements ...

As a member of Pfizer's quality assurance team, you will play a crucial role in ensuring the delivery of safe and effective products to patients. Your commitment to quality, compliance, and patient-centric approach will directly impact the lives of those who rely on our products. Your responsibilities will include evaluating and reviewing clinical and commercial drug batches to ensure they meet established specifications. You will conduct rigorous sampling and statistical process control procedures to identify deviations from standards and approve investigations and change control activities to maintain compliance with configuration management policies. In this role, you will contribute to m...

The Manufacturing Department is looking for a candidate to monitor and execute production activities during the shift. The main aim is to maintain cGMP and safety norms to achieve production targets effectively. Key responsibilities include executing production activities in a shift by managing available resources to meet production targets. It is essential to maintain standard process parameters as per BMRs and other supporting documents to ensure quality production. Additionally, preparing manufacturing records and updating online documentation to comply with production and cGMP requirements is crucial. Ensuring safe work processes and utilizing safety appliances during production activiti...

As a Production Manager at Kanath Engineering, you will play a crucial role in overseeing and managing the production processes at our Atgaon site. Your responsibilities will involve ensuring the efficiency of operations, maintaining quality assurance standards, and upholding safety protocols. You will be tasked with planning and organizing production schedules, collaborating with various departments, supervising production staff, and optimizing resource allocation to achieve production targets effectively. To excel in this role, you should bring a wealth of experience in production management and a strong background in process optimization. A solid grasp of manufacturing standards and safet...