4097 Gmp Jobs - Page 43

To follow the SOP and implementation on current Good Manufacturing Practices(cGMP). Reviewing the online documentation like BPR/BMR, Log Books, in process Formats,during self-inspection and QMS related query. To maintain the GMP, personnel safety and hygienic practices on shop floor. Involved in Process Validation of new products as well as revalidation of existingProducts, requalification of existing equipment. Ordering and inventory control of spare parts. Line clearance during batch change over(TYPE A) or product change over(TYPE B). Handling and supervision of dispensing, manufacturing and packing activities. Handling and manage manpower. Good knowledge of SAP. Supervision of manufacturi...

Financial Outcomes Evaluation and Validation : Monitor and control production costs, including labor, raw materials, and utilities. Optimize resource utilization to reduce waste and improve yield. Support cost-saving initiatives and continuous improvement projects. Customer Service Solution Development : Collaborate with QA/QC teams to ensure product quality meets customer expectations. Address customer complaints related to production issues and implement corrective actions. Participate in audits and customer visits to represent production capabilities What are the Critical success factors for the Role 1. Production Planning Execution Assist in daily production planning to meet output targe...

What are the Key Deliverables in this role Financial Outcomes Achieve and maintain production within allocated budgets by controlling raw material consumption, reducing wastage, and optimizing labor utilization. Drive improvements in yield and line efficiency to maximize output and minimize cost per unit. Ensure efficient use of machinery, manpower, and materials to achieve cost savings. Maintain optimal stock levels to reduce carrying costs and prevent overproduction or shortages. Maintain optimal levels of raw materials, packaging materials, and finished goods to balance production continuity with working capital management. Prepare timely and accurate MIS reports on production costs, vari...

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology At Cepheid, one of Danaher s 15+ operating companies, our work saves lives and we re all united by a shared commitment to innovate for tangible impact. You ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher s system of continuous improvement, you help turn ideas into impact innovating at the speed of life. At Cepheid, we are passionate about improving health care through fast, accurate, molecular diagnostic systems and tests. As a member of our team, you ll get to make an immediate, measurable impact on a global scale...

Title: Senior Executive/ Manager - Corporate Quality Compliance Business Unit: Global Quality and Compliance Job Grade: G10 Location: Vadodara Key Responsibilities At Sun Pharma, we commit to helping you “ Create your own sunshine ”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” ...

Responsibilities: Supervision of Production Operations: Oversee day-to-day operations on the production floor, ensuring efficient, smooth, and safe production processes. Supervise a team of operators and production workers, ensuring that production targets and quality standards are met. Ensure production timelines are followed, and tasks are assigned efficiently among the team. Quality Control and Improvement: Monitor product quality at various stages of production and ensure compliance with industry standards. Identify and resolve any issues or discrepancies related to product quality or process inefficiencies. Team Leadership and Development: Provide guidance and support to team members, f...

Primary Job Function To lead and manage all regulatory affairs activities at the manufacturing site located at Mumbai and LL locations, ensuring timely regulatory submissions, compliance with regulations, and providing strategic support to institutional and international business operations. The role is critical to maintaining business continuity and regulatory compliance. Core Job Responsibilities Regulatory Submissions and compliance Prepare and submit various applications such as additional product permission, Layout approval, facility modification approval, technical person approval, Test license, amendments in licenses, State GMP and GLP certificate applications, post approval changes e...

Production & Process Management Supervise the entire production process, ensuring smooth workflow and minimal downtime. Develop and implement production schedules to meet operational goals and delivery deadlines Monitor and analyze production metrics, ensuring adherence to efficiency and quality standards. Ensure proper functioning, maintenance, and calibration of manufacturing machinery. Identify and implement process improvements for enhanced productivity and cost efficiency. Quality Assurance & Compliance Maintain strict quality control measures to meet regulatory and ISO standards (ISO 9001 & ISO 13485). Ensure all manufacturing operations comply with GMP (Good Manufacturing Practices) a...

Receipt of raw marterial, packing materials and miscellaneous materials as per standard operating procedure. Preparation of Check list, Good receipt (in SAP) and labelling for raw materials and packing materials as per standard operating procedure. Responsible for submitting the RM/PM Invoice s to finance department. To maintain the online documentation related to warehouse receipt activities on daily basis.(Receipt area logbooks updating, Checklist updating). Responsible for preparation of Returnable Gatepass and Delivery Challan. Calibration of Weighing balance and Roll Label Counting Machine as per standard operating procedure. Distribution of material to various Departments. Handlinf of ...

Job Description Food Technologist As a Food Technologist, you'll play a key role in developing, optimizing, and maintaining our product offerings. You'll ensure that every meal we serve meets the highest standards of taste, safety, nutrition, and consistency. This is a hands-on role that blends culinary creativity with scientific precision. Key Responsibilities Product Development: Innovate and improve recipes, dressings, and toppings with a focus on taste, nutrition, and shelf life Collaborate with chefs and nutritionists to create seasonal and functional menu items Conduct sensory evaluations and trials to refine product quality Conduct pilot runs and defines the roadmap to scale-up of rec...

Responsible to ensure the cleaning and sanitization of machines, instruments and equipment s and area. Responsible for line clearance activity before commencing the operations as per SOP. Responsible to operate the machines, instruments, and equipment s of area. Inform immediately to concern supervisor for any observation/disturbance found in the aseptic area. Responsible to update on self-hygiene, cleaning & sanitization of area, follow SOPs, filled the document, of area. Responsible to fill the log of area as per SOP and work execution. Responsible to ensure UAF working in area. To follow the cGMP, Good Document Practice, and discipline in the department. Responsible to perform all the act...

We are currently seeking a Consumables Engineer for the design of single-use products. ETO service (Engineering to Order) allows our customers to benefit from Sartorius's consumable products perfectly adapted to their bioprocess need through a detailed customization. Work With Us - Your Responsibilities Manage ETO projects in an international environment from definition to final approval Coordinate all activities for the project and create the final design and pricing Define specifications in cooperation with other departments like product development, quality, procurement, MSAT,sales and marketing for more complex projects Making technical and feasibility analyzes of projects Design new cus...

Our vision is to transform how the world uses information to enrich life for all . Micron Technology is a world leader in innovating memory and storage solutions that accelerate the transformation of information into intelligence, inspiring the world to learn, communicate and advance faster than ever. JR58146 GEL Supervisor Designs, implements and maintains quality assurance protocols and methods for processing materials into partially finished or finished products. Responsible for planning, implementing and managing compliance of manufacturing and production processes with internal and external safety, quality and regulatory standards requirements for worldwide distribution. Designs methods...

Job Summary Experienced Quality Assurance professional with a strong background in the Active Pharmaceutical Ingredient (API) industry. Responsible for implementing and maintaining GMP-compliant Quality Management Systems to ensure product quality, regulatory compliance, and operational excellence. Key responsibilities include managing documentation, handling audits (regulatory and customer), overseeing batch release, deviation investigations, and ensuring adherence to global regulatory standards (cGMP, ICH, FDA, etc.). The role demands expertise in validation, change control, and continuous quality improvement within a highly regulated API manufacturing environment. Quality Planning and Sch...

Role & responsibilities Post - Sr Quality / QMS Engineer -Frozen Foods Location - Pune Jejuri Experience -05-08 yrs skills - QMS , Frozen Foods Contact - 9356395439 Email - jobpune22@gmail.com

Role & responsibilities Post - Sr Quality / QMS Engineer -Frozen Foods Location - Pune Jejuri Experience -05-08 yrs skills - QMS , Frozen Foods Contact - 9356395439 Email - jobpune22@gmail.com

We are seeking a proactive & detail-oriented Supply Chain Manager with strong knowledge of nutraceutical ingredients and industry trends.Familiarity with GMP, quality standards, & regulatory compliance.Excellent organizational & communication skills

We are seeking an experienced and detail-oriented Production Manager to oversee and manage the entire manufacturing process in our nutraceuticals production facility in Powder section. The ideal candidate will have 8 to 15 years of hands-on experience in nutraceutical or food supplement production, with a strong understanding of GMP, FSSAI regulatory compliance, and process optimization. 01. Role & Responsibilities Production Planning & Execution: 1. Develop and implement production schedules to meet demand forecasts. 2. Monitor daily production activities and ensure targets are met in terms of quantity, quality, and timelines. Process Optimization: 1. Identify and implement continuous impro...

Role & responsibilities To ensure incoming raw material as per quality specifications by adhering FIFO. Implementation and sustain of Good Manufacturing Practice and Good Hygiene Practice. Control of Monitoring and Measuring in OPRPs and CCP Pest control management tracking in the premises. Responsible for maintaining FSMS related documents (food safety manual, Adherence of yearly calendar, Internal Audit, CAPA, product traceability, MOM ) Conduct the internal quality audit & document control audit as per schedule Conduct the Mock recall and maintaining reports GMP and GHP training provide to Food handlers FSSAI statuary & regularity document maintaining reports. Fulfil the Food Safety Requi...

Qualified Actuarial Project Consultant Experience in UK/US DB Consulting sector Reviewer of complex calculation Experience with GMP Equalization/Rectification Documentation of calculation methodology, decision & assumption & ensure Quality assurance

As a Material Planning & Production Coordinator at Apotex Inc., your role involves ensuring effective and timely execution of material planning & production, lab scheduling, and regular review of materials inventory for expiring material. You will be responsible for creating Production and Lab Scheduling, collaborating with cross-functional teams, and identifying continuous improvement opportunities to streamline processes. Key Responsibilities: - Collaborate with cross-functional teams including Production, Lab, Warehouse, and Logistics - Drive continuous improvement opportunities to streamline processes and improve accuracy - Demonstrate knowledge of Supply Chain and Materials Management S...

Key Responsibilities: System Operation & Monitoring: Operate and monitor water systems including RO, EDI, Multi-effect distillation (MED), Pure Steam Generators, and related equipment. Perform routine checks and log system parameters (e.g., conductivity, flow, temperature, TOC) to ensure compliance. Monitor control systems (SCADA/BMS) and respond to alarms and deviations promptly. Preventive & Corrective Maintenance: Execute scheduled preventive maintenance of water treatment equipment and utility systems. Troubleshoot and resolve system breakdowns or performance issues with minimal downtime. Replace filters, cartridges, membranes, and perform sanitization as per SOPs. Compliance & Documenta...

Key Responsibilities: Instrumentation Setup & Maintenance: Oversee the installation, calibration, and maintenance of instrumentation systems used in formulation processes, including sensors, flow meters, pressure controllers, and temperature devices. Ensure the continuous functioning of all instruments, minimizing downtime, and troubleshooting any issues promptly. Support Formulation Processes: Assist the formulation engineering team with the technical setup and maintenance of equipment used for pharmaceutical formulations. Provide technical expertise and solutions for optimizing formulation processes, ensuring they meet safety and regulatory requirements. Documentation & Reporting: Maintain...

As a QC Chemist with 5 to 8 years of experience at Sinterx Pharma Private Limited, your role involves leading and executing complex analytical testing of API intermediates to ensure compliance with quality standards and regulatory guidelines. You will conduct advanced testing, review analytical data, support investigations, mentor junior analysts, and contribute to continual improvement initiatives. Collaboration with Quality Assurance, Production, and R&D teams is essential to maintain product quality throughout the production lifecycle. **Key Responsibilities:** - Perform routine and non-routine analysis of raw materials, intermediates, and in-process samples using validated methods and in...

You will be responsible for ensuring the quality of pharmaceutical formulations in the QA department. Your key responsibilities will include: - Minimum 3 to 5 years of experience in QA department of pharmaceutical formulation - Knowledge of In-Process Quality Assurance (IPQA) is required - Familiarity with Good Manufacturing Practices (GMP) - Preferable to have experience in Regulatory work No additional details of the company are mentioned in the job description.,