14 Bmr Preparation Jobs

As a Production Manager in the Ayurvedic & Nutraceutical industry, you will be responsible for the following key tasks: - Independently manage the production of syrups, tablets, and capsules. - Ensure production adheres to schedules, quality standards, and GMP compliance. - Prepare Batch Manufacturing Records (BMR) and maintain accurate documentation. - Oversee regulatory compliance and quality assurance processes. - Coordinate with teams to ensure smooth and efficient production workflows. To qualify for this role, you should meet the following requirements: - Minimum 3 years of experience in Ayurvedic and nutraceutical production. - Proficiency in manufacturing processes for syrups, tablet...

You will be responsible for: - Handling Quality Management System (QMS) for drug substance of bacterial products - Demonstrating good process understanding of upstream and downstream unit operations - Managing QMS documents including deviation, change control, and investigations through Track-wise software - Ensuring audit compliance and adherence to regulatory guidelines - Knowledge on documentation such as Standard Operating Procedures (SOP) and Batch Manufacturing Record (BMR) preparation Qualifications required: - Experience range of 3 years to 6 years in a similar role,

Role Overview: As a Quality Assurance officer at Sunrise Remedies, your role will involve various responsibilities related to ensuring the quality and compliance of products and processes within the organization. Key Responsibilities: - QA Documentation - Validation / Qualification - Documents Control and Archival of documents - Retain Sample Handling and Observation - SOP Preparation and Revision related Activities - BMR Preparation and Review - Monitoring of all the QA activities, test results, leaked defects, and identifying areas of improvement - Handling of QMS Related Activities (change control, deviation, Market Complaint, incident, OOS) - Knowledge of regulatory guidelines and requir...

As a candidate for the position, you will be responsible for handling the production area for Tablets and Capsules. This includes the preparation and filing of Batch Manufacturing Records (BMR) and Batch Packing Records (BPR). Additionally, you will oversee the management of Men Power within the production area. Your role will also involve coordinating with the In-Process Quality Assurance (IPQA) team and Quality Control (QC) department. The ideal candidate should have 2 to 4 years of relevant experience in this field. For any further details, you can reach out to hrd@stravahealthcare.com. As a candidate for the position, you will be responsible for handling the production area for Tablets a...

As a Manufacturing Technician at our company, you will be responsible for the following key tasks: - Manufacturing of Lyophilized Drug Product - Aseptic Blending & Filling - Injectable Filling - Lyophilization - BMR Preparation - Following cGMP Practices - Media Preparation - Vial Washing and De-pyrogenation - Validation, Labeling & Packaging - Documentation To qualify for this role, you will need the following qualifications and requirements: - M.Sc in Microbiologist / Biotechnology - 2 to 4 years of relevant experience The job location for this position is in Kadi, Gujarat. We also provide bus transportation facility for our employees. If you are interested in this position, please share y...

As a candidate for this position, you should have 3-5 years of hands-on experience in Granulation, Compression, and Coating processes. Your role will involve utilizing your good machine handling skills, specifically with RMG, FBD, Compression, and Coating equipment. Key Responsibilities: - Monitor and supervise production processes - Maintain online documentation - Ensure compliance with SOP and GMP standards - Prepare and review SOP, BMR, and BPR - Demonstrate skill in handling manpower - Plan and execute production activities - Utilize Pharma Cloud software for work tasks Qualifications Required: - 3-5 years of experience in Granulation, Compression, and Coating - Proficiency in machine ha...

Role Overview: As an R&D Executive in the Fill and Finish division, your main responsibility will be to prepare Batch Manufacturing Records (BMR), Batch Packaging Records (BPR), Standard Operating Procedures (SOPs), and General Protocols. Additionally, you will be tasked with handling Change Controls, Deviations, Corrective and Preventive Actions (CAPA), Out of Specification (OOS) and Out of Trend (OOT) investigations. Key Responsibilities: - Prepare Batch Manufacturing Records (BMR) - Prepare Batch Packaging Records (BPR) - Develop Standard Operating Procedures (SOPs) - Create General Protocols - Handle Change Controls - Manage Deviations - Implement Corrective and Preventive Actions (CAPA)...

As a Production Manager in the Ayurvedic & Nutraceutical industry, you will play a crucial role in overseeing the production process of syrups, tablets, and capsules. Your responsibilities will include: - Independently managing the production of syrups, tablets, and capsules. - Ensuring that production operations adhere to schedules, quality standards, and comply with Good Manufacturing Practices (GMP). - Preparing Batch Manufacturing Records (BMR) and maintaining accurate documentation. - Overseeing regulatory compliance and quality assurance processes. - Coordinating with teams to ensure smooth and efficient production workflows. To excel in this role, you must meet the following requireme...

As a member of the VTC MFG. QA team, your role will involve handling the Quality Management System (QMS) for drug substance of bacterial products. You are expected to have a strong understanding of the processes involved in both upstream and downstream unit operations. Your responsibilities will include: - Managing QMS documents including deviations, change controls, and investigations using Track-wise software. - Ensuring audit compliance and adherence to regulatory guidelines. - Proficiency in documentation tasks such as Standard Operating Procedure (SOP) development and Batch Manufacturing Record (BMR) preparation. Qualifications required for this role include: - A minimum of 3 to 6 years...

You will be responsible for managing the Quality Management System (QMS) for drug substance of bacterial products. It is essential to have a solid understanding of the process involved in both upstream and downstream unit operations. Your role will involve handling QMS documents including deviations, change controls, and investigations using Track-wise software. In addition, you should have experience in ensuring audit compliance, adherence to regulatory guidelines, and proficiency in documentation such as Standard Operating Procedures (SOPs) and Batch Manufacturing Record (BMR) preparation. This position requires a minimum of 5-8 years of experience in QMS, compliance, and documentation, wi...

As a Production Area Handling Specialist, you will be responsible for overseeing the manufacturing processes of tablets and capsules. This includes ensuring smooth operations, monitoring equipment performance, and maintaining quality standards. Your duties will also involve the preparation and filing of Batch Manufacturing Records (BMR) and Batch Packing Records (BPR) in compliance with regulatory guidelines. Attention to detail and accuracy are crucial in this aspect of the role. In addition, you will be tasked with managing the manpower within the production area, ensuring optimal utilization of resources and manpower efficiency. Effective communication and leadership skills will be essent...

You should have 3-5 years of hands-on experience in Granulation, Compression, and Coating processes. Additionally, you must possess good machine handling skills including RMG, FBD, Compression, and Coating equipment. Your responsibilities will include monitoring and supervising operations, ensuring online documentation, and maintaining compliance with SOP and GMP regulations. It is essential to have knowledge of SOP, BMR, and BPR preparation and review. Manpower handling skills and experience in production planning and execution are crucial for this role. Familiarity with Pharma Cloud software is required. This is a full-time position with benefits such as Provident Fund and a yearly bonus. ...

Responsible for preparing work instruction for Production and manufacturing activities Carry out production activities as per production plan Responsible for monitoring batch process Maintaining equipments and area cleanliness

Responsible for preparing work instruction for Production and manufacturing activities Carry out production activities as per production plan Responsible for monitoring batch process Maintaining equipments and area cleanliness