9 Bpr Preparation Jobs

Dr. Reddy's Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can't Wait . We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries. For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolve...

Job Title: Senior Officer to Senior Executive QMS (Production) Section: QMS - Production - API Mfg. Department: Production Qualification: M.Sc. (Chemistry) / B.E. (Chemical) Experience: 5 to10 years Location: Raks Pharma Pvt. Ltd. Dahej, Bharuch, Gujarat Job Description We are looking for an experienced QMS professional for our Production Department who will be responsible for ensuring compliance with cGMP, documentation practices, validations, and audit readiness. Key Responsibilities: Prepare new SOPs and revise existing SOPs as per requirements, periodic updates, and audit recommendations, including review and implementation for the Production department. Carry out process validation and ...

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 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)...

Role Overview: As a Packaging Planning Executive in the Sterile Manufacturing Department, your primary responsibility will be to prepare packaging planning on a monthly and daily basis based on material availability. You will also be responsible for updating self-hygiene practices, attending training sessions, and working in accordance with standard operating procedures. Key Responsibilities: - Prepare packaging planning on a monthly and daily basis according to material availability - Update self-hygiene practices - Attend training sessions as per schedule and ensure compliance with Training Needs Identification (TNI) - Adhere to standard operating procedures in the general area of the Ster...

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. ...

Outlines quality assurance procedures and policies Oversees implementation of quality assurance procedures Ensures the efficiency of inspections through hands-on guidance Ensures data integrity and accuracy Prepares reports on the results of quality inspections Evaluates outcomes of quality inspections and proposes corrective measures. Preferred skills : IPQA, Line clearance, BMR/BPR preparation and & Exposure in review Qualification of equipment and HVAC (DQ, IQ, OQ, PQ) Process validation, Protocol preparation and review Documentation, Change Control, deviation, Market Complaint, CAPA, etc.