360 Tablets Jobs

shall be responsible for maintaining and improving all QMS activity, GMP and GLP across the company Handling QMS activities like change control, validations, stability, qualifications, APQR and Risk assessment etc Label artwork review and management Required Candidate profile Assisting HOD in customer complaint analysis and preparation of customer complaint report. Investigation of incidents, deviations, OOS and ensure corrective actions in place.

Job Responsibilities: Development of oral solid dosage forms (tablets, capsules) including IR, MR, and coated products. Handling product development, optimization, and scale-up activities.

Key responsibilities: Executes online Batch Packing Records, online in process as per the parameters mentioned in the BPR, logbook, documents and other formats. take line clearance of area / machine as per respective SOPs. maintain / fill all area / machine related documents like Sequential, area cleaning, daily cleaning log books and other formats of machine & area as per SOP. verify and receiving of dispensed packing material. indent / receive / handle / verification / uses & destruction of stereo as per respective SOP. verify the Leak test of blister / strip as per frequency. If result not satisfactory, rectify the problems. maintain, handle / storage / labelling of machine spares /change...

Line Clearance for Dispensing, Manufacturing & Packing activities Dispensing of RM/PM for batch Mfg Monitoring of IPQA activities (Granulation, Blending, Capsulation, Compression, Coating, Packing Sampling of IP and FP Samples Batch documents review

Medicamen Biotech - SRL Pharma R&D Centre Required Formulations Profile Designation: Executive/ Scientist Qualifications: M. Pharma - Pharmaceutics Vacant Post: 6 Nos. Experience: 4 to 8 Years Please share profile on uday@shivalikrasayan.com Required Candidate profile Pharma R&D experience must in Formulation USFDA exposer prefer Preparation of Pharmaceutical Development Report Ready to relocate Bhiwadi, Rajasthan Ready to join Immediately Prefer Team Player Perks and benefits Best of Industries Salary based on Experience

Purpose/Objective Shift Manager - LT Operations is responsible for overseeing the entire product operation cycle, from berthing to the dispatch of products at the Liquid Terminal. Oversees managing daily shift operations, planning vessel activities, coordinating manpower, liaising with stakeholders, updating SOPs, accounting for stock, and maintaining cleanliness within the terminal. Key Responsibilities of Role Liquid Terminal Operations Management: Direct and manage daily shift operations at the Liquid Terminal, ensuring efficient and safe execution of all activities. . Resource Management: Evaluate operational needs and allocate the necessary manpower for effective Jetty and Tank Farm ope...

Purpose/Objective Shift Manager - LT Operations is responsible for overseeing the entire product operation cycle, from berthing to the dispatch of products at the Liquid Terminal. Oversees managing daily shift operations, planning vessel activities, coordinating manpower, liaising with stakeholders, updating SOPs, accounting for stock, and maintaining cleanliness within the terminal. Key Responsibilities of Role Liquid Terminal Operations Management: Direct and manage daily shift operations at the Liquid Terminal, ensuring efficient and safe execution of all activities. . Resource Management: Evaluate operational needs and allocate the necessary manpower for effective Jetty and Tank Farm ope...

Purpose/Objective Engineer - Automation and Instrumentation (Liquid Terminal) is responsible for the effective management and maintenance of automation and control systems specific to liquid terminal operations. This role is crucial for ensuring accurate and efficient handling of liquid cargo, maintaining safety standards, and optimizing the performance of liquid terminal facilities. Key Responsibilities of Role System Maintenance and Optimization: Conduct regular maintenance, troubleshooting, and optimization of automation and instrumentation systems to ensure uninterrupted liquid terminal operations. Technical Support: Provide expert support for automation systems, including programmable l...

Purpose/Objective Head of Section - Environment is responsible for ensuring compliance with environmental regulations, overseeing environmental monitoring and management systems, and leading initiatives to enhance environmental quality at the port. The role involves managing environmental projects, liaising with regulatory bodies, and ensuring the effective operation of treatment plants and waste management systems. Key Responsibilities of Role Environmental Monitoring: Oversee the regular collection and testing of air, sea water, ground water, treated water, and carbon emissions, ensuring they are within prescribed limits. Waste Management: Oversee the management, storage, and disposal of h...

Walk-In Interview: 14th December 2025 @ Sanand Job Location : Virochannagar Plant Venue : Hotel Veritas Grand, Sanand Vinayak Entice, Sanand - Viramgam Highway, Sanand, Ahmedabad - 382110 Time : 09:00 AM TO 03:00 PM Position: Technical Assistant / Executive Dept.: Quality Control (Formulation/Micro) Qual./ Exp.: B. Sc. / B. Pharm / M. Sc. / M. Pharm with 1 to 5 Years of relevant experience Area: Analysis /Qualification / Operations on HPLC/GC/FP/IP/RM/PM. Environment Monitoring, Media Preparation and Autoclaving, MLT, BET, Sterility Testing, Analytical Stability, Analytical method transfer Dept.: Quality Assurance (Formulation) Qual./ Exp.: B. Pharm / M. Pharm / M. Sc. with 1 to 5 Years of r...

We are thrilled to announce multiple exciting opportunities within our organization. The Zydus Skill Development Centre (ZSDC) is looking for passionate and skilled individuals with experience in QC to join our team as Technical Trainers. Role & responsibilities Responsible for training need analysis for identification of training topics w.r.t technical/soft skills/behavioural topics,. To impart training related to product/process, cGMP and GDP, SOPs, QMS, QC. Designing and preparation of training modules pertaining to QC. Tracking of scheduled training and training compliance. Planning skill development training activities of all sites through Annual calendar. Responsible for evaluating the...

Role & responsibilities JOB RESPONSIBILITY Your job responsibilities are listed below for your understanding and acceptance. In case of any system up-gradation in future, you will be simultaneously re-trained to understand the new implementation. 1. Responsible Manufacturing of Oral Solid Dosage Tablets and Capsule and for Production planning as per order or availability of material. 2. Responsible for Preparation of BMR for new product. 3. Responsible for verifying the filled BMR and yield reconciliation of each stage. 4. Responsible for preparation of Standard Operating Procedure (SOPs). 5. Responsible for Preparation MFR for new product development. 6. Responsible for coordinating with En...

Job Description Strong expertise in formulation development of sterile liquid injectable dosage forms, including end-to-end development and troubleshooting. Hands-on experience in drug device combination product development, with good understanding of device compatibility, functionality, and regulatory expectations. Proven experience in developing and handling lyophilized drug products (peptides, proteins, and small molecules), including cycle development and optimization.

As a Front-End Developer at ZURU Tech, you will play a crucial role in contributing to the front-end development of web applications. Your responsibilities will include handling production incidents, mentoring juniors when required, working closely with customers to ensure a smooth user experience, building reusable components and front-end libraries for future use, and translating designs and wireframes into high-quality code. Key Responsibilities: - Contribute to front-end development of web applications - Handle production incidents and ensure smooth operation - Mentor and guide junior team members - Work closely with customers to enhance user experience - Build reusable components and fr...

As a Front-end Web Developer at ZURU Tech, you will be contributing to the front-end development of web applications. Your responsibilities will include handling production incidents, mentoring juniors if required, working closely with customers to ensure a smooth user experience, building reusable components and front-end libraries for future use, and translating designs and wireframes into high-quality code. Key Responsibilities: - Contribute to front-end development of web applications - Handle production incidents - Mentor/guide juniors if required - Work closely with customers to ensure a smooth user experience - Build reusable components and front-end libraries for future use - Transla...

Roles and Responsibilities Plan production activities to meet customer requirements, ensuring compliance with GMP guidelines. Coordinate with various departments (QA, QC, Packing) for smooth plant operations. Ensure timely availability of raw materials and packaging materials through effective planning and coordination. Monitor daily production planning, shift planning, and manpower handling to achieve productivity targets. Oversee blister packing, granulation, compression machine operation, WHO inspections, and tablet/capsule filling processes. Desired Candidate Profile 10-12 years of experience in pharmaceutical production management or related field. Bachelor's degree in Pharmacy (B.Pharm...

Opening for Pharma Lifescience. Role & responsibilities : Candidate is having knowledge of OSD Formulation Plant. Depth knowledge of In Process Quality Assurance . Third Party Manufacturing Knowledge. Candidate is Ready for Within City Travelling for who are Manufacturing our Medicine. Qualification:-M-Pharma-QA or B-Pharma. Interested candidates shared resume on snehal@topgearconsultants.com

Formulation development and optimization for liquids and tablets Execute lab/pilot/commercial batches with complete documentation Perform stability studies and analytical/physical testing Troubleshoot formulation and manufacturing issues to improve product quality Support technology transfer and scale-up to production Ensure compliance with cGMP / WHO-GMP / regulatory requirements Maintain BMR, BPR, SOPs and technical reports Coordinate with QA/QC/Production/Regulatory for smooth execution of projects

Walk-In at Indore for Solid Oral - Production Production & Packing Solid Oral Plant Operator / Technical Assistant Tablet / Capsule - Granulation, Compression, Coating, Inspection, Capsule Filling and Wurster coater Blister Line (BQS) & Hicart Trainee Plant Operator Experience: 1 to 2 Years Qualifications: ITI Engineering Executive / Sr. Executive Process Equipment (Mechanical / Electrical / Instrumentation) Technician Instrument Technician - Process equipment's Fitter / Electrical / Instrumentation / Calibration Job location: Ahmedabad Qualification: BE / B.tech / B.Sc. / Diploma / IT Experience: up to 8 Years Date: 14th December 2025 (Sunday) Time: 9 am to 5 pm Venue: Papaya Tree Hotel, A....

Job Description: (Walk-in Drive Production Department): Coating Operator Production (OSD Formulations) We are hiring Coating Operators for tablet production. Responsible for operating tablet coating machines , monitoring process parameters, ensuring uniform coating , following GMP & SOPs , and maintaining equipment cleanliness. Experience in OSD formulations is preferred.

Role & responsibilities Formulation development (solid, semisolid, liquid oral) Tech transfer & scale-up Troubleshooting & problem-solving QbD, DoE, FMEA Strong documentation skills Knowledge of regulatory requirements Project management & cross-functional coordination

Hiring experienced IPQA professionals (48 years) for OSD formulation unit. Job Responsibilities: Line clearance, in-process checks, documentation (BPRs / Logbooks), Empower-3, Analytical Data Review, and QMS activities. Perform in-process checks during granulation, blending, compression, encapsulation & coating. Monitor IPC parameters: LOD, bulk density, blend uniformity, we Provide line clearance for manufacturing & packing operations Review BMR/BPR and ensure real-time documentation as per GMP/GDP . Verify equipment cleaning and ensure absence of cross-contamination . Conduct online sampling and coordinate with QC for testing. Support process validation & cleaning validation for OSD equipm...

As a Desktop Support Engineer at Wipro Technologies-Ireland, you will play a crucial role in maintaining the smooth operation of the technology environment. Your primary focus will be on providing exceptional support to clients and resolving technical issues promptly. Here are the key responsibilities associated with this role: - Demonstrate advanced technical expertise in troubleshooting and fault resolution to minimize user downtime. - Maintain proficiency in standard technology practices and tools to contribute to an effective IT environment. - Communicate complex technical solutions in a clear and friendly manner to non-technical audiences. - Possess in-depth technical knowledge of vario...

Job Description Relevant Experience : 1 To perform Operation activity of equipment and instruments as per SOP. 2. To affix the status label to equipments, instruments and IPC at each and every processing stage 3. To operate the equipment in safe and effective manner for production processing. 4. To follow and adhere to GDP and cGMP practices. 5.Inspect equipment to identify any replacement, and repairs. 6. Ensure that the equipment is maintained in good and safe working condition. 7. To Perform regular equipment maintenance to ensure production capacity and quality. 8. Identify and report unsafe operations and near misses to supervisor immediately. 9. Perform the activity as per SOP and inst...

Job Description Relevant Experience : Should have experience of Production for Formulation Plant of Oral Solids (Tablets, granules, powder) & Allied in PHARMACEUTICAL COMPANY / FACTORY. FDA Approval in Tablet Section Pharma Formulation plant would be preferred. 1. Batch Manufacturing Manufacture production batches as per Batch Manufacturing Record (BMR) and Batch Production Record (BPR). 2. BMR/BPR Documentation Complete the online BMR and BPR as per the respective activities. 3. Coordination with QA Coordinate with the Quality Assurance (QA) department for the issuance of monthly formats. 4. Manufacturing Parameters Review Review parameters during manufacturing stages such as compression, f...