338 Batch Manufacturing Jobs - Page 5

Role Overview: As a Research Associate in the API R&D-DBH department, your primary responsibility will be to ensure the smooth and efficient operation of various research activities in the manufacturing blocks. Your role will involve following strict guidelines and procedures to maintain safety, quality, and compliance with cGMP requirements. Key Responsibilities: - Acquire training for each activity/equipment before execution - Follow entry and exit procedures of manufacturing blocks, including chemical and Pharma areas - Perform all process operations as per Batch Manufacturing Records (BMR) - Clean all equipment as per cleaning Standard Operating Procedures (SOP), Procedure, and Process C...

To ensure the cleanliness of area and machines before starting the packing process. To perform challenge test of respective equipment & get it verified by packing officer To ensure availability of Batch manufacturing record before commencing the activity. To ensure the compliance of environmental conditions before commencing the activity. To ensure the line clearance from IPQA before commencing the activity. To run the machine as per approved SOP and in compliance with cGMP and record all the activities in the approved formats at the time of observation/activity is performed. To have knowledge of SOP of own working area and ensure to practice it. To escalate to supervisor for any non complia...

Job Title: Production Executive No. of Positions: 2 Company Name: The South Indian Manufacturing Company Company Website: www.saibol.com Location: Madurai (Local candidates preferred or must be willing to relocate) About the Company The South Indian Manufacturing Company is a reputed pharmaceutical manufacturer specializing in quality-driven processes and GMP-compliant production systems. Qualifications B.Pharm / M.Pharm / B.Sc Chemistry / M.Sc Chemistry Experience Freshers (0-2 years) are eligible Experienced candidates (3+ years) also welcome; higher salary will be offered based on profile Key Responsibilities Assist in ointment manufacturing (weighing, mixing, filling, packing, labeling) ...

To operate and monitor granulation equipment and processes in compliance with cGMP, SOPs, and safety standards, ensuring consistent production of high-quality pharmaceutical granules for tablet or capsule formulation. Key Responsibilities: Operate granulation equipment such as high-shear mixers, fluid bed dryers, oscillating mills, and blenders. Weigh, dispense, and mix raw materials as per batch manufacturing records (BMR). Monitor granulation parameters and adjust settings to maintain product quality. Perform in-process checks (e.g., moisture content, granule size) and document results accurately. Clean and maintain equipment and work areas as per SOPs. Execute machine changeovers and line...

With HOD and reliever discuss: - Special requirement/ instruction/target, last 2 shift issues, another 3 shifts schedule and additional task if any. Take quick round with the reliever in the entire area: - During round try to touch each and every people and have some specific question may be which are most critical to last 2 shifts issues/area etc. Charge will be taken during round physically area: - Any abnormality observed need to be objected; also, information should go to HOD. Abnormality should be cleared by the doer before leaving the workplace. Come to planning board well advanced (before shift start) and see the schedule status on the board updated and people reporting in the shift o...

Efficiencies to work long working hours (like as 10 to 11 Hrs.)Excellent knowledge of computer reservation process and MS Office.Shall be responsible for booking of Hotels/Flights/ Transportation as per the schedule sharedTo maintain the CRS on daily

Division Department Sub Department 1 Job Purpose Execute the production operations in line with safety and GMP requirements to meet the manufacturing targets in shift. Key Accountabilities (1/6) Operate the equipment efficiently without error and deviation as per SOP to meet shift targets Perform unit operations as per SOP and unit processes as per batch manufacturing record Optimize the utilization of available resources for achieving production in shift Maintain equipment, facility and block premises as per SOP for audit readiness Key Accountabilities (2/6) Provide suggestions for optimization of processes to manufacture quality product Identify the deficiency in area and errors in documen...

Role Overview: As a Production Chemist specializing in UV Gel Nail Paint, your main responsibility will be to oversee the scale-up and production of formulations from lab-scale to production-scale batches. You will create and adhere to batch manufacturing records (BMRs), monitor production floor procedures including mixing, heating, and filling processes. Key Responsibilities: - Convert lab-scale formulations to production-scale batches. - Create and follow batch manufacturing records (BMRs). - Monitor mixing, heating, and filling procedures on the production floor. Quality Control (QC): - Test raw materials, in-process batches, and final products for: - Viscosity - Cure speed (UV/LED) - Col...

As a Production Planning & Execution specialist, you will be responsible for executing daily production activities on the shop floor according to the approved production schedule. Your role will involve planning and allocating manpower shifts, distributing work effectively with proper supervision, and monitoring utilities to meet production schedules and ensure continuous functionality. Your coordination with various departments will be crucial for the smooth operation of production activities. You will liaise with Warehouse/Stores/Procurement to ensure timely availability of raw materials, coordinate with the QC Department for timely analysis and approval of samples, and work closely with t...

Job Description for Executive API Technology Transfer Responsibilities: To evaluate process and scale up studies/exhibit batch of commercial site. To understand chemistry reaction mechanism and process of APIs and Intermediate from Lab scientists. To observe lab batches and provide inputs for the process development that are safe, robust, scalable, reproducible, and commercially viable. To develop, optimize and integrate scalable chemical process technologies to pilot plant / commercial plant using Multimax, RC1e, Syrris and Lasentec (PAT Tool) To accomplish and review literature search for advanced tools used in scale up. To execute the pilot plant batches To conduct demonstration and valid...

As a QA Manager at Systacare, a trusted name in the pharmaceutical industry, your primary responsibility will be to ensure adherence to regulatory requirements and maintain the highest standards of compliance in injectable manufacturing. With a strong focus on innovation, compliance, and patient safety, Systacare is expanding its team and is seeking passionate professionals to join the organization. You will lead and manage the QA team to ensure compliance with cGMP, regulatory standards, and company SOPs. Your role will involve overseeing quality systems, including deviation management, change control, CAPA, OOS, and OOT investigations. It will be crucial for you to ensure quality assurance...

Greetings from FocusR...!!! Exciting Opportunity to Shift Your Career to an IT Sector. If you are currently working in Manufacturing, Production, Procurement, Logistics, Quality, Inventory or Supply Chain industries, this is your chance to shift your career into the IT sector!!! Great opportunity of becoming an "Oracle SCM Consultant" Complete On-Job Training will be given by FocusR (with salary) on ORACLE SCM MODULE as per of the permanent employment. Manufacturing sector experience: 2-5 years required Qualification: Any UG/PG Degree Notice Period: Immediate - 30 Days preferred Job Location: Salem and Chennai (Training will be mandatory in Salem) Willing to take Oracle Supply Chain Manageme...

Role & responsibilities Responsible for all in process Quality Assurance Activities Document issuance and control Preparation and review of SOPs, Protocols, Reports, BMR, BPR and QC Specifications Issuance and review of BMR and BPR and other quality system documents Internal audit and its compliance related activity Ensuring compliance to cGMP Prepare Annual Training Plan in co-ordination with Head of QA Schedule and coordinate the cGMP training session Assist in the delivery of new employee orientation training Assure training records are maintained for regular, temporary and contractors/consultants Check monthly log book and calibration of IPQA instrument and balance Stability and control ...

*Operate and monitor injectable (DPI)production equipment in compliance with cGMP standards. *Execute manufacturing processes compounding, aseptic filling, vial washing, autoclaving, and lyophilization. *Maintain (BMR) and related documentation. Required Candidate profile *Ensure adherence to safety, hygiene, & quality standards during production activities. *Familiarity with regulatory guidelines (USFDA, MHRA, WHO, etc.). *Good documentation and communication skills.

Junior Executive/ Executive - Production (API) Job Criteria: B.E-B.Tech (Chemical Engg.) / M.Sc./B.Sc. 1 to 5 years of experience Job Role: Ensure that the products are manufactured as per the cGMP and handle critical equipment like reactor, centrifuge, blender, sifter, multi-mill, etc. Maintain documentation as per regulatory requirement like change control, deviations. Highlight technical problems and take corrective actions, and maintain safety practices. Technical Officer/ Junior Executive/ Executive-Production+Packing (OSD) Production Job Criteria: M. Pharm/B. Pharm/DME/ITI 2 to 7 years of experience Job Role: Manage granulation, compression, coating, pelletization and capsule filling a...

As an Enterprise Domain Architect for CG&S Manufacturing, you will provide deep functional process and high-level technical expertise to analyze, define, design, and support the delivery of functional and technical capabilities for an application/group of applications in the manufacturing operations space for Consumer Goods and Services (CG&S) clients. This role involves collaborating with various teams and ecosystem partners to design and implement efficient, scalable, and secure solutions for CG&S clients. Conceptualization and design of manufacturing operations solutions for CG&S clients, from a functional process perspective as part of client pursuits and projects. Actively leading and p...

About The Role Project Role : Enterprise Technology Architect Project Role Description : Support sales teams in solution development, managing an internal matrix team to scope and price solutions. Lead customers through the design process. Work directly with Internal Accenture Domain Architects, Partner Architects, Client Architects, and Accenture project teams to design solutions. Must have skills : Manufacturing Operations Good to have skills : NA Minimum 15 year(s) of experience is required Educational Qualification : BE or BTech or MBA not mandatory Summary :As an Enterprise Domain Architect for CG&S Manufacturing, you will provide deep functional process and high-level technical experti...

1. Monitor raw material dispensing activity. 2. Perform daily IPQA activities as per SOP-defined frequency and ensure timely closure of IPQA observations. 3. Conduct validation sampling as per approved validation protocols. 4. Review BMR (Batch Manufacturing Record) and BPR (Batch Packing Record) for accuracy and compliance. 5. Perform ERP-related transactions of IPQA. 6. Check BSR (Batch Summary Record) and Shipper inspection as per SOP. 7. Manage issuance, review, and reconciliation of formats across all departments. 8. Conduct IPQA rounds and share observations with concerned HODs for corrective action and compliance. 9. Ensure cleaning, sanitation, and hygiene in all departments to maint...

Ensure the compliance of cGMP & EHS. Follow the cGMP requirement with appropriate housekeeping and documentation in manufacturing area. Co-ordination with other department for safe, successful and timely batch execution. Achieving plant production target w.r.t quality and yield. Active involvement in facing quality audits by vendor audit & regulatory audits. Lead from front to ensure safe behaviour / GMP culture on the shop floor. Comply with online documentation with complete data integrity. Undergo safety, quality and operational training & comply with requirement. Maintain housekeeping standard to ensure a clean and safe workplace. Follow the SOP practices. Preparation to comply statutory...

Responsible for Operation, cleaning and primary maintenance of negative isolator, Vibro sifter, Bin blenders and all other GEA granulation line equipment. Responsible for recording of activity in logbooks, Batch manufacturing record complete documentation as required in the manufacturing of product and the cleaning of facilities and equipment, following cGMP s and good documentation practices. To perform all in-process checks and monitoring of all intermediate processes in granulation. To select recipes and set process parameters in Blender HMI ensure its correctness before blender revolution. Responsible for Issuance, utilization, cleaning, and retrieval of sieves and proper handling of mac...

Hiring for one of the Largest Acrylic Emulsion Manufacturer in India supplying Adhesives & Emulsions all over India & Exports Experience:1 + Years CTC: Upto 3.5 LPA Roles and Responsibility Experience in emulsion / resins / adhesives reactor batch processing & basic trouble shooting. Able to run the reactors independently both in auto (SCADA / DCS) & manual mode. Able to manage team (at helpers level) & being a team player in the shifts. Others : SAP User experience, Quality Safety protocols inclined person. Taking batches as per the production planning with minimum batch cycle time. Timely escalation to shift in-charge and higher authorities in case of any machine related issue and cannot b...

Position: Production Officer Chemical Location: Kanpur (Rania), Uttar Pradesh Experience Required: 23 years in chemical manufacturing (adhesives, emulsions, resins, solvents, construction chemicals) with shift handling experience Salary Budget: 35,000 per month (Annual CTC: 4.20 Lakhs) Job Description: Astral Limited is hiring a Production Officer Chemical to manage shift operations at our chemical manufacturing facility in Kanpur (Rania). The ideal candidate should have hands-on experience in production processes related to adhesives, emulsions, resins, solvents, or construction chemicals, and should be capable of independently handling shift responsibilities. Key Responsibilities: Manage a...

Working Hours - 8 Hrs Role & responsibilities Dispensing, Manufacturing, Packaging and Dispatch activities. -Review and control of SOPs, BPR Issuance,Cleaning Validation,Line Clearance. -Master Formulae and records. -Good Documentation as per GLP,Preparation. -Review of process validation protocols and reports. -Familiar with Production machinery, Production floor working, pH meter, Refractometer, and GLP.

Job Description Key Responsibilities 1. Monitoring of IPQA activities in all functional departments. 2. Responsible for BMR correction/ quantity verification before batch execution along with QC. 3. Responsible for area and line clearance in production area. 4. Responsible for BMR verification for the completion and online inspection of batch execution at site. 5. Responsible for dispatch verification along with dispatch checklist, BMR, labels (at site and godown) 6. Site inspection for any abnormalities with respect to Raw materials, Packing materials, Products, labels, BMR, Dispatch. 7. Responsible for implementation of 5S at site. 8. Handling of Deviations, failure investigation, Change m...

Looking for Production Chemist for Vasai Location, daily production of colour cosmetics quality control and batch consistency formulation and process improvements understanding of manufacturing processes