338 Batch Manufacturing Jobs - Page 4

Job Title: API Production Block In-Charge Department: Manufacturing / Production Location: [Insert Location] Reports To: Production Manager / Plant Head Qualification: B.Sc / M.Sc in Chemistry, B.Tech / M.Tech in Chemical Engineering or related field. Job Purpose: To oversee and manage day-to-day operations of the API production block, ensuring efficient, safe, and compliant manufacturing of Active Pharmaceutical Ingredients in accordance with cGMP and regulatory requirements. Key Responsibilities: Production Management: Plan, coordinate, and execute API production schedules to meet manufacturing targets. Monitor daily production activities, troubleshoot process issues, and ensure minimal do...

Responsibilities: Ensure compliance with regulatory standards Collaborate with R&D team on new product development Develop and optimize production processes for APIs Monitor quality control procedures Annual bonus Provident fund

1-Lead QA/QC team,2-Implementation of QMS,3-implementation of good housekeeping, Safety in QC.4-Review & approval STP,SOP, Calibration record, CAPA, Audit compliance, Handling Training,Co-ordination with Production Warehouse,Quality Coordination.

1-Lead QA team,2-Implementation of QMS,3-implementation of good housekeeping, Safety .4-Review & approval STP,SOP, Calibration record, CAPA, Audit compliance, Handling Training,Co-ordination with Production Warehouse,Quality Coordination.

Responsibilities: * Collaborate with cross-functional teams on BPR and BMR. * Ensure compliance with CGMP and batch manufacturing standards. * Monitor production processes for quality and efficiency.

Key Deliverables Operate automated batch manufacturing using HMI as per SOPs Manage packaging, cleaning, and equipment preservation activities Ensure compliance with EHS, ISO, and IATF guidelines Maintain 5S standards and coordinate RM/PM availability Role Responsibilities Execute bulk batch production and packaging tasks Perform equipment cleaning and minor maintenance Follow safety and quality protocols across processes Report process deviations or abnormalities to supervisor

Job Summary We are seeking an individual to oversee batch manufacturing, ensuring adherence to cGMP (Current Good Manufacturing Practices), providing training, and coordinating day-to-day activities. Responsibilities include minimizing machine downtime, managing subordinate staff, assuring compliance with standards and SOPs (Standard Operating Procedure), leading regulatory audits, compiling reports, ensuring safety norms, and budget management. Roles & Responsibilities • You will be responsible for enforcing cGMP for batch manufacturing in order to obtain high-quality products and achieve targeted production within a span of control. • You will be responsible for imparting general and cGMP ...

Role Overview: The Shift Chemist at Pharma Manufacturing department is responsible for achieving the desired production yield of pharmaceutical APIs by ensuring all production activities in the shift comply with cGMP, cGLP, EHS requirements, and specified operating procedures. You will be required to properly take over shift operations as per defined procedures. This includes following the Gowning Procedure before entering the pharma area, indenting raw materials from stores, updating balance in Material Reconciliation Record, collecting Intermediate material, ensuring availability of Utilities before charging the batch, verifying and charging raw material quantities, executing production pr...

Role Overview: As a Production Operator in the granulation department, your main responsibilities will include: Key Responsibilities: - Operate, clean, and perform primary maintenance on negative isolator, Vibro sifter, Bin blenders, and all other GEA granulation line equipment. - Record activities in logbooks, Batch manufacturing record, and complete documentation following cGMPs and good documentation practices. - Perform all in-process checks and monitoring of intermediate processes in granulation. - Select recipes, set process parameters in Blender HMI, and ensure correctness before blender revolution. - Issue, utilize, clean, and retrieve sieves and handle machine change parts with inve...

Responsibilities: * Prepare SOPs, review BPRs, adhere to CGMP guidelines. * Collaborate with R&D on new product development. * Ensure compliance with GMP standards during production.

Role & responsibilities Chemical Batch Process ( Production ) Preferred candidate profile Monitoring day-to-day operations in the plant to ensure smooth production. Troubleshooting any production issues and implementing corrective measures to minimize downtime.

Role Overview: As a Manager-II in the MSTG department at Dadra, your primary responsibility will be to provide support in the execution and monitoring of trial, scale up, and exhibit process qualification batches. You will be involved in preparing and reviewing new product documents such as material requirement sheets, master formula cards, bill of materials, risk assessment reports, sampling protocols, reports, exhibit batch manufacturing records, and exhibit protocols. Sharing process knowledge with cross-functional departments through presentations to facilitate smooth technology transfer will also be a key aspect of your role. Key Responsibilities: - Review and evaluate product history a...

Qualification: Diploma / B.Tech / B.Pharma Experience: 38 years in Cartridge/PFS Line filling. Must have hands-on experience with Bausch Strobel or Syntegon filling machines (should be clearly mentioned in the resume)

We're Hiring!!!! Candidates with experience in API & Formulation are encouraged to attend our Walk in Interview. API MANUFACTURING Designation : Sterile Officer/Sr. Officer Experience: 5-10years Educational Qualification: B.Sc/M.Sc(Chemistry)/B.Pharma/M.Pharma Designation: Shift Incharge Experience: 10-12years Educational Qualification: B.Sc/M.Sc(Chemistry)/B.Pharma/M.Pharma Designation: Non-Sterile Operator/Officer Experience: 2-8years Educational Qualification: B.Sc/M.Sc(Chemistry)/BE/B.Tech Designation: Non- Sterile Shift Incharge Experience: 8 to 12 years Educational Qualification: B.Sc/M.Sc(Chemistry)/BE/B.Tech WAREHOUSE Designation: RM/PM - Head Experience: 12 to 15 years Educational Q...

Supervision of batch manufacturing & packing area in shifts Maintaining the production required documents in concerned area of working. Handling of manpower & training of works SOP Coordination with Q.A Handling of manufacturing activity of beta lactam product/packing operation, Sound knowledge of compression/coating/granulation etc., Knowledge of good manufacturing practices.

Oversee complete Production & Manufacturing operations at the Pharmaceutical Formulation Unit Ensure smooth execution of batch manufacturing for OSD (Tablets, Capsules, Dry Syrups) Ensure compliance with FDA regulations and GMP guidelines Monitor production efficiency, process optimization & manpower management Coordinate with QA, QC, and Regulatory teams for smooth operations Handle regulatory audits, validation, and documentation processes OSD Manufacturing Tablets, Capsules, Dry Syrups FDA Approval & Regulatory Compliance (WHO-GMP, Schedule M preferred) Production Planning & Process Optimization Team Leadership & Manpower Management

Job Description Requisition, receive, and verify raw materials as per batch requirements. Perform batch operations, charging, and utility operations. Maintain Batch Manufacturing Records, Batch Packing Records, and Equipment Cleaning Records. Operate all plant equipment as per SOPs and verify equipment status before use. Coordinate with QC for in-process and finished product testing. Liaise with Engineering for equipment calibration, AMC, and preventive maintenance. Ensure compliance with health, safety, and environmental regulations. Prevent spillage, contamination, and ensure proper labelling after batch completion. Participate in investigations and report discrepancies to the Production M...

Familiar with GMP guidelines and batch manufacturing processes. Skills: MS Office and effective communication. Responsible for managing daily production activities and documentation. Required Candidate profile Experience: 2-3 years in Pharma/API Qualification: B.Sc / M.Sc in Chemistry Experience in Oncology production preferred.

Role & responsibilities Should Have Knowledge on Batch Preparation, CIP, SIP, Autoclave, Filling, Knowledge on QMS Activities. Qualification Activities Preferred candidate profile B Pharma

Manufacturer chemist Shift - 9 am to 6 pm Package - 25 k to 40 k(3 year experience) location- patiala Skills- tablet and capsules(alopathy and pharma) Wtsapp me resume at 8295842337- MR. Bansal

Experience in Derma Formulations, Like Cream, ointment, gel Lotion etc. (Applicable for Non- Sterile) Experience in ophthalmic Formulations, Like eye ointment, eye Gel etc. (Applicable for Sterile). Know the aseptic Process and behaviors/Practices. Required Candidate profile Knowledge of SCADA system, in various manufacturing OEM equipment, like ADAM, IWK (High speed robotic tube filling machine), trac & trace system, IMA PG, OMAG, Sachet filling machine, /auto cartonator

Responsible for sampling of In-process sample, Process validation, rinse and swab sample,FG sample, Control sample, MLT sample and Stability sample and to ensure timely submit To make necessary entries into respective register/E- log book. Responsible for activities inline in ERP, LIMS, ELOG and EDCS as per requirement. To carry out Line clearance prior to start-up of any activity and verification of dailyequipment logs. Online checking of BMR its compliance. For carrying out in-process activity at Manufacturing stage as per BMR and relevant SOPs Checking of Environment monitoring of all respective areas on shop floor. To follow EHS policies. To ensure compliance of GDP and data integrity te...

The Production Chemist will be responsible for executing and monitoring API manufacturing processes, ensuring compliance with cGMP, SOPs, and regulatory guidelines . The role involves operating chemical process equipment, documentation, troubleshooting, and process optimization to achieve efficiency, safety, and quality standards. Key Responsibilities & Duties: Process Execution: Perform batch manufacturing activities in line with Standard Operating Procedures (SOPs), Batch Production Records (BPRs), and cGMP requirements. Equipment Operation: Operate and monitor reactors, centrifuges, multi-mill, shifter, tray dryer, filtration systems, GLR, and SSR equipment . Quality Assurance & Complianc...

Responsibilities: Responsible for creating, maintaining, managing accurate & compliant production-related documentation. This role ensures that all documentation adheres to internal standards and external regulatory requirements.

Maintaining good housekeeping and cGMP in shop floor Preparation of New documents like BPCR and SOP Deviation , change control, OOS, activity and is compliance Plant keeps ready for audit Overall responsibility of cGMP Production should be achieved as per target. Equipment cleaning Log book and Solvent log Book to be maintained. BPCR arrangements for running batches. Review and completion of all documents like BPCR, Equipment logbook, and format as per SOP