338 Batch Manufacturing Jobs - Page 2

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2.0 - 6.0 years

2 - 5 Lacs

dahej

Work from Office

Operate and monitor DCS (Distributed Control System) for process operations. Execute batch production as per SOPs and cGMP guidelines. Maintain Batch Manufacturing Records (BMR) and ensure all process parameters are properly recorded. Ensure line clearance , proper labeling, and area cleanliness before and after production. Carry out in-process checks and coordinate with QA for line clearance. Supervise charging, reaction, distillation, and filtration activities. Coordinate with Engineering for equipment maintenance and troubleshooting. Support process validation, deviation handling, and change control activities. Ensure compliance with safety, quality, and environmental norms (EHS) . Follow...

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8.0 - 13.0 years

7 - 12 Lacs

ankleshwar

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Plan, organize, and oversee daily production activities to meet production targets. Ensure compliance with cGMP, GDP, and safety standards across the production area. Supervise and guide officers/executives for efficient plant operations. Review and approve BMR/BPR, SOPs, deviation, and change control documentation. Monitor equipment performance , coordinate preventive maintenance , and ensure minimal downtime. Drive process optimization, yield improvement, and cost reduction initiatives. Coordinate with QA, QC, Engineering, SCM, and EHS departments for smooth operations. Prepare and analyze monthly production reports, KPIs, and productivity data. Ensure readiness for regulatory audits and p...

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20.0 - 30.0 years

500 - 1000 Lacs

baddi

Work from Office

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 ...

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2.0 - 5.0 years

2 - 5 Lacs

ankleshwar

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To carry out batch manufacturing and related production activities as per SOPs and cGMP requirements. Maintain and update Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR) . Ensure line clearance , proper labeling, and area cleanliness before and after production. Operate and monitor production equipment like RMG, FBD, Compression, Coating, Granulation, Packing machines , etc. Coordinate with QA, QC, and Engineering for daily operations and troubleshooting. Participate in process validation, deviation handling, and change control activities. Ensure compliance with safety, quality, and regulatory standards (USFDA / WHO / MHRA). Monitor manpower utilization, shift planning , ...

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20.0 - 30.0 years

500 - 1000 Lacs

baddi

Work from Office

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 ...

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3.0 - 8.0 years

2 - 6 Lacs

thane

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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 ...

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10.0 - 15.0 years

10 - 15 Lacs

aurangabad

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Interested Candidate please share your resume to atull@harmanfinochem.com Prepare monthly and daily production planning as per market requirements. Achieve production target within predesigned time with quality and safety. Ensure delivery of product on time as per production planning and market requirements. Prepare daily and monthly production reports. Check and monitor for the availability of raw materials and packing materials as per monthly production plan. Execution and monitoring of production plan and troubleshooting to avoid delay if any. Follow SOPs and implementing effective techniques to bring efficiency, improve/maintain quality standards and achieve maximum cost saving. De-bottl...

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4.0 - 9.0 years

3 - 4 Lacs

gandhidham, kachchh

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Roles and Responsibilities Plan production activities to meet customer requirements and company goals. Coordinate with cross-functional teams for smooth operation of production processes. Monitor and control daily production planning, ensuring timely completion of tasks. Develop and maintain accurate inventory management systems to minimize stockouts or overstocking. Ensure compliance with quality standards by implementing effective production supervision. Desired Candidate Profile 4-9 years of experience in Production Planning, Production Management, or related field. Strong understanding of Batch Planning, Batch Manufacturing, Daily Production Planning, Inventory Management, Production Eng...

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4.0 - 7.0 years

3 - 4 Lacs

hyderabad

Work from Office

To follow the safety rules in the premises according to the company norms To handle Quality Management Documents like Change Control, Deviation etc To prepare Failure Investigation Reports against Quality impacting deviations, Out-of- Specifications and Non-Conformances To ensure investigations are evaluated and closed out in a timely manner to meet business needs Responsible for cGMP compliance related to CAPA implementation and to ensure the timely closure of CAPA To review, develop and introduce systems, practices and cultural changes that enable the department to meet business demands within agreed time frames and expected GXP standards To perform risk analysis for different process or p...

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2.0 - 4.0 years

3 - 5 Lacs

rangpo, east district

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Preferred candidate profile Having IPQA experience in manufacturing & Packing Min 2 yrs of experience in Tablet/Capsule(OSD) Interested candidates may share profile at hr.plant@zuventus.com

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0.0 - 3.0 years

2 - 3 Lacs

ahmedabad

Work from Office

Supervise syrup/liquid manufacturing, packing & documentation. Ensure quality, equipment calibration, SOP compliance, and IPQA coordination. Conduct trial batches, train operators, and maintain smooth, safe, and compliant production operations. Provident fund

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20.0 - 30.0 years

500 - 1000 Lacs

baddi

Work from Office

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 ...

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2.0 - 6.0 years

0 Lacs

gujarat

On-site

Role Overview: As a Quality Assurance professional at our company, your primary responsibility will be to ensure the online documentation of batch manufacturing and batch packing records. You will also be in charge of carrying out in-process checks of pre-determined process parameters as per BMR/BPR and withdrawing in-process/FP/Reference & stability samples following SOP. Additionally, monitoring the environmental condition of critical areas and reviewing & approving QA SOPs will fall under your purview. Key Responsibilities: - Ensure online documentation of batch manufacturing and batch packing record - Carry out in-process checks of pre-determined process parameters as per BMR/BPR - Withd...

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8.0 - 11.0 years

19 - 25 Lacs

ahmedabad

Work from Office

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...

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0.0 - 2.0 years

1 - 2 Lacs

khanna

Work from Office

Assist in daily production activities related to polymer additives and chemical formulations. Monitor process parameters and ensure adherence to standard operating procedures (SOPs). Maintain proper documentation and production records. Required Candidate profile 0–1 year of experience in a chemical or polymer manufacturing unit (freshers may apply). Basic understanding of production processes, material handling, and lab practices.

Posted 3 weeks ago

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2.0 - 4.0 years

2 - 4 Lacs

mumbai suburban, vasai, virar

Work from Office

We are seeking a qualified Production Chemist to join our team at Harman Plastic Vasai (E). • Overseeing daily production of color cosmetics • Ensuring quality control and batch consistency experience (5-10 years) in color cosmetics production

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5.0 - 6.0 years

4 - 5 Lacs

kadi, ahmedabad

Work from Office

Role & responsibilities Cell Culture & Production Support: Perform aseptic handling and maintenance of cell cultures (e.g., Vero, BHK or other cell lines) in adherent and/or suspension formats. Prepare and sterilize culture media, buffers, and reagents as per batch requirements and SOPs. Monitor and record cell growth parameters, viability, and morphology. Scale-up cell cultures for downstream processing or viral seed production. Facility & Environmental Monitoring: Conduct routine facility checks including temperature, humidity, pressure differentials, and cleanroom conditions. Coordinate and ensure compliance with environmental monitoring schedules (viable/non-viable particles, surface, an...

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6.0 - 11.0 years

5 - 7 Lacs

ahmedabad

Work from Office

Role : Executive Small Volume Parenteral Manufacturing Location: Ahmedabad Department: Injectable / Sterile Production Key Responsibilities: Production Operations: Plan, organize, and execute the manufacturing batches of small volume injectable products. Operate / supervise key equipment: vial/ampoule washing, sterilization (autoclave, filtration), filling, sealing, capping, tunnel sterilizer, lyophilizer (if applicable) etc. Ensure line readiness, material dispensing, line clearance before/after operations. Aseptic Process & Sterility Assurance: Maintain cleanroom operations, gowning, environmental monitoring, microbial monitoring. Ensure correct operation of aseptic filling / sterile filtr...

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2.0 - 5.0 years

2 - 4 Lacs

vapi

Work from Office

Responsibilities: Documentation & Record Review: Review specifications, sampling instructions, test methods, and analytical reports. Review and approval of Batch Manufacturing Record (BMR), Batch Packing Record (BPR), Master Formula Record (MFR), and Equipment Qualification Records. Review completed Batch Production Records and Laboratory Control Records post-batch completion. Review analytical data, Calibration & Preventive Maintenance schedules, and external audit reports. Review and finalize Certificate of Analysis (CoA) for finished products. Review Draft Equipment Cleaning Records and Hold Time Study protocols/reports. Review Standard Operating Procedures (SOPs) and Annual Product Quali...

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3.0 - 6.0 years

5 - 6 Lacs

mehsana

Work from Office

Responsibilities: Report to the Production Manager on daily production activities and progress. Ensure adherence to Standard Operating Procedures (SOPs) for cleaning and equipment operations. Comply with Batch Manufacturing Record (BMR) specifications and promptly report any deviations. Enforce and maintain GMP compliance on the production floor. Participate in production planning, manpower allocation, staff training, and troubleshooting Out of Specification (OOS) issues. Supervise, verify, and approve 'Area Clearance' at the start and completion of production activities. Always maintain hygiene and cleanliness of the production floor. Meet production targets as per the approved production p...

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6.0 - 11.0 years

3 - 5 Lacs

vadodara, atladara, ekalbara

Work from Office

Function / Department - Production / Operations Department Job Purpose To operate chemical plant equipment safely and efficiently during batch manufacturing, ensuring proper handling of hazardous chemicals and strict adherence to PPE and safety protocols. Key Responsibilities 1. Operate and monitor chemical plant equipment (reactors, distillation columns, filters, dryers, etc.). 2. Execute batch manufacturing operations as per SOPs. 3. Handle and store hazardous chemicals with proper safety measures. 4. Ensure PPE kits are worn at all times and safety norms are followed. 5. Maintain process parameters and record operational data. 6. Support preventive maintenance and emergency response proce...

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0.0 - 3.0 years

1 - 4 Lacs

chennai

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Batch Preparation & Execution Prepare batches according to approved Master Formula Records (MFR/BMR). Ensure correct weighing, charging, and mixing of raw materials as per process. Monitor and record process parameters (temperature, time, pH, etc.).

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8.0 - 12.0 years

5 - 12 Lacs

aurangabad

Work from Office

Roles and Responsibilities Ensure compliance with cGMP guidelines during batch manufacturing of eye drops, injectables, parenteral products, and injections. Monitor production processes to ensure quality standards are met. Conduct regular audits to identify areas for improvement and implement corrective actions. Collaborate with cross-functional teams to resolve issues related to formulation development and process optimization. Develop and maintain documentation for batch records, SOPs, and other relevant documents. Desired Candidate Profile 8-12 years of experience in pharmaceutical industry with expertise in ophthalmic manufacturing. Bachelor's degree in Pharmacy (B.Pharma) or equivalent ...

Posted 4 weeks ago

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1.0 - 4.0 years

2 - 6 Lacs

bengaluru

Work from Office

Role & responsibilities We are looking for candidates who has hands on work experience in the API manufacturing sector to handle API Production activities like intermediate , Clean room , Second line shift incharge role . Also we are hiring fresh graduates who have passed in 2020 and above . Preferred candidate profile Freshers - BSC /Diploma in Chemical Engineering (Only male ) Junior officer & Officer - BSC ,MSc in Chemistry

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0.0 - 7.0 years

2 - 9 Lacs

baddi

Work from Office

Ensure daily production plans Vs actuals, ensure RM, PM and other material availability in accordance with the production schedule Manage and evaluate machine resources to ensure productivity and minimum downtime Provide motivation, support and guidance to all employees Recommend process improvements to enhance production quality and productivity and Provide job training to meet production goals Investigate problems, analyze root causes and define resolutions Ensure that final product meets quality standards and customer specifications Batch Manufacturing Liquid Injection Handling of Manufacturing Area BMR handling, & Monitoring and control of batch wise yield Strict follow up of GMP, cGMP, ...

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