343 Batch Manufacturing Jobs - Page 3

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...

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.).

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 ...

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

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, ...

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...

Role & responsibilities: •Raise material requisition and receive the materials from stores. •Prepare BMR for new products to be processed on the lines. •Online BMR, BPR entries to be updated and all formats of relevant SOPs to be completed. •Preparation of SOPs for the vials and cartridge processing area and ensure training of it for the line operators. •To improve the yield of the lines and to reduce the rejections. •To prepare the samples as per the customer requirements and complete the entries in BMR and logbooks. •To complete the SAP entries for the line activities online. •To ensure that the completed batch pallets are transferred to ready to ETO area/ nonsterile FG area and line is re...

JOB DESCRIPTION (Executive) Supervision of manufacturing, processing, packaging and holding of drug product as per define and approved procedures for stability batches and commercial batches. Maintaining the area and equipment in orderly manner as per cGMP requirements in a good state of repair and sanitized condition. To perform online documentation with respect to departmental procedures as per good documentation. To impart training of operation and cleaning related SOP to all subordinates and operators. Co-ordination for IQ / OQ for any new equipments / system. To perform PQ for any new equipments / system. To follow all concern departmental SOPs for day to day operation and cleaning. To ...

Supervision of manufacturing, processing, packaging and holding of drug product as per define and approved procedures for stability batches and commercial batches. Maintaining the area and equipment in orderly manner as per cGMP requirements in a good state of repair and sanitized condition. To perform online documentation with respect to departmental procedures as per good documentation. To impart training of operation and cleaning related SOP to all subordinates and operators. Co-ordination for IQ / OQ for any new equipments / system. To perform PQ for any new equipments / system. To follow all concern departmental SOPs for day to day operation and cleaning. To handle and manage material m...

ITI/Diploma with minimum 4 yrs of exp. in tablet manufacturing, filling & packing machines. Core skills in tablet plant equipment. Ensuring productivity, quality control, material management, safety & documentation. Required Candidate profile ITI/Diploma with experience in any Chemical/Pharma mfg. line. Ability to optimize production process & ensure Quality/GMP standard & regulatory requirements.

As an employee in this role, you will be responsible for the following tasks: - Scale-Up & Production - 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) - Color consistency - Shelf life stability - Ensure compliance with cosmetic regulations (e.g., FDA, EU, REACH). - Safety & Compliance - Handle hazardous chemicals (e.g., acrylates) safely. - Ensure MSDS/SDS are maintained. - Adhere to GMP and workplace safety standards. Additional...

JOB DESCRIPTION Job Title: IPQA Executive Job Location: Syngene International Limited, Bengaluru About Syngene : Syngene ( www. syngeneintl. com ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and proce...

Position: Trainee Production (Packaging dept) Location: Kanpur (Rania), Uttar Pradesh Experience Required: Fresher (01 year); candidates with internship or project experience preferred Job Description: Astral Limited is hiring Trainee Production (Packaging) for its packaging unit in Kanpur (Rania). This role is ideal for fresh diploma or engineering graduates who are looking to start their career in packaging operations and gain practical experience in production processes. Key Responsibilities: Assist in daily packaging operations under supervision. Learn to operate packaging machinery such as filling, sealing, labeling, and wrapping units. Support shift operations and follow safety and qua...

The role involves ensuring CGMP compliance and supervising lyophilizer activities in manufacturing area. Additionally, the position requires reviewing and maintaining online documents. Essential Functions: To plan line wise activity as per production schedule. Person shall be responsible for operation and handling of the general area. To follow SOPs and minimize the deviations. To follow GMP, GDP, Data Integrity as per respective SOP. To work with the GMP and compliance in manufacturing process. To maintain cleanroom with define cleaning frequency. To Report if abnormality/Deviation observed to immediate supervisor. To complete the short term and long-term goals / objective as set by H.O.D T...

Handling Batch process and process equipment, manpower handling, following safety rule. Responsible for consumption of Raw material, yield and quality of intermediate, semi-finished, finished product. Online BMR, BPR and ECR, Daily Records checking.

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 & responsibilities Manufacturing of Lyophilized Drug Product Aseptic Blending & Filling Injectable Filling Lyophilization BMR Preparation cGMP Practices, Media Preparation, Vial Washing and De-pyrogenation, Validation, Labeling & Packaging, Documentation Preferred candidate profile Aseptic handling Sound knowledge of QMS Sound knowledge of cGMP, GDP

We are currently seeking an Advance Technician Production Operations who will be responsible for supporting in manufacturing day-to-day activities in Dispensing/Packaging/Labeling. Candidate must be able to manage team or supervise their down line to ensure meeting daily output. The company is compliant with ISO 9001: 2015, ISO 13485: 2016 & EN ISO 13485: 2016, MDSAP and Beckman Coulter corporate Quality system requirements. In this role, you will be responsible for: Understand the process for labeling, Dispensing & Packaging and responsible to handle unit operation of Packaging instruments. Responsible to meet the FPY and OTD Targets for production as per planning schedule. Escalation to re...

Supervision of manufacturing, processing, packaging and holding of drug product as per define and approved procedures for stability batches and commercial batches. Maintaining the area and equipment in orderly manner as per cGMP requirements in a good state of repair and sanitized condition. To perform online documentation with respect to departmental procedures as per good documentation. To impart training of operation and cleaning related SOP to all subordinates and operators. Co-ordination for IQ / OQ for any new equipments / system. To perform PQ for any new equipments / system. To follow all concern departmental SOPs for day to day operation and cleaning. To handle and manage material m...

1. Responsible for Operation, cleaning, and primary maintenance of compression machine, metal detector, Lifting and positioning device, IPQC instrument. 2. Responsible for recording of activity in logbooks, Batch manufacturing record & Responsible for complete documentation as required in the manufacturing of product and the cleaning of facilities and equipment, following cGMP s and good documentation practices. 3. To Ensure equipment cleaning before line clearance as per standard operating procedure 4. To perform all in-process checks and monitoring all intermediate processes in compression stages. 5. To select recipes and set process parameters in PLC/SCADA of compression machine, IPQC ins...

Followings will be the Core Job Responsibilities of the position holder: 1. Responsible for Operation, cleaning and primary maintenance of negative isolator, Vibro sifter, Bin blenders and all other GEA granulation line equipment. 2. 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. 3. To perform all in-process checks and monitoring of all intermediate processes in granulation. 4. To select recipes and set process parameters in Blender HMI & ensure its correctness before blender revolution. 5. Respons...

Followings will be the Core Job Responsibilities of the position holder: 1. Responsible for Operation, cleaning, and primary maintenance of compression machine, metal detector, Lifting and positioning device, IPQC instrument. 2. Responsible for recording of activity in logbooks, Batch manufacturing record & Responsible for complete documentation as required in the manufacturing of product and the cleaning of facilities and equipment, following cGMP s and good documentation practices. 3. To Ensure equipment cleaning before line clearance as per standard operating procedure 4. To perform all in-process checks and monitoring all intermediate processes in compression stages. 5. To select recipes...

Job Description 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 depa...

Roles and Responsibilities * Manage production processes, ensuring compliance with GMP and batch planning. * Handle manpower effectively, including training and development of team members. * Oversee API manufacturing, reactors, centrifuges, BMRs, batch planning, hydrogenation, chlorination, distillation, centrifuges, GLRs, API production, pharma production, bulk drugs, and batch manufacturing. * Ensure solvent recovery and maintain a clean and safe working environment.

Topical Powder Manufacturing, Filling & Sec.Packing Activities oral Powder Manufacturing, Filling and Sec. Packing Activities Batch Initiation Manufacturing Secondary packing & tertiary Packing Share resume to hrd@stedmanpharma.com, Call - 7904827192 Required Candidate profile B.pharm Looking for candidate with Pharma formulation experience