1027 Cgmp Jobs - Page 26

Job Responsibilities : Area grading and land development Study the plot plan and lay out drawings and execution of the same in field, Coordinate with surveyor to establish plot boundary, initial RL of the plot and quantum of cutting/filling work, Sending of soil sample to laboratory for OMC and MDD testing and conduct regular field compaction test, Check the compaction utilization of resources Inform superiors in case of improper/less mobilization of P&M/resources by contractors Filling layer and proper level of cutting / filling activity, Check effective Verify contractors DPR and update report to Project control team, Ensure day to day execution; study of Project standards, specifications,...

Officer Production, Vapi, Gujarat Responsibilities: Equipment cleaning as per ECR/SOPs Ensure cGMP compliance Execute batch charging (BMR/BPR) Maintain records Complete BMR/BPR/ECR documentation Apply at talent@hireindians.com or call 8882212459. Required Candidate profile Qualifications & Skills: * B.Sc. / M.Sc. in Chemistry (Analytical/Organic/Industrial) or B. Pharma. * 1–4 years of experience in pharmaceutical formulation/API manufacturing.

Hi, Greetings Walk in Invitation: We are having face to face interview on 30th Aug 2025 Saturday in Banglore(Hosur Road) Interview location: Banglore (Hosur road- chandapura) Single day, Face to face( 2 rounds would be complted) Company : A leading Pharma API Unit - in Mysore Position - Production Department Associate Work Experience Min 3 yrs in API in current Hike would be appreciable on Current CTC \ If interested drop your CV to Jyotsna - 7780363938|| jyotsna@avaniconsulting.com Thanks & Regards Jyotsna

As a diligent team member, you are required to adhere to safety regulations within the premises as per company guidelines. Your responsibilities include conducting in-process checks during operations. You will be accountable for operating and cleaning various machines such as the Wrap-around labeling machine, Autocartonator machine, Online check weigher, track and trace system, Bopp taping machine with weighing balance, and machines in the PFS packing area. Additionally, you will be in charge of dispensing, checking, and receiving packing materials from the warehouse as needed. Your duties will also involve labeling and packing products according to the Batch Production Record (BPR). Timely ...

You are a passionate, dedicated, and detail-oriented professional, and an exciting opportunity awaits you to join the Quality Assurance Team at Zydus Takeda Healthcare Private Limited in Turbhe, Navi Mumbai. This joint venture between Zydus Lifesciences and Takeda Pharmaceuticals is committed to maintaining the highest level of quality and safety in its products. As a Senior Executive / Executive in Quality Assurance, based in Navi Mumbai, you will play a crucial role in In-Process Quality Assurance (IPQA). Your responsibilities will include monitoring and controlling the quality of products during the production process to ensure compliance with regulatory standards and company quality poli...

Lead and optimize sterile injectable production, ensuring cGMP compliance, timely delivery, and continuous improvement GMP compliance, planning, output/yield/OEE monitoring, team management, audits, BMR/BPR approval, coordination with QA/QC,

Wondering what's within Beckman Coulter Diagnostics Take a closer look. At first glance, you'll see that for more than 80 years we've been dedicated to advancing and optimizing the laboratory to move science and healthcare forward. Join a team where you can be heard, be supported, and always be yourself. We're building a culture that celebrates backgrounds, experiences, and perspectives of all our associates. Look again and you'll see we are invested in you, providing the opportunity to build a meaningful career, be creative, and try new things with the support you need to be successful. Beckman Coulter Diagnostics is proud to work alongside a community of six fellow Diagnostics Companies at...

Job Title: Quality Assurance Manager Location: Rabale, Navi Mumbai Experience: 10 15 years Department: Quality Assurance Employment Type: Full-time Reports To: Quality Head About Fusion Scientific Laboratories Fusion Scientific Laboratories is a USFDA and EMA accredited pharmaceutical laboratory based in Rabale, Navi Mumbai , offering world-class services in Formulation Development , Analytical Solutions , and Integrated Pharmaceutical Services (CDMO) . We partner with pharmaceutical companies globally to deliver compliant and innovative solutions across the drug development lifecycle. Position Overview We are looking for a highly experienced Quality Assurance Manager to lead quality oversig...

Job Description: We are seeking a dedicated and skilled Production Officer to join our team. The ideal candidate should have a minimum of 1 year of experience in a regulatory-approved manufacturing plant, with hands-on experience in handling critical production equipment and knowledge of cGMP standards. Key Responsibilities • Operate and manage production equipment such as reactors, centrifuges, dryers, multi-mills, and other machinery used in manufacturing processes. • Oversee and ensure thorough cleaning of production areas, maintaining compliance with cleanliness and hygiene standards. • Monitor and maintain environmental conditions on the shop floor, ensuring adherence to regulatory and ...

The ideal candidate will be responsible for overseeing the execution of production plans by utilizing pre-approved procedures, protocols, and manufacturing records. You will need to ensure strict adherence to cGMP and EHS (Environmental, Health, and Safety) norms to maintain compliance. Additionally, you will supervise and coordinate production activities, managing available resources effectively to meet production targets. Maintaining quality control is a key aspect of this role, where you will be required to uphold standard process parameters following Batch Manufacturing Records (BMRs) and other relevant documents to ensure high-quality production and compliance. Furthermore, you will be ...

You will be responsible for analyzing Vendor Approval samples and preparing Standardization of Solutions as needed. You will also need to implement GLP/GMP requirements and analyze Raw Materials, Finished Products, Stability samples, and Packing materials. Ensuring samples and related documentation meet cGMP requirements is crucial. Additionally, you will need to oversee the analysis of Raw Materials, Finished Products, and Stability Samples from outside commercial labs. Reviewing laboratory chemicals, calibrating instruments such as HPLC, UV, IR, Dissolution, KF Potentiometer, and performing Working standard qualification are part of your duties. Maintenance of Stability Incubators, loading...

As a Senior Manager Production at our Guwahati location, you will be responsible for overseeing all manufacturing operations to ensure smooth production processes and meeting quality standards. Your role involves planning, coordinating, and directing production activities while ensuring compliance with safety, regulatory, and company policies. Your key responsibilities will include planning and coordinating production and packing activities to achieve monthly targets. You will review daily production activities for various processes such as Granulation, Compression, Coating, Capsule filling, Inspection, Packing, and Nutra section. Ensuring Good Documentation Practices (GDP) at the shop floor...

The Chemist role involves performing standard chemical and physical analysis of inner and outer nutritional products in the quality control lab using wet chemistry techniques and instrumental analyses. As a Chemist, you will contribute by conducting laboratory testing, including qualitative and quantitative chemical and physical analysis of raw materials, finished products, and stability samples. You will be responsible for preparing standards and reagents, calibrating and operating sophisticated laboratory instrumentation such as HPLC, FTIR, UV-Visible spectrophotometer, and reviewing product certificates of analysis for accuracy and conformance. Additionally, you will perform routine calib...

The Quality Control department at Piramal Pharma Solution in Pithampur is seeking a dedicated individual to join their team as a QC Analyst. In this role, you will be responsible for performing testing on in-process samples, raw materials, finished drug products, and stability study samples to support production, packing release, and regulatory filings. You will report directly to the QC lab Supervisor. The ideal candidate should have 3 to 6 years of experience in a cGMP laboratory setting and be familiar with cGMP and FDA requirements. This position offers an exciting opportunity to contribute to the quality control processes in the pharmaceutical industry and work in a dynamic environment....

Job Title: Frontend Developer Job Type: Full-time Location: Hybrid Delhi | Pune | Bangalore Job Title: UI Engineer Job Type: Full-time, Contractor Location: Hybrid Bangalore, Pune, or Delhi Job Summary: Join one of our top customer's dynamic team as a UI Engineer, where you will take charge of crafting engaging and seamless user experiences You design, develop, and maintain both new and existing features, ensuring all phases of development are executed efficiently and effectively, Key Responsibilities: Develop and implement new UI features using JavaScript and React, Maintain and enhance existing features, ensuring optimal performance and scalability, Collaborate with cross-functional teams ...

Execute and monitor production activities as per SOPs and cGMP guidelines. Ensure compliance with safety, health, and environmental regulations during production operations. Handle day-to-day production activities for API and intermediate products. Required Candidate profile B.Sc. / M.Sc. (Chemistry) / B.E / B.Tech. (Chemical Engineering) with 2 to 7 years in API or Intermediates Manufacturing Strong knowledge of API / Intermediates manufacturing processes.

Oversee and manage daily production activities Ensure adherence to cGMP and EHS guidelines Coordinate with cross-functional teams for smooth operations Optimize processes for efficiency and quality

We are looking for a meticulous Junior Engineer to contribute to the efficient maintenance and operation of our API manufacturing facility at Synnat Pharma. As a Junior Engineer, you will be integral to ensuring the reliability of our mechanical and electrical systems, contributing to our commitment to quality and compliance. This role involves a blend of hands-on equipment maintenance, detailed record-keeping, and active participation in equipment validation and qualification processes. You will collaborate closely with senior technicians and engineers, assisting in breakdown maintenance, equipment installation, and process improvement projects. Your dedication to following safety procedure...

Interview For Production & QC Dept for API Pharma co in Bharuch on 29-08 at Dahej Qualification: Bsc/Msc Experience: 2 to 10 Years CTC: Up to 6 LPA EXP in API Is Must Send CV on sdpbharuch@gmail.com with Subject: Prod/QC Dahej No Job Charges Required Candidate profile Permanent Job Come Along with yr Friends Interview Venue: SDP HR Solution, 611, Golden Square Beside Dmart Near ABC Circle Bholav, Bharuch - 392001 Time : 9 to 3 Date : 29-08 Free Interview

Hiring for Production Chemist Job Location - Jammu (Sambha) Interview Location - Chandigarh Salary bar - 5LPA - 5.5LPA Max Industry pref. - Pharma (API) Interested one share resume on meenakshikandpal@tdsjobs.com 9041666549

The Opportunity: Officer - Quality Control is responsible to perform Quality Control activities at AQAL. What we are looking for :- Responsible for Timely analysis of under test samples giving timely results Coordination with tollar for quality related issues and clarification Sampling and analysis for RM/Intermediate/Finished Goods. Ensure compliance of ATR. Assisting team in ISO implementation Knowledge of calibration, standard preparation, standardization and relevant documentation. Handling knowledge of HPLC,GC and wet analysis. Education: B. Sc. M. Sc. (Chemistry) Experience: 2-5 years of experience in Quality including cGMP, ISO and regulatory Audits Preferred Skills/Qualifications: Kn...

As an Executive/Sr. Executive in the Engineering department at Liva Pharma's plant, you will be responsible for various tasks related to equipment maintenance and compliance procedures. Your key responsibilities will include: - Reviewing the plant equipment logbook and ensuring its accuracy. - Preparation and implementation of Standard Operating Procedures (SOPs) to maintain operational standards. - Ensuring compliance with relevant SOPs and performing necessary Preventive Maintenance (PM) and calibration before due dates. - Implementing corrective and preventive actions as required. - Recording and maintaining plant equipment maintenance activities. - Conducting training sessions for subord...

As a skilled Analytical Chemist, you will be responsible for various tasks related to method development, validation, and query response for finished products. Your duties will include preparing analytical method development reports, Certificates of Analysis (COA), and performing analysis of in-process samples, finished goods, and stability samples in accordance with cGMP requirements. It will be your responsibility to monitor the general laboratory and ensure its maintenance as needed. Your role will involve routine analysis and stability testing of finished products for parameters such as assay, related substances, dissolution, residual solvent, etc. Additionally, you will be required to r...

To implement cGMP QC labo. pharma regulatory standards.• FDA of small molecule & analytical methods/equipment: GC, LC, ICP-MS, KF, LOD, ROI, optical rotation, RI, stability analysis, light obscuration, potentiometric titrations, spectroscopy

Hi Greetings form Avani consulting , We have job opportunity with Apimanufacturing (pharma company) for production department mysore location . we are going to conduct Walk -in interview in Bangalore on 30- august-2025 . Job Description for Production-Associate Position- Associate Work Experience Min 3-9 yrs in API Location Mysore Gender Any Qualification- B.Tech Chemical Engineering/M Sc and Bsc Chemistry /Diploma in chemical Engg Roles & Responsibility 1. Responsible for appropriate production planning & execution of batches in line with targeted commitments complying cGMP& Safety requirements. 2. To ensure gowning practices, entry / exit procedures, usage of PPEs are followed by team whil...