1027 Cgmp Jobs - Page 29

You will be responsible for vaccine manufacturing activities related to cell culture, including cell revival, subculture, and cell counting of MRC-5 cells. Your role will involve the preparation of Master Cell Banks (MCB) and Working Cell Banks (WCB). You should have experience in handling Roller bottles, Cell stacks, and Tissue Culture Flasks (TCFs). Additionally, you will be required to prepare media and in-process buffers in media mixing vessels. Moreover, your duties will include experience in virus infection and virus harvesting procedures. You should be familiar with working on Chicken embryo fibroblast cells, involving tasks such as pooling embryos and seeding Roller bottles. In the Q...

You are looking for a QC Chemist with 4-5 years of experience or a Fresher in quality control lab. The ideal candidate should be familiar with operating sophisticated instruments such as HPLC, GC, and SPECTOPHOTOMETER. It is essential that the candidate has received training in cGMP. Salary is negotiable based on the candidate's experience. If you are interested in this position, please apply with your resume to the provided email address. This is a full-time, permanent role with benefits including Provident Fund. The preferred education level for this position is a Bachelor's degree. The preferred total work experience required is 2 years. The work location for this position is in person.,

As a Production Manager, you will be responsible for overseeing and managing day-to-day production operations to meet quality, cost, and delivery targets. You will develop and implement production schedules to ensure timely product delivery while ensuring adherence to Good Manufacturing Practices (GMP) and compliance with USFDA regulations. Your role will involve maintaining and ensuring compliance with USFDA, WHO, and other regulatory standards in all production processes. You will coordinate with the Quality Assurance (QA) team to prepare for and manage regulatory audits, inspections, and proper documentation of manufacturing processes. Leading, mentoring, and training the production team ...

You will be responsible for conducting site surveys and plotting layouts based on drawings. Additionally, you will interpret plans and specifications, monitor architectural, structural, and finishing work to ensure compliance with drawings. You will oversee work progress, quality, and adherence to building codes and regulations. It will be your duty to prepare and monitor schedules, ensuring timely project completion. You will manage contractors, review bills as per tender BOQ, and coordinate with seniors, contractors, and other professionals to achieve project objectives. Daily progress reports must be prepared and sent, and cross-functional teams will be collaborated with for timely projec...

As a maintenance engineer, your primary responsibilities will include maintaining facility and equipment, procuring engineering consumables and proprietary spares, and managing inventory. You will be responsible for performing and approving qualification studies for equipment and facilities, as well as scheduling and executing preventive maintenance programs for plant and utility equipment. Additionally, you will review and participate in process validation programs, update technical drawings such as plant layout and P & ID, and manage annual maintenance programs for utility and material handling equipment. You will also be involved in arranging instruments for plant equipment, ensuring comp...

The In-Process Quality Assurance Executive plays a crucial role in ensuring that all products adhere to cGMP and regulatory standards throughout the manufacturing and packaging processes. You will collaborate closely with production teams to uphold product quality and address any issues that arise in real-time. Your responsibilities will include overseeing the quality of products from the warehouse to production and packing stages, ensuring compliance with cGMP and regulatory requirements, identifying and resolving quality issues promptly, and participating in investigations of deviations and non-conformances. You will also be responsible for maintaining detailed documentation of quality-rel...

You will be responsible for Vaccine Manufacturing (Cell Culture), including tasks such as cell revival, subculture, and cell counting of MRC-5 cells. You will also be involved in the preparation of MCB/WCB and handling Roller bottles, Cell stacks, and TCFs. Experience in virus infection, virus harvesting procedures, and working with Chicken embryo fibroblast cells will be required. In the Quality Control department, you will be expected to perform various biochemical techniques, chromatography techniques, electrophoresis techniques, and immunoassay techniques. Your responsibilities will also include cell culture techniques, molecular techniques, analytical method validation (AMV), and analyt...

Trending Job Description To execute analysis of finished goods / Stability samples / Raw materials / Packing materials In-process and cleaning samples along with relevant laboratory documentation. Intimation & result reporting after completion of analysis & relevant documentation. Check all the instruments on the equipment required for the analysis are in working condition and are in calibrated state. Checking and ensuring proper status labels after confirming availability of all the requirements (as applicable) for analysis such as approved control procedure, analytical protocol, reference standards, chemicals, reagents, glassware, water preparation equipment, water bath, sonication baths, ...

You will be responsible for strictly following cGMP, Safety and Environmental Practices, as well as ensuring Good Manufacturing practices during operation. This includes filling Batch Manufacturing records and equipment cleaning records, maintaining proper personnel protective equipment usage, and ensuring good housekeeping in the respective plant area and its equipment. You will need to plan and ensure raw material availability for daily production as per the production plan, maintain documents like Issue and dispensing register, and carry out processes as per Batch Manufacturing Records (BMR) without any deviation. It is essential to adhere to data integrity in online documentation and han...

As a member of ACG Capsules in Shirwal, your primary responsibilities include checking the allocated post production line(s) such as ATS/Printing/camera in each shift according to the CTQ (critical to Quality) / CTP (Critical to Productivity) checklist. You will need to adhere to the plan outlined in the color change note, minimizing change over time at each sub-section. Following instructions from the shift lead is crucial for timely changeover, ensuring the availability of necessary equipment like roller(s) and ink. Furthermore, it is essential to execute In-Process Quality Control (IPQC) after each roller cleaning, checking camera rejections hourly to achieve zero defects. Operating the c...

You will be responsible for performing testing on in-process material, bulk drug substance, finished drug product, and stability samples in a cGMP laboratory setting. Your role will involve ensuring compliance with cGMP and FDA requirements. The position reports to the QC lab Supervisor. The ideal candidate should have 2 to 6 years of experience in a cGMP laboratory environment and be familiar with cGMP and FDA requirements.,

You will be joining our team as a Deputy Manager/Manager, Analytical method transfer, responsible for delivering developed analytical assays from R&D scale to GMP-compliant commercial quality control labs. Your role will involve overseeing projects related to analytical method transfer, collaborating with cross-functional teams, and ensuring technology transfer and assays qualification activities are conducted in compliance with GLP and GMP standards. The ideal candidate will possess expertise in cGMP, regulatory requirements, technical troubleshooting, method transfer, method validation, technology transfer, and laboratory techniques to support routine testing and release of research and cG...

Experience Required: You must have a strong background in contract manufacturing. Demonstrated experience in managing Greenfield and Brownfield projects is highly desirable. Primary Coordination And Execution: You will collaborate closely with cross-functional teams to ensure timely project delivery. It will be your responsibility to design and layout facilities for Greenfield and Brownfield projects, considering operational requirements and constraints. Additionally, you will be required to prepare detailed manufacturing documentation for new facilities and third-party (3P) manufacturing units. Supplier And Partner Management: You will oversee and streamline the operations of existing contr...

As a member of our team at Piramal Pharma Solutions (PPS), you will be responsible for ensuring strict adherence to cGMP, Statutory norms, and safety rules of the factory, taking on the role of a competent person under the Engineering Sr. Manager. Your key responsibilities will include reporting progress and issues on a daily basis, preparing and updating the list of equipment in line with Quality Assurance (QA) requirements, and creating the annual Preventive Maintenance (PM), Validation, and Qualification schedule for equipment. You will be expected to maintain the plant and equipment to ensure audit readiness at all times, engage team members productively, effectively manage contract work...

About Apotex Inc. Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions. For more information visit: www.apotex.com. Job Summary Storage and Dispensing of Packaging Materials. Job Responsibilities Supervise t...

Work Your Magic with us! Ready to explore, break barriers, and discover moreWe know youve got big plans so do we! Our colleagues across the globe love innovating with science and technology to enrich peoples lives with our solutions in Healthcare, Life Science, and Electronics Together, we dream big and are passionate about caring for our rich mix of people, customers, patients, and planet That's why we are always looking for curious minds that see themselves imagining the unimaginable with us, Your Role Leadership & Strategy Manage Sourcing Projects of high complexity and collaborates in cross functional teams Actively lead the development of the global / regional sourcing strategies and in...

Long Description The person should have knowledge in Manufacturing equipments. He should have exposure in equipment’s such as FBE,Fette/KORSCH M/C & auto coater M/C. He should be able to handle equipment trouble shoot in Manufacturing department. He should have exposure in regulatory organization . He must have faced the USFDA ,MHRA & other regulatory audits. He should have the exposure in Caliber QAMS, elog, track wise ,SAP ,WIND ,CDAS & other software. He should have the exposure in process simplification/optimization ,SABA ,elog & SCADA. Competencies Education Graduation in Pharmacy Work Experience 3-6 years of experience in Fette compression machine

Role & responsibilities Ensuring the cleanliness and housekeeping activities in the laboratory. Ensuring the laboratory safety. Calibration of analytical instruments like High Performance Liquid Chromatography (HPLC) and Gas Chromatography (GC). Analysis of raw material, in-process, finished product and stability samples using HPLC & GC. Analysis of vendor samples as part of vendor qualification. Analysis of cleaning samples using UV & HPLC. Analytical method validation, method transfer and verification analysis as per protocol. Analytical column performance and maintenance. Temperature and humidity daily check in HPLC room. Preferred candidate profile Analytical Chemistry Documentation skil...

The AGM / DGM Technical Services position requires a candidate with a B.Pharma / M.Pharma qualification and 15 to 20 years of experience in tech transfer activities of solid oral dosage forms for regulated markets. The ideal candidate should have experience in managing a team of 15 to 20 scientists, documentation officers, and technicians. As an AGM / DGM Technical Services in Kandivali, Mumbai, your responsibilities will include planning and executing scale-up and Exhibit batches of solid oral dosage forms for regulated markets such as US, EU, ROW, and Canada. You will be accountable for ensuring the timely initiation of stability studies for exhibit batches and overseeing the technical ser...

As a Quality Control (QC) Analyst at Jubilant Generics, you will be responsible for various tasks related to ensuring the quality and compliance of pharmaceutical products. Your role will involve sampling and analyzing packing materials and raw materials, conducting in-process quality control, and preparing specifications and test procedures. Additionally, you will be responsible for maintaining artwork and shade cards, as well as calibrating and validating instruments and equipment. Your attention to detail will be crucial in recording analytical data accurately and preparing records of analysis for both raw materials and finished products, including stability samples. In this role, it is e...

As a quality control professional, you will be expected to strictly adhere to cGMP norms and safety rules within the factory premises. Your key responsibilities will include verifying logbooks, records, and other analytical documents on a daily basis to ensure their correctness and completeness. It will be your duty to ensure the timely preparation and revision of SOPs, STPs, and other Quality Management System (QMS) documents. You will also be responsible for the prompt completion of investigation activities related to Quality Control (QC) aspects such as Out-of-Specification (OOS), Out-of-Trend (OOT), deviations, and out-of-compliance (OOC) activities. Moreover, you will be accountable for...

Summary Independent Project work less complexity, e.g. early phase projects. Lead or support smaller and less complex projects or support more complex projects with mentoring. Higher complex routine tasks e.g. failure investigations and deviation, change controls etc. Manage projects and processes to support departmental portfolio, projects and objectives according to agreed timelines and standards. Ensure that compliance with cGMP is maintained in TRD. About The Role Key Responsibilities Support a discipline and/or provide a service individually or within a team of associates. May provide functional expertise to Line Unit and other QA Units in area of responsibility Write review, decide on ...

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...

Division Department Sub Department 1 Job Purpose To execute the activities that are related to microbiology laboratory, Key Accountabilities (1/6) Involvement in all quality related activities Maintenance of all the area and the equipment, To ensure and monitor compliance with GLP and cGMP as per requirements of the respective authority, Key Accountabilities (2/6) Environment monitoring Monitoring of area to be carried out as per allocated schedule, Release and transfer within the timeframe mentioned in SOP, Follow the written procedure for Execution of aseptic process validation and testing of Aseptic process validation sample, Involvement in process Simulation, Key Accountabilities (3/6) I...

Role & responsibilities Knowledge of Operation & Maintenance of Instrumentation like HMI, PLC,SCADA in Pharmaceuticals (OSD) manufacturing facility and equipment upgradation. Basic knowledge on PLC (Programmable Logic Controller) and Computerized System (SCADA). Designing requirement in accordance with contract specification & desired performance. Ensure compliance to cGMP & Audit requirements. Leading a team of Electrical, Instrumentation & Software Engineers working in multiple projects. Note : Candidate who can Join Immediately are preferred and willingness to work in Shift basis. Candidate should have experience in Pharmaceutical Formulation - OSD - Tablets Manufacturing facility