2778 Gmp Jobs - Page 24

As a dedicated Qualification Professional, you will be responsible for overseeing the execution of Pre-Factory Acceptance Tests (Pre-FAT), Factory Acceptance Tests (FAT), and Site Acceptance Tests (SAT) in accordance with established test protocols. Your primary role will involve engaging directly with customers to ensure adherence to test specifications and securing necessary documentation and approvals during FAT at our facilities and SAT at customer locations. You will be expected to conduct thorough testing and troubleshooting of systems, including SCADA, to ensure optimal performance. Additionally, you will monitor and address Non-Conformance Reports (NCRs) arising during Pre-FAT, FAT, ...

Varex Imaging, headquartered in Salt Lake City, USA, is a leading innovator, developer, and manufacturer of X-ray imaging component solutions, which includes X-ray tubes, digital flat panel detectors, software, and other key components of X-ray imaging systems. We are looking for a Manufacturing Engineer - Braze and Furnace Specialist to join our rapidly growing team in Pune. Your Role Ensure work area meets established cleanliness and safety standards. Gather parts and fixtures and assemble as per product-specific work instructions. Mix, heat, monitor, and dispose various chemical mixtures including acids, alkaline, solvents, and detergents. Clean and prepare parts used in X-ray assemblies....

As a team member at Biocon Biologics Limited, a subsidiary of Biocon Limited, you will be part of a fully integrated global biosimilars organization dedicated to leveraging cutting-edge science and innovative tech platforms to enhance healthcare outcomes. With a strong research pipeline focusing on biosimilar molecules for diabetes, oncology, immunology, and other non-communicable diseases, we are committed to making treatment more accessible and affordable for patients worldwide. Your responsibilities will include performing line clearance for various manufacturing activities such as formulation, washing, filling, sealing, and others in designated areas. You will also be responsible for rev...

As a Pharmaceutical Manufacturing Chemist at Dior Pharmaceuticals in Mohali, your primary responsibility will be to supervise the manufacturing and formulation processes of Nutraceuticals and Ayurvedic products. It will be crucial to ensure strict adherence to Good Manufacturing Practices (GMP), WHO-GMP, and other regulatory standards to maintain product quality. Your role will involve monitoring the quality of raw materials, overseeing in-process production stages, and conducting thorough checks on finished goods to guarantee their quality and safety for consumers. This is a full-time, permanent position with benefits such as cell phone reimbursement and a fixed shift schedule. Additionally...

You are looking for a dedicated individual to fill the role of Officer-ETP at a location in Krishnapatnam, Andhra Pradesh, India. As an Officer-ETP, you will be responsible for ensuring the smooth operation of the effluent treatment plant and maintaining accurate records of chemical consumption and stock. Your main accountabilities will include overseeing the operations of the ETP plant, including preliminary treatment, primary treatment, and secondary treatment processes. You will also be responsible for the smooth operation of WWRP and ZLD operations, as well as maintaining chemical consumption and stock records. Additionally, you will be required to conduct regular backwashing of MGF, ACF...

The incumbent will be responsible for calibration activities related to injectable plant. You will lead and perform complex calibration tasks to ensure compliance with GMP and ISO standards. This will involve coordinating with OEM vendors and the engineering team to execute qualification, calibration, and requalification activities for QC equipment. Additionally, you will provide support for the installation and maintenance of pharmaceutical manufacturing and laboratory equipment. It is crucial to record data and results in accordance with Good Manufacturing Practices (GMPs) and ISO quality standards. Maintaining up-to-date calibration documentation and certificates will also be part of your...

Hi, We have an urgent opening in MNC company for Quality Head-Pune location. Bachelors or masters degree in engineering, Quality Management, Environment Science, or a related field. 20+ years of progressive experience in quality , sustainability or EHS roles, preferably across multiple industries (e.g., automation, etc.). At least 5 years in leadership role in a multinational company. Strong knowledge of quality systems, compliance standards (ISO 9001, ISO 13485, ISO/TS 16949, GMP, etc.), and industry regulations. Certified Quality Professional (e.g., Six Sigma Black Belt, ASQ CQE/CQM/OE) is highly desirable. Demonstrated success in leading quality transformations, continuous improvement ini...

Purpose of Job 1. Preparation and Review of PQR. 2. Statistical evaluation of identiifed CPP & CQA at Manufactuirng and Quality Control stage using Minitab software. Skill Required 1. Having basic knowledge on Microsoft Word and Microsoft Excell 2. Have knowledge of Minitab software for statstical evaluation of data. Roles and Responsibilites 1. Preparation and review of PQR schedule. 2. Planining of PQR compilation as per PQR schedule. 3. Collection of data from all the CFT teams for compilation of PQR. 4. Statistical evaluation of identiifed CPP & CQA at Manufactuirng and Quality Control stage using Minitab software. 5. Based of the PQR data recommendation to be recommended to concern depa...

Purpose of Job 1. Preparation of PQR. 2. Statistical evaluation of identiifed CPP & CQA at Manufactuirng and Quality Control stage using Minitab software. Skill Required 1. Utilization of Microsoft Word and Microsoft Excell 2. Using of Minitab software for statstical evaluation. Roles and Responsibilites 1. Preparation of PQR schedule. 2. Planining of PQR compilation as per PQR schedule. 3. Collection of data from all the CFT teams for compilation of PQR. 4. Statistical evaluation of identiifed CPP & CQA at Manufactuirng and Quality Control stage using Minitab software. 5. Based of the PQR data recommendation to be recommended to concern department and ensure implemenation of the same. Quali...

Skill Required 3 to 4 year Pharma background experience for FP , In process and PV samples. Roles and Responsibilites To analyze the samples of in process/FP/Process validation as per work allotted by section in charge/Designee. Preparation of report and submission of reports along with raw data to section in charge/Designee within time. Immediate reporting of any odd observation, incident, OOT and OOS result during analysis to section in charge/Designee. Qualification Required M.sc/B.pharm Relevant skills / Industry experience Should have 2 to 4 year experience. Relevant professional / Educational background M.sc/B.pharm

Candidate needs to handle all shop floor responsibilities of plant which includes batch and shift schedules preparation, planning and execution of batches, GMP documentation compliance, support in GMP audit compliance

Job Description Required for IPQA acitities. Required for Batch manufacturing record review. Required for line clearnace and other shop floor related activity of QA. Work Experience 3 to 8 years. Education Graduation in Pharmacy Competencies

Reviewing LIMS/ELN relevant documentation, SOP s, training presentations, and any other documents related to CSV requirement for any enhancements or new implementation/Modules. Collaborating with IT and QA to facilitate validation activities, writing/execution/review of Test Scripts, and effective implementation of LIMS. Ensuring the proper functioning of LIMS application as per the business needs through rigorous testing. Review of Specification, Standard Operating Procedure, Instrument Operating Procedures, General procedures. Observation data sheet, calibration data sheets, protocols and reports etc. Creation/ preparation of documents, master data/ static data creation in LIMS, ELN and LM...

Perform in-process quality checks during manufacturing and packaging stages Ensure compliance with GMP, ISO, and regulatory standards Review and verify batch manufacturing and packing records Identify and report non-conformances, and implement corrective and preventive actions (CAPA) Conduct line clearance, sampling, and documentation as per SOPs Coordinate with production, QC, and warehouse departments to ensure product quality Maintain documentation for internal audits and regulatory inspections Provide on-the-floor training to production staff on quality protocols Help maintain quality-related documents and SOPs. Support in internal audits and regulatory inspections.

In Process Monitoring, GMP Compliance, Verfication of Online Documentation

Role & responsibilities Experience in operation and trouble shooting of process in plant. Isolation and purification of different organic compound using column chromatographic and crystallization techniques. Optimize the process parameters, what-if studies, holding studies etc. for scale up. Investigation of OOS/OOT and stability related issues. Handled various reagents like NaH, NaBH4, Br2, BHA, n-BuLi,TMSCl, TFA,PPA, Raney Nickel, Pd/carbon & also hazardous chemicals like POCl3, SOCl2 etc. Reactions performed like Hydrogenation,Brominaion,Oxidation,Reduction and condensation. Handling of Moisture sensitive reactions. Study and understand the project requirements, identifying and collection...

Roles and Responsibilities Develop new APIs through organic synthesis, method development, and optimization. Conduct literature reviews to stay updated on latest research trends and technologies. Ensure compliance with GMP guidelines during API manufacturing processes. Collaborate with cross-functional teams for product development, scale-up, and commercialization. Perform impurity analysis using techniques like NMR, DSC, etc. Desired Candidate Profile MS/M.Sc(Science) degree in Chemistry or Ph.D/Doctorate in Chemical Sciences from a recognized university. Strong expertise in areas such as API synthesis, organic chemistry, method development/validation/transfer/methodology. 9-14 years of exp...

Experience in QMS Knowledge of Compliance BMR, BPR, Documentation Audits RA Knowledge

Ensuring that analytical methods are validated and verified in compliance with regulatory standards. Reviewing and approving validation protocols and reports to ensure accuracy and consistency. Reviewing and evaluating raw data from analytical testing to ensure compliance with specifications and standards. Identifying trends, deviations, and out-of-specification results in analytical data and recommending corrective actions. Ensuring that all analytical testing is performed according to SOPs (Standard Operating Procedures) and regulatory requirements. Coordinating with the QC (Quality Control) team to ensure proper execution of tests and maintenance of laboratory equipment. Reviewing and app...

: We are seeking a qualified Assistant Manager HVAC with expertise in managing cleanroom and utility HVAC systems for a pharmaceutical facility. The role involves overseeing HVAC operations, maintenance, and projects while ensuring compliance with GMP, cGMP, and regulatory guidelines. Essential Functions: Manage and monitor HVAC systems, AHUs, chillers, cooling towers, boilers, and related utilities. Ensure cleanroom HVAC compliance with regulatory requirements (temperature, humidity, differential pressure, filtration). Plan and execute preventive, predictive, and breakdown maintenance of HVAC equipment. Support installation, commissioning, qualification (IQ/OQ/PQ), and validation of HVAC sy...

Description: The Deputy Manager Mechanical Engineering will be responsible for ensuring reliable operation, preventive maintenance, and continuous improvement of plant utilities, process equipment, and mechanical systems in compliance with pharmaceutical industry standards (cGMP, USFDA, EHS). The role requires hands-on expertise in maintenance planning, project execution, vendor management, and team leadership. Key Functions 1. Maintenance & Reliability Plan, schedule, and oversee preventive, predictive, and breakdown maintenance of mechanical equipment. Ensure maximum uptime of critical utilities like chillers, AHUs, boilers, compressors, WFI systems, HVAC, and clean utilities. Troubleshoot...

Description : The role involves managing electrical operations, preventive and breakdown maintenance, and ensuring compliance with GMP and safety standards. The candidate will be responsible for handling HT/LT systems, DG sets, UPS, VFDs, HVAC electricals, and utility equipment like chillers, compressors, boilers, WTP/ETP. Essential Functions: Electrical Maintenance & Operations Ensure smooth operation of electrical systems, panels, HT/LT substations, transformers, DG sets, UPS, and VFDs. Carry out preventive, predictive, and breakdown maintenance of electrical equipment in compliance with GMP and safety standards. Monitor and maintain HVAC, cleanroom, and utility-related electrical systems ...

Division Department Sub Department 1 Job Purpose Monitor and execute the production activities in an area during the shift by maintaining cGMP and safety norms to achieve production targets Key Accountabilities (1/6) Execute production activities in a shift by managing available resources to achieve production target Execute assigned tasks as per planned production activity to meet production targets for a shift Regulate usage of consumables in the production process at optimum levels to save costs Increase the efficiency of area by utilization of equipment and by reducing downtime in manufacturing area Key Accountabilities (2/6) Maintain standard process parameters as per BMRs and other sup...

Division Department Sub Department 1 Job Purpose Monitor and execute the production activities in an area during the shift by maintaining cGMP and safety norms to achieve production targets Key Accountabilities (1/6) Execute production activities in a shift by managing available resources to achieve production target Execute assigned tasks as per planned production activity to meet production targets for a shift Regulate usage of consumables in the production process at optimum levels to save costs Increase the efficiency of area by utilization of equipment and by reducing downtime in manufacturing area Key Accountabilities (2/6) Maintain standard process parameters as per BMRs and other sup...

Experience: 02 to 05 Year Experience in Store (OSD Formulation) Education Qualification: B.Sc. | M.Sc. | B. Pham. Department: Store Location: Santej Ahmedabad. Gender: Male Only Facilities Provided: Transportation Facility Available (As Per Circumference Of Sunrise Remedies)* Mediclaim and Food Facility provide By Company.* Key Responsibilities: Monitoring the people for raw material sampling and analysis in day to day. Trouble shooting resolve during the analysis of raw material by analyst Handling of Raw material section, start from sampling to Release of raw material. Should have knowledge of ERP and LIMS Knowledge of chemical test as well as HPLC analysis Handling of QMS like incident, O...