2755 Gmp Jobs - Page 6

Walk-in at Matoda We are hiring multiple positions for our manufacturing facility at Matoda as mentioned below. Please find our current job requirements and venue details mentioned. If any of the requirements match your current job profile, kindly walk in with your latest resume. Role & responsibilities Injectable Manufacturing (Executive/Senior Officer / Officer) Experience - 02 to 08 Years Qualification - B. Pharmacy/ M Pharmacy / Msc / Bsc / Engineering - (Instrumentation / Process Equipment Maintenance) (Senior Executive / Executive / Senior Officer) Experience - 03 to 10 Years Qualification BE / B Tech QUALITY ASSURANCE IPQA (injectable) / QMS / Documentation (Officer / Senior Officer /...

Role Objective : To manage the production of polymer compound extrusion processes. The required skills for the Production Manager position include expertise in Kaizen, Total Quality Management (TQM), ISO documentation, process safety and audits, 8D reporting for failures, Failure Mode and Effects Analysis (FMEA), CPk and OEE calculations, efficiency data and yield calculations, and customer complaint management. Additionally, desired skills encompass leadership qualities, knowledge of IATF and GMP, techno-commercial acumen, being detail-oriented, and having experience in the polymer compound manufacturing industry. Production Management : Production planning, sequencing, and scheduling Varia...

To manage the team and manage the house keeping activities at the site Assign work duties, evaluate performance, and train new personnel in policies and procedures, as well as operation of cleaning and maintenance equipment. Handle complaints, and all housekeeping-related customer service concerns and resolve any problems efficiently. Maintain inventory records of cleaning and other supplies, and may handle purchasing of materials and equipment maintenance services. Keep track of room cleaning tasks to workers. Supervising a housekeeping department requires someone with good management and communication skills Location : Bachupally & Gachibowli

We have job opportunity with Pharma Manufacturing Industry for QA Trainee, Mysuru Location Position : - QA Trainee Qualification : MSc. (Chemistry)/ Life Science Experience : 1 Year experience in API Industry. Budget : upto 21000 /PM - stipend Male /Female candidates are considered. Ready to work in shifts (1st, 2nd and Night shift) Immediate joiners preferred. Preferred Skills: 1. Knowledge of API manufacturing processes and regulations. 2. Familiarity with quality management systems (QMS) and audit processes. 3. Strong communication and interpersonal skills. Key Responsibilities: 1. Assist in conducting audits and inspections of production areas, warehouses, and laboratories. 2. Support th...

Responsible for follow the health, safety & environment norms as per company policy & procedure Responsible for follow the Good Laboratory practices & Good Documentation practices Maintain laboratory discipline Preparation of COA, Raw material trend Required Candidate profile Operate and calibrate instruments like Gas Chromatography, HPLC, Analytical balance, PH meter, GCMS Validity of instrument calibration, reagents, volumetric solutions, working standard

Overview Location: Bangalore, Hyderabad, Chennai and Coimbatore Experience: 8 to 10 years Skills: CM360 - End to End campaign knowledge and Ad trafficking, Troubleshooting & Reporting, GAM, Team Handling, Stakeholder management Notice Period: Immediate Joiners This exciting role of a Manager - Ad Operations requires you to creatively manage digital media campaigns for our global brands. Your expertise of ad tech and knowledge of the Digital Market Cycle would make you a great fit for this position. This is a great opportunity to work closely with the Top Global brands and own large and reputed accounts. About us We are an integral part of Annalect Global and Omnicom Group, one of the largest...

1. To perform routine, preventive and breakdown maintenance of plant and Utility equipment. 2. Troubleshooting and maintaining healthiness of plant and Utility equipment. 3. Assisting engineer in modification and improvement activities. 4. Involvement during equipment qualification/validation related activities. 5. Adhere to all company policies & manuals. 6. Strictly adhere to all regulatory and legal compliance. 7. Follow GEP, GMP and GDP during maintenance and project activities. 8. Ensure safety compliance during maintenance of equipment. 9. To maintain equipment cleaning after completion of maintenance activity. 10. To carry out any job assigned by immediate supervisor / HOD.

1. To perform routine, preventive and breakdown maintenance of plant and Utility equipment. 2. Troubleshooting and maintaining healthiness of plant and Utility equipment. 3. Assisting engineer in modification and improvement activities. 4. Involvement during equipment qualification/validation related activities. 5. Adhere to all company policies & manuals. 6. Strictly adhere to all regulatory and legal compliance. 7. Follow GEP, GMP and GDP during maintenance and project activities. 8. Ensure safety compliance during maintenance of equipment. 9. To maintain equipment cleaning after completion of maintenance activity. 10. To carry out any job assigned by immediate supervisor / HOD.

1. To perform routine, preventive and breakdown maintenance of plant and Utility equipment. 2. Troubleshooting and maintaining healthiness of plant and Utility equipment. 3. Assisting engineer in modification and improvement activities. 4. Involvement during equipment qualification/validation related activities. 5. Adhere to all company policies & manuals. 6. Strictly adhere to all regulatory and legal compliance. 7. Follow GEP, GMP and GDP during maintenance and project activities. 8. Ensure safety compliance during maintenance of equipment. 9. To maintain equipment cleaning after completion of maintenance activity. 10. To carry out any job assigned by immediate supervisor / HOD.

Dishman Group is looking for Executive - Production to join our dynamic team and embark on a rewarding career journey. Production Planning : Developing production plans, schedules, and strategies to meet output goals and deadlines. Operations Management : Overseeing day-to-day manufacturing activities, ensuring adherence to production schedules, and resolving operational issues. Resource Allocation : Managing resources including manpower, equipment, and materials to optimize production efficiency. Quality Assurance : Implementing quality control measures, monitoring production standards, and ensuring product quality meets specified criteria. Process Optimization : Identifying areas for impro...

Dishman Group is looking for Officer - QA to join our dynamic team and embark on a rewarding career journey Develop and implement quality assurance policies and procedures Conduct regular audits and inspections to ensure compliance with standards Investigate and resolve quality issues and customer complaints Train staff on quality control processes and standards Maintain accurate records and documentation of quality activities

As a Technology Compliance Partner, you will be responsible for authoring SDLC documents and providing SDLC advice to IT colleagues regarding the practical application of the SDLC. This role is vital for IT product, engineering, and service teams to understand and implement technology and process controls to meet the company s policy and regulatory obligations. What will you do in this role: Engage with IT practitioners and acts as a consultant for the System Development Life Cycle (SDLC), Compliance Risk Profile, Digital SDLC, Good Documentation Practices and the IT Control Requirements Set including the adoption of agile ways of working. Provide compliance advice to IT colleagues regarding...

As a Quality Control (QC) Officer in the pharmaceutical (Formulation) industry located at Waghodia GIDC, Vadodara, your main responsibilities will include: - Performing quality checks on raw materials, in-process materials, and finished products. - Carrying out lab testing using instruments like HPLC, GC, UV, FTIR, etc. - Ensuring all work complies with GMP (Good Manufacturing Practices), GLP (Good Laboratory Practices), and other regulatory requirements. - Identifying and reporting any issues like defects, deviations, or non-conformities. - Maintaining accurate records, including test reports and documentation. - Working closely with production and QA teams to address and resolve quality-re...

As an Esco Lifesciences Group employee, you will play a crucial role in providing enabling technologies, products, and services to support the life sciences and healthcare industries. With headquarters in Singapore and a global presence, Esco is a leader in multiple categories within the fastest-growing segments, particularly excelling in the Chinese market. Your contributions will be instrumental in bridging technologies, products, and talent across the world. Key Responsibilities: - Demonstrate comprehensive product knowledge to support sales, marketing, and technical teams effectively. - Monitor production activities closely to ensure adherence to Good Manufacturing Practices (GMP) and re...

Ensuring best quality of product and minimum customer complaints through stringent on-line quality control checks and finished product inspection Implementing right quality control systems/standards for the processes, physical systems and environment. Trouble shooting during online production to minimize wastage and ensure quality. Responsible for maintaining GMP, GHK GLP and internal / external audits (HACCP, AIB, Personal Hygiene, Process audit) Root cause and failure analysis for quality defects and implementation of the corrective actions. Responsibilities Conducting online quality checks in the process area to ensure that all FLI standards of quality are followe'd during the production ...

Operate and monitor utility equipment including boilers, chillers, air compressors, cooling towers, RO/DM water systems, and HVAC units. Perform routine checks and logbook entries for pressure, temperature, flow rates, and other critical parameters. Ensure timely startup, shutdown, and smooth functioning of utility systems as per production requirements. Carry out preventive maintenance activities in coordination with the engineering team. Monitor fuel, water, and power consumption and escalate abnormalities. Support compliance with statutory and safety norms in utility operations. Respond promptly to breakdowns, deviations, and utility-related emergencies. Additional Responsibilities: Suppo...

Responsible for sampling of In-process sample, Process validation, rinse and swab sample,FG sample, Control sample, MLT sample and Stability sample and to ensure timely submit To make necessary entries into respective register/E- log book. Responsible for activities inline in ERP, LIMS, ELOG and EDCS as per requirement. To carry out Line clearance prior to start-up of any activity and verification of dailyequipment logs. Online checking of BMR its compliance. For carrying out in-process activity at Manufacturing stage as per BMR and relevant SOPs Checking of Environment monitoring of all respective areas on shop floor. To follow EHS policies. To ensure compliance of GDP and data integrity te...

Leadership & Team Management Lead and mentor a team of R&D scientists, chemists, and analysts. Drive project prioritization, resource allocation, and technical guidance. Research & Development Oversee design, development, and optimization of APIs, intermediates, and formulations . Ensure robust process development and technology transfer from lab to pilot to commercial scale. Integrate innovation in synthetic routes, green chemistry, and cost-effective process improvements. Regulatory & Compliance Ensure adherence to GMP, ICH, FDA, and other regulatory frameworks in all R&D activities. Partner with Quality and Regulatory teams to generate required documentation and filings. Collaboration & S...

Develop and implement sourcing strategies for APIs, key starting materials (KSMs), intermediates, and excipients . Identify, qualify, and onboard new suppliers globally, ensuring adherence to GMP, FDA, and regulatory standards . Negotiate supplier contracts covering pricing, lead times, quality, and delivery terms. Manage supplier relationships to ensure reliability, consistency, and risk mitigation. Conduct market analysis to track pricing trends, alternative sources, and supply chain risks. Work closely with QA/QC, R&D, and supply chain teams to align sourcing with technical and business requirements. Ensure compliance with pharma procurement regulations , sustainability standards, and int...

- Develop new branches - Make annual budget/plan - Develop beat-plan for individual team members based on prioritized customer segments - Liasion with underwriting team - Lead a team of sales professionals Required Candidate profile - Must have exp. in group health/ corporate health insurance - Should have exp. in brokerage firm - Should be comfortable in field for client meetings

Focus on Health clients/companies Responsibility of building and maintaining relation with clients. Sales process: lead generation, closing Lead and be accountable for the client proposals, Contracts & documentation following company procedures Required Candidate profile Must have exp. in Corporate helath insurance sales

Job Mission: To build and lead the operational backbone of our direct-to-consumer (D2C) baby food brand. You will be responsible for flawless execution from production support to final dispatch, ensuring the highest standards of quality, efficiency, and safety while building a culture of continuous improvement. This role has a clear path to a Head of Operations position within 18-24 months, based on demonstrated performance in building scalable systems and leading teams. Key Responsibilities: 1. Operational Excellence & Maintenance: Act as the first point of contact for all equipment breakdowns (AC, dehumidifier, band sealer, electrical issues), ensuring less than 1% machine downtime. Build ...

Effective operation and maintenance of equipment like autoclave, Garment cubicle, sealing machine, vessels CIP and SIP SKIDS To practice the c GMP activities and to follow the clean room discipline Cleaning and sterilization of the vessels and transfer lines using CIP & SIP equipment Preparation and filtration of disinfectant and cleaning of the area Monitoring of LAFU, AHU, Dynamic pass box, Garment cubicles and cold rooms Maintaining of all cGMP activities and housekeeping activities in the critical operations Maintenance and updating of equipment log books and GCRs Manual recording of the temperature and positive pressures Cleaning of equipment Blending of vaccines Preparation, Sanitizati...

.Create and maintain company Q.A documentation, manuals, procedures .Continuously improve QA processes and procedures. .Preparation of QA reports. .Responsible for Compliance of Medical Device Directive (MDD) 93/42/EEC, ISO 13485:2016, ISO 14971:2012 Required Candidate profile Thoroughly Knowledge of Medical Device Directive (MDD) 93/42/EEC, ISO 13485:2016, ISO 14971:2012 & Medical device Rules 2017

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