4089 Gmp Jobs - Page 25

Roles and Responsibility Develop and implement operational strategies to achieve business objectives. Manage and supervise a team of professionals to ensure efficient operations. Analyze operational data to identify areas for improvement and optimize processes. Coordinate with various departments to ensure seamless operations and resolve issues. Implement and maintain quality control measures to ensure high standards. Identify and mitigate risks to ensure compliance with regulatory requirements. Job Requirements Proven experience in operations management with a minimum of 5 years of experience. Strong knowledge of operational principles and practices. Excellent leadership, communication, and...

We are looking for a skilled Restaurant Manager to join our team in the hospitality industry. The ideal candidate will have 5-10 years of experience in managing restaurants and excellent leadership skills. Roles and Responsibility Manage daily restaurant operations, including staff supervision and customer service. Develop and implement strategies to improve customer satisfaction and increase sales. Maintain high standards of food quality, safety, and hygiene. Analyze sales reports and develop plans to boost revenue. Lead and motivate a team of servers, bartenders, and kitchen staff. Ensure compliance with health and safety regulations and company policies. Job Requirements Proven experience...

We are looking for a skilled Restaurant Manager to join our team, with 5-10 years of experience in the hospitality industry. The ideal candidate will have a strong background in managing restaurants and excellent leadership skills. Roles and Responsibility Manage daily restaurant operations, including staff supervision and customer service. Develop and implement strategies to improve customer satisfaction and increase sales. Maintain high standards of food quality, safety, and hygiene. Analyze sales reports and develop plans to boost revenue. Lead and motivate a team of servers, bartenders, and kitchen staff. Ensure compliance with health and safety regulations and company policies. Job Requ...

Responsible to provide oversight and completion of the site APQRs Responsible for authoring of APQRS assigned, per site APQRs per schedule Responsible for ensuring any site or CMO APQR is created following the effective process and procedures Provide in depth quality and compliance oversight during report authoring. Responsible for ensuring all elements of the AQPR procedure are fulfilled accurately. Responsible for facilitating review and approval meetings, problem-solving key issues, and effectively managing communications with key stakeholders. Responsible for collecting review feedback and resolving comments and questions. Responsible for projecting and communicating stakeholder actions ...

Operate and monitor DCS (Distributed Control System) for process operations. Execute batch production as per SOPs and cGMP guidelines. Maintain Batch Manufacturing Records (BMR) and ensure all process parameters are properly recorded. Ensure line clearance , proper labeling, and area cleanliness before and after production. Carry out in-process checks and coordinate with QA for line clearance. Supervise charging, reaction, distillation, and filtration activities. Coordinate with Engineering for equipment maintenance and troubleshooting. Support process validation, deviation handling, and change control activities. Ensure compliance with safety, quality, and environmental norms (EHS) . Follow...

Plan, organize, and oversee daily production activities to meet production targets. Ensure compliance with cGMP, GDP, and safety standards across the production area. Supervise and guide officers/executives for efficient plant operations. Review and approve BMR/BPR, SOPs, deviation, and change control documentation. Monitor equipment performance , coordinate preventive maintenance , and ensure minimal downtime. Drive process optimization, yield improvement, and cost reduction initiatives. Coordinate with QA, QC, Engineering, SCM, and EHS departments for smooth operations. Prepare and analyze monthly production reports, KPIs, and productivity data. Ensure readiness for regulatory audits and p...

To carry out batch manufacturing and related production activities as per SOPs and cGMP requirements. Maintain and update Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR) . Ensure line clearance , proper labeling, and area cleanliness before and after production. Operate and monitor production equipment like RMG, FBD, Compression, Coating, Granulation, Packing machines , etc. Coordinate with QA, QC, and Engineering for daily operations and troubleshooting. Participate in process validation, deviation handling, and change control activities. Ensure compliance with safety, quality, and regulatory standards (USFDA / WHO / MHRA). Monitor manpower utilization, shift planning , ...

Quality Assurance Executive- Female Location- Mohali Education- B.Pharm / M.Pharm / B.Sc / M.Sc Salary - 20K Experience - Min 1 year in quality control (in pharma) 6 days working Day Shift Required Candidate profile Candidate should have knowledge of GMP, GLP, validation, documentation, and regulatory compliance. Proficiency in MS Office and ERP systems

Design and conduct experiments to create and refine new drug compounds. Research new materials and compounds for potential medicinal use. Analyze how substances interact with biological systems and human tissue.

As a Production Planner in a pharmaceutical manufacturing environment, your role involves developing and managing efficient production schedules to meet demand forecasts, optimize resource utilization, ensure compliance with GMP and regulatory standards, and minimize downtime. Your key responsibilities include: - Developing and maintaining detailed production plans based on sales forecasts, inventory levels, and customer orders. - Coordinating with procurement, quality assurance, warehouse, and manufacturing teams to align production plans. - Monitoring production progress and adjusting schedules as necessary to avoid delays and ensure timely product delivery. - Ensuring planning aligns with...

As a Mechanical Maintenance Manager in a pharmaceutical manufacturing facility, your role will involve overseeing the maintenance activities of mechanical systems and utilities to ensure uninterrupted and compliant operations. Your key responsibilities will include: - Overseeing preventive, predictive, and breakdown maintenance of mechanical systems such as HVAC systems, compressors, boilers, pumps, water systems, process equipment, and cleanroom equipment to ensure they operate within required parameters and meet GMP compliance. - Ensuring all maintenance activities are compliant with cGMP, USFDA, MHRA, WHO, and other regulatory bodies by maintaining and reviewing maintenance documentation ...

Role Overview: You will be joining ValGenesis, the market leader in end-to-end digital validation, as a Lead Validation Engineer in Chennai. Your main responsibility will be to ensure that the cutting-edge products meet the highest quality standards through validation processes. Key Responsibilities: - Collaborate with Product, Engineering, and Testing teams to understand product functionalities thoroughly. - Review Product Requirements such as Epics, User Stories, and Software Requirements. - Develop comprehensive test cases in Operational Qualification (OQ) and Performance Qualification (PQ) protocols following guidelines. - Create realistic test cases and datasets based on real-world cust...

Azurity Pharmaceuticals is a privately held, specialty pharmaceutical company that focuses on innovative products that meet the needs of underserved patients. As an industry leader in providing unique, accessible, and high-quality medications, Azurity leverages its integrated capabilities and vast partner network to continually expand its broad commercial product portfolio and robust late-stage pipeline. The company's patient-centric products span the cardiovascular, neurology, endocrinology, gastro-intestinal, institutional, and orphan markets, and have benefited millions of patients. For more information, visit www.azurity.com. Azurity Pharmaceuticals is proud to be an inclusive workplace ...

Job Title: Formulation Expert Herbal / Nutraceutical / Cosmetics. Location: Lakkenahalli, Ramanagara district, Karnataka 562127. Experience: 12-15 Yearsof experience. Qualification: M. Pharm (Pharmaceutics) or M.Sc. (Chemistry) with experience in formulation development. Job Summary: We are seeking a skilled and innovativeFormulation Expertwith over 12-15 years of experience in the development of herbal, nutraceutical, or cosmetic formulations. The ideal candidate will be responsible for end-to-end formulation development, from ideation to scale-up and commercial transfer. Key Responsibilities: Develop and optimize novel formulations and product concepts based on project requirements. Develo...

Use Your Power for Purpose Our manufacturing logistics and supply team ensures that customers and patients receive the medicines they need precisely when they need them. By embracing challenges, imagining new possibilities, and taking decisive action, you'll help accelerate the delivery of medicines to the world. Your role is crucial in making sure that life-saving treatments are available promptly, meeting the needs of patients everywhere. What You Will Achieve In this role, you will: Take responsibility for individual contributions to achieve team deliverables, working effectively as a team member and coordinating with others. Manage personal time and professional development, taking accou...

We are looking for a highly skilled and experienced Executive to join our team in the Hospitality industry. The ideal candidate will have a strong background in Food and Beverage Service, with excellent communication and customer service skills. Roles and Responsibility Manage daily operations of the food and beverage service department. Coordinate with kitchen staff to ensure timely delivery of high-quality food products. Develop and implement effective inventory management systems to minimize waste and optimize resources. Maintain high standards of customer service and resolve complaints professionally. Collaborate with other departments to achieve business objectives. Analyze sales data a...

Hi, Greetings from Avani Consulting!! We have job opportunities with API Manufacturing Company for the Sr. Executive/Executive- Electrical position, Mysore Location. Position- Sr. Executive/Executive- Electrical & Instrumentation Work Experience +8 in API / Pharmaceutical / Chemical / FMCG / Continuous Process Industry Location Mysore Qualification- B.E. / B.Tech / Diploma in Electrical Engineering. Knowledge of SAP. Must Have Electrical Supervisor License Must have experience in 66KV Job Summary: To lead and manage all electrical maintenance activities and ensure optimal performance, reliability, and safety of electrical systems in an API manufacturing facility. The role also includes effic...

Title: Sr.Manager-2 Business Unit: SGO Job Grade 9B Location : Guwahati Key Responsibilities Primary Responsibility: 1.Overseeing the Entire OSD & NOSD Functions of Plant. 2.Co-ordination with Production & Project Personal, Contractors and Machine Manufacturers to Sort out Machine related problems, Major or Minor Modifications for Smooth running of Process. 3. Tracking & Maintaining the critical spares required for Preventive & routine Maintenance. 4. To facilitate safety in working Environment by implementing EHS policies. 5.Responsible for Sourcing of Machine, Tooling, Consumable pats and related service and interacting with user departments for Analyzing the required materials. 6.Facing c...

Job Title: Global Study Supply Support (GSSS) Role Overview Provide operational support to Clinical Supply Chain Study Leaders for multiple studies across all phases (set-up, follow-up, closure). Work independently and collaborate with multiple leaders and cross-functional teams. Key tasks include: Preparing and tracking transfer orders. Managing stock reconciliation. Performing quality checks. Preparing documentation for labeling and shipments. Monitoring needs for destruction. Archiving documents in the electronic Trial Master File. Key Responsibilities Support clinical supply chain operations for global studies. Ensure compliance with regulatory standards and protocols. Maintain accurate ...

Regulatory Documentation Specialist focused on IVF buffer media and sterile life science products . The ideal candidate will have strong expertise in regulatory compliance, documentation, and quality systems aligned with DCGI, ISO 13485, CE (MDR/IVDR) , and WHO-GMP standards. Qualifications: Masters in Biology / Biotechnology / Life Sciences 3–5 years’ experience in regulatory documentation for sterile or IVF-related products Key Skills: DCGI submissions & Product/ Site Master Files ISO 13485:2016 QMS documentation CE marking, MDR/IVDR compliance Knowledge of Drugs & Cosmetics Act, Medical Device Rules (2017) Responsibilities: Prepare and maintain regulatory dossiers, technical files & SOPs ...

Operate VNA (Very Narrow Aisle) equipment to handle materials in GMP-compliant warehouse racking systems. Perform accurate put-away and retrieval of pharmaceutical materials from designated storage locations. Ensure FIFO/FEFO (First In, First Out / First Expired, First Out) principles are followed. Carry out daily equipment checks and maintenance logs. Support stock counting, reconciliation, and inventory audits. Follow all safety procedures, especially within cleanroom or temperature-controlled areas, if applicable. Adhere to SOPs, GDP, and GMP guidelines during all operations. Assist in loading/unloading materials and ensure material labels and documentation are correct and intact.

About The Role Skill required: KYC Screening - Know Your Customer (KYC) Designation: Regulatory Compliance New Associate Qualifications: Any Graduation Years of Experience: 0 to 1 years What would you do? Help clients transform their compliance function from reactive to proactive through an intelligent compliance operating model powered by data, intelligent technologies and talentLooking for someone with KYC experience along with ECDD/OCDD knowledgeBusiness and regulatory requirements, governance, operating model, process and system controls to verify the identity, suitability, and risks involved with onboarding and/or maintaining a business / customer relationship. This includes driving cus...

About The Role Skill required: KYC Screening - Know Your Customer (KYC) Designation: Regulatory Compliance Associate Qualifications: Any Graduation Years of Experience: 1 to 3 years What would you do? Help clients transform their compliance function from reactive to proactive through an intelligent compliance operating model powered by data, intelligent technologies and talentLooking for someone with KYC experience along with ECDD/OCDD knowledgeBusiness and regulatory requirements, governance, operating model, process and system controls to verify the identity, suitability, and risks involved with onboarding and/or maintaining a business / customer relationship. This includes driving custome...

About The Role Skill required: KYC Screening - Sanctions Screening Designation: Regulatory Compliance Analyst Qualifications: Any Graduation Years of Experience: 3 to 5 years What would you do? Help clients transform their compliance function from reactive to proactive through an intelligent compliance operating model powered by data, intelligent technologies and talentLooking for someone with KYC experience along with ECDD/OCDD knowledgeAbility to effectively and efficiently conduct the process of screening individuals, entities, or transactions against lists of sanctioned or restricted parties. Sanctions screening involves using specialized software, understanding relevant regulations, and...

Role & responsibilities Manage and oversee all production documentation activities for API manufacturing, ensuring compliance with GMP and regulatory standards . Prepare, review, and maintain batch records, SOPs, and production reports , ensuring accuracy and completeness. Coordinate with production, quality, and regulatory teams to ensure smooth documentation flow and timely submission of records. Implement documentation control systems and train team members on best practices to maintain high-quality standards.