4062 Gmp Jobs - Page 6

As a Corticosteroid Production Manager at Krishang Pharma Private Limited in Ode, Anand, Gujarat, your role will involve leading corticosteroid API production with a strong focus on GMP compliance and quality. You will be responsible for guiding the team to efficiently achieve production targets, overseeing technology transfer, and scaling up manufacturing processes. Collaboration with QA will be essential to ensure regulatory compliance with bodies such as USFDA and EMEA. Additionally, you will be required to maintain batch records and optimize production workflows. Key Responsibilities: - Lead corticosteroid API production focusing on GMP compliance and quality. - Guide the team to efficie...

As an Equipment Maintenance Technician, your role involves the following responsibilities and qualifications: **Role Overview:** You will be responsible for maintaining and troubleshooting a variety of equipment, including injection molding machines, CNC milling machines, EDM machines, surface grinders, and utility equipment like transformers, generators, air handling units, and more. **Key Responsibilities:** - Carrying out routine scheduled maintenance work and responding to equipment faults promptly. - Designing maintenance strategies, procedures, and methods to ensure optimal equipment performance. - Providing accurate information and regular progress updates to the management team. - Un...

As a Capsule Filling Machine Operator at Lavanya Healthcare Limited in Dera Bassi, Punjab, your role is crucial in ensuring the accurate and efficient filling of hard gelatin capsules using the SA9 Capsule Filling Machine while adhering to cGMP, safety, and quality standards. Key Responsibilities: - Set up and operate the SA9 Capsule Filling Machine according to the daily production plan. - Load empty capsules and powder/blend into appropriate hoppers and magazines. - Monitor capsule weight, alignment, and sealing during production. - Perform in-process checks, document findings, and ensure compliance with SOPs and BMR. - Clean machine parts before and after each batch or product changeover....

As a QC RM Analyst, your role is crucial in ensuring the compliance of raw materials with quality specifications to maintain product safety, efficacy, and regulatory compliance for third-party manufacturing operations. Key Responsibilities: - Conduct routine and non-routine testing of incoming raw materials following SOPs. - Perform physical, chemical, and microbiological tests to verify material quality. - Ensure identification, purity, and conformity of raw materials to specifications. - Record, maintain, and report accurate test results in laboratory documentation systems. - Investigate deviations, non-conformances, and out-of-specification (OOS) results. - Coordinate with procurement, pr...

Role Overview: You will be designated as a Senior Executive - Quality (Audit and compliance) in the Corporate Quality department at Shalina Healthcare. Your main responsibility will be to conduct Vendor Quality Audits and ensure GMP and GLP compliance at various manufacturing and testing facilities. You will also be involved in preparing and presenting quality review meetings, conducting self-inspections, and coordinating with cross-functional teams for maintaining the quality system. Key Responsibilities: - Prepare and adhere to annual planner for Quality audits for Loan licence Units (LLU), Third Party Manufacturing Sites, public testing laboratories, and Shalina Operating units (OUs) - Re...

As a highly experienced Quality Assurance leader, you will drive Corporate QA initiatives across multiple formulation manufacturing sites. Your primary responsibility will be to strengthen the company's Audit, Compliance, and Validation/Qualification (VQ) framework, ensuring adherence to global regulatory standards, and maintaining continuous inspection readiness. This strategic corporate role requires close coordination with site QA, manufacturing, and regulatory teams to uphold a consistent culture of quality excellence and compliance across all units. Key Responsibilities: - Lead and manage internal and external audits across formulation sites (OSD, Injectables, Topicals). - Ensure full c...

As a Senior Manager in the R&D department at Gujarat Fluorochemicals Limited, your role will involve the following key responsibilities: - Leading a team of scientists and chemists for new product/process development and enhancing existing products. - Conducting literature surveys and identifying commercially viable and non-infringing routes for fluoro-specialty molecules targeted for commercialization within specified timelines. - Developing and standardizing industrially feasible processes while meeting cost targets. - Identifying and creating new products to meet market demands. - Preparing feasibility reports, cost analysis reports, monthly progress reports, and Technology Development Re...

As a Process Equipment Engineer, you will be responsible for designing and specifying process equipment systems for pharmaceutical manufacturing plants. Your role will involve ensuring alignment with project goals and regulatory standards such as GMP, FDA, and EMA. Your key responsibilities will include: - Selecting appropriate equipment based on factors such as material compatibility, process requirements, automation, and cost-effectiveness. - Developing equipment specifications, datasheets, and technical documentation for procurement and installation. - Having hands-on experience in installing isolator-based filling lines from manufacturers such as Bausch + Straubel, Syntegon, and Sterilin...

Job Description: As a Quality Compliance Officer in a manufacturing environment, your primary responsibility will be to ensure quality compliance, documentation, and adherence to industry standards. You will play a crucial role in maintaining the quality of products through various checks and inspections. Key Responsibilities: - Conduct quality checks and inspections of raw materials & finished products to maintain high standards. - Ensure compliance with Good Manufacturing Practices (GMP), International Organization for Standardization (ISO), and other regulatory standards. - Maintain quality documentation accurately and assist in audits to validate compliance. - Support process validation ...

As a Chemical Engineer at TFarms, you will be responsible for overseeing and optimizing the production processes in our spice processing plant, specifically focusing on managing solvent-based oleoresin extraction, powder manufacturing, and essential equipment operation such as boilers, cooling towers, reactors, and evaporators. Your role is crucial in ensuring production efficiency, safety compliance, quality standards, and cost control. **Key Responsibilities:** - Plan, coordinate, and supervise daily production activities including oleoresin extraction, powder manufacturing, and other processes. - Oversee the operation and maintenance of critical machinery like boilers, cooling towers, rea...

Department: Production Documentation - Investigations Location: Bidar,Karnakata Position: Executive / Senior Executive About Us: Sai Life Sciences is one of the fastest-growing Contract Research, Development, and Manufacturing Organizations (CRDMOs). As a pure-play, full-service partner, we collaborate with over 300 global innovator pharma and biotech companies to accelerate the discovery, development, and commercialization of their NCE programs. We have over 3000 employees across our facilities in India, the UK, and the USA, working together to deliver scientific excellence and customer success. We are a Great Place to Work certified organization with a culture of openness, mutual respect, ...

As a QA/QC Assistant at HempCann Solutions Private Limited, you will be responsible for overseeing manufacturing operations to ensure workflow efficiency, compliance, and continuous improvement. Your key duties will include production planning, quality assurance, maintenance, and statutory compliance. Your responsibilities will include: - Recording incoming Raw material, In-process product, and Finished Product samples as per requisition - Issuing test reports as per the intimation slip - Issuing analytical data sheets - Preparing Quality specifications of RM, In-process, and finished products - Preparing COA of finished products of Tablets, Capsules & Churna products - Preparing SOPs - Prep...

As a Quality Assurance Specialist, you will be responsible for ensuring GMP and GLP compliance through various audit activities at Loan Licence Units (LLU), Third Party Manufacturing Sites, public testing laboratories, and Shalina Operating Units (OUs). Your key responsibilities will include: - Preparation and adherence to annual planner for Quality audits to monitor overall performance and compliance. - Reviewing audit compliance reports for external/regulatory/customer audits and ensuring timely closure of observations. - Conducting self-inspections, compiling reports, and tracking compliance for timely closure. - Coordinating technical document evaluation from vendors, arranging sample an...

As a Document Controller at SEPAM in Chennai, your role involves managing project documentation, records, and communication tasks related to document management. Key Responsibilities: - Hands-on experience in GMP, Equipment Qualification, DQ/IQ/OQ/PQ - Experience in FMCG projects - Proficient in Document Management and Project Documentation - Skilled in Documentation and Records Management - Strong communication skills - Attention to detail and organizational skills - Proficiency in document control software - Ability to work effectively in a team environment Qualifications Required: - Bachelor's degree in a relevant field Note: Additional details about the company are not provided in the jo...

As a Quality Control Testing Technician in a Cell Therapy Lab, your primary responsibility is to ensure the quality and safety of cell therapy products through rigorous testing and analysis. You will work in a highly regulated environment, adhering to Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) to support the development and production of cell-based therapies. This role requires a strong attention to detail, analytical skills, and the ability to work collaboratively with cross-functional teams. - Execute a variety of tests to assess the quality, purity, and potency of cell therapy products, including but not limited to viability assays, sterility testing, endotoxin...

Role Overview: As an Associate Scientist in Analytical Chemistry at Kenvue, you will be responsible for handling analytical testing activities for new product development projects, supporting changes to commercial products, and specific research-based assignments as part of Global operations. Your main role will involve delivering analytical testing and related documentation activities with a focus on compliance under the supervision of the team leader. Key Responsibilities: - Ensure qualification on assigned analytical technologies and instrumentation for testing capabilities. - Conduct testing on assigned analytical technologies such as HPLC/ UPLC, GC, IC, AAS, etc. - Execute the assigned ...

As a Material Planning & Inventory Management professional, you will play a crucial role in ensuring the smooth flow of raw materials and packaging materials for production. Your responsibilities will include: - Monitoring and managing RM & PM stocks to align with production plans - Maintaining optimal inventory levels to prevent stock-out situations and excess stock - Coordinating with the Purchase team to ensure timely procurement - Ensuring FIFO / FEFO and proper storage practices are followed - Conducting daily stock reconciliation and reporting In terms of Warehouse & Handling Operations, you will be responsible for: - Proper receiving, inspecting, storing, and issuing of RM/PM - Mainta...

Role Overview: As an Officer-Ammonia at Bunge, your role involves ensuring the smooth running of utility equipments and Vanaspati Production with a focus on quality and food safety. You will be responsible for operating and maintaining packing utility equipment such as Chillers, air compressor, ammonia system, cold rooms, and cooling towers. Additionally, operating the refinery & bakery ammonia plant will be part of your key responsibilities. Key Responsibilities: - Operate and Maintain the packing utility equipment including Chillers, air compressor, ammonia system, cold rooms, cooling towers, and Air Dryer. - Maintain the cold room cycle and ensure timely Vanaspati FG delivery to dispatch....

1. Starting business in a new village a. Village identification within the radius b. Feasibility study of the village based on demographics, activities and financial needs of the customers c. Assist the MC-IC in making the village approval 2. Sourcing of business a. Identification of customers and forming of Joint Liability Groups b. Filling up of the application form c. Verification of the residence and business of the customer d. KYC verification e. Pre-disbursement training f. Visiting potential customers in order to develop business 3. Disbursements a. Collection of KYC documents b. Assisting the MC-IC for disbursement activity completion c. Loan documentation 4. Collection of current du...

Reporting To Branch Manager 1. Starting business in a new village a. Village identification within the radius b. Feasibility study of the village based on demographics, activities and financial needs of the customers c. Assist the MC-IC in making the village approval 2. Sourcing of business a. Identification of customers and forming of Joint Liability Groups b. Filling up of the application form c. Verification of the residence and business of the customer d. KYC verification e. Pre-disbursement training f. Visiting potential customers in order to develop business 3. Disbursements a. Collection of KYC documents b. Assisting the MC-IC for disbursement activity completion c. Loan documentation...

1. Starting business in a new village a. Village identification within the radius b. Feasibility study of the village based on demographics, activities and financial needs of the customers c. Assist the MC-IC in making the village approval 2. Sourcing of business a. Identification of customers and forming of Joint Liability Groups b. Filling up of the application form c. Verification of the residence and business of the customer d. KYC verification e. Pre-disbursement training f. Visiting potential customers in order to develop business 3. Disbursements a. Collection of KYC documents b. Assisting the MC-IC for disbursement activity completion c. Loan documentation 4. Collection of current du...

Reporting To Branch Manager 1. Starting business in a new village a. Village identification within the radius b. Feasibility study of the village based on demographics, activities and financial needs of the customers c. Assist the MC-IC in making the village approval 2. Sourcing of business a. Identification of customers and forming of Joint Liability Groups b. Filling up of the application form c. Verification of the residence and business of the customer d. KYC verification e. Pre-disbursement training f. Visiting potential customers in order to develop business 3. Disbursements a. Collection of KYC documents b. Assisting the MC-IC for disbursement activity completion c. Loan documentation...

1. Starting business in a new village a. Village identification within the radius b. Feasibility study of the village based on demographics, activities and financial needs of the customers c. Assist the MC-IC in making the village approval 2. Sourcing of business a. Identification of customers and forming of Joint Liability Groups b. Filling up of the application form c. Verification of the residence and business of the customer d. KYC verification e. Pre-disbursement training f. Visiting potential customers in order to develop business 3. Disbursements a. Collection of KYC documents b. Assisting the MC-IC for disbursement activity completion c. Loan documentation 4. Collection of current du...

1. Starting business in a new village a. Village identification within the radius b. Feasibility study of the village based on demographics, activities and financial needs of the customers c. Assist the MC-IC in making the village approval 2. Sourcing of business a. Identification of customers and forming of Joint Liability Groups b. Filling up of the application form c. Verification of the residence and business of the customer d. KYC verification e. Pre-disbursement training f. Visiting potential customers in order to develop business 3. Disbursements a. Collection of KYC documents b. Assisting the MC-IC for disbursement activity completion c. Loan documentation 4. Collection of current du...

1. Starting business in a new village a. Village identification within the radius b. Feasibility study of the village based on demographics, activities and financial needs of the customers c. Assist the MC-IC in making the village approval 2. Sourcing of business a. Identification of customers and forming of Joint Liability Groups b. Filling up of the application form c. Verification of the residence and business of the customer d. KYC verification e. Pre-disbursement training f. Visiting potential customers in order to develop business 3. Disbursements a. Collection of KYC documents b. Assisting the MC-IC for disbursement activity completion c. Loan documentation 4. Collection of current du...