4062 Gmp Jobs - Page 4

We are looking for a highly skilled and experienced F&B Associate to join our team at Ginger Hotels. The ideal candidate will have 2-5 years of experience in the hospitality industry, preferably in hotels and restaurants. Roles and Responsibility Manage food and beverage operations to ensure high-quality service and customer satisfaction. Coordinate with kitchen staff to prepare and cook food according to recipes and presentation standards. Maintain cleanliness and organization of food storage areas, refrigerators, and freezers. Ensure compliance with health and safety regulations and maintain a safe working environment. Collaborate with other departments to achieve sales targets and improve...

The Qualification Expert for Analytical Instrumentation is responsible for ensuring the accuracy and reliability of analytical instrumentation used in various scientific processes. They will be responsible for assessing and verifying the qualifications of these instruments, as well as documenting and maintaining the records. About the Role MAJOR RESPONSIBILITIES Perform qualification assessments on analytical instruments to ensure compliance with regulatory requirements and industry standards. Develop and execute qualification protocols, including installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ), for analytical instruments. Collaborate with ...

Department - Quality Assurance, Number of open positions - 4 Master s degree in finance, accounting, or related field.Qualified chartered accountant professional with minimum 2 years of experience Job requirements Key Responsibilities: Monitor and enforce Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP) on the shop floor Conduct in-process quality checks during manufacturing and filling operations Review batch manufacturing records (BMR) and batch packing records (BPR) for completeness and compliance Investigate non-conformities, deviations, and customer complaints, and assist in CAPA implementation Coordinate with production, QC, and R D to ensure adherence to SOPs and...

Mynvax is a biotechnology company focused on the discovery, development, and scalable manufacturing of thermostable recombinant vaccines against respiratory and emerging viral infections. The company collaborates closely with leading academic and translational partners including the Indian Institute of Science, Bangalore. Role Execute and optimize cell culture processes using E. coli and insect cell systems (Sf9, High Five, etc.) and baculovirus expression workflows. Operate and maintain bioreactors (1-50 L scale) for process development and optimization studies. Perform cell revival, maintenance and prepare cell banks. Perform media and feed optimization, infection kinetics, and yield analy...

Location : Rajpura City : Rajpura State : Punjab (IN-PB) Country : India (IN) Requisition Number : 42274 Business Title Technician - Production Reporting to AM - Production Role Purpose Statement: Responsible for performing various tasks to operate, monitor, troubleshoot, perform preventive maintenance, safety, food safety, chemical safety and GMP etc Main Accountabilities: Operate churn cum blending of VP refinery RO refinery in accordance with established procedure and guidelines. Operate short mix, bleacher, autoclave, deo, Fractionation, and acid oil plant in accordance with established procedure and guidelines. Perform necessary pre-operation activities to ensure proper equipment startu...

Specific Responsibilities: Drive the client and regulatory audits and address the audit finding related to BMP5 Facility. Facilitate and monitor the performance of regular facility walkthroughs and internal quality audits for biologics operations to ensure adherence to the implemented systems and compliance with regulatory requirements including data integrity assessment. Responsibility for establishment and implementation of a robust cleaning, sanitization sterilization process. Monitoring of equipment which are related to Facility Management and responsible for adherence to current SOP and safety requirements. Lead and monitor management of garments and general consumables as per BMP5 faci...

Job Summary To implement efficient, quality processes at ARPL in alignment with global standards that comply with heath authority requirements. IPQA activities, CCR initiation, Review, Approval, QA assessment, QA Responsible final closure of CCR in QMS Track wise. SME for Swab/Rinse sampling, AQL, Cross contamination, MMaR S / MPaR S MMaR S / MPaR s Review approval in live link. Job Responsibilities Ensure adherence to GMP regulatory requirements by one and all in the facility. Planning Co-ordination of daily activities in Manufacturing and Packing areas. Co-ordination ensuring timely execution of in-process activities for manufacturing packaging. Preparation and Review of SOP Routine monito...

Rsponsible for managing the initial and periodic validation and qualification activities for various areas and facilities. This includes drug substance and drug product manufacturing equipment, cold storage equipment, utilities, media fill of aseptic areas, and smoke studies. The role requires a seasoned professional with experience in validation and qualification processes within the pharmaceutical or biotechnology industry, specifically on injectables. Key Responsibilities: Validation and Qualification Management : Manage the validation and qualification activities for manufacturing equipment such as Autoclaves, Tunnels, Lyophilizers, Bioreactors, and Dry-heat Sterilizers. Handle the valid...

Hi We are hiring for Executive/ Sr. Executive (Production) for Gr. Noida and Panipat Location. Candidate must be from food processing industry with 2-6 yrs exp. in production with good knowledge of computer (word, Excel etc).

We are hiring for the role of Quality Executive Job Description / Key Responsibilities Inspect raw materials, in-process, and finished products to ensure compliance with quality standards. Monitor and enforce adherence to ISO, GMP, and HACCP quality standards. Identify defects and conduct root cause analysis to prevent recurrence. Develop and implement Standard Operating Procedures (SOPs) for quality control processes. Maintain detailed records of inspections, test results, and reports . Coordinate with the production and maintenance teams to address quality issues. Train and supervise quality control staff or line inspectors. Handle customer complaints related to quality and provide correct...

Role & responsibilities Ensure proper documentation and control of records related to incidents, deviations, change controls, and other QMS-related activities. Maintain and update records as per established SOPs and regulatory requirements. Oversee day-to-day warehouse activities, including material receipt, storage, issuance, and handling. Manage material handling activities through RF and GRN systems in SAP. Ensure proper segregation, identification, and traceability of materials. Coordinate with Sales and Supply Chain teams to ensure smooth and timely dispatch of goods. Prepare packing lists, consignment checklists, and related dispatch documents in line with SOPs.. Competencies Strong or...

Department: Production Tasks : Plan and execute shift-wise production schedules to meet output and quality targets. Supervise machine operation, material flow, and manpower allocation on the shop floor. Monitor process parameters and take corrective action to maintain product specifications. Maintain production logbooks, reports, and system entries accurately and timely. Coordinate with QA, Maintenance, and Stores for smooth plant operation. Ensure strict adherence to GMP, ISO, BIS (IS 5405) and Safety standards. Implement productivity improvement initiatives. Monitor wastage, yield, and process efficiency, and recommend improvements. Conduct training for operators and contract workers on ma...

We are seeking a qualified Production Chemist to join our team ac Vasai (E). • Overseeing daily production of color cosmetics • Ensuring quality control and batch consistency experience (5-10 years) in color cosmetics production

1.Production Manager- 12 to 15yrs in production with regulatory experience GMP,HACCP,FSSAI/USFDA guidelines Collaborate with R&D ,QC and Maintenance departments for smooth production flow troubleshoot manufacturing issues and implement continuous process improvements. 2. Shift Incharge- 5 to 8yrs in production with regulatory experience Maintain good housekeeping and cGMP in shop floor Preparation of new documents like BPCR and SOP etc 3.Operators- 3 to 5yrs in production ONLY MALE CANDIDATES ARE PREFFERED

We are looking for a highly motivated and enthusiastic F&B Steward to join our team at YAAN Wellness Retreat. The ideal candidate should have 0-2 years of experience in the hospitality industry. Roles and Responsibility Manage food and beverage service areas, including preparation and presentation. Ensure high-quality customer service by responding promptly to guests' needs and resolving issues professionally. Maintain cleanliness and organization of food and beverage equipment and supplies. Collaborate with other departments to ensure seamless service delivery. Participate in inventory management and stock control of food and beverage supplies. Develop and maintain knowledge of menu items, ...

Role Overview: As a Quality Assurance Specialist at this organization ranked among the top 500 global companies, you will play a crucial role in monitoring the overall Quality System status of the distribution center. Your compliance to drug, medical device, and local regulations will ensure the maintenance of quality processes through procedures, training, and inspections. Key Responsibilities: - Ensure all staff is trained in their job functions, including GMP standards. - Write and revise Standard Operating Procedures as necessary. - Conduct regular facility inspections, maintain records, summarize findings, and report them accordingly. - Coordinate or assist in corrective actions and pre...

Role Overview: You have the opportunity to join the Quality Assurance Team at Zydus Takeda Healthcare Private Limited as a Senior Executive / Executive - Quality Assurance. In this role, you will be responsible for In-Process Quality Assurance (IPQA), ensuring that manufacturing processes comply with regulatory standards and company quality policies to maintain the highest level of product integrity and safety. Key Responsibilities: - Perform real-time monitoring of production processes to ensure adherence to quality standards. - Conduct routine inspections and in-process checks to verify compliance with specifications and protocols. - Collaborate with production and quality control teams to...

Bachelor's degree with over 8 years of experience in designing and developing solutions in Trackwise Proven track record of successfully completing Trackwise project implementations, including stages such as discovery, design, development, testing, and deployment. Experience working in a GMP environment, 5+ years in an IT Systems Role. Expert knowledge of GMP Quality Management to include CAPA/Deviation, Lab Exception, Product Complaint, Audit, and Supplier Management. SDLC/GAMP, Business Analysis, and Enterprise Systems Management. General knowledge of GxP Quality Processes and Systems (GMP, GLP, GCP, GVP, GDP) Familiarity with other enterprise systems and modules such as ERP, SCM, and PLM,...

**Job Description:** **Role Overview:** As a Bench Scientist at our company, you will be responsible for conducting experimentation in the area of formulation research and development, process development, regulatory and intellectual property for global markets. You will play a crucial role in planning and executing experiments in line with Quality by Design (QbD) principles, using One Factor at a Time (OFATs) and Design of Experiments (DOE). Your work will involve applying scientific principles of QbD, DoE, statistics, and scale-up principles to products at different stages from selection to launch. Additionally, you will work on understanding intellectual property scenarios, developing str...

Job Description QC Manager (Plastic & Protective Packaging) Department: Quality Assurance / Quality Control Reporting To: Plant Head / General Manager Operations Location: Surajpur Industrial area ( Greater Noida ) Job Summary The QC Manager is responsible for planning, implementing, and overseeing all quality control activities within the packaging plant. This includes ensuring that plastic packaging products such as thermoformed trays, cutlery, foam, and shrink/poly wraps meet customer requirements, industry standards, and internal quality benchmarks. The role demands leadership in team management, process improvement, and compliance to regulatory and certification norms. Key Responsibilit...

We are seeking a highly experienced Quality Assurance leader to drive Corporate QA initiatives across multiple formulation manufacturing sites. The incumbent will be responsible for strengthening the company's Audit, Compliance, and Validation/Qualification (VQ) framework, ensuring adherence to global regulatory standards, and maintaining continuous inspection readiness . This is a strategic corporate role requiring 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). Ens...

About Hikal Ltd. Hikal is manufacturing Active pharmaceutical ingredients (APIs), custom manufacturing, intermediates and advanced intermediates. For more details login www.hikal.com Role & responsibilities Understanding of Reactor handling , BMR handling / BPCR Handling . Knowledge of Process handling, Documentation. set up and adjust the machine as per batchs requirement . Preparing of Area for Audits Sound Knowledge of Chemical Engineering. Hardworking and dedicated Preferred candidate profile Candidate should be from B.Sc(Chemistry) /B.E/B.Tech(Chemical Engineering) B.Sc/Diploma(Chemical Engineering) can also attend the interview Compensation will be paid as per company standreds Walk-in...

Key Responsibilities Perform routine analysis of Raw Materials (RM), Packaging Materials (PM) and Finished Goods (FG) to ensure compliance with product specifications and quality standards. Conduct validation and verification of all critical procedures related to new equipment, new processes and new product introductions. Implement, monitor and maintain hygiene and sanitation practices to ensure compliance with Good Manufacturing Practices (GMP) and Good Hygiene Practices (GHP). Organize and conduct training sessions for plant personnel on GMP, GHP and safety protocols to promote a culture of food safety and quality. Maintain accurate and up-to-date documentation as per HACCP and FSSC 22000 ...

We are looking for a skilled Demi Chef De Partie with 4 to 8 years of experience to join our team at Courtyard by Marriott, responsible for preparing high-quality Indian Curry and Tandoor dishes. The ideal candidate will have a strong background in cooking and a passion for delivering exceptional culinary experiences. Roles and Responsibility Assist the Head Chef in planning and preparing menus for special events and functions. Develop and maintain high standards of food quality, presentation, and taste. Collaborate with other kitchen staff to ensure seamless service delivery. Conduct regular menu costing and inventory management. Ensure compliance with health and safety regulations and comp...

Handling of Documentation, Issuance and retrieval of documents,Training software Employee should have Pharmaceutical QA doc cell experience.