2755 Gmp Jobs - Page 4

As an R&D Associate Cosmetics/Skincare at Vilvah, you will play a crucial role in researching, formulating, and developing high-quality skincare and haircare products that align with our clean beauty and sustainability values. Your expertise in cosmetic science, formulation skills, and creative approach to product innovation will be key to your success in this dynamic and rapidly growing Direct-to-Consumer Ecommerce brand. **Key Responsibilities:** - Research emerging consumer trends, active ingredients, product formats, and packaging innovations in the beauty & personal care industry. - Conduct bench-scale experiments for new product development and validate performance through standard tes...

As a Production Assistant at our food production line in Supa, Ahmednagar, you will play a crucial role in supporting daily operations. Your main responsibilities will include: - Assisting in food preparation, processing, and packaging - Maintaining quality control to ensure compliance with health and safety standards - Monitoring product quality and reporting any deviations or issues to the supervisor - Labeling, packaging, and storing products correctly - Maintaining cleanliness and sanitation in the work area according to food safety standards - Following standard operating procedures (SOPs) and production schedules - Assisting in inventory checks, restocking of supplies, and scheduling t...

Role Overview: You will be responsible for coordinating breakdown activities, improvement activities, preventive maintenance schedules, overseeing external contractors, and ensuring compliance with safety and quality standards in the Instrumentation section. Your role will involve reviewing production operations, training team members, managing spare parts inventory, and leading troubleshooting efforts to minimize downtime. Additionally, you will maintain budgets, support technical activities, and ensure regulatory compliance, contributing to the efficient and reliable operation of instruments, equipment, and facilities. Key Responsibilities: - Coordinate with cross-functional team members t...

You will be responsible for the following key accountabilities: - Initiating and leading production startups and change overs. - Trouble shooting of the injection molding process. - Planning and executing resin and tool changes based on production schedules/trials. - Participating in continuous improvement initiatives that support production efficiency, scrap reduction, proving of new tools, and alternative material evaluation. - Generating daily production documentation including end-of-shift production/scrap reports and collection of process control data. - Maintaining and practicing safe working habits and participating in safety initiatives. - Performing general tasks including but not l...

Job Title: Maintenance Engineer Location: HUL Chhindwara Plant Department: Engineering & Maintenance Req Id: Job Summary: The Instrumentation Engineer will be responsible for maintaining and optimizing instrumentation systems to ensure seamless plant operations. The role requires strong expertise in Industrial Automation, IT & Operational Technology (OT) to integrate and improve plant efficiency, safety, and reliability. Key Responsibilities: Instrumentation & Control Systems: Maintain, calibrate, and troubleshoot field instruments, sensors, and automation equipment (PLC, SCADA, DCS). IT & OT Integration: Develop and support industrial network architecture , ensuring effective communication ...

As a part of the Technology Transfer Team under the R&D vertical at Palli location, your primary responsibilities will include: - Preparing Master BMR and BPRs - Managing documents - Coordinating with various departments such as Regulatory Affairs, Manufacturing, Warehouse, Quality Assurance, Quality Control, and Engineering for the execution of Scale-up and Exhibit batches - Reviewing GMP related documents - Selecting equipment at the facility Your role will involve facilitating Change Controls for various reasons and initiating them due to revisions in BMR/BPRs and other PD related changes. You will also study critical parameters during scale-up batches to optimize the CPPs and CQAs, provi...

Job Description Summary This role is responsible for developing and implementing health and safety plans, enforcing policies, and evaluating practices and facilities to ensure compliance with legal guidelines. They conduct training sessions, monitor compliance, investigate accidents, and provide recommendations for improvement. They also communicate guidelines to employees, report on health and safety issues, and develop relevant policies to maintain a safe workplace. Their focus is on promoting occupational health and safety and minimizing risks for employees. Job Description About the Role: Implement and enforce HSSE policies, procedures, and practices in accordance with company, local, an...

Job Description Maintain receipt and dispensing of raw materials and packing materials. Update daily stock registers and bin cards. Prepare stock statements. Ensure cleaning, arrangement, and status labelling in packing material stores. Maintain humidity control, cleaning, and calibration. Handle materials properly and ensure safe storage of RM/PM. Receive and dispense materials as per GMP procedures.

Job Description Prepare and implement quality assurance policies and procedures. Ensure compliance with standards, quality policy, and safety regulations. Prepare, review, issue, distribute, and archive GMP documents for finished product manufacturing. Review and release raw materials, packing materials, intermediates, and finished products. Review BMR, BPR, ECR, and analytical raw data for product approval. Monitor cleanliness and labelling of finished product containers. Review and approve OOS, deviations, non-conformances, and investigations. Ensure all operations are performed according to SOPs and GMP requirements. Review and approve SOPs, protocols, and reports. Conduct and coordinate ...

About Company Job Description Roles and Responsibilities • Shop Floor Management • Manpower Planning • To maintain a proper ratio of trained and untrained employees • Improvement in FTF (First Test Failure) at different stages of production • To collect and analyze rejection data • Training of New Operator • Skill Matrix Preparation For Operator • To keep inventory control in the shop floor • Lead by example, ensuring a safe and efficient workplace is maintained at all times • Achieve the required company quality standards ensuring both internal and external customer satisfaction • Ensuring the KPIs are monitored and targets achieved. • Drive performance of team members, giving direction and...

Develop and design packaging materials in compliance with product, regulatory, and customer requirements. Coordinate with vendors for development of cartons, labels, foils, bottles, and other packaging components. Conduct trials for new packaging materials and evaluate their performance on production lines. Ensure packaging complies with GMP, regulatory guidelines, and stability study requirements. Prepare and review packaging material specifications, artworks, and BOMs. Collaborate with QA, RA, Production, and Supply Chain teams for smooth implementation. Monitor packaging innovations, cost optimization, and sustainability initiatives. Maintain packaging documentation, approvals, and record...

Familiar with GMP guidelines and batch manufacturing processes. Skills: MS Office and effective communication. Responsible for managing daily production activities and documentation. Required Candidate profile Experience: 2-3 years in Pharma/API Qualification: B.Sc / M.Sc in Chemistry Experience in Oncology production preferred.

Good knowledge of QC processes and GMP compliance. Skills: MS Office proficiency and strong communication skills. Responsible for quality testing, documentation, and ensuring product compliance with industry standards. Required Candidate profile Experience: 5-6 years in Pharma/API Education: B.Sc / M.Sc in Chemistry Must have hands-on experience with HPLC.

Role & responsibilities 1. To daily analytical planning within the team to deliver results to production team within agreed analytical timeline. 2. To monitor & procure the required essential items like, chemicals, reagent, glassware, columns, spares, consumables, gas cylinders etc. 3. To manage all qc equipments periodically servicing and maintenance at the time of break dawn. 4. Supervision of all chemists work which are distributed. 5. To ensure all qc instruments periodically calibrated & preventive maintenance program. 6. To ensure all raw material, in process & Finished products analysis report review and monitoring online analysis & its documentation. 7. To prepare the Standard Operat...

Role & responsibilities Sampling and analysis of Raw Materials, In-process samples, Finished Products , and Stability samples as per SOP and test methods. Preparation and standardization of volumetric solutions, reagents , and reference standards . Performing routine chemical, instrumental (HPLC, GC, UV, FTIR), and microbiological testing (for applicable roles). Equipment/instrument calibration and maintenance logs. Participation in method validation , stability studies, and process validation activities. Adherence to Good Laboratory Practices (GLP) and regulatory standards. Supporting internal and external regulatory audits (like USFDA, WHO-GMP). Reporting deviations, OOS results, and non-c...

Role & responsibilities 1. Develop and optimize cost-effective, scalable, and robust API processes suitable for GMP manufacturing 2. Conduct lab-scale and pilot-scale experiments to evaluate process parameters and critical quality attributes (CQAs) 3. Collaborate with R&D, Analytical, QA/QC, and Production teams for successful technology transfer 4. Prepare and review technology transfer documents 5. Provide on-site support during scale-up and commercial manufacturing, troubleshooting in case of any technical issues 6. Ensure compliance with regulatory guidelines (ICH, USFDA, EMA, etc.) during development and transfer 7. Identify and implement process improvements to enhance yield, purity an...

Roles and Responsibilities * Ensure compliance with food safety regulations, HACCP, and GMP guidelines. * Conduct regular audits and root cause analysis for quality issues. * Develop and implement corrective actions to prevent recurrence of non-conformities. * Collaborate with suppliers to ensure supplier quality standards are met.

A QC Officer performs visual inspections, tests, and measurements on raw materials, in-process products, and finished goods. This is done to identify any defects or deviations from the quality standards and specifications. Required Candidate profile Previous experience in a quality control, quality assurance, or manufacturing environment is highly valued. A strong understanding of quality control principles, testing methods

Role & responsibilities Review source documentation for master data objects such as laboratory methods and analysis Create/ build master data objects in the LIMS, including test methods, specifications, sample plans, and instruments Ensure data consistency, accuracy, and compliance with internal SOPs and external regulatory requirements (e.g., FDA, ISO, GxP) Support LIMS validation activities, including documentation and testing. Troubleshoot and resolve data-related issues within the LIMS Collaborate with a team of master data builders working across various sites for the LIMS deployment Preferred candidate profile 2+ years of experience working with LIMS platforms (Ideally, Caliber) Strong...

SAP Quality Management (QM) System Specialist responsible for implementing, configuring, and supporting SAP QM processes and solutions across manufacturing and quality operations. The role focuses on master data management, MICs, inspection planning, usage decisions, certificate profiles, and integration with external systems such as LIMS. Ensures compliance with GMP and internal quality standards. Act as regional IT Business Partner for SAP QM, supporting the global IT team. Responsible for securing project execution in adherence to Lonza standards and policies. Provide IT support for complex incidents and problems (3rd level support Role & responsibilities: : Configure and support SAP QM f...

Role & responsibilities Job Responsibility: 1. Responsible for Compliance as per ISO 9001:2015, ISO 14001:2015, ISO 45001:2018 2. Coordination with QA department for all QMS related activities. 3. Responsible for QRM, Change control, Deviation, CAPA etc. 4. Responsible for Protocol and Report Preparation and execution of Process Equipment Qualification. 5. Coordinate with other department to ensure timely closure of QMS elements. 6. Responsible for compliance of Internal as well as External Audits. 7. Co-ordination for Training of employees on efficient documentation practices. 8. Ensure Good Documentation practices across the Department. 9. Ensure indenting and raising departmental CAPEX an...

To perform microbiological testing of raw materials, in-process samples, finished products, water, and environmental monitoring to ensure compliance with regulatory and company standards. Required Candidate profile Requirements: Microbiology testing / analysis work Skills: MS Office, Communication Skills

About Us Scimplify is a specialty chemicals manufacturing company offering a full-stack solutionfrom R&D and custom synthesis to large-scale manufacturing and doorstep delivery. Headquartered in Bengaluru, India, we serve multiple industries ranging from pharmaceuticals to agrochemicals and industrial chemicals to personal care and fragrances. We enable 500+ businesses across 20+ countries to develop and scale innovative chemicals from lab to commercial production. We have raised over $54 million from top tier investors such as Accel and Bertelsmann, We are a team of 250+ professionals with entities in India, Japan, USA, UAE, and Indonesia. Learn more about why Forbes thinks we are the top 1...

Req ID: 329333 NTT DATA strives to hire exceptional, innovative and passionate individuals who want to grow with us. If you want to be part of an inclusive, adaptable, and forward-thinking organization, apply now. We are currently seeking a Business Intelligence Specialist to join our team in Bangalore, Karn?taka (IN-KA), India (IN). Trakwise support resource Trackwise L2 Support for onprimse and Digital version of trackwise for a lifesciences client. Strong understanding of drug discovery or related life science industry experience is required. Strong knowledge in GLP/ GMP process / GXP process Need overall 3/ 4 yrs experience in supporting L2 TrackWise . Work independently on the L2 suppor...

As a Manufacturing Associate at our company located in Turbhe, Navi Mumbai, you will play a crucial role in supporting manufacturing operations for high-quality diagnostic/research products. Your background in Medical Laboratory Technology (DMLT/BMLT) or Lifesciences will be valuable in ensuring compliance with quality and safety standards. Freshers are also encouraged to apply. **Key Responsibilities:** - Carry out routine manufacturing activities following SOPs and GMP guidelines. - Perform sample preparation, testing, and documentation. - Operate, clean, and maintain laboratory/manufacturing equipment. - Assist in batch preparation, labelling, and packaging activities. - Maintain accurate...