2755 Gmp Jobs - Page 17

Roles and Responsibilities Prepare dossiers, variations, renewals, and amendments for USFDA regulatory submissions. Coordinate with third-party agencies for audits and inspections (USFDA, WHO). Ensure compliance with GMP requirements through self-inspection and third-party audits. Maintain liaison with government authorities for licensing and approvals. Provide guidance on legal metrology regulations to ensure accurate product labeling. Desired Candidate Profile 7-12 years of experience in Regulatory Affairs or related field (nutraceutical industry). Bachelor's degree in Pharmacy (B.Pharma) from a recognized institution. Strong knowledge of FSMS, Food Safety, HACCP, FSSAI, Legal Metrology, a...

Production Planning: Doing Daily/Weekly & Monthly Planning ofProduction based on availability of PM, BM in the ERP. To share the firmplan with the procurement team for the current week and tentative planof following week to order packing materials. Check whether the blendsare approved before taking planning for Packing. Planning the Manpowersbased on the production plan for the Month. Production & Packaging Execution: Responsible for achieving monthlyProduction Goals. Estimating the amount of material, equipment, andlabor required for production. Promptly addressing and resolvingproduction issues to minimize delays in production, Monitor the MSH level& do the changes in planning accordingly....

HE should be able to implement Pharmaceutical SOP for Production department with help of Manpower and Materials, Shift wise produciton as per schedule . Implementaton SOP on ground level under guildelines -SOP of GMP /FDI in various Produciton lines Required Candidate profile HE should be able to implement Pharmaceutical SOP for Production department with help of Manpower and Materials, Shift wise produciton as per schedule under guildelines of GMP-FDI for production

1. Factory & Warehouse Hygiene and Pest Control Ensure strict implementation of hygiene and sanitation protocols across the factory and warehouse. Oversee pest control measures and maintain compliance with food safety standards. Monitor and verify routine cleaning and deep cleaning (ALC) schedules in production and packaging areas. 2. Production & Packaging Quality Assurance Ensure adherence to quality parameters throughout the production and packaging processes. Conduct regular verification of quality control checks, including for online processes, gifting, and customized orders. Monitor CCP and OPRP to ensure process safety and consistency. 3. Material Verification & Warehouse Monitoring M...

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 & Visual Inspection & Packing Aseptic operations/ QMS / SKID / Multi-vessel / SVP / Visual Inspection / Packing / VI (Senior Officer / Officer / Associate) Experience - 02 to 07 Years Qualification - B. Pharmacy/ M Pharmacy / Msc /Bsc / Diploma / ITI Engineering (Instrumentation / Process Equipment Maintenance) (Senior Executive / Executive / Senior Officer) Experienc...

1. Quality Systems & Documentation: Develop, implement, and maintain GMP-compliant QMS. Oversee change control, deviations, CAPA, incident management, risk assessment, and market complaints. Ensure GDP compliance in all QA documentation, including SOPs, batch records, specifications, and MOAs. Prepare and revise SOPs, distribute and retrieve old versions, and manage documentation control. Handle QMS activities like return goods, non-conformities, and investigation reports (5-Why, 6M method). 2. Validation & Qualification: Review and approve URS, IQ, DQ, OQ, and PQ protocols and reports. Manage process validation, cleaning validation, equipment qualification, and facility validation. Conduct ...

Lead end-to-end development of new products including concept development, prototyping,trials, and commercialization. Work closely with cross-functional teams (QA, Production, Marketing, Procurement, and SupplyChain) to ensure successful product rollouts. Develop and optimize recipes for popcorn, extruded snacks, roasted snacks, and flavouredvariants. Conduct shelf-life studies, sensory evaluations, and process validations. Source and evaluate new ingredients, flavours, seasonings, and packaging materials incollaboration with suppliers. Manage pilot trials and scale-up activities at the plant level. Monitor industry trends, competitor products, and consumer preferences to support innovationp...

Tasks Lead the Quality Assurance (QA) and Quality Control (QC) operations across all manufacturing units at HLL-KFB, ensuring compliance with cGMP, ISO 13485, WHO-GMP and other regulatory standards. Oversee batch release, deviation management, CAPA, change control, validation, and documentation systems. Ensure timely testing and release of raw materials, packing materials, in-process, and finished products through QC lab operations. Coordinate internal audits, external inspections (by CDSCO, State FDA, WHO, ISO), and ensure audit preparedness at all times. Guide the implementation of Quality Management Systems (QMS) and drive continual quality improvement initiatives. Lead the development an...

Key Responsibilities: Assist in monitoring daily quality parameters across raw material, in-process, and finished product stages. Conduct basic testing of raw materials, intermediates, and finished products as per quality standards. Ensure adherence to company quality systems, food safety norms, and regulatory requirements. Support implementation of GMP, HACCP, FSSAI and other quality/food safety standards. Maintain accurate lab records, documentation, and reports. Coordinate with production teams to ensure compliance with quality standards. Participate in audits, inspections, and sampling activities. Escalate deviations/non-conformities to seniors for corrective and preventive action

Microbiological Testing & Analysis: Perform microbiological testing of raw materials, processed chicken, water, air, and surface swabs as per standards. Identify and analyze microbial contamination, ensuring corrective actions are implemented. Maintain detailed records of microbiological reports and analysis. Food Safety & Hygiene Compliance: Monitor and enforce hygiene and sanitation practices across the slaughterhouse. Conduct routine checks to ensure compliance with FSSAI, HACCP, ISO, and GMP standards. Ensure proper functioning and calibration of laboratory equipment used for microbiological testing. Quality Control & Documentation: Maintain and update microbiological documentation as pe...

A Production Officer is responsible for carrying out shift production activities by following instructions from superiors like the AGM or Sr. Manager. A key part of the role is ensuring all raw materials and required batch sheets are available on time for planned batches. You will coordinate with the Engineering department for timely maintenance and with QC for in-process and finished product analysis. The position requires you to strictly follow GMP and safety norms, attend EHS training, and adhere to relevant Standard Operating Procedures (SOPs) . You will monitor and maintain stipulated parameters such as temperature, pH, and pressure during batch processing and record any observed abnorm...

Responsibilities: To receive operating instructions for the shift from Production Officer/Executive/Assistant Manager and above. Ensure batch processing is carried out strictly in accordance with batch records and as instructed. Operates the process ensuring that all parameters are strictly followed and within the specified limits. Shall submit the in process / intermediate sample to QC lab for analysis as per the batch instruction. Responsible for maintaining Good House Keeping in all the areas of Production department. Ensures that the equipment s are always clean from outside. Follow GMP and Safety Instructions during the work. To make entries in BPCR, BCLR, PDR and all cGMP related docum...

Your responsibilities will include, but are not limited to: Design, plan and interpret scientific experiments for projects at different clinical phases of drug substance and drug product development with minimal guidance. Well versed with regulatory guidelines, scientific literature, technology transfer and interpretation of the results to draw conclusions in reports. Provide scientific guidance to the laboratory associates Write, review and/or approve analytical documentation in timely and high-quality manner, such as releases, analytical batch records, method validations, stability, technical reports, SOP s etc. ensuring compliance with Novartis and health authorities guidelines Helping to...

Design, plan, perform, interpret and report results of scientific experiments for the preparation and timely delivery of drug substances (DS), drug products (DP), processes and procedures within a multifunctional project team coordinated by a Project Leader. Manage technical lab/plant activities. Management TrackLead a team for the development of pharmaceutical/biological/cell gene therapies working in a small manufacturing plant environment. Execute the functional strategy and drive operational excellence in line with TRD vision and strategy. Ensure full portfolio support in line with GDD, Sandoz, NTO and NIBR plans. SANDOZ: Associate Scientist: Design, plan, perform, interpret and report r...

Key Responsibilities: Participate in finalizing Basic and Detailed Engineering concepts (Electrical/ Instrumentation/ Extra low voltage- LAN /Telephone / CCTV / Access Control, Firefighting system & other fields, as applicable). Review/ Approve Electrical /Instrumentation/ Extra low voltage package services drawings & documents supplied by the consulting firm. Ensure Installation/ Execution of Electrical, Instrumentation & Extra low voltage package services inline to GMP, GEP, ISPE & other applicable standards as applicable. Perform in - depth review of the project to schedule work and estimate costs. Oversee all onsite and offsite Electrical & Instrumentation services to monitor compliance ...

Key Responsibilities: Managestechnical complaintsinvestigationsto determine root causes and implement corrective actions to prevent recurrence. Collaborate with cross-functional teams to gather data, lead, and perform Root Cause Analysis to identify the likely root cause of events. Review and approve complaints as the site Investigation approver. Manage multiple investigations concurrently. Periodically analyze trends in technical complaints. Participate in audits and inspections, including inspection readiness activities. Handle data integrity escalations. Implement and drive global Data Integrity (DI) network initiatives Essential Requirements: More than Over 10years of practical experienc...

Must-Have Skills: 2+ year s of experience in validation in a GMP-regulated environment (pharmaceutical, biotech, medical devices, etc.). 5+ to 9 Years overall experience in Testing with 2+ years of experience in validation experience is mandatory. Experience leading software validation projects. Proficiency in developing and executing validation protocols (IQ, OQ, PQ), reports, and related documentation. Familiarity with computer system validation and software validation is a plus Strong problem-solving and analytical skills Excellent communication and teamwork skills. Good-to-Have Skills: Experience with automated and computer-controlled systems validation (21 CFR Part 11) Education and Pro...

The Manager - Quality Control (QC) will be responsible for ensuring that all products manufactured for third-party clients meet quality standards, regulatory requirements, and client specifications. You will oversee all QC activities in the production process, lead a team, manage testing procedures, and ensure adherence to quality guidelines for skincare, hair care, body care, and personal care products. Your key responsibilities will include developing, implementing, and maintaining QC processes to ensure products meet quality and safety standards. You will monitor production processes, work closely with the production and R&D team to identify and resolve any quality-related issues, and ove...

About Alkem: Alkem Laboratories Limited is an Indian multinational pharmaceutical company headquartered in Mumbai, that manufactures and sells pharmaceutical generics, formulations and nutraceuticals in India and globally over 50 countries. The company has consistently been ranked amongst the top five pharmaceutical companies in India. Alkem's portfolio boasts renowned brands like Clavam, Pan, Pan-D, and Taxim-O, which are recognized among the top 50 pharmaceutical brands in India. Key Responsibilities: Conduct training needs analysis for both sales and non-sales teams to identify areas for development and enhancement. Design and deliver customized training programs tailored to enhance sales...

As a Project Engineer specializing in pharmaceutical machinery manufacturing at CoralPT Worldwide Pvt. Ltd., located in Ankleshwar, Gujarat, you will play a crucial role in managing projects from inception to completion with a focus on quality, efficiency, and adherence to industry standards. Your expertise in Blenders, Stainless steel reactors, fluid bed dryers, RMG/HSMG, Tray dryers, and other pharmaceutical equipment will be instrumental in ensuring the successful design, development, and execution of projects related to pharmaceutical machinery. Your key responsibilities will include overseeing the installation, commissioning, and validation of equipment, collaborating with cross-functio...

Instrument Analysis GC/HPLC for QC department Min 2-5 only API CO 1 to 3 year experiance HPLC/GC analysis like Assay, RS, Chiral, Purity, Residual solvent analysis Location- Nandesari, Vadodara, Gujarat, India.

Job Title : Executive COE Department : Operations / Strategy / Quality Location : [Insert Location] Experience : 35 Years Education : B.Sc / M.Sc / B.Tech Industry : Manufacturing / Wellness / FMCG / Ayurveda Job Summary We are seeking a dynamic Executive COE to lead strategic initiatives and drive operational excellence across departments. The ideal candidate will be responsible for implementing quality standards, optimizing processes, and supporting cost-efficiency and compliance across the organization. Role & responsibilities Drive improvement projects, policies, and strategic initiatives Implement and maintain standards such as ISO, FSSAI, AYUSH, and GMP Develop, update, and monitor SOP...

The Accounts Receivable Specialist is responsible for managing and maintaining the company-s accounts receivable process. This includes ensuring timely and accurate invoicing, handling queries from customers and internal business stakeholders. Responsibilities: Process Revenue invoices on Monthly/Daily etc. Coding/referencing Debtor invoices Generation of GMP Multiple kind of sales invoices Working with client to obtain relay Ad Hoc Analysis work of for the finance function Continuous improvement of this role within the finance department Completion/Updation of charging sheet Manage and support the funding/billing process. Month-End Closing via multiple Finance ad hoc reports. Take care of A...

The Packing Supervisor will oversee and manage the packaging operations of oral solid dosage pharmaceutical products in compliance with USFDA, cGMP, and company standards. This role ensures timely execution of packing activities, adherence to quality and safety norms, and coordination with cross-functional teams to meet production targets. Key Responsibilities Supervision & Operations Oversee day-to-day packaging operations for OSD products. Ensure compliance with USFDA, cGMP, and SOPs during all packing activities. Monitor and maintain the integrity of batch records and documentation. Quality & Compliance Ensure packaging processes meet quality standards and regulatory guidelines . Coordina...

Photon Interactive is looking for enthusiastic and detail-oriented Data Entry Operators (Freshers) to join our dynamic team on a 6-month contract . This role is ideal for candidates who are looking to start their career in the IT/Software industry and gain experience in a fast-paced, professional environment. Key Responsibilities: Accurately enter data into internal systems, spreadsheets, or databases Maintain and update records with high attention to detail Perform regular data backups and ensure data integrity Assist in verification, validation, and cleanup of data Coordinate with team members to ensure timely completion of tasks Maintain confidentiality and security of data Requirements: ...