309 Gmp Compliance Jobs - Page 5

Job Title: Production Manager Location: - Ecotech VI Greater Noida, U.P Shift: Day Shift Responsibilities: A Production Manager in a Nutraceutical company is responsible for overseeing the manufacturing process, ensuring efficiency, quality, and compliance with industry regulations. Their key responsibilities include: 1. Production Planning & Management Develop and implement production schedules to meet demand. Optimize resources (manpower, machinery, materials) for efficiency. Ensure timely production while minimizing waste and downtime. 2. Quality Assurance & Compliance Ensure all products meet GMP (Good Manufacturing Practices), FDA, and other regulatory standards. Work closely with the Q...

Oversee complete Production & Manufacturing operations at the Pharmaceutical Formulation Unit Ensure smooth execution of batch manufacturing for OSD (Tablets, Capsules, Dry Syrups) Ensure compliance with FDA regulations and GMP guidelines Monitor production efficiency, process optimization & manpower management Coordinate with QA, QC, and Regulatory teams for smooth operations Handle regulatory audits, validation, and documentation processes OSD Manufacturing Tablets, Capsules, Dry Syrups FDA Approval & Regulatory Compliance (WHO-GMP, Schedule M preferred) Production Planning & Process Optimization Team Leadership & Manpower Management

You are competent in two engineering disciplines and possess thorough site knowledge. Your responsibilities include: - Diagnosing and correcting equipment problems - Maintaining facilities and production equipment - Involvement in installation, testing, inspecting, and commissioning new electrical equipment - Calibration of instrumentation - Rectification of regulatory deviations Accountability is key as you will be responsible for: - Maintaining and documenting maintenance work - Improving maintenance procedures in compliance with GMP - Communicating effectively any issues during handover - Providing feedback on completed engineering tasks, including root causes and outstanding issues You w...

As a Deputy Manager at Syngene International Ltd., your main responsibility will be handling QMS documentations like CC, CAPA, and Investigations, as well as managing EDMS documents, study protocols, and qualification protocols. You will be in charge of performing activities related to Engineering & maintenance at Biologics Unit 03 while ensuring GMP compliance and error-free operations. It will be crucial for you to follow all EHS requirements at the workplace to ensure individual and plant safety. - Complete all assigned mandatory trainings related to data integrity, health, and safety measures on time - Ensure compliance to quality systems and current good manufacturing practices - Develo...

Experience in maintenance and repair is must. Responsible for equipment preventive & breakdown maintenance. Responsible for boiler & Utility operation and maintenance. Technician and fitter shift planning. QMS Documentation & Logbook preparation Perks and benefits Accommodation & Transportation Mediclaim Policy

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.

Job Description As the Head of Quality Assurance at Instrumentation & Control Solutions in Indore, you will be responsible for leading and managing all Quality Assurance activities within the pharmaceutical unit. Your primary focus will be to ensure compliance with cGMP, regulatory standards such as WHO-GMP, USFDA, EU, and internal Quality Management System (QMS) protocols. Key Responsibilities - Lead QA operations, overseeing documentation, audits, and ensuring compliance. - Manage deviations, Corrective and Preventive Actions (CAPA), Out of Specification (OOS) investigations, and regulatory audits. - Supervise Standard Operating Procedures (SOPs), validations, and training programs. - Ensu...

Role Overview: As a Trainee / Jr. Officer at our company, you will be responsible for supporting pharmaceutical operations by utilizing your educational background in B. Pharm / M. Pharm. Your key responsibilities will include having a basic knowledge of various pharmaceutical processes such as Granulation, Blending, Compression, Capsule Filling, Coating, and Bottle Packing. Additionally, you will be required to demonstrate hands-on understanding of equipment like Glatt Integrated Line, Blenders, Sifter, Mill, Fette Compression Machine, Capsule Filling, Auto Coater, Bottle Filling Line, etc. It is essential to have knowledge of preparation & execution of SOPs, BMR/BPR documentation, equipmen...

Possesses a comprehensive understanding of Good Manufacturing Practice (GMP) regulations, guidelines, and safety standards. Demonstrates the capability to oversee equipment operations within the designated Kilo lab manufacturing area. Ensuring adherence to critical process parameters as outlined in the Batch Manufacturing Record (BMR). Able to coordinate with service departments to meet the requirement(s) of the Kilo lab. Knowledge of basic engineering calculations, Piping and Instrumentation Diagram (P&ID) preparation, equipment sizing, and mapping. Strong analytical and problem-solving skills. Excellent communication and interpersonal skills.

Design and execute validation protocols for process and cleaning validation activities, including IQ (Installation Qualification), OQ (Operational Qualification), PQ (Performance Qualification), and CV (Cleaning Validation). Develop and maintain a validation master plan (VMP) that aligns with regulatory requirements and organizational goals. Conduct process validation studies to ensure manufacturing processes consistently produce products that meet predefined quality attributes. Analyze process performance and critical parameters during validation runs and document results. Ensure adherence to Good Manufacturing Practices (GMP) during all validation activities. Develop and execute cleaning v...

Shop floor experience is required in the Tablets and Capsules section and sound knowledge of solid oral equipment functioning and operating principle Perform real-time monitoring of manufacturing and packaging processes to ensure adherence to GMP, SOPs, and regulatory requirements. Conduct in-process checks for critical quality attributes (e.g., weight, hardness, uniformity, and packaging integrity) at defined stages of production. Ensure timely documentation and approval of batch manufacturing records (BMR) and batch packaging records (BPR). Lead and coordinate qualification activities, including Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification ...

Job Title: Senior Executive RM/PM Store & Warehouse Department: Production Warehouse Location: RM/PM Store – Manesar - Gurugram Reporting To: Sr. Associate: RM/PM-Warehouse Key Responsibilities: Oversee receipt, storage, and issue of Raw Material (RM) & Packaging Material (PM). Ensure proper documentation (GRN, issue slips, stock registers, SAP/ERP entries). Monitor material handling, stacking, FIFO/FEFO compliance. Maintain stock accuracy through regular cycle counts and physical verification. Coordinate with Purchase, QC, Production teams for smooth material flow. Ensure compliance with GMP, safety, and audit requirements. Manage space utilization and housekeeping in the warehouse. Supervi...

Handling Quality management system and regulatory support & reviewer. Change control, CAPA,OOS,APQR. Compliance verification at Site. Dispatch compliance. BMR and Work sheet compliance before release. Document and Data control and training.

Job Description Summary Manages all Quality Assurance activities associated with the product development and product support processes in BD TCI. Ensures that all Design Control quality elements are established and documented to provide a safe and effective product that meets customer needs. Lead evolution and improvement of the product development process, policies and procedures which will enable design teams to respond rapidly to customer needs. Runs multiple projects directly while managing other quality engineering resources running separate projects. Provides leadership, quality oversight and direction, scheduling, decision-making, problem-solving and team-building capabilities. Mainta...

Roles : To ensure GMP compliance to approved procedures / practices as per SOP. Responsible for review of analytical records, handling of QMS related activities for Quality control. Ensure compliance for Quality Control (Analytical, Bioassay and Microbiology sections). Review of Specifications & STPs related to Quality Control department. Compliance verification in Quality control department by frequent lab visits. To ensure compliance to Retention/control sample management and document cell management in line with SOP for retention, destruction and withdrawals. Periodic review of Water & EMP trends and escalation if any abnormalities/OOT/OOS observed. Preparation, Review of stability schedu...

Position Summary: The Deputy Manager Warehouse will be responsible for planning, organizing, and overseeing all warehouse operations, ensuring efficient receipt, storage, dispensing, and dispatch of materials. The role requires strict adherence to cGMP and GDP standards, effective audit management, and strong leadership to guide the warehouse team. Key Responsibilities: Manage end-to-end warehouse activities, including material receipt, storage, dispensing, and dispatch . Ensure compliance with cGMP, GDP, and regulatory guidelines in all warehouse operations. Prepare for and actively participate in regulatory and customer audits ; implement corrective and preventive actions. Develop and moni...

This role is responsible for technology transfer, process scale-up, equipment selection, and process validation in API manufacturing. The position ensures that the selected equipment aligns with process requirements, product quality, safety, and regulatory compliance, while supporting continuous improvement and operational excellence. Key Responsibilities: 1. Technology Transfer & Scale-up Lead the transfer of chemical processes from R&D to manufacturing. Evaluate and optimize process parameters for scale-up using mass and energy balances. Collaborate with Engineering for facility fitment, equipment readiness, and plant execution. 2. Equipment Selection & Sizing Analyse process requirements ...

Oversee QA For Contract Manufacturing: Draft Agreements, Review Batch Docs, CoAs, Deviations, And Artwork. Ensure GMP Compliance, Traceability, And Regulatory Alignment. Support IPQA Checks, Sampling, Audits, And Real-Time Issue Resolution. Required Candidate profile Skilled in corporate QA documentation, third-party coordination, and artwork review Manage change control, audit readiness, and traceability Ensure regulatory compliance and product release approval

Responsibilities: * Ensure GMP compliance at all times * Monitor production costs & optimize efficiency * Collaborate with R&D on new product launches * Manage material planning & inventory levels Provident fund

Role & responsibilities The incumbent must have experienced working on microbial cell culture, recombinant antibody manufacturing from microbial expression systems. Should have experience in manufacturing on 1000L bioreactor and handling automated CIP, CIP and TFF systems. Experience on manufacturing of consistency and commercial scale up batches. Good knowledge of technology transfer from R&D scale to commercial plant manufacturing. Should be responsible for qualification of equipments and facility. Sound knowledge on GMP and working in close with cross functional departments for execution of manufacturing activities within specified timelines. Should lead, motivate and train the team in GM...

Job Description Summary Manages all Quality Assurance activities associated with the product development and product support processes in BD TCI. Ensures that all Design Control quality elements are established and documented to provide a safe and effective product that meets customer needs. Lead evolution and improvement of the product development process, policies and procedures which will enable design teams to respond rapidly to customer needs. Runs multiple projects directly while managing other quality engineering resources running separate projects. Provides leadership, quality oversight and direction, scheduling, decision-making, problem-solving and team-building capabilities. Mainta...

Job Title: Production Executive No. of Positions: 2 Company Name: The South Indian Manufacturing Company Company Website: www.saibol.com Location: Madurai (Local candidates preferred or must be willing to relocate) About the Company The South Indian Manufacturing Company is a reputed pharmaceutical manufacturer specializing in quality-driven processes and GMP-compliant production systems. Qualifications B.Pharm / M.Pharm / B.Sc Chemistry / M.Sc Chemistry Experience Freshers (0-2 years) are eligible Experienced candidates (3+ years) also welcome; higher salary will be offered based on profile Key Responsibilities Assist in ointment manufacturing (weighing, mixing, filling, packing, labeling) ...

Conduct regular inspections and audits of products, processes, and systems.Identify quality issues and implement corrective actions.Develop and maintain quality documentation, including SOPs and checklists.

Perform routine and non-routine quality control tests using analytical techniques such as HPLC, GC, UV-Vis, IR, titration, and others.Develop, validate, and optimize analytical methods as per regulatory guidelines.

Conduct regular inspections and audits of products, processes, and systems.Identify quality issues and implement corrective actions.Develop and maintain quality documentation, including SOPs and checklists.