35 Gmp Guidelines Jobs - Page 2

This is a full-time on-site role for a Quality Control Officer. As a Quality Control Officer, you will be responsible for ensuring the quality and safety of products through laboratory testing and data analysis. Your primary duties will include conducting analytical tests using instruments such as HPLC, GC, UV, IR, Water content by KF, Auto titrator, and Dissolution Apparatus. Additionally, you will be responsible for quality assurance activities and effectively communicating results with team members and clients. To excel in this role, you should possess strong analytical and laboratory skills, along with hands-on experience in operating various testing instruments. Your ability to follow S...

As a Production Chemist at our WHO-GMP Pharma Factory, you will play a crucial role in overseeing the production processes of tablet medicines to ensure quality and efficiency in manufacturing. Your responsibilities will include managing manufacturing operations, maintaining quality control standards, optimizing processes, documenting production activities, ensuring equipment maintenance, adhering to safety protocols, and collaborating with the quality assurance and production teams for seamless operations. To qualify for this role, you should hold a Bachelor's degree in Pharmacy, Chemistry, Biotechnology, or a related field, along with a minimum of 2 years of experience in a production chem...

As a Supply Chain Specialist for the Active Product Ingredient (API), Excipients, consumables, and component sourcing in the fast-growing clinical division, your main role involves identifying and agreeing upon the supply chain. You will be responsible for sourcing new products and suppliers, ensuring compliance with regulatory requirements and staying informed about market trends. Negotiating competitive prices is essential to support the business in achieving its targets and margins efficiently. Your responsibilities also include processing orders from other departments, managing the supply chain effectively, and maintaining a supplier base aligned with the company's commercial objectives....

Key Responsibilities : Technical Skills Candidate should have good understanding of Chemistry and biology pharma R&D lab. Candidate should have exposure of lab computing support in handling lab instruments needs. Candidate should have implementation experience of Electronic Lab notebooks (ELN) preferably Biovia or Perkin Elmer Candidate should be familiar with GMP guidelines. Experience in demonstrating a track record of delivering scientific solutions in the pharmaceutical and CRO industry. Experience in the implementation of Informatic applications like (Electronic Laboratory Notebooks(elNB), Laboratory Information Management System, Chromatography Data system (CDS) and other scientific ap...

As a Quality Assurance Officer at our organization, your primary responsibility will be to review and ensure compliance of Standard Operating Procedures (SOPs), Batch Manufacturing Records (BMRs), and protocols across all our sites. You will also be required to conduct internal audits and provide support during external regulatory audits from bodies such as USFDA, WHO, MHRA, and others. Monitoring Corrective and Preventive Actions (CAPA) implementation and change controls will be part of your duties to ensure data integrity and Good Manufacturing Practice (GMP) compliance across our manufacturing units. You will also be responsible for evaluating product quality trends and preparing quality ...

As a Sr. Executive / Asst Manager (Shift Incharge) in the Production Fermentation (Upstream) department at Natural Biogenex Pvt. Ltd., you will play a crucial role in overseeing and leading shift-wise operations effectively. With 6 to 10 years of experience and a background in M.Sc. / B.Tech. / B.Sc. in Biotechnology, Microbiology, or Industrial Microbiology, you will be responsible for ensuring the smooth functioning of fermentation processes in compliance with SOPs and production schedules. Your key responsibilities will include supervising and monitoring shift activities, ensuring operational efficiency, timely escalation of issues, maintaining documentation as per GMP standards, managing...

You are urgently required to join Lavanya Healthcare Limited as a Sachet Packing Machine Operator. Your responsibilities will include operating, cleaning, and performing minor maintenance on sachet packaging machines. It is essential that you have 1 to 2 years of experience in sachet packing or similar machine operation and possess a 10th or 12th pass education qualification. Your role will be in the Production / Packaging department, and you should be well-versed with GMP guidelines. The work schedule is Monday to Saturday from 9:00 AM to 6:00 PM. The job type is full-time, and the work location is in person at Near Phillanto Company, Behra Road, Dera Bassi, Punjab. In addition to a competi...

The Form-Fill-Seal (FFS) Operator position entails operating and maintaining Form-Fill-Seal machines utilized in the production of IV Fluids. Your primary responsibility will be to ensure the smooth and efficient operation of these machines, along with monitoring the production process to uphold high standards of quality and safety. You will be tasked with operating and monitoring the Form-Fill-Seal machines, making necessary adjustments, and conducting routine maintenance procedures as required. It is crucial to ensure the proper functioning of the machines, troubleshoot and address any issues that may arise during production, and maintain compliance with standard operating procedures (SOPs...

Trending Job Description Key responsibilities. Responsible for working with Technology Transfer, Production, and the Client to generate, revise, and approve master production records (MPRs) and any other documents associated with the commercial products in the manufacturing, e.g., SOPs, material specifications, technical reports, etc. Preparing unplanned and planned deviations for responsible processes and forming the investigation team. Collaborates with Process Development (PD), Technology Transfer (TT), Operations, Quality Control (QC), and Quality Assurance (QA) in problem-solving activities, including deviation writing and CAPA closure. Work with project and engineering teams to replace...

As a Project Manager in the pharmaceutical industry with a PhD (Doctor of Philosophy), your role involves overseeing and managing projects related to drug development, clinical trials, regulatory compliance, or other pharmaceutical initiatives Your advanced academic background in pharmaceutical sciences provides you with a deep understanding of the industry and scientific principles You develop project plans, timelines, and budgets, considering the specific objectives, deliverables, and resource requirements of pharmaceutical projects You coordinate with cross-functional teams and stakeholders to ensure effective project execution Risk Assessment and Management: You identify potential risks ...