38 Gmp Standards Jobs - Page 2

Receipt of Material- Physical Receipt & Entries in System ( Books) Proper Handling & Storage of Raw Material (Chemicals) As per Material Data Sheet. Working Knowledge of SAP/ERP. Follow QMS/TQM as per Standards. Adherence to GMP & Safety Standards. Required Candidate profile Ensure Compliance to ISO & OHSAS Procedures for Storage & Preservation of Material. Coordination with F&A for Timely invoice submission

As the Design Head of Packaging Machinery, you will be responsible for leading mechanical design and research & development activities for high-speed packaging and bottling machinery to ensure continuous innovation, superior quality, and optimal performance. Your key role will involve overseeing the design of various components such as moulds, conveyors, filling lines, and packaging machinery. You will be tasked with managing the entire product development lifecycle from conceptualization to commissioning. It will be your responsibility to ensure compliance with CE, ISO, GMP standards, and customer specifications. Additionally, you will be expected to implement design automation, CAD best pr...

At Cepheid, we are dedicated to enhancing healthcare by providing rapid and precise diagnostic testing solutions. Our relentless mission inspires us every day as we strive to develop innovative and scalable technologies to address the most challenging health issues worldwide. Join our team and be part of the journey to revolutionize molecular diagnostics from concept to delivery, ultimately improving patient outcomes in various healthcare settings. Working with us offers you the opportunity to make a significant global impact in an environment that nurtures professional growth and advancement. As a Process Engineer, your primary responsibility is to develop and implement strategies to enhanc...

As a Design Draftsman at Truvera, a concept to commissioning company in the Pharma and speciality chemical field, located in Vadodara, you will be responsible for creating technical, engineering, and architectural drawings. Your main tasks will include utilizing Computer-Aided Design (CAD) software to produce detailed plans and blueprints, collaborating with engineers and architects, ensuring drawings adhere to industry standards, and making revisions as needed to meet project specifications. To excel in this role, you should have proficiency in Technical Drawing and Engineering Drawings, experience with Architectural Drawings and Drawing principles, familiarity with GMP standards and regula...

As a Draftsman/woman in the pharmaceutical industry, you will play a crucial role in creating detailed technical drawings and documentation essential for various aspects of pharmaceutical facility design, including equipment layout, process flow, and other engineering requirements. Your responsibilities will encompass producing 2D and 3D CAD drawings for architectural, mechanical, piping, electrical, and HVAC systems. Your work will involve preparing layouts for cleanrooms, labs, production suites, and utility areas based on Good Manufacturing Practice (GMP) standards. Your role will also entail collaborating with project engineers and architects to interpret technical designs and specificat...

You are passionate about improving health care through fast, accurate diagnostic testing. Your mission at Cepheid drives you every moment of every day as you develop scalable solutions to solve complex health challenges across the world. You are involved in every stage of molecular diagnostics, from ideation to the delivery of testing advancements that enhance patient outcomes. As a member of the team at Cepheid, you have the opportunity to make an immediate impact on a global scale in an environment that promotes career growth and development. Cepheid collaborates with six fellow Danaher Diagnostics companies to address the world's major health challenges by developing diagnostic tools that...

As an experienced and proactive Environment, Health & Safety (EHS) Manager, you will lead and manage all EHS initiatives in our dairy processing facility. Your responsibilities include developing, implementing, and maintaining programs to ensure a safe and compliant work environment in alignment with regulatory standards and company policies. A deep understanding of food-grade processing, hygiene protocols, waste management, and regulatory compliance specific to the dairy industry is essential for this role. Your key responsibilities will involve EHS program development & management, overseeing health & safety initiatives, ensuring environmental compliance, managing emergency preparedness, a...

As a Supervisor at Sigachi located in Dahej, you will play a crucial role in ensuring the smooth production operations in line with GMP standards. Sigachi, a renowned manufacturer of Excipients for Pharma, Nutra, and food industries, has been a key player in the market since its inception in 1989. With multiple facilities in Telangana and Gujarat, Sigachi has solidified its position as a leading producer of Microcrystalline Cellulose globally. Operating under various certifications like EXCiPACT GMP, SGMP, HACCP, EDQM CEP, and ISO 9001:2015, Sigachi has built a reputation for delivering high-quality products across continents. Your primary responsibilities will include planning and organizin...

You should have an ITI or Diploma in Electrical Engineering or equivalent qualification. Additionally, you should possess at least 3 years of experience working as an industrial electrician in a pharmaceutical or GMP-regulated manufacturing environment. Your role will require a strong understanding of industrial wiring, control panels, and basic PLC operations. It is essential that you can read and interpret electrical drawings and schematics proficiently. Knowledge of GMP standards is mandatory, and you should be willing to work in shifts if required. Preferred skills for this role include basic knowledge of automation systems, familiarity with cleanroom operations, and pharma-grade equipme...

As a Production Manager at Natural Biogenex Pvt. Ltd. (NBPL), a subsidiary of Natural Capsules Limited, located in Vasanthnarasapura KIADB Industrial Area, Tumkur, Karnataka, you will play a crucial role in overseeing and managing API production operations. With 10-15 years of experience in the industry and a background in MSc.(Organic Chemistry)/ MTech Chemical (Technology)/ BSc.(Chemistry), you will ensure the highest quality standards for pharmaceutical ingredients in compliance with international regulatory bodies such as USFDA, WHO, and ICH-Q7A. Your responsibilities will include supervising day-to-day shop floor operations, workforce management, batch planning, and execution. Your expe...

The job involves being a team member of the Engineering Maintenance & Reliability Team within the Active Pharmaceutical Ingredient department of the Manufacturing division. Your primary responsibility is to execute maintenance activities in the plant, ensuring minimal breakdowns and maximum efficiency while adhering to safety and GMP standards. You will support the Senior Engineer in planning, scheduling, and executing maintenance activities to ensure plant and equipment availability, capacity, integrity, and reliability as per company policies and procedures. Additionally, you will be responsible for maintenance tasks in the Manufacturing, Packing, and utility areas as assigned by the Senio...

Key Responsibilities: Create and review Process and Instrumentation Diagrams (P&IDs) following industry standards and GMP requirements. Develop 3D models for process skids and plant piping systems using industry-standard software (e.g., AutoCAD Plant 3D, REVIT). Coordinate with multi-disciplinary teams including process, mechanical, and automation engineers. Ensure compliance with ASME BPE standards. Essential Skills: Experience with modular/skid design. Knowledge of cleaning and sterilization processes. Strong analytical and problem-solving abilities. Excellent attention to detail. Good communication and documentation skills. Ability to work independently and as part of a team.

KEY RESPONSIBILITIES The incumbent will work closely with the Corporate Quality Assurance teams under the supervision of the Digital Business Partner, leading articulation of key technology and digital requirements and ensuring successful rollouts. More specifically s/he will lead the following responsibilities: Business Analysis: Point of contact and between business, IT, end user and other cross functional teams during the project or maintenance phase. Collect data, analyse & define the business and user requirements. Analyse business problems and facilitate in IT solution evaluation. Work closely with managers and end users to have buy-in for the proposed solution. Creating a detailed bus...