2778 Gmp Jobs - Page 25

Required For Manufacturing Role Production Support for instruments and applications in manufacturing area for Life Science customer. Should have Knowledge of ITSM ticketing tool including handling of service requests and incidents in GxP managed environment. SKILLS: Life Science domain ,GMP and GDP Knowledge ,ITSM tool, Backup and restoration activities of GxP systems, Desktop engineering support.

JOB DESCRIPTION Jubilant Bhartia Group Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S Bhartia and Mr. Hari S Bhartia with strong presence in diverse sectors like Pharmaceuticals, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Jubilant Bhartia Group has four flagships Companies- Jubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited. Currently the group has a global workforce of around 43,000 employees. About Jubilant Ingrevia Limited Jubilant Ingrevi...

Seeking a IPQA Executive to ensure skincare products meet regulatory, safety & quality standards. Work closely with manufacturing, R&D, and QC teams. Requirement: 2+ years of QA experience, preferably in cosmetics or pharma manufacturing. Required Candidate profile Skincare manufacturing & QC expertise Knowledge of FDA, GMP, ISO regulations Attention to detail & procedural compliance Strong analytical, problem-solving & com skills Ability to work with GMP proces

Production planning & line balancing Process Control & Improvement Quality & GMP Compliance Resource & Inventory Management Team Supervision

Dear Applicants, Greeting from Biophore India pharmaceutical Pvt Ltd, We have opening for Formulation DQA Department Development Quality Assurance / Formulation Quality Assurance R&D: Handling of QMS documents and Ensure the SOP compliance Review of Formulation Analytical Development Documents & Formulation Product Development Documents. Method Validation and Transfer Protocols and Reports Product development with QbD approach Responsible for ensuring GMP/GLP/GDP compliance in the Formulation and Analytical areas as per the respective SOPs. Review of FRD activities (LNBs, BDRs, PDRs, MFRs and MPR) SOPs and Guidelines Preparation and Review and Approval of SOPs. Responsible for conducting Int...

R.K.Hospital (Gajuwaka Hospitals Pvt. Ltd.,) is looking for Quality Executive to join our dynamic team and embark on a rewarding career journey Understand customer needs and requirements to develop effective quality control processes Devise and review specifications for products or processes Set requirements for raw material or intermediate products for suppliers and monitor their compliance Ensure adherence to health and safety guidelines as well as legal obligations Supervise inspectors, technicians and other staff and provide guidance and feedback Oversee all product development procedures to identify deviations from quality standards Inspect final output and compare properties to require...

Aquachem Industries Private Limited is looking for QC Chemist to join our dynamic team and embark on a rewarding career journey Chemical Analysis: Conduct chemical and physical testing on raw materials, in-process samples, and finished products to assess their quality and compliance with specifications Instrument Operation: Operate and maintain laboratory equipment and instruments, such as HPLC, GC, UV-Vis spectrophotometers, and other analytical instruments Data Analysis: Analyze and interpret test results, ensuring accuracy and consistency in data reporting Quality Control: Implement and maintain quality control standards and procedures to ensure that products meet regulatory and quality r...

Job description 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

Job Description Receipt and Storage of Raw and Packing Materials. Dispensing of Raw and Packing materials. Should have knowledge of SAP . Should have good communication skills. Exposure to regulatory enviornment. Work Experience Should have experience of 2 to 5 years in dispensing of raw and packing materials. Education Diploma in Pharmacy Competencies

As a Quality Assurance professional in the Pharmaceutical & Life Sciences industry, your primary responsibilities will revolve around the review and approval of Supplier Qualification documents, including NSQR, VQ Documents, etc., from Raw material / Packing material manufacturers and external service providers. You will be tasked with preparing and distributing corporate approved supplier lists, New product tentative approved supplier lists, and Tentative approved supplier lists to all SQAs. Your role will also involve providing support to site QA for regulatory audits and Customer audits, reviewing vendor notifications, and coordinating with RA & SCM for further requirements. Additionally,...

As a QA/QC Assistant at HempCann Solutions Private Limited, located at Plot No. 266/3328, Gangadhar Meher Marg, Post KIIT, Bhubaneswar - 751024, your primary responsibility will be to oversee manufacturing operations to ensure workflow efficiency, compliance, and continuous improvement. This role involves key duties such as production planning, quality assurance, maintenance, and statutory compliance. Your responsibilities will include recording incoming raw materials, in-process products, and finished product samples as per requisition. You will be issuing test reports based on intimation slips and analytical data sheets. Additionally, you will be responsible for preparing quality specifica...

As a Capsule Filling Machine Operator SA9 at Lavanya Healthcare Limited in Dera Bassi, Punjab, your main responsibility is to efficiently operate and maintain the SA9 Capsule Filling Machine. You will be tasked with ensuring the accurate filling of hard gelatin capsules in accordance with cGMP, safety, and quality standards. Your key responsibilities will include setting up and running the SA9 Capsule Filling Machine according to the daily production plan, loading empty capsules and powder/blend into appropriate hoppers and magazines, monitoring capsule weight, alignment, and sealing during production runs, conducting in-process checks, ensuring cleanliness and line clearance of machine part...

As a Process Equipment Systems Engineer in the pharmaceutical manufacturing industry, your primary responsibility will be to design and specify process equipment systems for manufacturing plants. This involves ensuring that the equipment aligns with project goals and meets regulatory standards such as GMP, FDA, and EMA. You will need to select appropriate equipment based on factors like material compatibility, process requirements, automation, and cost-effectiveness. Your role will also involve developing equipment specifications, datasheets, and technical documentation for procurement and installation purposes. It is essential to have hands-on experience in installing isolator-based filling...

The role of Site Quality Head within the Global Quality & Compliance business unit at Ahmednagar involves ensuring the supply of high-quality, GMP compliant products. Your main responsibilities will include defining operational strategies for quality system management, finalizing quality assurance and quality control goals, and ensuring alignment with Sun Pharma compliance standards and regulatory requirements. You will provide leadership to achieve all quality accountabilities for QA, QC, and Stability at the site. Proactively assessing quality issues, ensuring compliance with regulatory requirements, and tracking quality assurance/control metrics will be crucial aspects of your role. Your ...

As a Senior Executive Process at our Krishnapatnam location in India, your role will involve taking overall responsibility for shift production and planning. You will be accountable for various key tasks including production planning and scheduling, material balance management for oil, chemicals, and by-products, as well as ensuring that variable costs are maintained within approved budget levels. In this position, you will collaborate with the commercial and purchase departments to facilitate the dispatch of co-products, by-products, and hazardous waste, ensuring the smooth operation of the plant. Additionally, you will work closely with the engineering department to implement preventive ma...

You are a passionate, dedicated, and detail-oriented professional, and an exciting opportunity awaits you to join the Quality Assurance Team at Zydus Takeda Healthcare Private Limited in Turbhe, Navi Mumbai. This joint venture between Zydus Lifesciences and Takeda Pharmaceuticals is committed to maintaining the highest level of quality and safety in its products. As a Senior Executive / Executive in Quality Assurance, based in Navi Mumbai, you will play a crucial role in In-Process Quality Assurance (IPQA). Your responsibilities will include monitoring and controlling the quality of products during the production process to ensure compliance with regulatory standards and company quality poli...

At Elanco (NYSE: ELAN) - it all starts with animals! As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets. We're driven by our vision of Food and Companionship Enriching Life and our approach to sustainability - the Elanco Healthy Purpose - to advance the health of animals, people, the planet and our enterprise. At Elanco, we pride ourselves on fostering a diverse and inclusive work environment. We believe that diversity is the driving force behind innovation, creativity, and overall business success. Here, you'll be part of a company that values and champions new ways of thinking, work ...

You will be joining Kenvue as an Associate Scientist, Analytical Chemistry based in Mumbai. At Kenvue, we are passionate about everyday care and science, with a global team of diverse individuals dedicated to delivering the best products to our customers. As a Kenvuer, you will have the opportunity to impact the lives of millions of people every day. We prioritize people, care, trust, and courage, offering brilliant opportunities for you to shape our future and yours. In this role, you will be responsible for various analytical deliverables in new product development projects, supporting changes to commercial products, and specific research-based activities as part of Global operations. Your...

The Document Controller position at SEPAM in Chennai is a full-time on-site role that involves managing project documentation, records, and communication tasks related to document management. The ideal candidate should possess hands-on experience in GMP, Equipment Qualification, DQ/IQ/OQ/PQ, as well as experience in FMCG projects. Key responsibilities include document management, project documentation, and records management. The successful candidate will need to demonstrate strong communication skills, attention to detail, and organizational skills. Proficiency in document control software is essential for this role. Additionally, the ability to work effectively in a team environment is cru...

Lead and optimize sterile injectable production, ensuring cGMP compliance, timely delivery, and continuous improvement GMP compliance, planning, output/yield/OEE monitoring, team management, audits, BMR/BPR approval, coordination with QA/QC,

Ensures Products meet established standards by developing and implementing quality control procedures, conducting audits, monitoring performance metrics, and resolving quality issues. Maintain documentation, Ensure compliance with Pharma regulations Required Candidate profile M.Sc - B. Pharma - M. Pharma - BE - Chemical Good knowledge Of Quality Assurance Good Command over English And Computer Must be ready to face customers Inquiries And Local And US FDA Authority

At Cepheid, we are passionate about improving health care through fast, accurate diagnostic testing. Our mission drives us, every moment of every day, as we develop scalable, groundbreaking solutions to solve the world's most complex health challenges. Our associates are involved in every stage of molecular diagnostics, from ideation to development and delivery of testing advancements that improve patient outcomes across a range of settings. As a member of our team, you can make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development. Cepheid is proud to work alongside a community of six fellow Danaher Diagnostics companies. Togethe...

Designs, implements and maintains quality assurance protocols and methods for processing materials into partially finished or finished products Responsible for planning, implementing and managing compliance of manufacturing and production processes with internal and external safety, quality and regulatory standards requirements for worldwide distribution Designs methods and procedures for inspecting, testing and evaluating the precision and accuracy of production processes, production equipment and finished products Performs analysis of reports and production data to identify trends and recommend updates or changes to quality standards and procedures when necessary May assure compliance to i...

Blancher area: ensure that equipment is set to the standard required for the specific product process. Monitor water levels, quality, and usage. o Ensure temperature, retention times, alarms are all set within the RS view system. Monitor / record yield loss, colour, texture and any breakage. SAAP / Dextrose System: ensure that equipment is set to the standard required for the specific product process. Monitor Dextrose / SAPP percentage, water quality and ingredient usage. Ensure temperature and alarms are all set within the RS view system. Monitor / record colour and any breakage. Dryer Area: ensure that equipment is set to the standard required for the specific product process. Ensure tempe...

Should handle stores activities independently. Inward of material and entries Goods Inward Memo Preparation Handle Engineering Stores Inwards, Inspection, rejection, Issue, Bill review Experience in ERP / SAP HANA for entries Service Entry / Desktop items ordering. Compliance: Ensuring compliance with regulatory requirements, Good Manufacturing Practices (GMP), and other relevant standards. Coordination with various Department like Purchase, Finance and Suppliers Spare management Documentation: Maintaining accurate records of stock movements, expiry dates, and other relevant information. Compliance and Regulations: Ensuring compliance with all relevant regulations and industry standards Docu...