4089 Gmp Jobs - Page 33

Eligibility Criteria Work Experience: Minimum 1 year (QA / QC in Manufacturing preferred) Qualification: M.Sc. / B.Sc. (Chemistry) Age: Up to 26 years Gender: Open (Any) Language Preference: English Hindi (good in English) Industry Preference: Manufacturing / Chemicals / Pharma Key Responsibilities Ensure compliance with QA standards, SOPs, and regulatory guidelines . Conduct sampling, testing, and analysis of raw materials, in-process, and finished products. Prepare and maintain QA documentation, reports, and audit records . Perform in-process quality checks to ensure production consistency. Coordinate with Production, QC, RD, and Supply Chain for quality-related activities. Support impleme...

You will be responsible for providing operational support to business functions in managing contractors and external services, as well as representing an interface between the internal community and external partners. Acting as a single point of contact for all activities in accordance with legislation, internal regulations, good practices, and business objectives via NOCC Engineering project team. - Provide operational and administrative support to the organization in coordinating and managing external contractors, and activities between internal stakeholders and external partners. - Create purchase orders and order equipment in SAP/ESHOP. - Care for and maintain electronic databases (Share...

In this leadership role, you are an internal technical master at the line level who ensures the line team is performing at a level that sustains and improves business results on one or more of 6 stars model. You model priority setting, manage the plan-do-check- adjust cycle and provide coaching and training for your team. How you will contribute You are a key ingredient in helping us change how the world snacks. You will operate and maintain equipment to build technical mastery and to deliver on safety, quality, cost, delivery, sustainability and morale targets, understanding losses in your area and taking the appropriate action to eliminate them. You will use autonomous and progressive main...

Role & responsibilities Prepare, review and submit regulatory documents for new drug applications, product registrations, amendments and renewals to the US, Brazil, EU, India and State Level authorities. Regulatory Submissions : Prepare and submit regulatory documents, including INDs (Investigational New Drug Applications) and NDAs (New Drug Applications) to regulatory authorities. Compliance and Licensing: Ensure compliance with regulatory requirements of US, Brazil, EU & India. Liaise with regulatory authorities for drug licensing, including product registrations, renewals and manufacturing licenses for local and international markets. Ensure timely submission of import licenses and NOcs (...

Role & responsibilities Key Responsibilities Execution of experiments: Conduct experiments to evaluate water purifier-based components such as sediment, carbon blocks, RO membranes, etc. Also need to evaluate product performance as per specifications. He/She will be working under guidance of scientists/chemists. Documentation: Maintain comprehensive and accurate records of all experiments, results, and observations in lab computer. Reporting: Summarize experimental findings and project progress to seniors regularly. Safety and Compliance: Strictly adhere to all laboratory health, safety, and regulatory protocols, including Good Laboratory Practices (GLPs) and Good Manufacturing Practices (GM...

Overview This role will assist the AMESA Supplier Quality Assurance team by conducting re-approvals annually for low risk designated suppliers located in AMESA that supply ingredients to Pepsico. This role will contact suppliers, request, and review returned pre-requisite data and documents, and re-approve the supplier site (3-year reapproval cycle). The role will update the required database(s) to support the re-approval. The expectation is ~200 supplier sites per year. The role will also support ancillary programs in AMESA SQA such as gathering program evidence from suppliers and brokers related to Food Fraud, Quality and Food safety Certifications and Contaminants programs as well as upda...

Job Title: ESO QA Specialist Location: Ankleshwar, Gujarat, India Seeking experienced QA professionals with 5+ years in GMP environments. Responsible for quality lifecycle management, audits, CAPAs, change control, and regulatory compliance.

Food Safety, FSSAI requirements, Maintenance of FSSC 22K Mgt. system, 3rd Party off-Role, Handling Customer complaints of unit and carry out RCA & CAPA, QMS/Verification/Validation, share results for SAP recording, Quality protocols are made-salt

Follow Good Manufacturing Practices (GMP) and Good Laboratory Practices (GLP). Review scientific literature and patents to identify new product development opportunities. Required Candidate profile Specialty Chemicals / Excipients / Pharmaceutical Field Whatsapp CV on 9724346949

Responsibilities: Production & Compliance: Oversight of External Preparations, and Oral Liquid Finished Formulations Ensure adherence to batch manufacturing records (BMR), batch packing records (BPR), and standard operating procedures (SOPs). Monitor and optimize production schedules to meet output targets and minimize downtime. In-process Quality Assurance (IPQA) and documentation control (DOC - QMS) Handling regulatory audits and ensuring compliance (PICs, EU, MHRA, WHO GMP etc.) electronic documentation systems including E-BMR, E-BPR, and E-Logbooks. Lead deviation investigations, CAPA implementation, and change control processes. Technical Expertise: Execute and document Design Qualifica...

Responsibilities: Analytical Operations: Perform and supervise analysis of Raw Materials (RM), Packing Materials (PM), and Finished Goods (FG). Operate and maintain analytical instruments :- HPLC, GC, UV-Vis, FTIR, Dissolution Apparatus Ensure compliance with GLP, 21 CFR Part 11, and data integrity standards. Review and approve analytical reports and LIMS entries , Quality Systems & Compliance Implement and monitor Quality Management Systems (QMS). Lead investigations for OOS, OOT, Deviations, and Laboratory Incidents. Prepare and review SOPs, STPs, and validation protocols. Ensure audit readiness and support regulatory inspections (USFDA, WHO-GMP, etc.) Documentation & Reporting Maintain ac...

Responsibilities: Assist in the preparation and compilation of regulatory dossiers (CTD / ACTD / eCTD) for product registration in various markets. Support the collection and review of technical documents from R&D, QA, QC, and Production departments. Help maintain regulatory databases, tracking sheets , and product registration status logs. Learn and follow current regulatory guidelines (USFDA, WHO, MHRA, EU, CDSCO) . Assist in the submission of post-approval changes , annual updates, and renewal applications. Draft and format regulatory documents, letters, and summaries . Help respond to regulatory agency queries and deficiencies under guidance. Ensure compliance with documentation practice...

Responsibilities: To manage day to day activities of quality control. To distribute QC related work as per production planning Preparation & reviewing of QC SOPs. To monitoring of all the Q.C. testing & its complete follow up. To approve all the Raw materials, packing materials, inprocess & finished goods after proper testing with its online documents. To review SOP and STP. Checking out daily & monthly calibrations as per designed SOPs. To prepare and execute calibration calendar of QC instruments. Review out of Specification results and its documents for final conclusion. To participate in investigate of market complaint, product recall Sample. Coordinate training of workers and staff for ...

Responsibilities: Project & Team Management Lead and manage multiple API development projects across various stages (Route scouting, lab development, scale-up, validation). Plan and allocate resources effectively among chemists and analysts. Mentor and guide junior scientists on technical and professional development. Process Development & Optimization Design and optimize synthetic routes with focus on yield improvement, impurity profile, and cost reduction. Identify and develop alternate synthetic strategies to mitigate IP challenges or improve process efficiency. Develop robust and scalable processes suitable for commercial production. Technology Transfer Prepare technology transfer docume...

Responsibilities: Documentation & Record Review: Review specifications, sampling instructions, test methods, and analytical reports. Review and approval of Batch Manufacturing Record (BMR), Batch Packing Record (BPR), Master Formula Record (MFR), and Equipment Qualification Records. Review completed Batch Production Records and Laboratory Control Records post-batch completion. Review analytical data, Calibration & Preventive Maintenance schedules, and external audit reports. Review and finalize Certificate of Analysis (CoA) for finished products. Review Draft Equipment Cleaning Records and Hold Time Study protocols/reports. Review Standard Operating Procedures (SOPs) and Annual Product Quali...

Responsibilities: Maintain database on regular basis. Verify data and correct database. Review and verify the entries. Respond to queries for information and access relevant files Comply with data integrity and security policies Required Skills: Logical thinking. Organizing. Good Computer knowledge Good communication.

Responsibilities: Report to the Production Manager on daily production activities and progress. Ensure adherence to Standard Operating Procedures (SOPs) for cleaning and equipment operations. Comply with Batch Manufacturing Record (BMR) specifications and promptly report any deviations. Enforce and maintain GMP compliance on the production floor. Participate in production planning, manpower allocation, staff training, and troubleshooting Out of Specification (OOS) issues. Supervise, verify, and approve 'Area Clearance' at the start and completion of production activities. Always maintain hygiene and cleanliness of the production floor. Meet production targets as per the approved production p...

We are looking for a Data Analyst to join our Employer Data Team in Bangalore . This is an amazing opportunity to work on U.S. Market Access landscape and evolving payer/employer models . The team consists of three colleagues and is reporting to th e Manager . We have a great skill set in data analysis , primary and secondary research , SQL , advanced Excel, and we would love to speak with you if you have skills in the US healthcare space and a penchant for working with data. About You experience, education, skills, and accomplishments Experience in US healthcaremarket with familiarity with healthcare datasets, U.S. payers, PBMs or employer benefits Exposure to SQL Proven experience in prima...

Managing and leading team and Implement and enhance Quality Management Systems, managing all QA dep activities. Monitor laboratory activities to ensure strict adherence to GLP/cGMP procedures, promoting a culture of quality.

As a Scientist I at the U.S. Pharmacopeial Convention (USP), you will play a crucial role in supporting the development of Reference materials. Your responsibilities will include: - Supporting reaction monitoring, scale up, and final analysis of samples as per monograph/in-house procedures, including method development if required. - Preparing development reports for Synthetic Support projects and being involved in project acceptance. Executing projects per approved test protocols when assigned. - Preparing, executing, and completing IQ/OQ/PQ of new instruments. Indenting the required glassware, chemicals, and columns for the ARD projects. Maintaining GLP and implementing safety procedures w...

As an intern at Vivimed Labs Limited, you will have the opportunity to be involved in various day-to-day responsibilities, which include: - Ensure compliance with GMP and regulatory guidelines. - Assist in documentation and record-keeping activities. - Support day-to-day operations across multiple departments such as QA, QC, MIS, production, sourcing, and packaging. - Conduct quality checks and maintain process standards. - Learn about pharmaceutical manufacturing processes and best practices. - Maintain logs, reports, and necessary documentation. - Adhere to safety and operational protocols in all tasks. - Collaborate with cross-functional teams to ensure efficiency. - Gain equal opportunit...

You will be joining an organization with a reputable history of over 10 years in the Pharma raw material industry, specializing in excipient products. As a Regulatory Affairs Associate, you will play a crucial role in handling technical queries and regulatory documentation for the company's newly launched E-commerce platform, CLYZO. - Manage the entire regulatory documents of excipients. - Resolve technical queries from prominent pharmaceutical clients. - Handle technical matters and document-related work for the excipient manufacturer. - Prepare in-house technical documents required for the promotion of excipient products. - Provide specific technical documents for manufacturer and product ...

As an Officer / Executive in the Engineering Department at the Indore Plant, your responsibilities will include handling various functions such as Electrical, Instrumentation, Mechanical, HVAC, Utilities, Engineering Stores, Control Systems, Documentation, and Equipment Qualification/Validation in a regulated Pharmaceutical / API / Chemical industry. Key Responsibilities: - Maintenance and troubleshooting of electrical panels, drives, and control systems (PLC/SCADA). - Calibration and validation of instruments and sensors to ensure accuracy. - Ensuring power supply reliability and effective energy management. - Compliance with electrical safety standards and audit requirements. For Mechanica...

About Apotex Inc. Apotex is a Canadian-based global health company. We improve everyday access to affordable, innovative medicines and health products for millions of people worldwide, with a broad portfolio of generic, biosimilar, innovative branded pharmaceuticals and consumer health products. Headquartered in Toronto, with regional offices globally, including in the United States, Mexico and India, we are the largest Canadian-based pharmaceutical company and a health partner of choice for the Americas for pharmaceutical licensing and product acquisitions. For more information visit: www.apotex.com. Job Summary Under the guidance of Manager-Instrumentation/R&D, responsible for installation...

Job Title Senior Manager - Production Business Unit Sun Global Operations Function Production (OSD) Location : Mohali Key Responsibilities At Sun Pharma, we commit to helping you Create your own sunshine by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine As you enter the Sun Pharma world, you'll find yourself becoming Better every day through continuous progress. Exhibit self-drive as you Take charge and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we Thrive together and support each other's journeys. Position Summary Planning of Productio...