4097 Gmp Jobs - Page 45

We are looking for a Computer System Validation (CSV) Specialist to ensure that GxP-regulated systems meet compliance requirements in line with 21 CFR Part 11 , EU Annex 11 , and GAMP 5 . The role involves validation of systems used in Quality Control (e.g., LIMS, Chromeleon) and/or Manufacturing operations (e.g., SAP, MES) . The ideal candidate should have hands-on experience preparing and executing validation documents (URS, IQ/OQ/PQ), and strong knowledge of data integrity and GxP practices in the pharmaceutical or life sciences industry.

Handling Batch process and process equipment, manpower handling, following safety rule. Responsible for consumption of Raw material, yield and quality of intermediate, semi-finished, finished product. Online BMR, BPR and ECR, Daily Records checking.

KATURI MEDICAL COLLEGE & HOSPITAL is looking for CSSD Technician to join our dynamic team and embark on a rewarding career journey Operating and maintaining sterilization equipment Cleaning, inspecting, and assembling surgical instruments and equipment Ensuring that all instruments and equipment are properly sterilized and packaged for use Managing inventory and restocking supplies as needed Maintaining accurate records and documentation of all sterilization procedures and equipment maintenance Adhering to infection control policies and procedures to prevent the spread of infection Collaborating with other departments, such as surgery and nursing, to ensure the timely delivery of sterilized ...

Role & responsibilities Manufacturing of Lyophilized Drug Product Aseptic Blending & Filling Injectable Filling Lyophilization BMR Preparation cGMP Practices, Media Preparation, Vial Washing and De-pyrogenation, Validation, Labeling & Packaging, Documentation Preferred candidate profile Aseptic handling Sound knowledge of QMS Sound knowledge of cGMP, GDP

Role Overview: You will be responsible for overseeing the production of ice creams, gelato, bars, mini bites, macarons, popsicles, choco tacos, and other frozen treats. Your main tasks will include developing and implementing production plans, organizing daily production activities, monitoring ingredient inventory, and leading production teams to meet goals. Additionally, you will be required to ensure facility and equipment maintenance, collaborate with cross-functional teams, manage compliance and risk, oversee culinary and product development, and provide team leadership and training. Key Responsibilities: - Develop and implement detailed production plans to meet demand forecasts and ensu...

You will be responsible for preparing detailed 2D and 3D drawings of pharmaceutical and medical equipment using AutoCAD or similar CAD software. Your role will involve working closely with design engineers to translate concepts and prototypes into technical drawings. Additionally, you will need to revise drawings based on engineering changes and production feedback, ensure compliance with industry standards, and assist in preparing technical manuals, BOMs (Bill of Materials), and assembly instructions. Furthermore, you will coordinate with production teams to address any drawing-related issues during fabrication and provide support to R&D and quality teams for design validation and improveme...

About the job About us/Company overview: mCaffeine is India's 1st caffeinated personal care brand with an exciting range of caffeinated products for young and aspiring millennials. We believe in confidence over all skin and body biases. Redefining age-old notions of beauty associated with colour, we never sell insecurities. We have vowed not to make fairness products. At mCaffeine, beauty has no colour or gender it's about you .You are a revolution, a culture, a routine, a high, and essentially now a lifestyle . You are Bold, Young, and Confident . Come, join the pack! Role Overview: We are looking for a Senior Executive QA & QC with strong experience in cosmetic manufacturing and a deep und...

Site Name: Bengaluru Luxor North Tower Posted Date: Sep 26 2025 Be You at GSK At GSK, we unite science, technology, and talent to get ahead of diseases together. We are a world leader in infectious diseases, including vaccines and HIV, with the broadest portfolio in the industry, pushing the frontiers of respiratory science and improving the lives of millions of patients. Recognized for our ESG leadership, we are making an impact on society's most urgent challenges. We're confident that together we can make a positive impact on the health of more than 2.5 billion people by 2031. When you set out on your adventure at GSK, we make a deal. You commit to living our values and performing against ...

As a QA Manager in an OSD (Oral Solid Dosage) plant, your role involves overseeing all quality-related activities to ensure products meet required standards and regulations. This includes developing and implementing quality management systems, conducting audits, managing quality control, and leading the QA team. Your key responsibility is to play a crucial role in ensuring compliance with GMP, regulatory standards, and continuous improvement initiatives. Key Responsibilities: - Developing and Implementing Quality Management Systems: - Establishing and maintaining quality policies, procedures, and standards for the OSD plant. - Ensuring Compliance: - Ensuring all products and processes adhere...

You will become a part of a quality-driven and compliance-focused production team responsible for manufacturing high-quality pharmaceutical products. Your role will contribute directly to ensuring uninterrupted production, regulatory compliance, and delivery of safe, effective medicines to patients. You will work in a GMP-regulated facility and collaborate closely with cross-functional teams like QA, Engineering, and Planning. Key Responsibilities: - Execute daily production activities (granulation, compression, coating, or packaging) as per approved batch manufacturing records (BMRs). - Ensure compliance with cGMP, safety, and regulatory guidelines during all production operations. - Superv...

As a Vendor Quality Assurance Specialist, your role is crucial in ensuring that all vendors supplying materials meet the company's quality standards and regulatory requirements through a structured vendor qualification and evaluation process. Key Responsibilities: - Initiate and coordinate vendor qualification activities for both new and existing vendors. - Prepare and maintain vendor qualification dossiers and files to ensure documentation accuracy. - Coordinate with procurement and other departments to gather necessary vendor data and documentation efficiently. - Ensure vendors comply with Good Manufacturing Practices (GMP), regulatory requirements, and company quality standards to uphold ...

As a Documentation Officer at our company located in Ecotech-XI, Greater Noida, you will play a crucial role in managing various documentation tasks to ensure compliance with industry standards and maintain the confidentiality of technical and regulatory documents. Key Responsibilities: - Maintain and update inventory records for Impurities, APIs, and Chemicals, ensuring proper filing, placement, and retrieval on the company server. - Upload and manage product information on agnitio.co.in and company social media platforms for effective information management. - Develop and manage product labels, Material Safety Data Sheets (MSDS), and issue Certificates of Analysis (CoA) from raw data as pa...

As a Quality Assurance Coordinator, you will play a crucial role in ensuring the quality standards of the products by implementing and monitoring quality assurance policies and procedures. Your responsibilities will include: - Assisting in planning and implementing quality assurance policies and procedures. - Monitoring and analyzing quality performance metrics to identify trends and areas for improvement. - Supervising quality control operations, including inspections, audits, and testing procedures. - Working closely with production, R&D, and supply chain teams to resolve quality-related issues. - Leading root cause analysis (RCA) and corrective/preventive action (CAPA) initiatives. - Coor...

Role Overview: As a Production Supervisor in Pharmaceutical Manufacturing at Makshi, Madhya Pradesh, your role will involve supervising daily production operations to ensure compliance with Good Manufacturing Practices (GMP). You will be responsible for overseeing the production of tablets, capsules, liquids, or injectables, ensuring adherence to Batch Manufacturing Records (BMR), Batch Packing Records (BPR), and Standard Operating Procedures (SOPs). Additionally, you will monitor equipment readiness, coordinate with Quality Assurance/Quality Control (QA/QC) for in-process checks, maintain shop floor hygiene and discipline, and train staff on GMP, Good Distribution Practices (GDP), and safet...

Role Overview: As a Formulations Scientist in Hyderabad, India, you will be responsible for the development of oral solid dosage forms of Non-DEA and DEA substances. Your key functions will include conducting Literature Search, Pre-Formulation, Formulation Design, and Development of stable, Bioequivalent, and Manufacturable generic solid oral formulations. Key Responsibilities: - Act as a mentor and motivator to the team. - Develop robust formulations and processes for immediate release and modified release tablet and capsule dosage forms. - Evaluate patents and develop non-infringement strategies, including the capability of developing Paragraph IV products. - Scale-up and optimize manufact...

1) Understand quality concepts and work on continual improvement.2) Support new product development and nutrition studies.4) Have knowledge of FG, raw material, and packaging material testing.5)Maintain good GMP and GHP at the manufacturing location.

B.Sc./M.Sc. with 1–4 years in QC (API). Hands-on with HPLC, GC, UV, and wet analysis. Experienced in raw material, in-process, and finished product testing. Strong in GMP, documentation, and analytical techniques. Required Candidate profile B.Sc./M.Sc. with 1–4 years’ QC experience in API. Proficient in HPLC, GC, wet lab testing, and GMP documentation. Detail-oriented, accurate, and skilled in analytical methods. Perks and benefits GMP GLP plant| Growth| Safety| Compliance| Perks

Key Responsibilities: Operate and monitor production equipment such as reactors, centrifuges, dryers, and filters for API manufacturing. Ensure adherence to cGMP, safety, and regulatory guidelines during production operations.

Role Overview: As the Deputy Manager Quality, your primary responsibility is to support the Quality Manager in ensuring that all products, processes, and services meet established quality standards and regulatory requirements. You will be leading a team of quality professionals, driving continuous improvement initiatives, and ensuring compliance with internal and external quality standards. Key Responsibilities: - Assist the Quality Manager in developing, implementing, and maintaining quality management systems (QMS) in compliance with ISO, GMP, or other relevant standards. - Supervise day-to-day quality operations including incoming inspection, in-process quality checks, and final product a...

As a Site Quality Head at our reputed pharmaceutical manufacturing company in Vapi, Gujarat, you will be responsible for leading and overseeing the Quality Assurance and Quality Control functions at our Oral Solid Dosage (OSD) facility. Your role will involve full ownership of quality systems, lab operations, regulatory compliance, and audit readiness. To excel in this position, you should currently hold a site-level quality head role and have hands-on experience managing QA and QC teams in a regulated pharmaceutical environment. **Key Responsibilities:** - Lead and manage the complete Quality function (QA and QC) at the site - Ensure compliance with GMP, regulatory, and customer requirement...

Role Overview: At Dameasy, you will be part of a dynamic team reimagining how modern consumers experience food. As a Quality & Operations Executive, you will play a crucial role in ensuring quality control, lab testing, and operational execution at our manufacturing unit. This hands-on, cross-functional position will involve direct involvement in production, compliance, and new product development, contributing to shaping the future of food manufacturing. Key Responsibilities: - Quality Oversight - Monitor GMP, hygiene, and food safety standards on the production floor - Conduct quality checks during production and on finished goods - Lab Testing & Analysis - Run lab tests on raw materials a...

As a Laboratory Operations professional at Piramal Pharma Solutions (PPS) in Morpeth, United Kingdom, your role involves the following critical tasks: - Preparation of samples and associated reagents, performing basic analysis accurately and on time - Gathering, generating, analyzing, and interpreting data - Organizing and planning your work efficiently - Preparing samples, reagents, and equipment required for analysis - Ensuring the laboratory is well stocked and resourced - Performing a variety of analytical testing using wet chemical and instrumental techniques - Conducting routine equipment maintenance and calibration - Writing and reviewing SOPs, sampling and testing procedures, analyti...

Work Location: Caldic Specialties India Private Limited B-06-E, ESR TALOJA Industrial & Logistics Park, Village Usatane, Khoni Taloja Road, Taluka Ambernath, District Thane & Village Nitlas, Taluka Panvel, District Raigad, 421 306, Maharashtra, India. Shift work is required Working days: 6 days per week Position Overview: The Quality Assurance Supervisor has the responsibility of supporting the implementation and ongoing maintenance of the quality and food safety systems used by the company at their Manufacturing Plant. The quality and food safety systems including: FSSC 22000, ISO9001, HACCP, Kosher, Halal, Eco Vadis and GMP. Key Responsibilities: Ensure compliance with company Food Safety ...

lead&plan projects-pellets/mups,meet TPP, timelines,budget-FRD(FBC,RMG,Coating,Nano),interpret ARD results,delegate & monitor teams, Ensure compliance: MFR,scale-up,stability protocols,PDRs,SOPs,GMP,SHE Technical discussions-DQA, ARD, Marketing, Required Candidate profile FRD pellets/modified release, QbD,cGMPs, GLPs, expertise in process and formulation optimization,tech transfer&scale-up -FBC,RMG,coating,extrusion,nanotech, DIPO qualification, validation, spec review

We are looking for a skilled CSV Lead with 15-25 years of experience to join our team. The ideal candidate will have expertise in ServiceNow and HPALM. Roles and Responsibility Manage and implement CSV solutions using ServiceNow and HPALM. Collaborate with cross-functional teams to ensure seamless integration of CSV with other systems. Develop and maintain documentation for CSV processes and procedures. Troubleshoot and resolve issues related to CSV implementation. Provide training and support to end-users on CSV tools and features. Ensure compliance with industry standards and best practices for CSV management. Job Requirements Strong knowledge of ServiceNow and HPALM. Experience in managin...