1074 Glp Jobs - Page 16

As a Manufacturing Associate at our company located in Turbhe, Navi Mumbai, you will play a crucial role in supporting manufacturing operations for high-quality diagnostic/research products. Your background in Medical Laboratory Technology (DMLT/BMLT) or Lifesciences will be valuable in ensuring compliance with quality and safety standards. Freshers are also encouraged to apply. **Key Responsibilities:** - Carry out routine manufacturing activities following SOPs and GMP guidelines. - Perform sample preparation, testing, and documentation. - Operate, clean, and maintain laboratory/manufacturing equipment. - Assist in batch preparation, labelling, and packaging activities. - Maintain accurate...

Core responsibility related to GLP: Anesthesia / euthanasia of laboratory animals as per SOP Blood collection preparation Collection of blood from laboratory animals as per SOP and study plan Preparation of blood smears Necropsy & organ collection from laboratory animals (rat, mice, rabbit & guinea pig). Preparation of fixative solutions. Tissue sectioning and maintaining various histopathological instruments. Labeling of micro centrifuge and bottle according to study plan. Preparation of surgical instruments for necropsy. Opening of carcass and collection of organ according to study plan requirement. Tissue trimming according to SOP and study plan requirement. Processing of animal tissue ac...

Role Overview: As a Raw Material Quality Control Analyst, your main responsibility will be to ensure that all raw materials (API & excipients) used in manufacturing are sampled, tested, and released according to pharmacopeial/in-house specifications and regulatory standards before they are utilized in production. You will play a crucial role in maintaining the quality and integrity of raw materials used in pharmaceutical manufacturing processes. Key Responsibilities: - Receive and verify raw material intimation from the warehouse. - Conduct GMP-compliant sampling using appropriate tools and in classified environments (if applicable). - Properly label samples and maintain sampling logbooks. -...

Conduct final inspection and testing of finished products to ensure compliance with quality standards and customer specifications. Hands-on experience in testing of Finished products Instruments must be handled like HPLC, GC, KF, IR, DT, and Dissolution. Hands-on experience like software like Empower and LIMS. Qualification M.SC/B.Pharma 3 to 6 years Additional Information

B.Sc/M.Sc Chemistry, 1–8 yrs exp in API/Pharma QC. Must handle HPLC/GC/UV/IR, cGMP, stability, and docs. Local preferred Dahej. Only male candidates are required. Only pharma experience required.

As a Lab Incharge, you will be responsible for overseeing the daily operations of the chemistry laboratory. Your role will involve managing laboratory activities, ensuring safety protocols, and maintaining high standards of quality. Key Responsibilities: - Supervise laboratory staff and students to ensure adherence to safety protocols and standard operating procedures. - Manage laboratory inventory, equipment, and supplies efficiently. - Develop and implement laboratory procedures, protocols, and safety guidelines. - Conduct regular safety audits and risk assessments within the laboratory. - Collaborate with faculty and researchers to develop and implement research projects effectively. - Pr...

Exciting Career Opportunities at Natco Pharma Limited for the following requirements Work Location: Kothur (Formulation Division) Interview Date: Saturday, 20th September 2025 Time: 9:00 AM to 2:00 PM Venue: Natco House, Road No.-2, Banjara Hills, Hyderabad 500034 (Opp. A.P. Productivity Council) Open Positions: Analyst - Quality Control (OSD & Sterile) Experience: 3 to 5 Years Qualification: B. Pharmacy / M. Pharmacy / M.Sc (Organic/Analytical/General) Chemistry Key Responsibilities: Adherence to GLP, GDP, cGMP, and ALCOA+ standards. Analysis of RM / IP / FP samples, Operation and troubleshooting of instruments such as HPLC, UV, KF, IR, and Dissolution Apparatus. Demonstration of QC testing...

Please note that this position is for QC and not for QA. Candidates with API/Bulk Drugs experience shall apply. Job description-Quality Control Lead Role & responsibilities 1. Responsible to lead functions of Quality Control department at site. 2. Responsible to establish, implement and maintain Quality Control department in the state of compliance with statutory and regulatory expectations. 3. Responsible to ensure data integrity in quality control laboratory. 4. Responsible for handling Internal/External/Regulatory audits in Quality Control department at site. 5. Responsible for Preparation/ review of Compliance Report and appropriate CAPA implementation w.r.t. quality control observations...

Walk-in at Matoda We are hiring multiple positions for our manufacturing facility at Matoda as mentioned below. Please find our current job requirements and venue details mentioned. If any of the requirements match your current job profile, kindly walk in with your latest resume. Role & responsibilities Injectable Manufacturing (Executive/Senior Officer / Officer) Experience - 02 to 08 Years Qualification - B. Pharmacy/ M Pharmacy / Msc / Bsc / Engineering - (Instrumentation / Process Equipment Maintenance) (Senior Executive / Executive / Senior Officer) Experience - 03 to 10 Years Qualification BE / B Tech QUALITY ASSURANCE IPQA (injectable) / QMS / Documentation (Officer / Senior Officer /...

Job Alert Sr. GM / Associate Vice President – Quality Control Location: North India Industry: API / Chemicals Manufacturing Salary: Open (Attractive hike on current package) Experience: 16+ Years | Age: 50 Years We are seeking a dynamic Quality Control leader for a reputed API Manufacturing organization . The candidate must have strong exposure to regulatory-driven companies with proven expertise in leading global regulatory audits (USFDA, EMA, MHRA, etc.) and managing large QC operations. Key Responsibilities: Head the Quality Control department ensuring compliance with cGMP & international regulatory guidelines. Lead a QC team of 150–200 employees , driving efficiency, compliance, and tech...

Responsible for follow the health, safety & environment norms as per company policy & procedure Responsible for follow the Good Laboratory practices & Good Documentation practices Maintain laboratory discipline Preparation of COA, Raw material trend Required Candidate profile Operate and calibrate instruments like Gas Chromatography, HPLC, Analytical balance, PH meter, GCMS Validity of instrument calibration, reagents, volumetric solutions, working standard

Key Responsibilities: 1. Stability Study Design & Planning Define study protocols, including time points, conditions (temperature, humidity, light exposure), and container types. Collaborate with formulation scientists and regulatory affairs teams to ensure studies align with regulatory guidelines (e.g., ICH, FDA). Plan long-term and accelerated stability testing for new and existing products 2. Compliance & Documentation Document study protocols, deviations, results, and reports. Maintain comprehensive stability study records for internal reference and regulatory submissions. Prepare stability data for inclusion in regulatory filings, ensuring compliance with ICH, FDA, or other relevant gui...

As a Quality Control (QC) Officer in the pharmaceutical (Formulation) industry located at Waghodia GIDC, Vadodara, your main responsibilities will include: - Performing quality checks on raw materials, in-process materials, and finished products. - Carrying out lab testing using instruments like HPLC, GC, UV, FTIR, etc. - Ensuring all work complies with GMP (Good Manufacturing Practices), GLP (Good Laboratory Practices), and other regulatory requirements. - Identifying and reporting any issues like defects, deviations, or non-conformities. - Maintaining accurate records, including test reports and documentation. - Working closely with production and QA teams to address and resolve quality-re...

Role Overview: As an experienced analytical development scientist at Dr. Reddys Laboratories Ltd., your main responsibility will be to execute analytical activities based on priorities and established timelines. You will be required to provide timely analytical delivery for stability testing, test method development/validation, method transfers, and other related requests from Research & Development (R&D) or formulation development. Key Responsibilities: - Conduct Literature survey and prepare analytical strategy for assigned projects. Should have a minimum understanding of DMF and test methods of drug substance, etc. - Perform analytical method development of Viscosity, PSD, GSD, Assay, RS,...

As a Chemical Research Scientist C in the R&D Department in Bangalore, your role involves conducting literature search and review using basic software knowledge like Sci-Finder, Chem-draw, and other databases. You will also need to have a basic understanding of AI & Chat GPT. Your responsibilities include: - Executing synthesis and scale up of small organic molecules/intermediates, active ingredient/polymers/dispersions to multi-kilogram quantities under the supervision of the department head, adapting to evolving project requirements. - Employing techniques such as column chromatography, recrystallization, fractional, column & vacuum distillation, and different techniques. - Utilizing HPLC,...

Ensuring best quality of product and minimum customer complaints through stringent on-line quality control checks and finished product inspection Implementing right quality control systems/standards for the processes, physical systems and environment. Trouble shooting during online production to minimize wastage and ensure quality. Responsible for maintaining GMP, GHK GLP and internal / external audits (HACCP, AIB, Personal Hygiene, Process audit) Root cause and failure analysis for quality defects and implementation of the corrective actions. Responsibilities Conducting online quality checks in the process area to ensure that all FLI standards of quality are followe'd during the production ...

Ensure cost-effective, non-infringing route selection and process development for both existing and new products. Conduct feasibility assessments, optimization studies, and process validation in the lab, followed by seamless tech-pack transfer. Design and execute experiments involving a wide range of organic reactions, including product characterization and process condition optimization. Lead the end-to-end development of new products from concept through to commercialization. Manage R&D projects from ideation to execution, including planning, experimentation, data analysis, and reporting. Perform 2 3 chemical reactions daily while providing leadership and guidance to Research Associates (R...

1) Responsible for managing and organizing laboratory operations of respective section i.e all aspect of analytical related activities including TAT and budget preparation. 2) Executing the first line supervision of laboratory personnel to ensure the analytical works are professionally carried out, to ensure accuracy & reliability of analytical results. Responsible for cross checking and validating the analytical results for release to customer. 3) Developing and maintaining an effective laboratory workforce by constantly improving the work methods and analytical competence of subordinates. 4) Implement and maintain quality system according to the ISO /IEC17025 requirements and the Nestl Qua...

Role & responsibilities Can handle the shift independently. Responsible for all ink testing like viscosity, shade strength, gloss, Transparency, Grinding. Inspection of all raw material and packing material. Can develop new raw material and Packing material with new vendors. Maintain all quality standard and documentation as per ISO 9001:2015. Carry out quality assessment measures of all the products ready to be shipped and incoming raw materials. Can handle the customer complaint and make report. Maintain very close communication and coordination with Production Monitor the production phase at various levels. Comply all safety requirements in the working environment EHS. Do Equipment mainte...

ORGANISATIONAL OVERVIEW Lambda Therapeutic Research is a full-service Global Clinical Research Organization (CRO) with its headquarters in Ahmedabad, India. With facilities and operations strategically located in Mehsana (India), Las Vegas (USA), Pittsburgh (USA), Toronto (Canada), Warsaw (Poland) and London (UK), we offer comprehensive end-to-end clinical research services to the global innovator, biotech, and generic pharmaceutical industries. JOB DETAILS Department: Bioanalytical Operations Designation: Research Associate Job Location: Ahmedabad (Gujarat) KEY DELIVERABLES To develop and validate Bioanalytical methods. To process / analyze samples of allotted projects. To operate, calibrat...

Conduct quality checks of raw materials, in-process, and finished goods Maintain QC documentation and test records Assist in audits and ensure compliance with standards Coordinate with production for quality improvements Required Candidate profile Job Title: Quality Executive Location: Merta, Rajasthan Experience: 2–4 Years Salary: 30,000 – 35,000/month Type: Full-Time Industry: [Manufacturing/FMCG/Pharma] Joiners: Immediate preferred

As a Production Planning & MIS professional, your role will involve preparing and executing production plans, managing material requirements, controlling inventory, and maintaining MIS reports to support decision-making. You will closely coordinate with Production, QA, QC, Procurement, Regulatory Affairs, and Sales teams while ensuring compliance with GMP/cGMP and regulatory requirements for both Vizag and Dahej Locations. Key responsibilities include: - Developing and implementing production plans. - Conducting Material Requirement Planning (MRP). - Managing inventory levels effectively. - Coordinating and communicating with cross-functional teams. - Ensuring documentation and compliance st...

Sample collection &Testing : Assist in collection and testing raw materials and finished product as per SOP regular guidelines. Instrument Handling : Learn and support basic operation and maintenance of laboratory instruments.

Job Title : Veterinarian for Preclinical research organisation Location: Pregnapur, Hyderabad Experience : Freshers Reports To : Head Preclinical Research / Study Director / TFM Job Summary: We are seeking a qualified and experienced Veterinarian to support preclinical research programs within a GLP-compliant Contract Research Organization environment. The veterinarian will be responsible for the care, welfare, and regulatory compliance of laboratory animals used in safety, pharmacology, and toxicology studies, ensuring adherence to OECD GLP guidelines and sponsor requirements. Key Responsibilities: Animal Care & Welfare Oversee the health and welfare of laboratory animals (rodents, rabbits,...

Overview Ensuring best quality of product and minimum customer complaints through stringent on-line quality control checks and finished product inspection Implementing right quality control systems/standards for the processes, physical systems and environment. Trouble shooting during online production to minimize wastage and ensure quality. Responsible for maintaining GMP, GHK GLP and internal / external audits (HACCP, AIB, Personal Hygiene, Process audit) Root cause and failure analysis for quality defects and implementation of the corrective actions. Responsibilities Conducting online quality checks in the process area to ensure that all FLI standards of quality are followed during the pro...