1079 Glp Jobs - Page 23

Qualification : ITI/B. Tech/M. Tech Experience : 1. ITI with minimum 5 to 6 years of relevant experience (Required minimum 2 3 years experience in Biomedical department at Multi specialty hospitals). 2. B. Tech minimum 2 to 4 years of relevant experience (Required minimum 2 3 years experience in Biomedical department at Multi specialty hospitals). 3. M. Tech minimum 2 to 3 years of relevant experience (Required minimum 2 years’ experience in Biomedical department at Multi specialty hospitals).

QC officer -04 Qc Executive - 01 Perform chromatographic analyses and tests, including HPLC, Gas Chromatography (GC), and Thin-Layer Chromatography (TLC), on raw materials, in-process materials, and finished products. LIMS knowledge preferred. Required Candidate profile We are looking for Male candidate due to work in rotation shift ( First/Second/Night) preferred B.Sc./MSc chemist & required experience of pharma formulation Sterile/Non Sterile product.

Dear Candidate, Greetings of the Days!!!! We are having Job Openings for the Post of Officer-QC. Required Skills- GLP, AMV, Chemical Testing, HPLC, RA work Under QC. Qualification:- Bsc/ Msc/B-harma/M-Pharma. Interview Schedule:- Address:-198/2 and 198/3, Saga Lifesciences Limited Vasna, Ahmedabad. Contact Number-8347011134/79. Salary:- Depends on Interview and who can join within 30 Days. Please visit our website www.sagalifesciences.com Those Candidate who are interested please share their resume on hr@sagalifesciences.com. Regards, Devendra Dawande

Required QC Analyst exp 4-5 year, Finish Good HPLC salary -Hike on current salary Male only Location - Baddi Call at -9818040604

Work Schedule Standard (Mon-Fri) Environmental Conditions Laboratory Setting, Office Job Description Job Title: Lab Operations and Workflow Manager & Training Coordinator Location: CEC ,Hydreabad], India Position Summary: At Thermo Fisher Scientific, our mission is to enable our customers to make the world healthier, cleaner, and safer. This role is essential in delivering that mission by ensuring operational excellence in our laboratory environment. The Lab Operations and Workflow Coordinator will play a critical role in managing laboratory readiness, instrumentation, workflow alignment, and cross-functional coordination to support impactful customer demonstrations and internal technical ac...

Job Summary: We are looking for a highly competent and experienced Senior Formulation & Development (F&D) Chemist with extensive hands-on exposure in the development of solid oral dosage forms , specifically tablets and pellets . The candidate must possess in-depth knowledge of formulation strategies, process optimization, and regulatory documentation, with a strong command over the preparation of Product Development Reports (PDRs) in line with global regulatory expectations. Key Responsibilities: Formulation Development (Tablets & Pellets Focus): Develop robust and scalable formulations for immediate-release (IR), modified-release (MR), and delayed-release (DR) tablets as well as multi-part...

Post: Officer - QC Experience: 1-5 Years Qualification: M.Sc No. of Vacancy: 3 Nos. JOB RESPONSIBILITY :- Responsible for sampling and Instrumental/chemical analysis of RM, In-Process, Intermediate, Finished product, Cleaning samples, Validation samples, Market samples and Stability samples. Responsible to perform the calibration of instrument/equipment available in Quality Control laboratory. Maintain the laboratory as per GLP and GMP System. Sampling, Analysis, and review of raw material/packing material, Wet analysis i.e., water content, IR, UV, LOD, Assay by potentiometry, Sulphated ash etc, finished goods sampling, working on HPLC & GC instrument. Interested candidates can share CVs at ...

Hiring For QC AM For Formulation Co in Khambhat Location Qualification: BSc / MSc / B.Ph / M.Pharm Exp : 8 to 18 Years CTC: Good Salary Experience in Formulation Is Must Send CV on sdpbharuch@gmail.com with Subject: QC Khambhat Share with Friends Required Candidate profile SDP HR SOLUTION 611, Golden Square, Beside DMART, Near ABC Circle, Bholav, Bharuch - 392001 Free Jobs !!1 Share with Your Friends & Colleagues!!!

Eurofins Advinus is a premier preclinical and early development CRO offering drug discovery, preclinical and development stage contract research services in the areas of discovery services, regulatory Toxicology (Safety Assessment), DMPK, Analytical R&D Services and API CDMO. Eurofins Advinus manufactures drug substances to support Toxicology and early clinical studies. Job description: Planning/performing and reporting of acute toxicology studies Assist in preparation of SOP"™s, Protocols and Reports Participate in GLP / AAALAC related activities Literature search Maintenance of animal house and relevant documents as per GLP and AAALAC norms. To Assist and work along with SD and TC in Plann...

Eurofins Advinus is a premier preclinical and early development CRO offering drug discovery, preclinical and development stage contract research services in the areas of discovery services, regulatory Toxicology (Safety Assessment), DMPK, Analytical R&D Services and API CDMO. Eurofins Advinus manufactures drug substances to support Toxicology and early clinical studies. Experience (years) 20-22+ years relevant experience or PhD in Microbiology with at least 15+ years of relevant industry experience. Job description: In-depth scientific expertise in Genotoxicology, with significant experience in designing, executing, and interpreting genetic toxicology studies in both regulatory (FDA, EMA, IC...

Eurofins Advinus is a R&D services company that supports the discovery and development of compounds for diverse industries including Pharmaceuticals, Biologicals, Agrochemicals, Nutraceuticals and Cosmetics. Eurofins Advinus is part of Eurofins Scientific, a EUR 4.5 Billion leading international group of laboratories providing a unique range of analytical testing services to the pharmaceutical, food, environmental and consumer products industries and to governments. Eurofins Advinus facility has over 30 years of GLP experience in conducting regulatory studies in compliance with global regulations for supporting clinical trials and registration of substances and products globally. For the pha...

Eurofins Advinus is a R&D services company that supports the discovery and development of compounds for diverse industries including Pharmaceuticals, Biologicals, Agrochemicals, Nutraceuticals and Cosmetics. Eurofins Advinus is part of Eurofins Scientific, a EUR 4.5 Billion leading international group of laboratories providing a unique range of analytical testing services to the pharmaceutical, food, environmental and consumer products industries and to governments. Eurofins Advinus facility has over 30 years of GLP experience in conducting regulatory studies in compliance with global regulations for supporting clinical trials and registration of substances and products globally. For the pha...

We are looking for a highly skilled and experienced Analyst-QC to join our team at eClerx Services Ltd. The ideal candidate will have a strong background in IT Services & Consulting, with excellent analytical and quality control skills. Roles and Responsibility Collaborate with cross-functional teams to identify and prioritize testing requirements. Develop and implement comprehensive test plans and cases to ensure high-quality deliverables. Conduct thorough analysis of test results and identify areas for improvement. Work closely with the development team to resolve defects and enhance overall product quality. Participate in continuous improvement initiatives to optimize testing processes. M...

Chemical and physical tests on in-process samples, and finished products using techniques like HPLC, GC, and titrations. Maintaining accurate records of analytical data, preparing reports, and ensuring compliance with GLP and GMP. Required Candidate profile Developing & validating analytical methods and procedures to ensure accuracy Following all safety guidelines, regulatory standards Contact Mr Deep at 9867038868, Email Id: ops@empowerrecruitments.com

Analyse the assigned samples and chromatographic tests for analysis by using the suitable valid procedure and calibrated instruments to ensure the compliance to the set specification / standards Perform analysis for release of RM, PM, FP & water analysis and process/cleaning validation as per commitment dates Perform analysis for stability samples without any errors as per schedule Check the results of the tests performed, evaluate them against the specifications Review the TDS printed through LIMS for its completion before release Key Accountabilities (2/6) Perform all activities as per current standard procedures by referring to all approved procedures/specifications to ensure compliance t...

Requisition for Executive for the implementation and monitoring of GLP in TIC. Skills Required : Good Laboratory Practice, Quality Assurance, MS Office Package, Communication Skills Roles and Responsibilities : Preparation of documents related to applying GLP (Good Laboratory Practices). Ensure the upkeep and maintenance of the laboratory by implementing GLP. Ensure compliance with GLP standards. Logbook management, sample management, SOP management, and other document management related to GLP. Any other work related to Quality assurance assigned by the manager. GLP-trained person or experience working in GLP labs. Must have good verbal and written skills.

Roles and Responsibilities: - Authorize release of test report based on the Buyers protocol & test methods - On time responds to Buyers & clients queries, emails and calls - Responsible for reviewing revisions, updates on test parameters, protocols and regulations, etc. and circulating these to the concerned lab team - Training lab staff as per updated, revised protocol received from clients and brands - Support team to develop capability on new test parameters as received in buyer protocol - Training & Supervising the handling, operating and maintenance of test equipment. - Supervising preparation and maintenance of document as per requirement of ISO 17025 - Monitor accuracy of ILC/ PT prog...

Roles and Responsibilities: - Authorize release of test report based on the Buyers protocol & test methods - On time responds to Buyers & clients queries, emails and calls - Responsible for reviewing revisions, updates on test parameters, protocols and regulations, etc. and circulating these to the concerned lab team - Training lab staff as per updated, revised protocol received from clients and brands - Support team to develop capability on new test parameters as received in buyer protocol - Training & Supervising the handling, operating and maintenance of test equipment. - Supervising preparation and maintenance of document as per requirement of ISO 17025 - Monitor accuracy of ILC/ PT prog...

Roles and Responsibilities Conduct analytical testing of finished products, including dissolution, UV-Vis, KF, FTIR, and GLP compliance. Develop and validate analytical methods for solid oral OSD products using techniques such as GC, HPLC, and UV spectroscopy. Perform method transfer and validation activities to ensure accuracy and reliability of test results. Collaborate with cross-functional teams to resolve OOS/OOT issues and implement corrective actions. Maintain accurate records of laboratory data, reports, and documentation in accordance with cGMP guidelines.

Develop SOPs for production, filling, packaging & QA/QC; ensure FDA, EU, BIS & Drug Act compliance; conduct audits; review BMR, BPR & MFR; implement QMS; train staff on GMP/GLP; manage labelling, claims & documentation for regulatory compliance.

Develop and optimize analytical methods (HPLC, UPLC, GC, UV, Dissolution, KF, IR, etc.) for oral solid and oral liquid formulations. Perform analytical method validation and transfer to Quality Control / manufacturing sites.

Job Description: We are seeking a detail-oriented and skilled Analytical Scientist (Five Batch Analysis) with hands-on experience in conducting Phy-Chem and validation studies for agrochemicals and pharmaceutical compounds. The ideal candidate will have strong knowledge of global regulatory guidelines and be capable of preparing study-related documentation while maintaining audit readiness at all times. Key Responsibilities: Conduct Physico-Chemical studies for agrochemical compounds in accordance with regulatory requirements. Act as Study Director for Five Batch Analysis studies in accordance with CRO and GLP regulatory requirements. Develop study plans, protocols, and schedules for analyti...

We are seeking a meticulous and quality-focused QC Analyst to join our team at Nymbioz Biotech Pvt Ltd in JP Nagar, Bangalore. As a QC Analyst, you will play a crucial role in ensuring the safety, consistency, and compliance of our products through rigorous quality control processes. If you have a passion for precision and scientific standards, we would be delighted to have you on board. Your responsibilities will include conducting routine analysis of raw materials, in-process, and finished products using standard laboratory techniques. It will be essential to ensure that all quality control procedures comply with regulatory requirements and internal protocols. Maintaining accurate document...

At Godrej Industries Group (GIG), you have the privilege to serve over 1.1 billion consumers globally through businesses with market leadership positions in various industries including consumer products, real estate, agriculture, financial services, and chemicals. The group is known for its commitment to excellence and innovation. You can learn more about us at https://www.godrejindustries.com/. Godrej Pet Care (GPC) is a new chapter in the pet foods industry, a 100% subsidiary of Godrej Consumer Products Limited. GPC is poised to make a significant impact in the thriving pet food industry, which is a 5,000 crore category and expected to experience robust double-digit growth in the coming y...

As a bench scientist at our organization, you will be responsible for conducting experimentation in the field of formulation research and development for global markets. Your role will involve working with scientific principles such as Quality by Design (QbD), Design of Experiments (DoE), statistics, and scale-up principles. You will be required to analyze data from literature reviews and effectively present information for decision-making purposes. Understanding the Intellectual Property (IP) scenario and working on design strategies, prior art searches, and establishing proof of concept through experiments will be a key part of your responsibilities. You will collaborate with cross-functio...