1074 Glp Jobs - Page 13

Dear Candidate , we are hiring for the Position Jr Executive .(Instrumentation,Hematology,Activity,Potency Based Assays,Bio chemical group) 1.Candidate have good hands on experience in HPLC, electroscopic test methods. 2.should be able to handle liquid chromatography instrument and relevant 21 CFR softwares 3.should be able to handle ELISA Reader ,microscope,basic QC Instruments . 4.candidate should have good hands experience in colorimetric ,spectrophotometric. 5. should be have a idea on GLP compliance requirements. for more details please reach out Venkat -9381915043 /Manasa - 9502434725

DEAR CANDIDATE , WE ARE HIRING! LET'S JOIN OUR TEAM NOW! Department: R&D Position: Research Trainee / Research Associate Preferred Qualification: M.Sc. Biotechnology / M.Sc. Biochemistry Preferred candidate: Male Preferred Experience: 2 to 3 years of experience Should have good documentation skills and knowledge of GDP, GMP, GLP. Should have basic knowledge about proteins and protein purification. Should be a good team player with good interpersonal skills. Job description: Perform R&D related documentation like SOP preparation, data management and data analysis. Perform routine laboratory procedures, including buffer preparation, gel electrophoresis, western blot. Operation and maintenance ...

Position: Executive TSD (Technology Support / Technology Transfer) Department: TSD Location: Ahmedabad Reports to: TSD Manager / Head of Department Experience: 510 Years Education: B.E / M.E Chemical / Chemical Engineering Key Responsibilities: Execute technology transfer from R&D to pilot and commercial production. Support process scale-up and optimization for cost, yield, and safety. Prepare and review tech transfer protocols, BMR/BPR, SOPs, and risk assessments . Troubleshoot and resolve issues during pilot and commercial batch production . Ensure compliance with cGMP, GLP, QbD, and regulatory guidelines . Liaise with R&D, QA, AR&D, Production, and Regulatory Affairs teams. Support audits...

Job Title: Sr. Executive/Executive Department: DQA Job Summary, Duties/Responsibilities: Ensure proper guidance on quality issues to the Product Development Teams Review the documents received from R&D, AR&D, etc. so that the same can be shared with authorities and customers . coordination communication and to respond customer complaint/query and regulatory authority. Review the process change proposals and help the team members provide guidance on change proposals Review the in-house expert reports/Quality overall summary (QOS) prepared by the team members Ensure proper stage gate compliance at various stages of product development Ensure that internal audits are conducted properly Review t...

Walk-in Drive @ SEZ-Matoda|| Ahmedabad on 28th Sep '25 (Sunday) for Quality Control Department. We are having excellent job opportunities for Quality Control Department at Amneal Pharmaceuticals, SEZ Matoda Injectable. Interview Venue Details: Date: 28th Sep 25 (Sunday) Time: - 9:00 AM to 3:00 PM Venue : Amneal Pharmaceuticals Plot No 15, 16, 17 Pharmez | Village: Matoda | Sarkhej Bavla Road | Ahmedabad Gujarat - 382220. REQUIREMENT FOR INJECTABLE QUALITY CONTROL DEPARTMENT Designation: Officer/ Sr. Officer /Executive/ Sr. Executive Department: Quality Control Qualification: Diploma/ B.Sc./ M.Sc/ B. Pharm/ M. Pharm Total Experience: 02 to 07 years (Pharma experience only) Desired Profile: GL...

Responsible for maintaining compliance and to ensure GLP in lab Responsible for preparation of AMV protocols and reports Responsible to provide request to section head for issuance of AWR and to record analysis related activities Responsible for execution of Analytical Method Validation/Verification activities in lab Responsible to carry out AMV activities as per planning Responsible to participate in investigation generated during AMV activities Responsible to participate in investigation of OOS/OOT to find out the root cause like verification of force degradation data. Responsible for preparation calibration and preventive maintenance planner. Responsible for daily temperature monitoring o...

Job Profile: Responsible for analysis of IP/FP/,PV, Semifinished products, hold time samples Responsible for maintaining compliance and to ensure GLP in lab. Responsible for analysis of samples on HPLC/GC etc. Responsible to provide request to section head for issuance of AWR and to record analysis related activities Responsible to receive samples of FP/IP/inprocess/,holdtime samples and maintain the record. Responsible for reconciliation and destruction of laboratory samples. Responsible to maintain records for FP/IP/PV/SFG/Holdtime samples Responsible for preparation of COAs Responsible to maintain individual training record Responsible for record details of OOS/OOT/OOC/Incidents and to pa...

Position: IA Computer System Validation (CSV) Engineer (CE25SF RM 3581) Job Summary: The Computer System Validation (CSV) Engineer is responsible for ensuring that computerized systems used in regulated environments (e.g., GMP, GCP, GLP) are validated in compliance with applicable regulatory requirements such as 21 CFR Part 11, Annex 11, GAMP 5. This role involves planning, authoring, reviewing, and executing validation deliverables, and supporting cross-functional teams. Key Responsibilities: Develop and execute validation strategies and plans for new and existing computerized systems. Create and maintain validation documents including: User Requirements Specifications (URS) Functional Spec...

" Jubilant Biosys is looking for Research Associate II - In Vivo, DMPK Location : Bengaluru Experience : 3 to 5 years Qualification : M Pharmacy Key Responsibilties : Read and understand various in vivo study protocols Good knowledge of various in vivo animal models employed in DMPK arena Handling of laboratory animals (mice, rats, guinea pigs, rabbits, hamsters etc.) Conduct various in vivo ADME studies (IV and PO studies, excretion studies etc.) Ability to administer compound via various routes in rodents (IV, PO, IP, SC, tropical, intravitreal etc.). Should be adept at conducting IV studies employing infusion pumps Should be able good at rodent cannulations (jugular, carotid, femoral) and...

Role Overview: You will be responsible for overseeing and supporting the overall activities during the product development life cycle from a quality perspective in R&D (API and intermediates). Your role will involve understanding the site needs for system establishment and sustainability, authoring/reviewing/approving SOPs/work directions, and ensuring effective implementation of quality systems in R&D activities as per GLP and regulatory requirements. Additionally, you will be required to review and approve various reports, conduct periodic audits of the R&D laboratory, ensure effective maintenance of records, and perform cGMP audits of R&D facilities and operations. Training the R&D team f...

As a Quality Control professional at Medivisual Healthworld in the Pharmaceutical & Cosmetic Manufacturing industry, you will be responsible for: - Performing testing of raw materials, in-process, and finished products such as tablets, syrups, skin care products, etc. - Ensuring quality checks are conducted following laid Standard Operating Procedures (SOPs) and regulatory standards - Making independent quality decisions (accept/reject) based on control parameters - Maintaining and updating all test records, reports, and logbooks in compliance with regulatory norms - Ensuring compliance with legal, safety, and quality standards Key Skills Required: - Hands-on experience in HPLC / GLC - Profi...

As an Analytical Scientist C at BacAlt, you will play a crucial role in the Research and Development Department. Your primary responsibility will be to develop and validate analytical methods for various instruments such as HPLC, GC, GC-MS, IR, UV-Visible Spectroscopy, Particle Size Analyser, and more. Additionally, you will be responsible for conducting wet analysis in the lab, planning stability studies, and performing testing according to established protocols for formulations, APIs, and excipients. Key Responsibilities: - Develop and validate analytical methods for various instruments including HPLC, GC, GC-MS, IR, UV-Visible Spectroscopy, and more. - Conduct wet analysis in the lab and ...

We are looking for QC Chemist to join our QC. The role involves analysis of raw materials, in-process samples, and finished products in compliance with regulatory standards.Freshers candidates can apply.

1. Amino acid validation. 2. In-Process and finished products analysis. 3. Product development product analysis. 4. Documentation. 5. Responsible for method process Share resume to hrd@stedmanpharma.com, Call 7904827192/9786920463 Perks and benefits Canteen and other welfare benefits.

Stedman Pharmaceuticals is looking for a dynamic and experienced candidate for the Quality Control (QC) department with hands-on experience in Analytical Method Validation for various dosage forms. Share your Resume to hrd@stedmanpharma.com

Role & responsibilities 1. Hands-on experience in HPLC, GC and Kjeldahl equipment is preferable. 2. Ensure all laboratory activities comply with GLP standards, maintaining high-quality and reliable results.

Job Title: Quality Assurance (QA) Clinical Research Experience: 810 years Location: Indiranagar, Bangalore Department: Quality Assurance About the Role MSCR is seeking an experienced QA professional with strong expertise in ICH-GCP and GLP principles to ensure the highest standards of quality and compliance across clinical research and laboratory operations. The ideal candidate will be well-versed in regulatory guidelines, clinical QA processes, and GLP compliance, with proven experience in audits, CAPA management, and continuous quality improvement initiatives. Key Responsibilities Clinical QA (ICH-GCP Focus) Develop and maintain ICH/GCP-compliant processes to control the quality of work an...

Opening in Medicamen Biotech Ltd(ANVISA & EU), Bhiwadi, Raj. Pharma formulation exp. Preferred Qualification: B.Sc./B.Pharma Vacant Post: 10 Nos. QA - IPQA/Documentation/Validation QC - IPQC/HPLC/Chemical Testing/GC/KF Mail-ID: hrd@medicamen.com Required Candidate profile Immediate joiner prefer Experience : 2 to 8 Years Ready to Relocate Bhiwadi Self Motivated/ Team Player/ Committed for Performance. E-Mail: hr-ho@medicamen.com Mob: +91 7240001632/ 9992395009

Skills Required: Graduate / PG in management With a minimum of 4-7 years of experience in managing the Admin function. Must have hands on experience into Advance Excel Key Responsibilities Making MIS Reports of collated data Meticulously working on the data collated from various sources of department and preparing comprehensive reports Ensuring the precision of the reports Preparing Delivery Files Extensive work on Excel Preparing necessary dashboards for day to day operations Monitor & analyses data for business trends & prepare monthly revenue & collection report Provide cross functional quality oversight from a compliance perspective fo testing and disposition, quality investigations, val...

Sample Preparation & Analysis : Collect, process, and analyze biological samples (e.g., blood, serum, plasma) using ELISA and related immunoassay techniques. GoMediaJobs Assay Execution : Perform both manual and automated ELISA procedures, including direct, indirect, sandwich, and competitive formats, ensuring accurate and reproducible results. Quality Control & Documentation : Monitor assay quality control parameters, document results meticulously, and maintain compliance with Good Laboratory Practices (GLP) and Standard Operating Procedures (SOPs). Indeed+1ICON+1 Equipment Maintenance : Calibrate, maintain, and troubleshoot laboratory instruments such as microplate readers, pipettes, and w...

As an experienced Quality Assurance (QA) professional with 8-10 years of experience in clinical research, pharmaceuticals, or life sciences, you will play a crucial role in ensuring the highest standards of quality and compliance at MSCR. Your expertise in ICH-GCP and GLP principles will be essential to maintain regulatory guidelines, clinical QA processes, and GLP compliance throughout the organization. Key Responsibilities: - Develop and maintain ICH/GCP-compliant processes to control the quality of work and clinical studies at MSCR. - Lead and manage internal quality audits, CAPA activities, and quality management reviews. - Conduct study audits to ensure adherence to sponsor protocols, G...

Roles and Responsibility Conduct thorough reviews of patient data to ensure accuracy and compliance with regulatory standards. Analyze complex data sets to identify trends and patterns that inform business decisions. Develop and implement effective data visualization techniques to communicate insights to stakeholders. Collaborate with cross-functional teams to design and implement process improvements. Provide expert guidance on data management best practices to junior team members. Stay up-to-date with industry developments and emerging trends in health data analytics. Job Requirements Strong understanding of healthcare operations and regulations. Proficiency in data analysis and visualizat...

Quality Control (Wet Lab / HPLC-GC / Reviewer) - Officer to Sr. Executive Education: B.Sc. M.Sc. (Chemistry or related discipline) Job Overview We are seeking skilled and detail-oriented professionals to join our Quality Control (QC) team across multiple functions including Wet Lab Analysis, HPLC/GC, and Analytical Data Review. The ideal candidates should have a strong background in QC testing, regulatory compliance, and documentation practices, with the ability to contribute to continuous improvement in laboratory processes. Key Responsibilities Wet Lab (Officer Senior Officer) Perform routine wet lab analysis and testing of raw materials, intermediates, and finished products. Ensure compli...

Key Responsibilities: Perform and oversee Quality Control activities in compliance with GLP, GMP, and regulatory guidelines. Conduct analytical testing, review of results, and ensure adherence to internal QC procedures. Review, maintain, and control QC documentation, ensuring accuracy, completeness, and compliance. Ensure timely preparation, issuance, archival, and retrieval of quality records and documents. Support internal and external audits/inspections by providing accurate data and documentation. Investigate deviations, OOS, and non-conformances, ensuring timely closure and preventive actions. Collaborate with cross-functional teams to drive continuous improvement and maintain high-qual...

We are looking for a skilled ECRF Data Reviewer to join our team at Gratitude India Manpower Consultants Pvt. Ltd., with 347 references. The ideal candidate will have experience in the IT Service & Consulting industry. Roles and Responsibility Review and analyze electronic case report forms (ECRF) data for accuracy and completeness. Identify and resolve discrepancies or errors in ECRF data. Collaborate with cross-functional teams to ensure data quality and integrity. Develop and implement processes to improve ECRF data review efficiency. Provide feedback and recommendations to stakeholders on data quality improvements. Maintain accurate records of ECRF data reviews and findings. Job Requirem...