1074 Glp Jobs - Page 4

Role: Support Analyst / Application Administrator We are seeking a highly motivated Support Analyst to provide application administration, user support, and issue resolution for computer systems used across Early Development. This role acts as a technical liaison between IT and end users, ensuring optimal system performance and compliance with regulatory standards. Key Responsibilities: Act as SME for assigned applicationssupporting users, troubleshooting issues, and managing system documentation. Handle user access control, perform audits, and maintain compliance documentation (GLP/SOP). Coordinate application deployments, upgrades, validations, and decommissioning. Collaborate with stakeho...

Job Title: Senior QC + QA Trainer (Pharma / Biotech Laboratory) Location: Remote Job type: Part-time Job Summary: We are seeking a highly experienced and knowledgeable QC + QA Trainer to design, develop, and deliver technical training programs for quality control and quality assurance teams. The trainer will be responsible for building competence in analytical testing, documentation practices, GMP compliance, and QA/QC systems within a regulated laboratory environment. Key Responsibilities: Training & Development Develop and deliver structured training programs on QC laboratory techniques, QA systems, and GMP compliance . Conduct practical laboratory training (analytical instruments, wet che...

Required Analysts for Quality Control Department We are having excellent job opportunities for Quality Control (QC) Department at Amneal Pharmaceuticals, SEZ Matoda Injectable. 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 05 years (Pharma experience only-Injectable is mandatory) Desired Profile: GLP : Operation and Calibration of HPLC (Waters and SHIMADZU), GC, UV, FTIR, K/F, AAS, IC. RM-PM : Analysis of Raw material and Excipients and handling of HPLC (Waters and SHIMADZU), GC(Agilent), UV, FTIR, K/F, AAS, IC. IP-FP ...

We are seeking a candidate with knowledge of clinical trials and the end-to-end management of biospecimens. You will be an independent contributor who will work closely with our Clinical Teams to develop and implement biospecimen management plan for BMS-sponsored Phase 1-4 clinical trials. Critical to this role is the ability to oversee timelines for specimen data delivery and thereby, enabling quick decision-making and ensuring BMS s continuous competitive advantage. Key Responsibilities Oversee and manage the complete lifecycle of biospecimens collected for clinical studies with minimal supervision. Clinical Team member responsible for providing shipping/sample movement and management incl...

Job Overview: The UPLC-MS Analyst is responsible for conducting ultra-performance liquid chromatography and mass spectrometry analyses on a wide variety of samples, including pharmaceutical, environmental, and biological samples. The role involves sample preparation, method development, and analysis using UPLC-MS techniques to identify, quantify, and characterize compounds. The analyst works closely with research and development teams to support studies, ensuring accurate and timely results. Key Responsibilities: Operate and maintain UPLC-MS/LCMS systems for the separation, identification, and quantification of compounds in various sample matrices. Perform routine analyses and troubleshoot i...

The Sr. Research Associate/ Sr. Executive/ Sr. Analyst for the Small Molecule Bioanalytical Laboratory is a technical role responsible for conducting BA/BE studies in the laboratory. Job responsibilities include performing critical method development and validation programs, technical and regulatory compliance of all studies. This role requires an individual with a robust background in pharmaceutics, or other related life sciences, coupled with extensive experience in the bioanalytical field, particularly within small molecule bioanalysis. This role demands an individual with a strong commitment to compliance, integrity, and excellence in bioanalytical research, particularly in small molecul...

5 7 years of experience in Analytical Method Development especially in handling HPLC, GC, ICP OES & LCMS , GCMS, NMR. Worked on Chemical Safety, GLP practice & documentation. Experience of Method development, Methods of analysis to maintain all testing records in line with ISO-9001 and cGMP requirements.

Sample Analysis of Pharmaceutical Dosages for Particle size determination by using the Optical microscope with 21 CFR Part 11 Compliant software Documentation of Analysis Research on new method development for different types of samples Interaction with customers related to analysis Following Laboratory practises as per GLP requirement Software application testing on real samples Eligibility: Education: Final Year M.Sc./B.Tech Biotechnology students (or passed out students who want internship and Project) Location: ImageProVision Headquarter at Baner, Pune Working Hrs: 9am to 6pm, Monday to Friday Duration: 6 months

Role Description This is a full-time role for a Quality Control Analyst, based on-site in Pune. The Quality Control Analyst will be responsible for conducting quality control tests, operating laboratory equipment, and ensuring compliance with quality assurance protocols. Day-to-day tasks include analyzing test results, preparing analytical test reports, and maintaining laboratory records. The role requires strict adherence to standard operating procedures to guarantee the accuracy and integrity of data. Skills required - Proficient in Analytical Skills, Quality Control, and Quality Assurance Hands-on experience with Laboratory Skills and Laboratory Equipment Strong attention to detail and pr...

Key Responsibilities: 1. Routine Analysis & Testing: Perform analysis of raw materials, in-process, finished products, and stability samples as per approved specifications and test procedures. Conduct analysis using instruments such as HPLC, GC, UV-Vis Spectrophotometer, FTIR, Dissolution Tester, pH Meter, and KF Titrator . Ensure analytical results are recorded accurately and reviewed as per GLP and cGMP standards. 2. Documentation & Record Keeping: Prepare and review analytical reports, COAs, and test records. Maintain logbooks, stability registers, and instrument usage records. Ensure compliance with Good Documentation Practices (GDP) and data integrity requirements. 3. Instrument Calibra...

Date: 16 Oct 2025 Location: Bangalore, KA, IN, 560100 Division: Discovery Services Job Description Designation: Sr. Research Associate/ Sr. Executive/ Sr. Analyst, Small Molecule Bioanalytical Research Laboratory, Translational and Clinical Research Job Location: Bangalore, India Reporting to: Project Leader / Group Leader of Small Molecule Bioanalytical Laboratory Job Grade: Level 9-II The Company Syngene International Ltd. (BSE: 539268, NSE: SYNGENE, ISIN: INE398R01022), is an integrated research, development, and manufacturing solutions company serving the global pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical sectors. Syngene's 4500+ scient...

Company Description At TAPI, we're not just a companywe're a community committed to advancing health from the core. As the world's leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we're shaping the future of health worldwide. Our strength lies in our peoplea team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that t...

HPLC, Prep HPLC, LCMS, UPLC, and Flash Chromatography. HPLC method development and validation, SOP/IOP preparation, calibration, and documentation. Knowledge of raw material, intermediate, and finished product testing.

Role & responsibilities Serve as the primary subject matter expert for all bioanalytical methods, including method development, validation, and sample analysis. Design and execute complex experiments for the quantification of drug candidates, metabolites, and biomarkers in biological matrices using a variety of platforms (e.g., Ligand Binding Assays, cell-based functional assays). Lead the evaluation, implementation, and troubleshooting of new analytical platforms and technologies to advance the laboratory's capabilities. Develop and influence bioanalytical strategies for multiple projects across the drug development pipeline. Manage project timelines and resources, serving as the bioanalyti...

Role & responsibilities : *Able to handle team planning and execution of shift schedule *Good knowledge on all QC related techniques like HPLC,Electro phoresis,Physiochemical, Biochemical, Immunochemical and cell based techniques *Good knowledge on QC equipment and related software *Need to ensure GLP&GDP Compliance *Good knowledge on sample management, Training Activities and QMS Elements

Scientific Leadership: Drive adoption of new technologies and methodologies to improve study accuracy and efficiency. Example, adopting best practices, standardizing workflow, eliminating unrequired steps. Standardized templates will reduce manual errors and cut turnaround time. Regulatory and Compliance: Provide expert toxicological risk assessments for new compounds and formulations to support regulatory submission. Example, in silico modelling, read-across techniques, literature reviews, and derivation of PDE and OEL values. Ensure timely submission of regulatory responses to meet 98% on-time compliance rate. Example, CAPAs, and deviation closures using TrackWise. Reinforce GLP adherence ...

Utility Operator HVAC / Water / Electrical (01 Position) based in Vapi, Gujarat. The ideal candidate brings 5 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvemen...

The ideal candidate brings 15-20 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen). Plan resources, ensure statutory compliance, drive traini...

The ideal candidate brings 5 to 10 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen) Additional info: Key Skills: DMF Compilation, QA Coordinat...

Micro Head based in Kathua, Jammu & Kashmir. The ideal candidate brings 12 - 15 yrs exp. and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen). Lead mi...

Assistant Manager / Sr. Executive based in Kadi, Mehsana District, Gujarat. The ideal candidate brings 5 to 10 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improveme...

Chemist (On Contract) (MP 25/20) based in Narmada, Gujarat. The ideal candidate brings 15-20 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen...

HVAC & Water System Engineers 2 Posts based in Amritsar. The ideal candidate brings 2 - 4 yrs exp and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen)...

HPLC Operator (01 Position) based in Vapi, Gujarat. The ideal candidate brings 5 to 10 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen). Ope...

Autocad Operator 1 Pos based in Amritsar. The ideal candidate brings 6-7 yrs exp and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improvement (5S/Lean/Kaizen). Operate and tro...