706 Glp Jobs - Page 28

Mechanical testing & analysis, test planning, sample prep, equipment setup/maintenance, IQ/OQ/PQ, calibration, RCA, SOP/WI prep, GLP/GDP/5S compliance, safety, experiment coordination, and quality/specification support.

1. Quality Management Systems: Implementing, monitoring, and maintaining Quality Management Systems to ensure compliance with CGMP/regulatory guidelines. 2. Documentation: Reviewing and approving technical and quality documents. Required Candidate profile Should be minimum Post Graduation in Science having the work experience of about 10 Yrs in Chemical .

Role & responsibilities: Responsible for creating, coordinating and maintaining the Master Study Schedule for all Cliantha sites. Working with all Head of Departments (HODs) of Cliantha Research on a regular basis to ensure the relevant project milestones are discussed and needs of Sponsor and functional areas are not compromised. Create, plan and monitor all project activities in PM database ensuring accuracy at all times. Responsible for identifying interdependencies for all projects and facilitate communication among functional areas where required. Understands time-sensitive nature of critical path project activities and notifies the relevant teams, and/or management of related issues. W...

IITR is currently looking for a highly skilled ADL Officer for one of the pharmaceutical Co. Location - Vapi, Gujarat. If you are interested and for further information, please share your updated CV to talent@hireindians.com/call on 8700944544. Required Candidate profile Min Exp - 2-4 yrs of experience. Qualification - BSc/MSc in pharma

Job Duties This is a full-time on-site role as a Transfer Pricing Senior Associate located in Bengaluru at BDO RISE Private Limited. The Transfer Pricing Senior Associate will be responsible for preparing and reviewing transfer pricing projects, ensuring compliance with US Transfer Pricing Regulations. Qualifications Bachelors or Masters degree in Accounting, Finance, Economics, Law or related field. Minimum 2 years of relevant experience in transfer pricing, preferably with a Big 4 or leading consulting firm. Strong technical knowledge of US transfer pricing regulations, OECD guidelines, and BEPS framework. Experience in preparing and reviewing transfer pricing documentation and economic an...

Candidates should have good hands on Experience on HPLC, GC, Stability, Wet Lab, RM Sampling & Analysis, Documentation, Standardization of Karl fisher Titrator. Responsible for Calibration of Instruments. Can handle QMS & AMV activities Required Candidate profile Preferred immediate Joiners. USFDA preferable. Interested candidate can share CV on sachin.kapte@enaltec.com Mob.8976826875

To effectively operate and leverage cutting-edge AI-driven drug discovery platforms. Familiarity with machine learning techniques and statistical data analysis. Solid foundation in computational drug discovery methodologies.

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 applications—supporting 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 sta...

About The Role Position Summary: Ensuring that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations Essential Duties and Responsibilities Applies GMP/GLP in all areas of responsibility, as appropriate Demonstrate and promote the company vision Regular attendance and punctuality Read and understand analytical procedures Review documentation, generated data, calculated results, and final reports according to departmental, corporate, and client SOPs Gain a technical understanding of the techniques in which review is being performed Use MS Windows applications such as EXCEL, Word, Access, Outlook email Conducts all activ...

Job Opening: QC Chemist – Executive Level Company: Dalas Biotech Limited Qualification: B.Sc. / M.Sc. in Chemistry or related field Experience: 2 to 7 Years Instrumental Analysis using HPLC, GC, KF, UV Spectrophotometry

Grade / Level III Division / Department - R&D Job Purpose URGENT OPENING FOR THE ROLE OF GENERAL MANAGER - R&D Job Accountability: We are actively looking for credible team members who would be primarily responsible for: Encompassing literature survey. Identifying techno commercially attractive and non infringing route for fluoro-specialty molecules identified for commercialization in time bound manner. Develop & standardize industrially feasible processes and also meet long term cost targets. Identify & develop new products. Prepare feasibility report, cost analysis report, monthly progress report and TDR Demonstrate/validate the lab scale process up to commercial scale.. Essential Lead a t...

Job Title: Senior IT Administrator Bioanalytical Support Experience: 3-5 Years Job Summary: The Senior IT Administrator will be responsible for managing and supporting the IT infrastructure, systems, and applications critical to bioanalytical operations within a GLP/GxP-compliant CRO. The role ensures high availability, compliance, and performance of IT services supporting regulated lab environments, including LIMS, chromatography software, and instrument data acquisition systems. Infrastructure & System Support Manage and maintain lab-related IT infrastructure including servers, workstations, storage, and backup systems. Administer Windows Server environments, Active Directory, Group Polici...

Job Title: Junior IT Administrator Bioanalytical Lab Support Experience: 2-3 Years Job Summary: The Junior IT Administrator will assist in maintaining the IT infrastructure and systems used in regulated bioanalytical operations within a GLP/GxP-compliant CRO laboratory. This role involves daily user support, troubleshooting, and basic system administration related to lab instruments, LIMS, and networked IT systems. Key Responsibilities: User & System Support Provide first-level IT support for lab users on desktops, applications, and hardware. Troubleshoot issues with instrument PCs, printers, and lab software (e.g., LIMS, Lab Solution, Analyst software). Ensure timely resolution of support t...

Roles and Responsibilities Conduct quality control tests on raw materials, in-process samples, finished products, and stability studies using HPLC, GC, UV, Dissolution, LIMS, Microbiology techniques. Ensure compliance with GLP guidelines for laboratory operations and maintain accurate records of test results. Collaborate with cross-functional teams to resolve quality issues and implement corrective actions. Develop and execute protocols for wet analysis testing of pharmaceutical products. Participate in audits conducted by regulatory authorities or internal stakeholders.

Principal task: Analytical Method Development by HPLC for all Project. Review the analytical method development data, validation study data and method transfer protocol and reports. Calibration of HPLC system. To maintain GLP/GDP in working environment. Preparation of analytical data and submit for review. Analytical Method Development and Validation. Responsibilities: Calibration of HPLC’s as per SOP and maintenance of HPLC Systems. Maintaining record for all analytical reports by entering all the data in raw data note book and timely release of analytical reports. Preparation & Review of analytical method validation protocol and report as per the current regulatory requirement. As per Prot...

Responsibilities: Individually handling department & manpower. Strong leadership skills to guide, supervise work activities, and help team members develop their skills. Work allocation / Planning and Review of documents. Preparation of SOP, Specification, Standard Test Procedures (STP), Raw Data Sheet (Protocol), Excel worksheet validation etc. Preparation and review of Analytical Method Validation protocol & Report. Preparation and review of equipment qualification documents. Handling of QMS documents like Change control, Deviation, Incidents, OOS, OOT etc. To investigate, identify the root cause and troubleshoot. To maintain GLP and discipline in the QC department. Required Skills Change C...

Responsibilities: Participate in management review meetings. Review of department trend analysis reports and internal studies or investigations. Ensure corrective action is initiated when required. Provide complete analysis of test results, investigation or information studies. Be capable of assuming study director responsibilities for all routine testing as well as certain advanced or specialized studies as requested by clients. Duties may include test scheduling, test preparation, proper application of test method(s), data collection, data review, and approval of final report of analysis. Maintain thorough knowledge and understanding of all SOPs pertaining to microbiology/sterility assuran...

Responsibilities: Schedule daily production and Manufacturing work centres based on sales priorities and material availability. Resource Management To assist production head to qualify manufacturing work stations and resources. Establish and maintain quality standards for all products. strickly adhere the product and in process quality standards on shop floor Ensure compliance with cGMP guidelines to maintain production and quality standards. Documentation ( all statutory and internals) are upto date on day to day basis Supervise. Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and plant housekeeping on a daily basis while ensuring proper record maintenance. Required Ski...

Position: Pre-Clinical Designation: Research Associate Job Location: Dholka, Gujarat 1. Study Sample Analysis- Clinical studies 2. Method Development and Method Validation - Preparation of STP And MVP 3. Coordinate with QA & QC department for timely completion of Projects reports 4. Preparation of SOP and method development and method validation documents 5. Maintaining GLP & ensure 100% compliance

We are seeking a diligent and skilled QC Analyst to join our Quality Control Department. The ideal candidate will have hands-on experience in analytical techniques, a strong foundation in chemical analysis. Number : 9687066537

Open Positions: Chemist Wet Analysis (1-4 yrs) Reviewer Shift Incharge cum Reviewer FP/SF/RM/AMV/Water/Stability (6 8 yrs) Documentation Validation & COA (3 5 yrs) Instrumentation HPLC/GC/ICP-MS/AAS (3 6 yrs) Eligibility: M.Sc. Chemistry Knowledge of GMP/GLP and lab safety practices Willingness to work in shifts (role-specific)

Beckman Coulter LS Beckman Coulter Life Sciences is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives. Position Summary and Overview: Responsible for managing the sites Non-conformance (NC) and deviation processes. This includes reviewing and approving NC records, containing non-conforming material, conducting trend analysis, managing related CAPAs, and driving root cause investigations. The role maintains compliant Quality Management System (QMS) procedures for NCs and supports internal and external audits and inspections. Es...

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), Barcelona (Spain), London (UK) and Warsaw (Poland), 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) Education: M.Pharm/B.Pharm or M.Sc. Experience: 2 to 3 years CTC Range: 4 to 5 Lacs Job Description: To develop and ...

Job Title: Associate Manager Job Location: Bangalore About Syngene : Syngene ( www. syngeneintl. com ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, safety and sustainability (EHS) mindset and operational discipl...

Implements, manages and maintains an Engineering Change Notice System which includes master data management, document management and facilitation of the change control processes over the product lifecycle in Agilents ERP systems. Documents changes related to product improvements, repairs, and new product development for all parts, products and tools. Coordinates the interaction between R&D Engineering, Manufacturing, Procurement, Planning, and Finance to ensure appropriate changes are documented. May provide documentation such as good manufacturing practices (GMP), good laboratory practices (GLP), and good clinical practices (GCP) procedure manuals and change authorization in accordance with...