1088 Glp Jobs - Page 43

Job Band: Job Band 13 (JB13) Hiring Manager: Akhil Kodiyamtharappel Sadasivan Lead Recruiter: Tino Manimuthu Country: India Our ability to grow, develop new capabilities and serve even more patients around the world depends on associates like you, who are passionate about our mission. Thank you for considering this new opportunity to further unlock your potential. JOB SUMMARY: - Ontime completion of testing, analysis, and documentation with respect to regulatory guidelines. REPORTING: - Reports to Deputy Manager QC ESSENTIAL DUTIES: - Administration/Internal Communications: Responsible for completing testing as part of Chemical, Functional and incoming inspection. Responsible for Document Re...

Job summary We are seeking an individual to perform the Preventive Maintenance and Break Down Maintenance of Analytical Equipment's present in Quality Control . Roles & Responsibilities To perform the preventive and breakdown maintenance of analytical equipment's or Instruments like HPLC, UPLC, GC-HSS, Dissolution Test Appratus, Titrators, FTIR, UV-VIS Spectrophotometer,.... To update the preventive maintenance plan whenever addition of instruments or match the calibration schedule. To prepare the task lists for all analytical equipment's and update them in SAP. To perform the preventive maintenance as per the PM schedule. To make sure of closing the generated PM orders in SAP after performi...

QA/QC Executive Qualification Candidates with the following academic qualification may apply:- B.Tech/M.Tech - Food Technology B.Sc/M.Sc - Food Technology B.Sc./M.Sc - Microbiology B.Sc./M.Sc - Chemistry B.Sc./M.Sc - Biochemistry Roles & Responsibilities Preparation of Syrp/Batches for Production Quality Checks, Analysis, and Documentation of Incoming and Outgoing Material Quality Checks during production process & finished material Assurance of Quality Standards of the Products as well as the Facility as a whole Preparation and Maintenance of various Documents involved in Production activities Personal hygiene and factory hygiene supervision as well as supervising the housekeeping team RCA ...

#hiring . Know anyone who might be interested? "Ahmedabad Location" Veeda Lifesciences is seeking a passionate "Junior It Administrator". Experience Required: 2-4 years Interested candidates can share an updated CV to mahendra.t3705@veedalifesciences.com 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. Role & responsibilities Infrastructure...

Review & approval of laboratory analytical data, test reports, and chromatographic data HPLC/GC/UV. Ensure GLP & cGMP standards, Participate in investigations of Out of Specification & Out of Trend, deviations, & lab incidents. SOP Review, CAPA.

Job Title : Veterinarian Preclinical (CRO & GLP) Location: Pregnapur, Hyderabad Experience : 1-3 years of experience in preclinical CRO 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 animal...

Role & responsibilities 1. Good knowledge about QC compliance GLP related activity. 2. Review all specification & testing procedures and test data sheet for raw materials, intermediates, finish goods, stability, in process and packing materials. 3. Good knowledge about verification of COAs as per specification. 4. Review of analytical data and audit trail prior to batch release of finished products and stability data. 5. Maintain records of daily monitoring temperature & humidity of stability chamber. 6. Good knowledge about batch release related activity. 7. Good knowledge of ensure QC specification and analytical method are confirming to the tested pharmacopoeia & customer requirements. 8....

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...