Quality Control InspectionsHplcQuality Control ToolsPharmaceutical Quality ControlQUALITY CONTROL
Location: On-site Nalagarh, Himachal PradeshExperience: 12 years (Mandatory)Qualification: B.Sc. in Chemistry / Microbiology / Biotechnology / Life SciencesAbout the Role:We are looking for a dedicated Quality Control (QC) Officer to join our pharmaceutical manufacturing team at our Nalagarh facility. The ideal candidate will have hands-on experience with laboratory testing and strong documentation practices in a GMP-regulated environment.Key Responsibilities:Conduct testing of raw materials, in-process samples, and finished products.Operate and maintain analytical instruments like HPLC, UV, IR, pH meter, etc.Ensure accurate and timely documentation as per cGMP and GLP guidelines.Perform stability studies and environmental monitoring (if required).Participate in lab audits, calibration, and equipment qualification.Maintain safety and hygiene in the lab environment.Desired Profile:B.Sc. in Chemistry / Microbiology / Biotechnology or relevant field12 years of QC experience in a pharmaceutical formulation unit (mandatory)Sound knowledge of GMP practices and analytical techniquesAttention to detail, good documentation habits, and strong analytical skillsMandatory Proficiency in written and verbal EnglishJoin a team committed to delivering high-quality, affordable medicines.Apply now to become part of our quality-driven organization!#QualityControl #PharmaJobs #ChemistryJobs #QCOfficer #PharmaceuticalIndustry #HimachalJobs #BScJobs #NalagarhJobs #PharmaCareers #GMPCompliance
QTP-Quick Test Professional QC - Quality ControlQuality ControlHPLCWalk in
Key Responsibilities(Performance Indicators)Knowledge about IMS system (ISO 9001:2015, ISO 14001:2015 OHSAS 18001:2007, and cGMP.Analytical skill for QC instrument, i.e. GLC, HPLC, UV-Visible, FTIR, ICP, K/F, Melting point etc.Regularize the QC activities as per cGMP requirements.RM, PKG, In-process and FG sampling and Analysis.Co-ordination with QC staff, R and D, Commercial and production for quality and dispatch related activities for on time dispatches.Day to day monitoring and execution online all IPQC and FG analysis activities.Resolve the trouble shooting related to QC activities.Knowledge about 21 CFR Part 211, 111 with data integrity (Part-11)Awareness about responsible care (Environment, Health, Safety and Security)
We have vacant of 2 QC Officer Jobs in Baddi Experience Required : 1 Year Educational Qualification : B.Pharma, B.Sc, M.Pharma, M.Sc Skill QA-Quality Assurance,QC - Quality Control,HPLC etc.
Performing HPLC Analysis: Running samples through HPLC instruments, interpreting results, and documenting findings. Maintaining Equipment: Ensuring HPLC systems are calibrated, maintained, and operating correctly. Method Development and Validation: Contributing to the development and validation of HPLC methods for various applications. Data Handling and Reporting: Managing raw data, compiling results, and generating reports as needed. Compliance with GLP/GMP: Adhering to Good Laboratory Practices (GLP) or Good Manufacturing Practices (GMP) guidelines. Troubleshooting: Addressing any issues or problems that arise during HPLC analysis. Safety and Housekeeping: Maintaining a safe and organized laboratory environment. Documentation: Keeping accurate records of all analytical activities and data.