Method Validation Jobs

Designation :- Analytical Method ValidationQualifications:- BSc/MScExperience :- 6 Years To 8 YearsSalary:- As Per interview Gender:- MaleJob Location:- Vapi, Gujarat Industry:- Manufacturing Industry/Reputed Engineer Company

Job Opening: Quality Assurance (QA) Officer with IPQA ResponsibilitiesLocation: On-site Nalagarh, Himachal PradeshExperience: 3+ years mandatory experienceQualification: B. Pharm / M. PharmLanguage & Software Skills: Proficiency in English and Microsoft Office (Word, Excel, PowerPoint) MandatoryAbout the Role:We are hiring a knowledgeable and proactive Quality Assurance (QA) Officer to join our pharmaceutical manufacturing unit in Nalagarh. This role combines core QA responsibilities with In-Process Quality Assurance (IPQA) oversight on the production floor. The ideal candidate will ensure regulatory compliance, documentation accuracy, and continuous quality improvement throughout the production lifecycle.Key Responsibilities: Core QA Functions:Review and approve Batch Manufacturing Records (BMR) and Batch Packaging Records (BPR).Manage deviations, validations (mandatory), change controls, CAPAs, and maintain documentation as per regulatory norms.Conduct internal quality audits and assist in external audits by clients or regulatory agencies.Maintain and update SOPs, manuals, and master documents in accordance with current regulations.Oversee document control systems and archival processes.Train employees on cGMP practices and quality systems.In-Process QA (IPQA) Responsibilities:Monitor critical stages of manufacturing and packing operations to ensure GMP compliance.Line clearance before batch start-up and between changeovers.Sampling of in-process materials and verification of critical process parameters.Real-time review and recording of BMR/BPR entries during production.Ensure proper gowning, hygiene, and sanitation compliance on the shop floor.Immediate reporting and documentation of any deviation or non-conformance observed.Desired Profile:B. Pharm / M. Pharm with a strong academic and technical background.Minimum 3 years of QA experience in a regulated pharmaceutical manufacturing unit.Hands-on experience with IPQA activities and on-floor quality monitoring.Excellent written and spoken English communication skills MandatoryProficiency in Microsoft Office (Word, Excel, PowerPoint) MandatoryGood understanding of WHO-GMP, Schedule M, and other applicable quality regulations.Strong coordination skills, attention to detail, and documentation accuracy.Join a team committed to delivering excellence through quality-first manufacturing.If you're passionate about compliance, process integrity, and hands-on QA work we invite you to apply!#QualityAssurance #IPQA #PharmaJobs #QAOfficer #BPharmJobs #MPharmJobs #PharmaCareers #GMPCompliance #NalagarhJobs #QualityFirst #IndianPharma #HimachalPharmaJobs #AuditReady

We are seeking a motivated and detail-oriented Chemical Analyst to join our team. As an analyst, you will support our team in conducting chemical tests, analyzing samples, and maintaining lab equipment. The ideal candidate must have foundational understanding of chemistry principles and laboratory procedures, to apply their knowledge in a professional laboratory environment. The role requires attention to detail, a strong commitment to safety standards, and the ability to collaborate with senior team members.Key Responsibilities: Chemical Analysis & Testing:Perform routine chemical tests and analyses on raw materials, in-process samples, and finished products to ensure they meet the required specifications. Data Documentation & Reporting:Record and document results in a clear and organized manner, ensuring accuracy in all data entries. Prepare reports for senior analysts or supervisors with findings, conclusions, and recommendations. Sample Preparation & Handling:Prepare and handle chemical samples by following established lab procedures. This includes weighing, mixing, and maintaining proper sample storage conditions. Lab Equipment Maintenance & Calibration:Maintain, calibrate, and troubleshoot laboratory equipment and instruments. Ensure proper use of equipment and adherence to all safety guidelines. Method Development & Validation Support:Assist in the development and validation of new chemical analysis methods, under the guidance of senior analysts. Contribute to method improvements based on findings from experimental tests. Adherence to Safety & Quality Standards:Follow all safety guidelines and laboratory protocols. Ensure compliance with health, safety, and environmental regulations. Maintain a clean, organized, and safe working environment at all times. Collaboration & Communication:Work closely with senior analysts and lab managers to troubleshoot problems, analyze trends, and implement improvements.

must have knowledge to perform analysis of Development, Routine and stability sample.

To ensure analytical data generated is adequate and accurate for purpose.To perform analysis of stability study,working standard samples.To perform the analytical method validation.To work as per GMP/GLP in the laboratory

Job Responsibility: 1. To ensure that GLPs followed in the laboratory. 2. To establish, develop, validate testing Procedures. 3. To Prepare protocols, reports and monitor samples of Method validation andMethod Development. To perform the calibration of instrument/equipment. To ensure that instruments andequipment are calibrated as per given schedule and records are maintained accordingly. To perform analysis for Raw material, finish products and stability samples. To ensure that samples are analysed in time and results are conveyed todepartment head or reviewer as per requirement and as per the procedure. To maintain documentation for Regulatory Submission Maintaining of SOP as per regulatory requirements and periodically reviewed. To ensure all record are maintained as per the procedures. Any other work assigned by the superiors. To prepare Method of analysis (MOA) and Specification and any otherdocuments of new drug product. To perform Method transfer to Q.C Department.Qualification :B. Pharm / M. PharmExperience : 2-3 YearsJob Location :Vadodara

Collaborate with design, validation, and architecture teams for IP content coverage, test pattern and test program development, validation, and debugDevelop test program infrastructure incorporating latest Best-Known MethodsValidate new product features, test conditions, test methodologies, and test contents during first silicon bring-upPerform silicon characterization across process, voltage, and temperaturePerform test program correlation and release for high volume productionDrive Key Performance Indicators such as test time reduction, yield debug, and quality improvement across productsSupport qualification activities and customer return debugRequirements:More than 4 years of experience in semiconductor product developmentExperience with ATE test program and pattern development Advantest 93K, a must.HBM, Scan, Bist and test program integrations experiences.Proficient in software programming and scripting languages (C, C++, Java, Ruby, Perl, Python)Knowledgeable in version control tools (Git, SVN, CVS)Knowledgeable in statistical analysisProficient in Windows, Unix, and Linux operating systemsStrong written and verbal communication skills

1. Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC etc and automation2. Communicate with synthesis-R&D and lead assist in analytical method remediation/troubleshooting3. Perform analytical characterization and data interpretation for complex organic compounds4. Experience in making lab SOPs and study reports5. Develop analytical methods that are accurate, precise, specific, and robust6. Calibration of the Analytical instruments as per the master calibration schedule7. Preparation and review of Specifications, Method of analysis procedures and Analytical development reports8. Discuss work plan on daily basis with supervisor/ manager and Mentor junior lab personnel9. Preparation and review of analytical protocols and reports (Analytical method validation, Method feasibility, Analytical method transfer, etc.).10.Participate in project meetings and prepare weekly and monthly reports and submit to Manager11. Preparation of analytical technical documents for dossier / Technology transfer executions of the projects.12. Regular lab duties including equipment maintenance, chemical inventory and lab clean-up13. Maintain strict IP Confidentiality and adhere to all related data privacy policies

Plan and manage all activities of Laboratory (analysis, chemical management, calibrations, standards management, investigations, incidents or out of specifications, method optimizations, validations .Manpower Planning ,Preferred candidate profile Having 2 to 3 Years of experience as a manager(Only Male).

Hi,we have an urgent opening in ADL for pharmaceutical ltd.Location:- Rudrapurexperience: 1-5 yrssalary 3.0 LPAinterested candidate, please share your resume on

Job descriptionPreparing test solutions, compounds, and reagents for conducting tests and advising and coordinating test procedures(qualitative and quantitative chemical and collect/physical analysis of raw materialsRequired Candidate profileExperience in handling instruments like UPLC, LC-MS , GC, ICP-OES, XRD and DSC.Role: QA / QC ExecutiveIndustry Type: Fertilizers / Pesticides / Agro chemicalsRole Category: Production & ManufacturingSheetal Tanwar