16 Amv Jobs

Responsibilities: * Conduct analytical research using GLP principles. * Develop, validate, transfer methods through AMV/AMT processes. * Collaborate with cross-functional teams on method development and validation. Health insurance Provident fund

Preparation of Validation Master plan, Quality Manual & SOP’s. FAT, URS, IQ, OQ, PQ and requalification protocol and reports of all instruments, calibration and validation schedule. Email CV - hr.rabale@galentic.com Job Location -Rabale Navi Mumbai Required Candidate profile Operation of EPIQ software, DOCS IQ and Learn IQ., Review in LIMS, Review of protocol APQR, CMD, CMV, AMD, AMV, AMT& method. Issuance of MFR, Batch Manufacturing Record,Batch Filling Record, Risk Mgt

Analytical method validation and Stability studies. Day to day trouble shooting QC sophisticated Equipment's like GC-MS, UPLC, HPLC, GC, GC-HS, Dissolution etc. Designation - Executive/Senior Executive/Deputy Manager/Manager

Job Opening @ leading OSD Pharmaceutical Company Seabird Staffing Solution is looking for its reputed client who have-state-of-the-art Pharmaceutical Organization involved in Research, Manufacturing, Marketing, Sales and Distribution of Medicinal Formulations and Products. Job Title - Analytical Development- Officer / Executive Location - Chhatrapati Sambhajinagar, Maharashtra Exp. - 5 to 10 Years Qualification - M.Sc. (Chemistry) CTC- No bar for suitable candidate Key skill - AMV / AMT Job Description- Method Development :Develop and optimize analytical methods for drug products using techniques like HPLC, GC, GC-MS, and LC-MS. Method Validation and Transfer: Execute and manage method valid...

Seabird Staffing Solution is looking for its reputed client who have- state-of-the-art Pharmaceutical Organization involved in Research, Manufacturing, Marketing, Sales and Distribution of Medicinal Formulations and Products. Job Title - Analytical Development- Officer / Executive Location - Chhatrapati Sambhajinagar, Maharashtra Exp. - 5 to 10 Years Qualification - M.Sc. (Chemistry) CTC - No bar for suitable candidate Key skill - AMV / AMT Job Description- Method Development: Develop and optimize analytical methods for drug products using techniques like HPLC, GC, GC-MS, and LC-MS. Method Validation and Transfer: Execute and manage method validation, including creating protocols and reports...

Experienced in independent instrumental analysis of raw material, in process samples, finished product and stability samples of pharmaceutical products. Well versed in analysis of Tablets, capsules, liquids samples, for common test as Assay, Related substances, Dissolution and preservative content analysis as per controlled specification and method of analysis. Should able to operate, calibrate and maintain instruments like HPLC, GC, Dissolution apparatus, UV and FTIR etc. Experience of Empower, Lab solution software shall be recommended. Exposure to perform AMV or development shall be preferred. Aware about on line & good documentation practices. vii. Should have knowledge of Data integrity...

Analytical Techniques: Versatile handling of HPLC, GC, PSD, UV, and FT-IR analysis, with hands-on experience in troubleshooting, calibration, and method validation. Statistical Analysis: Familiar with statistical concepts relevant to analytical method validation. Software: Skilled in MS Word and Excel for technical documentation, data analysis ( Excel-based statistical functions), and reporting. Regulatory Compliance: Experienced in managing USFDA and other international regulatory audits. Cross-Functional Collaboration: Strong ability to work effectively with QA, QC, and R&D teams to ensure method robustness and regulatory compliance. Must be having experience in API Designation - Executive...

Role & responsibilities 1. Knowledge of calibration and operation of HPLC with empower software. 2. Sound knowledge of analytical method development and Analytical method validation of OVI, purity, and assay method by HPLC as per pharma guidelines. 3. Knowledge of caliberation and operations of all equipments like balance, ph meter, in analytical opeartion. 4. good knowledge of sample preperation as per GLP. 5. Knowledge of retreival and storage working standards and columns. 6. Handling of final compilation of raw data, chromatographic data complying with GLP requirements. 7. Recording all analytical activities, approximately in respective raw data forms. 8. knowledge of preperation of gene...

Hands-on experience in - Perform the Analytical Method Validation by HPLC/GC Preparation and review of AMV Protocol and Reports Operations and calibration of the instruments like HPLC, GC etc. Preferred candidate - Having 5 - 10 yrs of experience in Quality control and must have at least 2 years in AMV

Role Overview: As a QC Team Leader at our company located in Ambernath, Maharashtra, your primary responsibility will be to lead a team of 30+ members in the QC-AMV team, including LC-MS, Nasal, and FT-NIR teams, for regular testing and method validation activities. You will also provide backup support to the QC Head of Department (HOD) by managing daily updates, commercial output, monthly sample status, training, review meetings, and coordination with stakeholders to align work requirements. Your role will involve executing and approving various types of Quality Management System (QMS) processes, identifying scientific root causes, implementing corrective and preventive actions (CAPA), and ...

Roles and Responsibilities Conduct analytical method validation, including preparing methods, running samples, and reporting results. Perform routine maintenance of laboratory equipment such as GC-MS, HPLC, LCMS, and other chromatography systems. Develop and maintain calibration protocols for instrument qualification and preventive maintenance schedules. Collaborate with cross-functional teams to resolve issues related to analytical testing and method development. Ensure compliance with regulatory requirements by maintaining accurate records of test data and reports.

Role & responsibilities 1. Knowledge of calibration and operation of HPLC with empower software. 2. Sound knowledge of analytical method development and Analytical method validation of OVI, purity, and assay method by HPLC as per pharma guidelines. 3. Knowledge of caliberation and operations of all equipments like balance, ph meter, in analytical opeartion. 4. good knowledge of sample preperation as per GLP. 5. Knowledge of retreival and storage working standards and columns. 6. Handling of final compilation of raw data, chromatographic data complying with GLP requirements. 7. Recording all analytical activities, approximately in respective raw data forms. 8. knowledge of preperation of gene...

Role & responsibilities 1. Knowledge of calibration and operation of HPLC with empower software. 2. Sound knowledge of analytical method development and Analytical method validation of OVI, purity, and assay method by HPLC as per pharma guidelines. 3. Knowledge of caliberation and operations of all equipments like balance, ph meter, in analytical opeartion. 4. good knowledge of sample preperation as per GLP. 5. Knowledge of retreival and storage working standards and columns. 6. Handling of final compilation of raw data, chromatographic data complying with GLP requirements. 7. Recording all analytical activities, approximately in respective raw data forms. 8. knowledge of preperation of gene...

Job Overview To lead and execute analytical method validation, transfer, and verification activities in compliance with regulatory and cGMP standards, ensuring robust analytical support for product development, regulatory submissions, and commercial manufacturing. Competencies Plan, perform, and document Analytical Method Validation (AMV) and Analytical Method Transfer (AMT) for raw materials, intermediates, and finished drug products. Prepare and review protocols and reports related to method validation/verification/transfer in alignment with ICH guidelines. Coordinate with R&D, AR&D, QA, RA, and manufacturing units for method transfer and troubleshooting activities. Perform routine and non...

Hands-on experience in - Perform the Analytical Method Validation by HPLC/GC Preparation and review of AMV Protocol and Reports Operations and calibration of the instruments like HPLC, GC etc. Preferred candidate - Having 5 - 10 yrs of experience in Quality control and must have at least 2 years in AMV

Company Overview: We are a reputed pharmaceutical company specializing in the manufacturing of Oral Solid Dosage (OSD) formulations. Committed to high-quality standards and regulatory compliance, we are looking for a dynamic and experienced professional to join our Quality Control team. Job Purpose: The Assistant Manager Quality Control will oversee and manage day-to-day QC operations to ensure compliance with cGMP, GLP, and regulatory requirements for OSD manufacturing. This role is critical for maintaining product quality and supporting internal and external audits. Key Responsibilities: Supervise and lead a team of QC analysts and chemists in routine testing of raw materials, in-process s...