945 Method Validation Jobs - Page 2

As a Quality Control Analyst in the chemical industry at Gait Naurish (I) Ltd., located in Sector 155, Noida, Uttar Pradesh, you will play a crucial role in ensuring the quality and regulatory compliance of our fine chemicals and flavour intermediate synthesis products for the food, fragrance, and nutraceutical industries. **Key Responsibilities:** - Conduct and interpret chromatographic analyses using GC (Gas Chromatography) and HPLC (High-Performance Liquid Chromatography). - Perform moisture determination via Karl Fischer titration. - Execute TLC (Thin-Layer Chromatography) for rapid qualitative assessments. - Assist in developing, optimizing, and validating new analytical methods in acco...

Description At USP, we value inclusive scientific collaboration and recognize that attracting diverse expertise strengthens our ability to develop trusted public health standards. We foster an organizational culture that supports equitable access to mentorship, professional development, and leadership opportunities. Our partnerships, standards, and research reflect our belief that ensuring broad participation in scientific leadership results in stronger, more impactful outcomes for global health. USP is proud to be an equal employment opportunity employer (EEOE) and is committed to ensuring fair, merit-based selection processes that enable the best scientific mindsregardless of backgroundto ...

Perform analysis of RM/IP/FP/API samples using HPLC/GC. Conduct method validation, stability studies, documentation, and ensure cGMP, GLP & data integrity compliance. Handle OOS/OOT, maintain instruments, and support audits.

Plan and execute advanced microbiological research to develop new products and optimize existing processes. Conduct microbial culturing, isolation, identification, and characterization using classical and molecular biology techniques. Required Candidate profile Must have experience in conducting antimicrobial assays by MIC/MBC and also handled in-vitro enzyme assays.

To Prepare sample for the determination of heavy metals, micro minerals and minerals in Food and Agriculture samples as per ISO, IS and Customer specific requirements adopting test methods ISO, AOAC and IS methods using Microwave digestor. Maintenance of standard Reference Materials, Chemicals, Reagents and Glassware used in the laboratory. Responsible for all the instruments related to Metal analysis. Maintaining samples; before, during and after analysis. Qualifications 3-4 years experience of working in food testing laboratory. Proficient in handling ICP-MS and method validation for heavy metals analysis Graduate B.Sc/M.Sc in Chemistry Good interpersonal and communication skills. Energeti...

Job Purpose: To design, develop, and validate HPLC, GC, and other analytical test methods that support the scale-up and manufacturing of new products, ensuring all project activities are completed within defined timelines and quality standards. Key Responsibilities: Operate analytical instrumentation including GC, HPLC/UPLC, UV/VIS, and other relevant laboratory equipment. Develop and validate analytical methods for new and existing products, including in-process samples for product development. Develop and validate test methods for use in cleaning validation studies. Prepare comprehensive method development, validation, and analytical test reports. Perform routine calibration and verificati...

Education: M.Pharm, M.Sc. (Chemistry), Ph.D. Experience: 5 to 12 years Location: Gurgaon An Analytical R&D Scientist in formulation is responsible for developing and validating analytical methods, conducting complex testing on various formulations, and ensuring product quality and stability. This includes designing and executing experiments, interpreting data, mentoring junior scientists, and collaborating with cross-functional teams to meet project and regulatory goals. Responsibilities Method development and validation: Design, perform, and validate new analytical methods for release and stability testing, ensuring compliance with regulatory guidelines like ICH. Testing and analysis: Indep...

Experience in crop protection, pharma, specialty chemicals, fine chemicals, Quality control Department Hands on experience in instrument and classical method of analysis. Good knowledge and experience in GLP and GMP. Good knowledge and experience of customer and regulatory audits. Handling customer complaints. Compliance with RCA and CAPA. Good knowledge and experience to establish QMS documentation.

Key Job Responsibilities: Lead Analytical Research and Development (ARD) activities, including method development, validation, stability studies, and method transfers. Review SOPs, STPs, protocols, raw data, and analytical reports. Provide analytical support to formulation development and manufacturing for product development, exhibit, and commercial batches within timelines. Mentor team members, allocate resources, monitor progress, conduct performance reviews, and arrange training. Manage internal and regulatory audits. Ensure compliance with standards, procedures, and data integrity across the department. Coordinate with external laboratories for specialized services and instrument calibr...

As a Quality Control Laboratory Compliance Specialist, your role involves ensuring compliance with SOPs and regulatory requirements. Your responsibilities will include: - Imparting training to QC Associates on SOPs and current regulatory requirements based on review observations. - Reviewing Analytical data such as Finished, Intermediate, Raw material, and Stability. - Ensuring accuracy of analytical data by reviewing electronic data and sequence audit trail against hard copy. - Reviewing Stability Protocols, Stability schedules, and Stability data sheets. - Reviewing master list of instruments, equipments, and Qualification documents. - Reviewing Preventive maintenance schedules, Calibratio...

Walk-In Drive For Formulation Analytical Research & Development(FAR&D)- MSN Laboratories, R&D Center, Pashamylaram, Hyderabad on Saturday 20-12-2025. Requirement for Executive - FAR&D - Formulation Analytical Research & Development(FAR&D) Undertake method development, troubleshooting and method validation to GMP and ICH. Investigation of non-conforming samples, CAPAs, data evaluation and reporting. Write cGMP Quality documents including Standard Operating Procedures, laboratory equipment procedures and investigational protocols. Excellent, enthusiastic, clear communication skills, both written and verbal, with a diverse audience are critical to the success of this position. Proven ability to...

Role Overview: As a Senior Executive - AQA at Jubilant Pharmova Limited in Nanjangud, Mysore, you will play a crucial role in ensuring analytical compliance in alignment with regulatory guidelines, monograph requirements, customer needs, and internal procedures. Your responsibilities will involve reviewing laboratory metrics to identify areas for improvement, ensuring right first-time laboratory performance, and overseeing various quality management system processes such as OOS, OOT, deviations, change management, incidents, CAPA, and effectiveness checks. Additionally, you will be responsible for reviewing and approving SOPs, specifications, analytical procedures, and conducting training on...

Role & responsibilities Perform analytical method validation for all tests like dissolution, Assay , Organic Impurities , Residual Solvents by HPLC or GC Method Transfer to QC sites Perform Calibration of analytical equipment like pH meter, Balance, HPLC, GC etc Maintain GLP Preparation of AMV protocols and reports Involve into lab incidence or investigations. Management of standards, chemicals/reagents, columns. Preferred candidate profile Candidate should have hands on experience in Method validation, Transfer, Protocol preparation etc. Immediate joiners preferable. Interested candidates may apply on madhura.patil@rubicon.co.in

Industry Name: Alivira Animal Health Limited Location: Parawada,Visakhapatnam Department: Quality Control Designation: Officer . Positions- 05 Role & responsibilities: 1. Should have a good knowledge in HPLC,GC,Wet Analysis,Method Validations and Method transfers. Preferred candidate profile: 1. Education: B.Pharm/B.Sc/M.Sc (Chemistry). 2. Experience: 2 to 5 Years. 3.Preferable Male Candidates. 4.Willing to work in shifts. 5.Pharma Exposure mandatory. 6.Immediate Joiners Preferred. Benefits: 1.Free Transport and Canteen facility. 2.Permanent roles,Uniform,Mediclaim,Statutory benefits. 3.Career growth and Competitive Salary. WALK-IN INTERVIEWS: Date and Day: 13/12/2025 & Saturday. Time: 10:30...

An ADL (Analytical Development Laboratory) role in API job responsibilities includes developing and validating analytical methods for raw materials, intermediates, and finished APIs, performing routine

Walk-In Interview: 14th December 2025 @ Sanand Job Location : Virochannagar Plant Venue : Hotel Veritas Grand, Sanand Vinayak Entice, Sanand - Viramgam Highway, Sanand, Ahmedabad - 382110 Time : 09:00 AM TO 03:00 PM Position: Technical Assistant / Executive Dept.: Quality Control (Formulation/Micro) Qual./ Exp.: B. Sc. / B. Pharm / M. Sc. / M. Pharm with 1 to 5 Years of relevant experience Area: Analysis /Qualification / Operations on HPLC/GC/FP/IP/RM/PM. Environment Monitoring, Media Preparation and Autoclaving, MLT, BET, Sterility Testing, Analytical Stability, Analytical method transfer Dept.: Quality Assurance (Formulation) Qual./ Exp.: B. Pharm / M. Pharm / M. Sc. with 1 to 5 Years of r...

Troubleshoot and identify solutions to resolve system issues. Manage spares ordering and replacement. Handle complaints and ensure timely resolution. Provide pre-sales support and install medical equipment. Achieve service targets through sales of contracts, consumables, and spares. Maintain accurate records of maintenance activities and follow standard operating procedures (SOP) for opening, attending calls, and closing them on time. Escalate unresolved issues to appropriate internal teams. Job Requirements Graduate or Diploma Holder in Biomedical / Electronics / Electrical / Instrumentation / Industrial Electronics. 1-3+ years of customer service in Medical Device/Equipment is preferred. P...

Develop and execute multi-channel strategies to maximize customer repeat purchase rates and average order frequency. Conduct deep dive analysis into customer cohorts to identify key churn indicators and develop timely, targeted intervention campaigns. Design, implement, and test personalized winback and reactivation flows for lapsed customers. Oversee the optimization and performance of loyalty and rewards programs, ensuring high enrollment and redemption rates. Track retention KPIs such as Churn Rate, CLV, and Repeat Purchase Rate, and utilize CRM tools for advanced customer segmentation. Optimize the entire subscription lifecycle, from onboarding to managing cancellation flows, for applica...

We are looking for a highly skilled and experienced professional to join our team as an Expert in Science & Technology at Novartis Healthcare Pvt. Ltd. The ideal candidate will have a strong background in science and technology, with excellent analytical and problem-solving skills. Roles and Responsibility Collaborate with cross-functional teams to develop innovative solutions using cutting-edge technologies. Conduct thorough analysis of complex data sets to identify trends and patterns. Develop and implement new methods and techniques to enhance existing processes. Provide expert guidance on scientific and technological matters to junior team members. Stay up-to-date with industry developme...

ARKRAY Healthcare Pvt. Ltd. Surat, India Document Control OP/F/046, Ver. 01, Effective date: 01.09.2022, Due date: 31.08.2027 Job Description (Reference Procedure: OP/S/001) JD No. JD-QLT-020Organization Level Division / Department / Team / Supervisor / Team MemberJob TitleExecutive BGMJob PurposeTo test and release all product at Semi-finished, In Process & Finish Stage Biochemistry & BGM Products and manage Quality Control Activity in Arkray Healthcare Pvt Ltd. Job ImportanceTo test, review and release the biochemistry product range & BGM Product range Job Responsibilities Ensuring that all the in process (IPQC) and semi-finished products (HALB) are tested in time (as per TAT) and release ...

Plan and execute reactions independently with proper reagents and according to applicable SOPs. Follow safety protocols and guidelines in the lab. Record analytical observations, necessary data, and accurate calculations. Prepare standard solutions and maintain CRM. Maintain laboratory documents and records. Validate methods for new matrices for metals and minerals parameters. Job Requirements Expertise in Operation of ICP-MS, ICP-OES for minerals and metals testing. Validation and verification as per EC regulation guidelines. Sample preparation and extraction of metals and minerals from various food and agricultural products. Quantification of metals & minerals by ICP-OES & ICP-MS technique...

We are looking for a highly skilled and experienced Analyst to join our Inorganic Lab team in Bangalore. The ideal candidate will have 2-7 years of experience in the field. Roles and Responsibility Operate ICP-OES for minerals and metals testing with expertise. Validate and verify samples according to EC regulation guidelines. Prepare and extract metals and minerals from various food and agricultural products. Quantify metals and minerals using ICP-OES techniques independently. Plan and execute reactions following applicable SOPs. Follow safety protocols and guidelines in the lab. Record analytical observations, data, and accurate calculations. Maintain CRM and laboratory documents and recor...

1) Excellent knowledge in HPLC Method development 2) Excellent knowledge of Good Laboratory Practices (GLP), Quality systems, Standard Operating Procedures. 3) Ability to independently handle HPLC systems Post Graduation M.Sc Graduation B.Sc

Good communication skills. Basic analytical chemistry knowledge. Hands on experience with HPLC/ LCMS / GCMS Method development skills Qualification Groups Post Graduation M.Sc Post Graduation MHRM

1. Responsible for procedures impacting the quality of products. 2. Issuing and receiving Standard Operating Procedures, Formats, Batch Production Records, Batch cleaning Records, Raw material, In-Process, Intermediate raw datas and maintain the logbooks. 3. Review of executed batch production records, Batch Cleaning records, Raw material, In-process, Intermediate, finished raw datas and archiving in systematic manner. 4. Review and ensure that the stability data, holding data supports to retest/expiry dates, storage on APIs and Intermediates. 5. Reviewing of method transfer/method verification/method validation related protocols, raw data, and report. 6. Reviewing of SpecMoA and related for...