133 Analytical Testing Jobs - Page 5

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Role & responsibilities: Formulation and drug product development for biosimilar products with special focus on insulin and insulin analogues Design and execute the experiments for pre-formulation and formulation process development for biosimilars and optimization ensuring its stability and efficacy Conduct stability studies as per guidelines and Perform analytical testing using advanced analytical instruments such as SEC-HPLC, RP-HPLC etc. Document experimental data and preparation of SOPs, protocols and Reports Preferred candidate profile: Must have basic understanding of container closure system like vial, cartridge, PFS etc. Must be familiar with regulatory requirements (USFDA, EMA) for...

Business: PPL Digwal Department: PTS Job Overview: To perform AR&D actives as per GMP & Safety Travel Requirements: NA Reporting Structure: Reports to Research Scientist - AR&D (Service) Key Stakeholders: Internal: QC, QA, SCM & Safety Experience: 4-8 Year Experience in manufacturing (API) as per Pharma Manufacturing GMP requirements. Responsibilities for Internal Candidates Key Roles & Responsibilities 1. Capable to handle independent projects 2. Analytical testing support to PDG synthetic group. 3. Coordinate with QA regarding method transfer, CCF and investigation reports. 4. Experience of handling of HPLC, GC, Potentiometer, Polarimeter instruments. 5. API Stability knowledge. 6. Capable...

Department: PTS Job Overview: To perform AR&D actives as per GMP & Safety Travel Requirements: NA Reporting Structure: Reports to Research Scientist - AR&D (Service) Key Stakeholders: Internal: QC, QA, SCM & Safety Experience: 4-8 Year Experience in manufacturing (API) as per Pharma Manufacturing GMP requirements. Responsibilities for Internal Candidates Key Roles & Responsibilities 1. Capable to handle independent projects 2. Analytical testing support to PDG synthetic group. 3. Coordinate with QA regarding method transfer, CCF and investigation reports. 4. Experience of handling of HPLC, GC, Potentiometer, Polarimeter instruments. 5. API Stability knowledge. 6. Capable to handle analytical...

Experience: 4-8 Year Experience in manufacturing (API) as per Pharma Manufacturing GMP requirements. Responsibilities for Internal Candidates Key Roles & Responsibilities 1. Capable to handle independent projects 2. Analytical testing support to PDG synthetic group. 3. Coordinate with QA regarding method transfer, CCF and investigation reports. 4. Experience of handling of HPLC, GC, Potentiometer, Polarimeter instruments. 5. API Stability knowledge. 6. Capable to handle analytical method development, Implementation, Validation as per requirement. 7. Should have experience of Analytical method transfer to QC. 8. Experience of making documents like method transfer protocol & report, method val...

Job Description Business: PPL Digwal Department: PTS Location: Digwal Job Overview: To perform AR&D actives as per GMP & Safety Travel Requirements: NA Reporting Structure: Reports to Research Scientist - AR&D (Service) Key Stakeholders: Internal: QC, QA, SCM & Safety External: NA Experience: 4-8 Year Experience in manufacturing (API) as per Pharma Manufacturing GMP requirements. Responsibilities for Internal Candidates Key Roles & Responsibilities 1. Capable to handle independent projects 2. Analytical testing support to PDG synthetic group. 3. Coordinate with QA regarding method transfer, CCF and investigation reports. 4. Experience of handling of HPLC, GC, Potentiometer, Polarimeter instr...

Key Responsibilities: Perform analytical testing and analysis of raw materials, intermediates, and finished pharmaceutical products. Conduct instrumental and wet chemistry techniques, including HPLC, GC, UV-Vis, FTIR, and titrations. Develop and validate analytical methods for new and existing pharmaceutical formulations. Conduct stability studies and ensure proper documentation of results. Maintain and calibrate laboratory instruments and equipment. Prepare and review standard operating procedures (SOPs) for analytical testing and instrument operation. Ensure compliance with cGMP (current Good Manufacturing Practices), ICH guidelines, and other relevant regulatory standards. Support analyti...

Hello Candidate, Greetings from Hungry Bird IT Consulting Services Pvt. Ltd.! We're hiring a Quality Control Head for our client. Qualification: MSc in Chemistry, Biochemistry, or a related field Location: Vikarabad District, Telangana Experience: 5 to 8 Years Salary: 3.5 lakhs to 4 lakhs per annum Required: Male Note: Preferably with strong experience in the pharmaceutical or ethanol industry. Job Summary: We are seeking an experienced Quality Control Head to lead the QC team at our client's facility. The ideal candidate will have a strong background in analytical techniques, including Gas Chromatography (GC) and High-Performance Liquid Chromatography (HPLC), and will be responsible for ens...

Role & responsibilities An experienced customer service professional for a role that includes technical knowledge in mechanical and chemical/analytical testing. Customer-facing strengths with enough domain understanding to engage clients confidently, solve problems, and identify business opportunities. Preferred candidate profile Qualifications: Essential: B.Sc./Diploma/B.tech in textile/Graduation Desirable: Good communication skills Experience Profile : Minimum Years : 3 Years ; Maximum Years : 15 Years Industry/ Sector: Textile Testing Scope of job /Activities handled: Customer Services Key Results Areas ( KRAs) & Key Deliverables : Handle day to day operations in a timely, complete and p...

Experience: 4-8 Year Experience in manufacturing (API) as per Pharma Manufacturing GMP requirements. Responsibilities for Internal Candidates Key Roles & Responsibilities 1. Capable to handle independent projects 2. Analytical testing support to PDG synthetic group. 3. Coordinate with QA regarding method transfer, CCF and investigation reports. 4. Experience of handling of HPLC, GC, Potentiometer, Polarimeter instruments. 5. API Stability knowledge. 6. Capable to handle analytical method development, Implementation, Validation as per requirement. 7. Should have experience of Analytical method transfer to QC. 8. Experience of making documents like method transfer protocol & report, method val...

Should able to perform and supervise following routine tests of general chemical nature:- To perform all tests on water i.e. pH, TDS, TSS, harnesses, alkalinity, BOD, COD etc. Pigment testing, Chemical Testing, application, analytical testing

Should be able to guide chemists and supervisor of the Laboratory to carry out Analytical tests and Application tests for Pigments. Analytical Testing Application Testing Pilot and R&D Testing Required Candidate profile Minimum 20 years’ experience in a Phthalocyanine Pigment Industry manufacturing Alpha, Beta Blues and Green Pigments.

As a QC Chemist, your primary role is to ensure the quality and integrity of raw materials, intermediates, and finished products in a chemical manufacturing setting. You'll be responsible for performing various analytical tests, interpreting results.

Long Description 1 Exposure to perform the testing of Inprocess, Finished product, Stability and Cleaning validation samples etc. 2 Having knowledge of Analytical Instruments to perform the testing by HPLC, GC, UV, IR, KARL FISCHER etc. 3 Having Analytical testing skills to perform the MDI/DPI Products test like Assay, APSD, DDU, RS, Spray Pattern, FPM and physical testing etc. 4 Exposure of Laboratory investigation like OOS, OOT, Incidence, Deviation. 5 Exposure of Stability sample management & Regulatory Audits. 6 Exposure of Analytical method transfer, Analytical method validation / Verification activity. 7 Knowledge of GLP and Good documentation Practices. Competencies Innovation & Creat...

FSSAI Approved 1.Perform chemical analysis of food samples. 2.Operate instruments like HPLC,GC-MS. 3.Ensure compliance with FSSAI, NABL & ISO standards 4.Conduct method validation 5.Preapre test reports and audit documentation 6. Supervise lab staff

Eurofins Scientific is an international life sciences company that provides a wide range of analytical testing services to clients across multiple industries. From food and pharmaceuticals to environmental and cosmetic products, Eurofins ensures safety, authenticity, and accuracy. With a global presence and over 900 laboratories, Eurofins is a leader in food, environmental, pharmaceutical and cosmetic product testing, as well as in genomics, clinical studies support, and other specialized diagnostic testing. Support processing of incoming samples by accurate and timely entry and review of sample information in LIMS. Employee Responsibilities: Audit sample information, including the formal re...

- Having experience in manufacturing cosmetics related products such as Cream, Lotion, Shampoo, Face Wash, Cleaner, Skincare, Nailpolis etc. - Supervising in-process quality control and managing bulk approvals and finished goods (FG) release. Required Candidate profile - Hands-on experience in instrumental and analytical testing of raw materials (RMs). Maintaining comprehensive records of quality tests, inspections, and other related activities.

About the Role: Responsible for analytical testing, documentation, and lab operations as per GMP standards. Key Responsibilities: Conduct chemical and instrumental analysis (HPLC, GC, UV, etc.) Ensure compliance with SOPs and GLP Prepare COAs and maintain records Calibrate and maintain lab instruments Coordinate with QA and production teams Qualifications & Skills: B.Sc / M.Sc / B.Pharm / M.Pharm 23 years experience in QC lab (pharma/chemical) Proficiency in analytical instruments and documentation Application Process: Interested candidates can send their resume, current CTC, and expected CTC to omshrilabs.hr@gmail.com Email Subject Format: Role: QC Officer | Name: [Your Name] | Experience: ...

A dynamic and result-oriented Scientist R&D to lead the research and development activities of plant nutrition and bio stimulant products. The ideal candidate will be responsible for formulation development, innovation, process optimization, quality control, and regulatory compliance to bring next-generation products to market. Key Responsibilities: • Lead R&D projects on the development of bio stimulants, micronutrient formulations, specialty plant nutrition products and bio botanicals. • Identify and validate new active ingredients from natural sources. • Drive scientific innovation to improve product performance and process improvement of the existing products and new product development....

Role & responsibilities We are seeking a skilled and proactive Instrumentation Maintenance Engineer to manage the complete maintenance lifecycle of analytical instruments and lab equipment. The ideal candidate will ensure optimal performance, calibration, and compliance of instruments used in quality control and R&D labs. Preferred candidate profile

Ensuring the quality of APIs through testing, analysis, & documentation Sample & inspect raw materials Maintain an accurate & complete record of testing, analysis Investigate deviations from the quality standard Ensure compliance with GMP regulations Required Candidate profile Bachelor's degree in B.Sc/M.Sc Chemistry, B.Pharm/M.Pharm. Previous experience in QC in API pharma manufacturing Strong knowledge of analytical techniques & instrumentation, e.g., HPLC, GC, UV-Vis

• Site analytical testing , evaluation and Development • Implementation of Pharmacopeial Updates and Source Change Document. • Managing master data operations within the LIMS and SAP system. • Developing, Optimizing, Validating, Verifying and Method transfer of analytical methods. • Ensuring discipline in Track Wise by monitoring pending tasks and facilitating the closure of quality events. • Ensuring adherence to regulations and maintaining the completeness of relevant logbooks or registers.

ABOUT AGRATAS Agratas is a wholly owned subsidiary of Tata Sons. We design, develop and manufacture high-quality, high-performance, sustainable batteries applied to multiple use cases in the mobility and energy sectors, to match our customers requirements. Agratas is a scale-up business with a start-up mentality, driven by our pursuit of green growth and technological progress. We develop next-generation battery technologies at our state-of-the-art R&D Innovation Hubs in India and the UK. JOB SUMMARY The In-Process Quality Manager is crucial in ensuring the quality and reliability of EV battery cells throughout the manufacturing process. Reporting to the Site Quality Head, this role involves...

Product Development/Product performance/Process Parameter Knowledge on modification of activated carbon structure Develop specialty carbons for gas phase potable waters Testing as per international testing procedures Establishment of Quality system Required Candidate profile Contact: 8939813208 Mail ID: finadsorbent@carbons.in

Walk-in Drive @ Ahmedabad on 18th May'25 (Sunday) for Quality Control Department We are looking for suitable candidates for OSD Quality Control for Ahmedabad location Unit Interview Venue Details: Date: 18th May 25 (Sunday), Time: - 9:00 AM to 1:00 PM Venue : Amneal Pharmaceuticals Pvt. Ltd Survey No. 634,637-641 Village: Rajoda Tal: Bavla Dist: Ahmedabad -Gujarat - 382220 1) REQUIREMENT FOR OSD QUALITY CONTROL DEPARTMENT Total Experience: 02 to 7 years (Pharma experience only) Qualification: B.Sc./ M.Sc/ B. Pharm/ M. Pharm Designation: Officer/ Sr. Officer /Executive/ Sr. Executive Department: Quality Control Desired Profile: Test RM, PM, in-process, finished & stability samples (various do...