1437 Gc Jobs - Page 16

Eurofins Advinus is a premier preclinical and early development CRO offering drug discovery, preclinical and development stage contract research services in the areas of discovery services, regulatory Toxicology (Safety Assessment), DMPK, Analytical R&D Services and API CDMO. Eurofins Advinus manufactures drug substances to support Toxicology and early clinical studies. Job description: Leadership role to manage team size of 10+ scientists (Ph.D. and M.Sc.) Extensive knowledge in E&L Extractable and Leachable experience in CCS as per USP monograph and medical devices as per ISO guidelines Managing multiple instruments (LC-MSMS, GC-MSMS, ICP-MS, IC etc.) Method development experience in LC-MS...

About The Role Project Role : Application Developer Project Role Description : Design, build and configure applications to meet business process and application requirements. Must have skills : Java Full Stack Development Good to have skills : Spring BootMinimum 7.5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Developer, you will design, build, and configure applications to meet business process and application requirements. Your typical day will involve collaborating with team members to develop innovative solutions and ensure seamless application functionality. Roles & Responsibilities:- Expected to perform independen...

About The Role Project Role : Application Developer Project Role Description : Design, build and configure applications to meet business process and application requirements. Must have skills : Java Full Stack Development Good to have skills : Spring BootMinimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Developer, you will design, build, and configure applications to meet business process and application requirements. Your typical day will involve collaborating with team members to develop innovative solutions and ensure seamless application functionality. Roles & Responsibilities:- Expected to perform independentl...

This Position reports to: Production Manager Your role and responsibilities You will be working as Quality Control Specialist look after Consistency and quality are top priorities for any manufacturer. But even with standards and specifications in place for employees to follow, businesses depend on quality engineers to verify that those standards are always met and that only the best products make it to market. The work model for the role is: #Li-Onsite This role is contributing to the ABB India, Smart Power, as a Quality Control Specialist for Nelamangala Bangalore Location. You will be mainly accountable for: Safety & Compliance: Assess risks, ensure safety for people and equipment, verify...

Note: Walk In Interview at Vadodara. Date: - 28.09.2025 (Sunday) Job Location: Daman & Dahej Qualification:- M.Sc. (Chemistry)/ B. Pharma/ M. Pharma Experience:- 2-6 Years in (API or Solid Oral) Required Candidate profile * 2-6 years of experience into LCMS, HPLC, GC & Wet Chemical sections, Analytical Validation, Finished Goods, Raw Material, Stability & GLP

Role & responsibilities Strong knowledge of TQM, ISO-IMS Standards. Hands-on experience with analytical instruments such as HPLC, GC, UV-Vis, FTIR, etc. Chemistry knowledge, Chemical analysis and Pesticide-Tech & Various formulation sample test procedure and regulation. Good knowledge of Operational Excellence methodologies such as 5S, TPM, FMEA, and related tools. Preferred candidate profile Strong knowledge of TQM, ISO-IMS Standards. Hands-on experience with analytical instruments such as HPLC, GC, UV-Vis, FTIR, etc. Chemistry knowledge, Chemical analysis and Pesticide-Tech & Various formulation sample test procedure and regulation. Good knowledge of Operational Excellence methodologies su...

We are looking for a highly skilled and experienced Analyst-QC to join our team at eClerx Services Ltd. The ideal candidate will have a strong background in IT Services & Consulting, with excellent analytical and quality control skills. Roles and Responsibility Collaborate with cross-functional teams to identify and prioritize testing requirements. Develop and implement comprehensive test plans and cases to ensure high-quality deliverables. Conduct thorough analysis of test results and identify areas for improvement. Work closely with the development team to resolve defects and enhance overall product quality. Participate in continuous improvement initiatives to optimize testing processes. M...

Exp: 2- 6 yrs • Knowledge in Method Development on Assay, RS, dissolution for formulation complex molecules. • understanding of Q1/Q2 evaluation • PEQ processes and characterization • Instruments: HPLC, GC, KF, UV, IR, etc. kiran.k@orbicular.co.in

Responsibilities: * Collaborate with production team on quality control measures. * Conduct HPLC, GC, Gas Chromatography tests on products. * Ensure compliance with industry standards and regulations. Free meal Accidental insurance

About The Role : Job TitleSenior Engineer, AVP LocationPune, India Corporate TitleAVP Role Description Technology underpins our entire business. Our Technology, Data and Innovation (TDI) strategy is focused on strengthening engineering expertise, introducing an agile delivery model, as well as modernising the bank's IT infrastructure. We continue to invest and build a team of visionary tech talent, providing you with the training, freedom and opportunity to do pioneering work. As an [Engineer] you will develop and deliver significant components of engineering solutions to satisfy complex and diverse business goals. You will engage and partner with the business whilst working within a broader...

About The Role Project Role : Application Lead Project Role Description : Lead the effort to design, build and configure applications, acting as the primary point of contact. Must have skills : SAP S/4HANA Group Reporting Good to have skills : NA Minimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As an Application Lead, you will lead the effort to design, build, and configure applications, acting as the primary point of contact. Your typical day will involve collaborating with various teams to ensure that application requirements are met, overseeing the development process, and providing guidance to team members. You will also engage...

Opportunity for ADL Officer at Pharmaceuticals Manufacturing Company in Vapi, Gujarat. Minimum 3 years of experience required Qualification - B.Sc. / M.Sc. degree preferred Attractive Salary Required Candidate profile Interested candidates can share their updated CV at hire@hireindians.com OR Call/ WhatsApp on +918882212450.

About the Role We are looking for a meticulous Web Application Reviewer to ensure the accuracy, quality, and usability of data and content within our web applications. The role involves reviewing images, validating extracted data, comparing records, and making acceptance or rejection decisions with clear reasoning. The ideal candidate should be comfortable navigating web applications, understanding their functionalities, and leveraging related technologies to efficiently complete tasks. Key Responsibilities Review images and data uploaded into the web application with attention to detail. Validate extracted information against source images or documents. Accept or reject records within the a...

Walk In drive for Formulation Analytical Research & Development - Department (FAR&D) - ASQA & ASRD : MSN Laboratories, R&D Center on Friday 26-09-2025. Roles & Responsibilities : ASRD Responsibilities : 1) Execution of Analytical Method validations for drug products for various markets. 2) Execution of DPDM Method validations for drug products. 3) Analytical method transfers to the Quality control labs. 4) Performing the calibrations of the analytical instruments. 5) Preparation & review of Analytical Method validations protocols and reports. 6) Responsible for cGLP, documentation and implementation of departmental quality systems. AQA Responsibilities : 1. Preparation and Review of AQA SOPs...

As an Executive or Senior Executive at Syngene, your primary responsibility will be method development, validation, and stability testing of drug substance/drug product. You should have strong hands-on experience in developing and validating Assay & related substances methods for drug substance/drug product. Additionally, you should be willing to work with complex injectables and be open to working in shifts. - Handle instruments such as HPLC, UPLC, GC, UV Visible spectrophotometer, balances, Potentiometer, and stability chambers. - Well-versed in Good documentation/laboratory practices like ALCOA+. - Experience in calibration and qualification of laboratory instruments. - Prepare and review...

As a Fill and Finish QC at our company, you will play a crucial role in ensuring the quality of our pharmaceutical products. Your responsibilities will include: - Performing quality control tests using equipment such as HPLC, GC, Dissolution apparatus, and UV Visible Spectrometer. - Conducting weight analysis and stability studies for Injectable dosage forms. To excel in this role, you should possess the following qualifications: - B.Pharm/B.Sc/M.Sc. degree. - 2 to 6 years of hands-on experience in a similar role. - Proficiency in using HPLC, GC, Dissolution apparatus, and UV Visible Spectrometer. Join our team and contribute to the production of high-quality pharmaceutical products.,

As a Pharmaceutical Documents Associate at our company, you will play a crucial role in ensuring the quality and compliance of our pharmaceutical products. Your responsibilities will include: - Having experience or sound knowledge in Active Pharmaceutical Ingredients, Finish Product, Packaging Material Standards, Quality Management, and Quality Control. - Demonstrating knowledge or experience in Quality control tests for various formulations and APIs such as Assay, Dissolution, Disintegration, Uniformity of Weight/dosage, Impurity testing, Water content, etc using methods like HPLC, GC, TLC, IR/UV, Disso, etc. - Understanding pharmacopoeia applications and all documentation relevant to QA/QC...

As an Assistant Manager or Team Leader at Synnat Pharma in Visakhapatnam, you will play a crucial role in leading method development, validation, stability studies, and technology transfer activities. Your meticulous nature and extensive experience will be essential in collaborating closely with R&D, QC, and Regulatory teams to support product development and ensure compliance with global pharmaceutical standards. You should possess strong analytical expertise, leadership skills, and a dedication to regulatory compliance and continuous improvement. - Developing, optimizing, and validating analytical methods such as HPLC, GC, UV-Vis, and Dissolution according to ICH and regulatory guidelines....

Company Name Gangwal healthcare Job Title Quality Control Manager Job Location: Maharashtra Description Job Summary: We are seeking an experienced and detail-oriented Quality Control professional with strong expertise in Nutraceutical products testing, nutritional profiling, and regulatory compliance. The ideal candidate will ensure all raw materials, in-process samples, and finished goods meet internal quality standards, statutory requirements, and international regulations. Key Responsibilities Testing & Analysis Perform qualitative and quantitative analysis of nutraceutical and food products. Conduct nutritional profile testing including macronutrients, micronutrients, vitamins, and miner...

Job Description: - Possess a minimum of 2 years to a maximum of 6 years of experience in handling Analytical instruments such as HPLC and GC. - Conduct routine analysis using these instruments and participating in method development processes. - Expertise in analytical techniques will be essential in ensuring accurate and reliable results.,

Date: 15 Sept 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Development Services Job Location: Bangalore Department: Analytical Development Drug Product About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical industries around the world. Syngene s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work ...

Job Summary IWMS Analyst GCS We are seeking a motivated IWMS analyst who is an excellent multitasker with exceptional time management skills. CADD Coordinator can expect to assist the Blackstone Global Corporate Services team in modifying and creating as-built floor plans in AutoCAD application, AutoCAD drawing clean-up, linking AutoCAD drawing entities to IWMS databases, update of completed MACs and new hires into system, and assist with output of FM Systems reports. The ideal candidate for this role should possess excellent computer skills, organizational skills, and experience in working with AutoCAD. Responsibilities and Duties Provide AutoCAD support to the Blackstone IWMS Director in m...

Note: Walk In Interview at Vadodara. Date: - 28.09.2025 (Sunday) Job Location: Daman & Dahej Qualification:- M.Sc. (Chemistry)/ B. Pharma/ M. Pharma Experience:- 2-6 Years in (API or Solid Oral) Required Candidate profile * 2-6 years of experience into LCMS, HPLC, GC & Wet Chemical sections, Analytical Validation, Finished Goods, Raw Material, Stability & GLP

Role & responsibilities Analytical testing of chemicals, Reagents, Raw materials and other Pharmaceutical products. Preparation, Standardization and stability evaluation of volumetric solutions/Reagents/Indicators. Performing computerized system validation (CSV) as per current regulatory requirements. Testing of Raw materials, In-process, Intermediates and APIs using Chromatographic Data system. Analytical Testing of Related substances/Content/Assay/Purity testing and Calculation by HPLC Using Empower/Lab Solutions. Data generation, Integration and Review of Chromatographic data generated by Chromatographic data system. Method Transfers & Holding time Studies. Testing of Raw materials, In-pr...

Analysis of routine samples (product development batches, stability study samples, raw materials etc.). Operation and Calibration of analytical instruments/equipment s. Analytical activities related to Quality control department. Qualification of working standards. Documentation of analytical activities as per good documentation practices. Work in laboratory as per good laboratory practices. To use PPEs and follow safe practices in lab. Any other task assigned by management. Sampling of raw materials from pilot plant dispensing area. Analysis of samples in quality control laboratory. Operation and Calibration of instruments in quality control laboratory