1459 Gc Jobs - Page 27

The position of Assistant/Executive in the Analytical PRD department of the R&D Business Division is located in Udaipur. Reporting to the Group Leader - Analytical PRD, you will be responsible for assisting in the analytical method development of assigned projects within the given timeframe while adhering to safety and environmental regulations. Your duties will include raw materials and finished products analysis, generating Certificate of Analysis (COA), and troubleshooting any complexities during analysis proactively. You will play a crucial role in understanding the analytical scope of the assigned projects, providing inputs for analytical support planning, ensuring proper maintenance of...

As a member of our team, you will be responsible for the synthesis and purification of assigned molecules/experiments. You will also actively participate in process development activities for the assigned molecule, as well as provide support for scaling up developed processes in the pilot plant and large-scale manufacturing processes. Your role will be crucial in ensuring complete support for Tech Transfer activities by closely collaborating with cross-functional teams. An essential aspect of your responsibilities will be to add value to processes through innovation. You will be expected to understand and analyze reports received from the Analytical department, which may include NMR, Mass Sp...

As an Analytical Chemist at our leading Contract Research Organization (CRO), you will have the opportunity to assist in conducting analytical testing of samples using instruments such as HPLC, GC, LC-MS/MS, and UV Spectrophotometer under supervision. You will play a crucial role in preparing reagents, solutions, and standards following Standard Operating Procedures (SOPs) with precision and attention to detail. Your responsibility will include accurately recording and maintaining raw data, logs, and reports in compliance with GLP/GMP standards. By ensuring proper documentation, you will play a pivotal role in meeting regulatory and internal audit requirements. You will provide essential sup...

As a Senior Manager in the Research and Development department at Gujarat Fluorochemicals Limited, you will play a crucial role in leading a team to drive innovation and growth. Your main responsibilities will include conducting thorough literature surveys, identifying viable and non-infringing routes for commercializing fluoro-specialty molecules, developing and standardizing industrial processes, and meeting cost targets within specified timelines. Additionally, you will be expected to discover and develop new products, prepare various reports, and scale up lab processes to commercial levels. To excel in this role, you must have strong leadership skills to manage a team of scientists and c...

You are invited to join Global Calcium Pvt. Ltd., a prominent API manufacturing company located in Bangalore, India, specializing in speciality API's, benzodiazepines, ophthalmics, oncology, chelated minerals, and organic mineral salts. We are currently seeking talented individuals to fill various roles in the QC Department. Open Positions: - QC ICP-MS Analyst (2 openings) - QC DMF Support (2 openings) - QC Analytical Validation Support (2 openings) - QC Wet Analysis (2 openings) Qualifications: - B.Sc./M.Sc. in Chemistry or related fields - 1 to 4 years of relevant pharmaceutical QC experience - Familiarity with cGMP practices and regulatory compliance Responsibilities: - Perform routine an...

Date: 1 Aug 2025 Location: Bangalore, KA, IN, 560099 Custom Field 1: Development Services Job Description Job Title: Junior Analytical Development Scientist Oral Solids Job Location: Bangalore Department: Analytical Development Drug Product About Syngene: Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SO...

Department : Quality control Open Position : ( HPLC, GC ,Wet Lab ) Work Location: Bidar Key Responsibilities Responsible to perform the HPLC / GC/Wet analysis of Raw material & intermediates, in process/cleaning, intermediate, finished product and stability samples as per the work allotment. method validation, protocols & preparation, review, data review and planning, troubleshooting worked on Empower Software. Good communication& Interpersonal skills. Check the Calibration, Preventive maintenance and status tag of the instruments prior to use. Operate and calibrate the instruments as per SOP. Print the ARDS from GMP Pro and enter the test results after completion of the analysis. Ensure the...

About The Role Project Role : VIS & BI Strategy Practitioner Project Role Description : Develop a VIS/BI vision, business case, and modernization strategy; discover and assess VIS/BI opportunities; identify industry- and function-centered VIS/BI use cases; guide clients on industry and function relevant measures and metrics; develop a VIS/BI roadmap and operating model; help drive adoption, decision making and behavior change; measure VIS/BI value. Must have skills : Kinaxis Good to have skills : NAMinimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a VIS & BI Strategy Practitioner, you will engage in the development of a comprehen...

Job Description 1. Analysis of stability/Finished product samples and compile the report as per ALCOA procedure, other miscellaneous samples and compile their report. 2. To maintain the instrument usage and maintenance of instrument like Dissolution Test apparatus, UV spectrophotometer, balance, PH meter and Sonicator etc. 3. Ensuring data integrity policy, GDP and its effectiveness up to compliance 4. To maintain the stability chamber and tracker. 5. To maintain the stability chamber and tracker. 6. To ensure charging and withdrawal of stability samples as per approved protocols. Work Experience Education :- B.Pharm/ MSC/ M. Pharm Experience :- 2 to 4 yrs. Education Others Competencies

Role Description: Quality control executive Location: Mil Laboratories Pvt. Ltd. 541, GIDC, Manjusar, Ta. Savli, Dist. Vadodara - 391775 Experience: 5 to 6 years Roles Responsibilities:- To perform all the testing related to RM, bulk, FP and stability samples To perform all the testing of packaging materials Handling of QMS documents like SOP, CAPA, repeat analysis, Deviation etc. To manage and lead the team To perform analytical method validation To prepare specifications for different materials New vendor approval Should have working experience of HPLC, GC, UV spectrophotometer, centrifuge etc. What will you need to be successful Preferred experience in sterile pharma plant. Extensive unde...

Scope of Role- The DVA Engineer is responsible for Dimensional Variation Analysis and Tolerance stack up for ongoing and new projects. Knowledge / Experience: 7+ Years Area of Responsibility: DVA Engineer creates and maintains analysis models representing the assembly process, tolerances, and CAD data used for the virtual assembly of a vehicle. He will be responsible for creating reports, communicating results, issues, and recommendations to the customer. Job Requirements: Should have experience in Body Components /Interior Trims/Exterior Trims Domains Should have good working knowledge of GD&T & Tolerance Stack up Analysis Should have good knowledge of GD&T Standard preferred ASME Should ha...

Well Experience on validation work on GC & HPLC

Role & responsibilities Should able to handle HPLC & GC,PH Meter, Knowledge on GMP&GLP Preferred candidate profile Familiarity with analytical testing techniques using HPLC/GC/FTIR/Dissolution/UV. Performing calibration of instrumentations Testing of finished product, raw materials, packaging and stability Perform analytical testing - HPLC, FTIR, UV

As a Lab Technician based in Bahadurgarh (HR), you will be responsible for conducting various laboratory tests using analytical instruments such as HPLC, GC, Titrator, and others. Your duties will include receiving, labeling, and analyzing samples, executing laboratory testing procedures, making observations, and interpreting findings. It is essential to maintain day-to-day testing records and have prior experience in oil testing or pharmaceutical lab environments. In this role, you will be required to organize and store chemicals, substances, fluids, and compressed gases following safety guidelines. Accurate recording of all data and results in specified forms, both paper-based and electron...

As a Lab Chemist at our Oil & Refinery facility located in Kheda, Ahmedabad, you will be responsible for conducting routine and non-routine laboratory tests on crude oil, intermediates, and finished products. Your key responsibilities will include analyzing samples using instruments such as GC, HPLC, AAS, FTIR, and other standard lab equipment while ensuring that all testing is performed in accordance with established safety and quality standards such as ASTM, BIS, and ISO. You will be expected to maintain accurate documentation of test results and prepare detailed reports for internal use, supporting quality control and quality assurance processes to ensure compliance with regulatory requir...

Hiring For QC Manager in Jhagadia MSC Chemistry / PhD / BE Chemical 15 to 20 Years Up to 18.0 LPA Budget Experience in Phthalic Anhydride must Send CV on sdpbharuch@gmail.com with Subject: QC Manager Jhagadia No Charges Share with your Friends Required Candidate profile Share Job with Your Friends Interview Venue: SDP HR Solution, Sixth Floor, 610, Golden Square, Beside Dmart, Near ABC Circle, Bholav, Bharuch Best Job Placement Consultancy in Gujarat

Skill Required 3 to 4 year Pharma background experience for FP , In process and PV samples. Roles and Responsibilites To analyze the samples of in process/FP/Process validation as per work allotted by section in charge/Designee. Preparation of report and submission of reports along with raw data to section in charge/Designee within time. Immediate reporting of any odd observation, incident, OOT and OOS result during analysis to section in charge/Designee. Qualification Required M.sc/B.pharm Relevant skills / Industry experience Should have 2 to 4 year experience. Relevant professional / Educational background M.sc/B.pharm

Division Department Sub Department 1 Job Purpose Part of the TA COE responsible to manage and support global leadership hiring through extensive market research, candidate sourcing, preliminary screening and support the end-to-end recruitment process, ensuring a seamless experience for both candidates and internal stakeholders Also support enablers in global leadership hiring like compliance & governance, liaisoning with cross functional teams and other operational requisites of the role Key Accountabilities (1/6) Market Research/Mapping for key leadership roles including global talent trends Independently c onduct deep-dive research on global leadership talent landscape including proactive ...

Company Description Colliers (NASDAQ, TSX: CIGI) is a global diversified professional services and investment management company Operating through three industry-leading platforms Real Estate Services, Engineering, and Investment Management we have a proven business model, an enterprising culture, and a unique partnership philosophy that drives growth and value creation For 30 years, Colliers has consistently delivered approximately 20% compound annual returns for shareholders, fuelled by visionary leadership, significant inside ownership and substantial recurring earnings With nearly $5 0 billion in annual revenues, a team of 23,000 professionals, and more than $100 billion in assets under ...

What You Will Enjoy Doing What makes you great Overall Line Responsibility (Production to Packaging): Start and stop machines as per operation schedule Perform parison controls and monitor material usage (weight distribution, regrind levels, tail lengths) Conduct regular visual and technical quality checks throughout the shift Check and record process parameters (e g , machine cycle time, mold cooling water temperature, process temperature) Weigh waste materials/lumps and document in daily reports Prepare machines for mold changes Ensure accurate production as per quantity and quality specifications Place rejected bottles in designated bins only Record packing details (pallet no , quantity, ...

Conduct final inspection and testing of finished products to ensure compliance with quality standards and customer specifications. Hands-on experience in testing of Finished products Instruments must be handled like HPLC, GC, KF, IR, DT, and Dissolution. Hands-on experience like software like Empower and LIMS. Qualification M.SC/B.Pharma 3 to 6 years Additional Information

Design & develop API/intermediate processes, optimize & validate methods, analyze data (HPLC, GC, NMR, IR, MS), impurity profiling, documentation, lab record management & equipment maintenance. Required Candidate profile 1 - 5 years of experience BSc./ MSc. in Chemistry

Job Description: 24 7 audit readiness. Participation in internal, external, regulatory audits. Ensure 100% participation in trainings against CAPAs. Responsible for initiation and investigation on LIR, OOS, OOT & boarder line results and reporting them to the in-charge. Supporting to share required documents from QC to RA/ other requirement. Determining team priorities in accordance with the plants needs, while coordinating with the team leader /Manger. Follow up the housekeeping, cGMP, GLP and Safety Guideline in laboratory. Sampling and analysis of RM / FG / intermediates / cleaning samples based on requirement and result entry in analytical sheet, QA form, LIMS and online documentation as...

Aquachem Industries Private Limited is looking for QC Chemist to join our dynamic team and embark on a rewarding career journey Chemical Analysis: Conduct chemical and physical testing on raw materials, in-process samples, and finished products to assess their quality and compliance with specifications Instrument Operation: Operate and maintain laboratory equipment and instruments, such as HPLC, GC, UV-Vis spectrophotometers, and other analytical instruments Data Analysis: Analyze and interpret test results, ensuring accuracy and consistency in data reporting Quality Control: Implement and maintain quality control standards and procedures to ensure that products meet regulatory and quality r...

We are seeking an experienced AM R&D Executive to join our team. The ideal candidate will be responsible for planning and executing chemical reactions, monitoring their progress, and optimizing conditions to ensure high-quality output. This role requires a hands-on approach to research and development, including scaling up products and ensuring all activities are meticulously documented. Roles and Responsibilities Plan, set up, monitor, and work up chemical reactions. Monitor the progress of reactions using standard analytical techniques such as TLC, GC, HPLC , and LCMS . Isolate products and optimize reaction conditions to improve yields and output. Purify compounds using various methods, i...