1474 Gc Jobs - Page 39

The ideal candidate should possess strong communication skills and be well-versed in analytical techniques such as HPLC, GC, IR, UV, and Wet analysis.,

Long Description 1. Perform characterization of peptides , nucleic acids-based (oligonucleotides) or other injectable drug products using High Resolution Mass Spectrometry (LC-HRMS) . Experience with QToF/Orbitrap instruments and Ion Mobility will be preferred. Additional experience in Fluorescence, particle size analysis (DLS), and other relevant techniques (e.g. SEC-MALS) are desirable. 2. Analyze and interpret LC-MS and MS/MS data for impurity profiling and characterization. Solve problems and implement new research methods through literature search, coordinate with cross-functional teams (formulation, QA, QC, regulatory, etc.), application specialists, etc. to complete analytical tasks. ...

Work with Us. Change the World. At AECOM, we're delivering a better world. Whether improving your commute, keeping the lights on, providing access to clean water, or transforming skylines, our work helps people and communities thrive. We are the world's trusted infrastructure consulting firm, partnering with clients to solve the world’s most complex challenges and build legacies for future generations. There has never been a better time to be at AECOM. With accelerating infrastructure investment worldwide, our services are in great demand. We invite you to bring your bold ideas and big dreams and become part of a global team of over 50,000 planners, designers, engineers, scientists, digital ...

Aforeserve Technologies Pvt Ltd (XtraCover) is looking for Quality Control Executive (QC) to join our dynamic team and embark on a rewarding career journey Assist in quality control tasks and activities. Develop and implement quality control policies and procedures. Monitor and report on quality control performance metrics. Collaborate with quality control teams and stakeholders. Ensure compliance with quality control standards and regulations.

QC Role & responsibilities : Handling of QC instruments, Such as HPLC, GC, UV, FTIR, Dissolution Apparatus, Melting point, Karl Fischer apparatus, Auto titration, Analytical weighing Balance, Polari meter, Disintegration Apparatus, pH Meter etc. Analysis of In process, validation, Hold time study, finished products and stability samples according to related specifications Daily as well as monthly calibration of analytical balance of instrumentation section To maintain the daily logs adhering to the Good Laboratory Practices. Daily standardization of Karl Fischer reagent. Daily temp recording of instrumentation room, chemical room & refrigerator. Daily preparation of 0.4% NaoH for discarded p...

Role & responsibilities Operate and maintain QC instruments, including HPLC, GC, UV, FTIR, Dissolution Apparatus, Melting Point Apparatus, Karl Fischer Apparatus, Auto Titration, Analytical Weighing Balance, Polarimeter, Disintegration Apparatus, pH Meter, etc. Perform analysis of in-process samples, validation, hold-time study, finished products, and stability samples as per relevant specifications. Conduct daily and monthly calibration of analytical balances in the instrumentation section. Maintain daily logs and ensure adherence to Good Laboratory Practices (GLP). Perform daily standardization of Karl Fischer reagent. Monitor and record daily temperature readings of the instrumentation ro...

We are seeking a highly motivated and experienced Study Director to oversee chemical characterization studies within our research and development team. The ideal candidate will have a strong background in analytical chemistry, extensive knowledge of chemical characterization techniques, and a proven track record in managing complex projects. This position offers a competitive salary and benefits package, along with opportunities for professional growth and development. If you are passionate about advancing scientific research and thrive in a collaborative environment, we encourage you to apply. Roles and Responsibilities 1. Oversee and manage chemical characterization studies from initiation...

Urgent opening for QC Officer-Sr. Officer in Dahej, Bharuch. Note: Walk In Interview at Ahmedabad Date & Time: 20th July, 2025 at 09:00 AM Onwards Job Location: Dahej, Bharuch Experience: 2 to 7 years in API Qualification: M.Sc./B.Pharm/M. Pharm Required Candidate profile Roles and Responsibilities: -Experience in Section LCMS / PSD / HPLC / GC /Method Validation -Candidate preferred from Pharma API (Active Pharmaceutical Ingredient).

At SCIEX, our work at one of Danaher's 15 operating companies plays a vital role in saving lives. We are driven by a shared commitment to innovate for real-world impact. As a global leader in mass spectrometry, SCIEX provides cutting-edge solutions for precise detection. With a history spanning over 50 years, SCIEX has been at the forefront of developing revolutionary technologies and solutions in mass spectrometry and capillary electrophoresis. Our products empower customers to swiftly address environmental threats, gain deeper insights into disease-related biomarkers, enhance patient care in clinical settings, expedite the introduction of relevant drugs to the market, and ensure the safety...

You will be responsible for conducting lab testing and analysis in a Pharma Laboratory located in Gurugram. The ideal candidate should possess an MSc in Chemistry, B.Pharma, or a related field with 2 to 10 years of experience. Your main duties will include chemical testing of raw materials, finished products, cosmetics, Ayurveda, Sidha, and Unani products. You should also have knowledge and experience in handling instruments such as HPLC, GC, GC-MS/MS, ICP-MS, and Dissolution equipment. Additionally, you will be required to maintain documentation in accordance with NABL Audit standards. This role requires attention to detail, strong analytical skills, and the ability to work effectively in a...

Post – Assistant Manager (QC) Location: Ahmedabad (Kathwada) Gender – Male Experience- HPLC, GC, KF Education – BSC Chemistry / BE, B. Tech (Chemical) Experience – 6 to 10 yrs Preference – Food / Pharma industry

Project Managers are responsible for overseeing the project/engagement/activity on a daily basis and are responsible for delivering high-quality results within the identified objectives and constraints, ensuring the effective use of the allocated resources. They are responsible for risk and issue management, project communication and stakeholder management. Project managers perform the activities of planning, organising, securing, monitoring and managing the resources and work necessary to deliver specific project goals and objectives in an effective and efficient way. - Grade Specific Senior Project Manager - Responsible for leading either a large project or a definable segment of a very la...

Analyse raw, in-process, and finished products using GC, HPLC, and other instruments. Role includes sampling, testing, equipment calibration, and ensuring compliance with SOPs in a pharma QC environment. Required Candidate profile (Minimum 2 years’ experience, preferably in ADL within the pharmaceutical industry)

Qualification :- B.Sc / M.Sc Chemistry Experience :-2 to 4 year in Formulation Plant Location :- Padra (Vadodara) Experience in Formulation Plant , HPLC Handling .

Organica Water is looking for Project Engineer to join our dynamic team and embark on a rewarding career journeyPrepare, schedule, coordinate, monitor and control the assigned engineering projects.Monitor compliance to applicable codes, practices, QA/QC policies, performance standards and specifications.Cooperate and communicate effectively with the client and project team.Functional planning and execution of particular work packages within the given parameters.Implementing Project driven changes and requests.Evaluation of customers specifications.Ability to lead multiple projects and partner with management / functional managers to resolve conflicts and obtain resources for project.Excellen...

Role Overview Responsible for qualification & calibration activities for defined instruments and equipment as per schedule & procedures with QMS. Illustrative Responsibilities Ensure that qualification & calibration activities are planned and executed within time frame defined by the procedure and equipments are released on time as per the pre-defined schedule. Responsible for coordinating with lab supervisors / system owners for handling of any non-conformances or escalations Handling of QMS related activities like, Change control, CAPA and Deviation with its effectiveness check. Responsible for quality compliance activities for laboratory instruments qualification and calibration. Summariz...

Role & responsibilities Regular & development Analytical support for R&D projects Method development using HPLC & GC Should Handle Instruments (HPLC, GC, IR, UV, KF & Potentiometer) independently. Preferred candidate profile Exposure to handle analytical equipments like GC, HPLC, KF, Potentiometer, IR & UV. Basic knowledge on ICH guidelines. Good Development Knowledge Awareness of Industry practices in Analytical domain. Basic regulatory knowledge.

Long Description 1 Exposure of execution of planning of Inprocess, Finished product, stability and cleaning validation samples of MDI / DPI formulation. 2 Exposure of compliance to all cGMP, GxP or any other regulatory requirements, including EHS requirements. 3 Maintenance of GLP in the Laboratory. 4 Having knowledge of Analytical Instruments like HPLC, GC, GCMS, LCMS, UV, IR, KF, ACI, NGI, DUSA, Spray Pattern etc. 5 Exposure of Laboratory investigation like OOS, OOT, Incidence, Deviation, CAPA, Change control etc. 6 Exposure of Stability sample management & Regulatory Audits. 7 Exposure of Analytical method transfer, Analytical method validation / Verification activity. 8 Exposure of Calib...

Key Responsibilities: Drive sales of laboratory products, particularly microbiology and chromatography items, including HPLC/GC vials and columns. Build and maintain strong relationships with clients across the assigned territory. Conduct regular client visits to follow up on leads and ensure order closures. Consistently improve sales performance by nurturing both existing accounts and identifying new business opportunities. Travel extensively within Telangana to engage with customers and ensure satisfaction. Lead and mentor a team of field sales executives, providing direction and support. Track team performance, coach team members, and help achieve set sales targets. Work closely with seni...

Preparation and Standardization of Volumetric solutions. Knowledge about capa analysis and customer audits Handling to instrument such as GC, HPLC, KF, PH Meter Sampling of Raw materials and Finish Goods. Maintain QC instruments ISO Documentation.

Job Description Summary This analyst role is responsible to perform analysis of stability samples, Raw materials, analytical method validation/verification and method transfer studies Job Description To perform Nitrosamine & extractable and leachable analysis of analytical method development / validation / verification and method transfer. Handling of LCMS, ICPMS instruments. Knowledge on nitrosamine method development / validation / verification. Experience: 7 to 9 years with M.Sc./ M. Pharm

Your Role and Responsibilities 1. Hands on work on custom layout for analog blocks like High Speed SerDes and General purpose IO designs with Cadence Virtuoso on latest technologies like 5nm and below and also take leadership roles in delivery of IPs 2. Work on Floor planning, power design, signal routing strategy, EMIR awareness andparasitic optimisations 3. Understand and apply analog Layout techniques to ensure the design meets performance with minimum possible area and good yield. 4. Participate in building and enhancing layout flow for faster, higher quality design process. 5. Checking physical verifications like DRC/LVS/ERC/ANT/DFM and other IBM internal checks 6. Collaborate with Circ...

Educational Master Of Technology,Bachelor Of Science,Bachelor Of Technology,Bachelor of Engineering,Bachelor of Pharmacy (Honors),Master of Pharmacy Service Line Application Development and Maintenance Responsibilities Key components of the responsibilities are as mentioned below but not limited to:6+ yrs. of Professional experience and strong knowledge with real time experience in IT Quality & Compliance, Computer System Validation / Software Testing / System Implementation in the Life Sciences industry. Leads the effort to manage, and/or maintains validation of the GxP computerized systems. Create Validation Plan, Validation Report and Reviews validation documents such as URS, FS, FRA, DD,...

Role & responsibilities :- 1) Knowing HPLC/ GC, Dissolution, UV, FT-IR, Potentiometer Troubleshooting, Calibration, Method Validation and Method Development. 2) Perform the analysis individually for In process and stability samples as per plan. 3) Follow Good manufacturing practices, Good laboratory practices and Good documentation practices in ADL. 4) Method Development of new products for test like Cleaning, Assay, Residual solvent, Dissolution & organic impurities. 5) Preparation, storage and usage of Volumetric / Reagent / Standard / Indicator solution. 6) Perform the calibration and verification of all instrument / equipment as per calibration scheduled. Preferred candidate profile :- P...

Job Summary We are seeking an associate for the Quality Control team responsible for conducting investigations in case of any failure, incidents, market complaint, OOS & OOT. The role involves ensuring accuracy in investigation, technical report writing/documentation, adherence to safety procedures and reporting discrepancies. Roles & Responsibilities • You will be responsible for conducting investigations in case of any failure, incidents, market complaint, OOS & OOT. The role involves ensuring accuracy in investigation, technical report writing/documentation, adherence to safety procedures and reporting discrepancies. • You will ensure accuracy of the documentation before submitting it for...