1426 Gc Jobs - Page 5

As an experienced candidate with 2-5 years of experience in HPLC/GC in the pharmaceutical industry, you will be responsible for the following key responsibilities: - Conducting HPLC and GC analysis as per industry standards - Analyzing and interpreting test results accurately - Maintaining and troubleshooting laboratory equipment - Ensuring compliance with safety regulations and quality standards To qualify for this role, you must have the following educational background: - Bachelor's or Master's degree in Pharmacy (B.Pharm/M.Pharm) or Science (B.Sc/M.Sc) If you are interested in applying for this position, please email your resume to hr@elysiumpharma.com or info@elysiumpharma.com. Kindly e...

Job Description: You should be a good communicator with knowledge of analytical techniques like HPLC, GC, IR, UV, and Wet analysis. Key Responsibilities: - Perform HPLC, GC, IR, UV, and Wet analysis. - Communicate effectively with team members and stakeholders. Qualifications Required: - Proficiency in analytical techniques like HPLC, GC, IR, UV, and Wet analysis. - Strong communication skills.,

You will be responsible for preparing customer files, reviewing batch records, and releasing batch records. You will act as a liaison to our customer's quality assurance groups for batch record review and release. You will manage communication between operations/production, project management, and other quality groups. Additionally, you will approve all batch records prior to production to ensure they conform to cGMP requirements. - Timely analysis of under test samples and providing timely results - Coordinating with production for quality-related issues and clarification - Sampling and analysis for RM/Intermediate/Finished Goods - Ensuring compliance of ATR - Assisting the team in ISO impl...

As an Executive/ Sr. Executive in Quality Management System (Analytical Assurance), your role will involve leading the Out of Specification investigations and managing core QMS activities related to QC. Your responsibilities will include: - Triggering out of specification investigations when test results fall outside predefined specifications. You will be required to design and conduct tests to confirm or eliminate suspected root causes. - Handling QMS documents such as Incidents & Deviations. - Evaluating change control & CAPA processes. - Reviewing analytical documents like worksheets, specifications, methods of analysis, stability protocols & summary reports, and logbooks from the Quality...

Job Description He should be a good communicator and should know the Analytical techniques liks HPLC,GC ,IR ,UV and Wet analysis Qualifications Master's degree in Analytical/General Chemistry About Us In the three decades of its existence, Piramal Group has pursued a twin strategy of both organic and inorganic growth. Driven by its core values, Piramal Group steadfastly pursues inclusive growth, while adhering to ethical and values-driven practices. Equal employment opportunity Piramal Group is proud to be an Equal Employment Opportunity and Affirmative Action employer. We do not discriminate based upon race, ethnicity, religion, color, national origin, gender (including pregnancy, childbirt...

The Opportunity The person will be responsible in preparing customer files, review batch records, and release batch records. Liaison to our customer's quality assurance groups for batch record review and release. Manage the communication between the operations/production, project management, and other quality groups. Approve all batch records prior to production to ensure that they conform to requirements of cGMP. What We Are Looking For Responsible for Timely analysis of under test samples giving timely results Coordination with production for quality related issues and clarification Sampling and analysis for RM/Intermediate/Finished Goods. Ensure compliance of ATR. Assisting team in ISO im...

As a Quality professional at Piramal Pharma Solutions, your role will involve remote support to PPL sites, reviewing analytical data, preparing master build in LIMS, and document preparation. Your key responsibilities will include: - Preparation of Master Build in LIMS. - Overseeing track-wise operations for QMS activities. - Preparation and review of Method Validation, Method Transfer, Method Verification, and Equivalency documents. - Preparation and review of Test Methods, STPs, and Specifications. - Operational knowledge of eDMS and ensure application compliance. - Monitoring compendial changes and preparing evaluation reports. - Reviewing analytical data, raw data, chromatography, and LI...

This is where your work makes a difference. At Baxter, we believe every personregardless of who they are or where they are fromdeserves a chance to live a healthy life. It was our founding belief in 1931 and continues to be our guiding principle. We are redefining healthcare delivery to make a greater impact today, tomorrow, and beyond. Our Baxter colleagues are united by our Mission to Save and Sustain Lives. Together, our community is driven by a culture of courage, trust, and collaboration. Every individual is empowered to take ownership and make a meaningful impact. We strive for efficient and effective operations, and we hold each other accountable for delivering exceptional results. He...

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 ...

Key Responsibilities: Manage full-cycle IT recruitment, from job requisition to onboarding, for public and state government clients. Source qualified candidates using platforms such as Monster, Dice, CB, and LinkedIn. Develop and maintain pipelines of cleared and compliant IT professionals for contract. Conduct thorough screenings to ensure candidates meet technical and eligibility criteria. Collaborate with managers and other team members to define role requirements, salary ranges, and contract terms. Negotiate pay rates and terms aligned with client budget structures and agency standards. Schedule and coordinate interviews between candidates and client hiring panels. Maintain recruitment d...

Main Purpose Lead Testing Engineer to oversee the testing and validation of ourelectromechanical components, including relays, contactors, MCBs, and otherlow-voltage switchgear The ideal candidate will have a strong background intesting electromechanical devices and a deep understanding of internationalstandards Responsibilities Experience in verification and Validation of Low voltage switchgear productslike Relays or similar productsStrong knowledge on Lab instruments like Power source, Oscilloscope, Dataloggers etc Develop comprehensive testing and validation plans for new and existingelectromechanical components Identify and document boundary conditions and worst-case scenarios to ensure ...

Laxmi Organic Industries Limited. We are looking for candidates interested in Technical Associate-Quality for Chiplun. Job Title: Technical Associate-Quality Department: Quality Control/ Quality Assurance Location: Lote. Job Purpose *To provide analytical(ADL), quality control (QC) support to Manufacturing* Role and Responsibilities Operational: Use analytical techniques and instrumentation, such as GC, HPLC, IR, UV-Visible Spectrophotometer, Potentiometer, KF, Melting point. Calibration of instruments like IC, Fluoride analyser, HPLC, GC, IR, UV-Visible Spectrophotometer, Potentiometer, KF, Melting point. Analysis samples like finish product, raw material and in-process. Report the results ...

We are currently seeking a data-driven and detail-oriented Program Intern to join Leap. This role will involve critical thinking, problem-solving, and analytical thinking to drive operational improvements and support strategic initiatives. The charter for this role will include: Work closely with the founder/senior leaders to turn ideas into validated experiments. Dive into industry trends, discover competitor insights while also working on user research. Build a hypothesis to solve the different problem statements, execute, validate and scale the results Align with stakeholders across the org to drive the actionables; be a driving force in cross-functional teams Present findings, recommenda...

IT Recruiter will be responsible for full-cycle recruitment of technology professionals for state, local, and public sector clients across the United States. This role involves sourcing, screening, qualifying, and onboarding IT candidates. Key Responsibilities: Manage full-cycle IT recruitment, from job requisition to onboarding, for public and state government clients. Source qualified candidates using platforms such as Monster, Dice, CB, and LinkedIn. Develop and maintain pipelines of cleared and compliant IT professionals for contract. Conduct thorough screenings to ensure candidates meet technical and eligibility criteria. Collaborate with managers and other team members to define role r...

As the Lead of the Residue Analysis & Instrumentation section in the laboratory, your role involves overseeing and managing the analysis of pesticides, antibiotics, veterinary drugs, mycotoxins, heavy metals, and other contaminants in food samples. You will be responsible for operating, supervising, and maintaining advanced analytical instruments such as LC-MS/MS, GC-MS/MS, ICP-MS / ICP-OES, HPLC, GC, AAS, UV-Vis, and FTIR. Your duties include ensuring compliance with NABL (ISO/IEC 17025:2017), FSSAI guidelines, Codex, and BIS standards. You will also be involved in method validation, verification, calibration, and measurement of uncertainty. Reviewing and authorizing test reports as an Auth...

For over 50 years, SCIEX has been developing groundbreaking technologies and solutions in mass spectrometry and capillary electrophoresis. Our products enable our customers to quickly respond to environmental hazards, better understand biomarkers relevant to disease, improve patient care in the clinic, bring relevant drugs to market faster and keep food healthier and safer. At SCIEX, you'll find a rewarding role that amplifies your impact on the world and helps you realize life's potential. SCIEX is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we're pioneering the future of science and medicine, developing products that enable researchers in t...

For over 50 years, SCIEX has been developing groundbreaking technologies and solutions in mass spectrometry and capillary electrophoresis. Our products enable our customers to quickly respond to environmental hazards, better understand biomarkers relevant to disease, improve patient care in the clinic, bring relevant drugs to market faster and keep food healthier and safer. At SCIEX, you'll find a rewarding role that amplifies your impact on the world and helps you realize life's potential. SCIEX is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we're pioneering the future of science and medicine, developing products that enable researchers in t...

Signore Technologies Pvt. Ltd. is looking for . Net Software Engineer to join our dynamic team and embark on a rewarding career journey Collaborate with cross-functional teams to achieve strategic outcomes. Apply subject expertise to support operations, planning, and decision-making. Utilize tools, analytics, or platforms relevant to the job domain. Ensure compliance with policies while improving efficiency and outcomes.

Job Requirements Ensuring the timely release of the PDIS for introduction of New products as per Category requirements for both DEC and Vendor Pick-up. Validation of GC & AMC-Crafting Charges for all new products Coordinate with NPI & Factory NPD teams for Timely completion of proto products Dashboard maintenance and tracking the stage gate completion of designs and effectively communicating to all relevant stakeholders NPD spoc of Brief to PDIS release for DEC designs and co-ordinate with category managers for vendor pick-ups. Ensuring proto bin liquidation through periodic inputs to the category teams Ensure the smooth implementation of newly developed NPD portal across vendors for both pl...

Choosing Capgemini means choosing a company where you will be empowered to shape your career in the way youd like, where youll be supported and inspired bya collaborative community of colleagues around the world, and where youll be able to reimagine whats possible. Join us and help the worlds leading organizationsunlock the value of technology and build a more sustainable, more inclusive world. Job Role Very good Understanding of current work and the tools and technologies being used. Comprehensive knowledge and clarity on Bigquery, ETL, GCS, Airflow/Composer, SQL, Python. Experience working with Fact and Dimension tables, SCD. Minimum 3 years" experience in GCP Data Engineering. Java/ Pytho...

Job Summary We are seeking a highly skilled Analytical Scientist in to join our Research and Development team for Injectable Division for developing and validating analytical methods for injectable products, ensuring compliance with the regulatory requirements, conducting literature reviews, scaling up for manufacturing of batches, coordinating manufacturing readiness, overseeing plant execution, and facilitating seamless technology transfer. This role demands a strong understanding of analytical principles, excellent documentation skills, and the ability to work effectively in a collaborative team environment. scaling up for manufacturing of batches, coordinating manufacturing readiness, ov...

Analytical test including physical and wet analysis. Expertise in handling of HPLC, GC , UV and IR Knowledge on OOS and OOT Calibration of laboratory Instruments. Preparation and standardization of Reagents/Volumetric solutions. To ensure cGLP compliance and Data Integrity

Position: Junior Officer / Chemist Quality Control (QC) Industry: Pharmaceutical – API Manufacturing Location: Ankleshwar, Gujarat Department: Quality Control Experience: Minimum 2 Years (Pharma – API Experience Mandatory) No. of Positions: 2 Job Description: We are seeking a detail-oriented and experienced Junior Officer / Chemist – QC to support our API manufacturing unit's Quality Control operations. Key Responsibilities: Perform and monitor all QC activities including analysis of Raw Materials (RM) , Intermediates , and Finished Products Operate and calibrate laboratory instruments such as: HPLC GC UV Spectrophotometer FTIR Karl Fischer Titrator pH Meter Conductivity Meter Auto Titrator ...

Analysis of Raw Material, In-Process & Product samples as per standard test methods,Operation of polymer testing equipment (MFI, Impact, Molding), GC, Spectrophotometer etc ISO 9K, 14K,SAP CTC :5-&7 LPA Exp- 4-6 Years

Job Description Jubilant Bhartia Group Jubilant Bhartia Group is a global conglomerate founded by Mr. Shyam S Bhartia and Mr. Hari S Bhartia with strong presence in diverse sectors like Pharmaceuticals, Contract Research and Development Services, Proprietary Novel Drugs, Life Science Ingredients, Agri Products, Performance Polymers, Food Service (QSR), Food, Auto, Consulting in Aerospace and Oilfield Services. Jubilant Bhartia Group has four flagships Companies- Jubilant Pharmova Limited, Jubilant Ingrevia Limited, Jubilant FoodWorks Limited and Jubilant Industries Limited. Currently the group has a global workforce of around 43,000 employees. About Jubilant Biosys Jubilant Biosys Ltd is a p...