1437 Gc Jobs - Page 17

To ensure and carry out the analysis of sample and all other activities as per Standard Operating Procedure (SOP). To follow and ensure Good Laboratory Practices (GLP), Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP) inside lab. To check, verify and review the calibration of all the analysis instruments whether performed as per the schedule. To ensure recording of all the data related to the testing online, on day-to-day basis and ensure traceability of the same. To work for lab readiness for audit and ensure compliance in Laboratory.

To ensure and carry out the analysis of stability sample and all other activities as per Standard Operating Procedure (SOP). To get involve and support in investigation of failure of any material or product in case of any out of specification (OOS) or Out of trend (OOT) or laboratory incident or non-conformity and take corrective and preventive actions. To raise and implement change control or document change request wherever necessary. To follow and ensure Good Laboratory Practices (GLP), Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP) inside Stability lab. To ensure availability of the working & impurities standards as per various pharmacopoeia. To assist Supervis...

To ensure and carry out the analysis of stability sample and all other activities as per Standard Operating Procedure (SOP). To get involve and support in investigation of failure of any material or product in case of any out of specification (OOS) or Out of trend (OOT) or laboratory incident or non-conformity and take corrective and preventive actions. To raise and implement change control or document change request wherever necessary. To follow and ensure Good Laboratory Practices (GLP), Good Documentation Practices (GDP) and Good Manufacturing Practices (GMP) inside Stability lab. To ensure availability of the working & impurities standards as per various pharmacopoeia. To assist Supervis...

Position: Assistant manager Department: QC Location: Ankleshwar, Gujarat Joining : Within 1 Month Roles & Responsibilities: Ensure adherence to GLP, cGMP, safety, and data integrity practices in the laboratory. Perform routine and stability analysis of Raw Materials, Packing Materials, Intermediates, APIs, In-process samples, Finished Products, Returned Goods, Hold Time studies, Working Standards as per specifications, SOPs, and test procedures. Execute HPLC-related analysis with proper online documentation in LIMS. Maintain compliance with CFR 21 Part-11 and good chromatography practices during analysis, integration, and review. Record analytical results in worksheets/protocols, ensuring ac...

Multiple requirements as Analyst for HPLC, GC and ICP at middle and senior level. Experience from public testing lab will be an added advantage. Preference will be given to immediate joiners or who are ready to join in short notice period. Required Candidate profile It is on the rolls of Cotecna Life Sciences India Pvt Ltd(Erstwhile Geochem Laboratories) If interested please share profiles on nilesh.kadam@geochem.net.in or any more information call on 9870476784

We are seeking a skilled Analyst with hands-on experience in FTIR/Disso/UV/KF/HPLC techniques(Multiple requirements). The candidate should be well versed with Method Development, Method Validation and routine analysis. Required Candidate profile It is on the rolls of Cotecna Life Sciences India Pvt Ltd(Erstwhile Geochem Laboratories) Walk-in interview 22-Sept to 26-Sept 9.30am to 5pm on 27-Sept-25(Saturday) from 9.30am to 3pm

Position: US IT Recruiter (Work from Office) Experience Required: 3-4 Years Location: Hyderabad (HITEC City) Timings: 06:30 PM - 03:30 AM Notice Period: Immediate to 15 Days Qualification: Graduation in any stream Note: Exceptional proficiency in communication is a critical requirement for this role. Role & Responsibilities: Lead end-to-end recruitment for IT positions, including sourcing, screening, interviewing, and offer negotiation. Collaborate with hiring managers to understand job requirements, ensuring a tailored and efficient recruitment process. Leverage a variety of sourcing channels (job boards, LinkedIn, social media, and networking) to identify top IT talent. Conduct thorough in...

Position: US IT Recruiter (Fresher) Location: Hyderabad (HITEC City) Timings: 06:30 PM 03:30 AM IST Notice Period: Immediate Joiners Preferred Qualification: Graduation in any stream Note: Exceptional communication skills are mandatory for this role. This is a purely night-shift position . Role & Responsibilities Support end-to-end recruitment for IT positions under the guidance of senior recruiters. Collaborate with the team to understand job requirements and candidate profiles. Source potential candidates using job portals, LinkedIn, and internal databases. Conduct initial screening calls to evaluate candidate suitability. Coordinate interview scheduling, follow-ups, and feedback with cand...

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

As an Analytical Chemist at the Pharma Division of a Chemical Manufacturing Company in Ahmedabad, you will be responsible for handling analytical instruments such as HPLC, GC, UV, IR. Your key responsibilities will include performing instrument calibration, analyzing finished products and raw materials, and conducting wet lab analysis. **Key Responsibilities:** - Handle analytical instruments such as HPLC, GC, UV, IR - Perform instrument calibration - Analyze finished products and raw materials - Conduct wet lab analysis **Qualifications Required:** - 2 to 7 years of experience in Analytical Chemistry - Knowledge of analytical instruments and techniques - Educational background in Chemistry ...

Job Description: You should possess strong communication skills and be well-versed in analytical techniques such as HPLC, GC, IR, UV, and Wet analysis. Key Responsibilities: - Perform analytical testing using techniques such as HPLC, GC, IR, UV, and Wet analysis. - Communicate effectively with team members and stakeholders. - Maintain accurate records of all analytical tests conducted. Qualifications Required: - Proficiency in analytical techniques such as HPLC, GC, IR, UV, and Wet analysis. - Strong communication skills. - Prior experience in a similar role would be an advantage.,

A Quality Control Manager oversees and manages quality control processes to ensure products and services meet established standards, customer expectations, and regulatory requirements. Responsibilities include developing and implementing QMS policies Required Candidate profile M.Sc - B. Sc - M. Pharma - B. Pharma Must be able handle department independently in Medium Scale Pharma Company Knowledge to get Prepare necessary documents for Pharma Company FDA requirements

Dear Coder's Greetings From Qway Technologies Hiring for Group Coordinator Experience Required: 3 to 10 Yrs Location: Chennai (Guindy) Salary: As per Norms Notice Period: 15 Days Max Designation - Group Coordinator Required Speciality: E/M Coding Flexible towards shift timings Must be a good team player Looking for Immediate joiners Interview Mode: Direct Walkin/Online If you are interested, please share your updated resume below Whatsapp Number. 7397746781 Contact us on Monday to Friday between 11.30 am to 8.30 pm Regards HR Team Qway Technologies

Perform AMD & AMV for API dosage forms, handle HPLC/GC, develop stability-indicating methods (ICH, USP, EP, JP), impurity profiling, forced degradation, residual solvent analysis, method transfer, troubleshooting & compliance with GLP/GMP.

Operating Gas chromatography, HPLC general knowledge of GLP and GMP, wet analysis

As a Validation Specialist at our company, your primary responsibility will be to plan, execute, and document analytical method validation activities for raw materials, in-process samples, finished products, and cleaning validation. This will involve assessing various parameters like accuracy, precision, specificity, linearity, robustness, LOD/LOQ, and others. You will also review and approve validation protocols and reports to ensure compliance with ICH Q2(R1), USP, and other regulatory standards, maintaining adherence to GMP, GLP, and cGMP guidelines. Your role will require collaboration with R&D, QA, and Production teams to facilitate seamless tech transfer and validation support. Trouble...

Our Company At Teradata, we believe that people thrive when empowered with better information Thats why we built the most complete cloud analytics and data platform for AI By delivering harmonized data, trusted AI, and faster innovation, we uplift and empower our customers?and our customerscustomers?to make better, more confident decisions The worlds top companies across every major industry trust Teradata to improve business performance, enrich customer experiences, and fully integrate data across the enterprise, What Youll Do Create integration test specs and plans to validate product features and releases, Collaborate with feature teams to assess the system test scope and coverage for new...

As a Senior Manager - Quality Analyst at AB InBev India, based in Aurangabad, Maharashtra, you will be responsible for handling various instruments such as GC, Alcolyser, DMA, Sodium Meter, pH Meter, and Gas Generators. Your primary tasks will involve calibration and maintenance of all BQA instruments while strictly adhering to BQA SOPs. You will analyze in-process samples, identify deviations, and inspect incoming brewing raw materials. Your role will also include ensuring the reliability and accuracy of data by following SOPs for all analysis, utilizing BWC and control charting. It will be your duty to maintain records, update the AB datasheet regularly, conduct PRP audits, and 5S Audits p...

Home The University Job Opportunities and Working At Swansea Current Vacancies Research Officer in Antihydrogen Physics Back to list Research Officer in Antihydrogen Physics Related pages Current Vacancies Benefits & Rewards Equality Diversity & Inclusion Information for Applicants Information for for colleagues from around the world Our reward and benefits, and ways of working enable those who join us to have enriching careers, matched by an excellent work-life balance, About The Role The group is a leading member of the ALPHA collaboration with responsibility for positrons, antihydrogen synthesis, laser-spectroscopy and frequency metrology Recent research highlights include the first laser...

Role & responsibilities 1. Knowledge of calibration and operation of HPLC with empower software. 2. Sound knowledge of analytical method development and Analytical method validation of OVI, purity, and assay method by HPLC as per pharma guidelines. 3. Knowledge of caliberation and operations of all equipments like balance, ph meter, in analytical opeartion. 4. good knowledge of sample preperation as per GLP. 5. Knowledge of retreival and storage working standards and columns. 6. Handling of final compilation of raw data, chromatographic data complying with GLP requirements. 7. Recording all analytical activities, approximately in respective raw data forms. 8. knowledge of preperation of gene...

Role & responsibilities Preferred candidate profile

quality control with experiance of hplc,gc,karlfisher,uv,spectometer

Role & responsibilities Carry out RM, In process, Finish material testing, Follow laid down SOP for testing, keeping records, Raw material Sampling, testing and approval, Reagent preparation Preferred candidate profile Only male candidate can apply for the post. candidate should have min 3 yrs of experience in chemical industry in QC department.

On-site assessment and selection of target trainees and hospitals to ensure the selections result in optimal quantity and quality of trainees and Phaco conversion rates for the Phaco Development Program. Onsite (Operating Room) and wet lab instruction and consultation of trainees in the entire process of converting from ECCE and SICS to Phaco. This includes working with designated outside-Alcon consultants (course instructors and on-site proctors) to ensure effective trainee Phaco conversion rates and high quality surgical results Demonstrate product and procedural excellence to best technical model and coach trainees and affiliated personnel how to achieve optimal surgical and patient resul...

Walk-in Drive | TIL Healthcare | Multiple Openings in Production, QA, Engineering & QC TIL Healthcare is a part of "Jhaver Group of Companies" having a turnover of USD 450mn whose core activities include Manufacturing, Marketing, Engineering, Construction and Trading like diversified businesses. Our plants are accredited approvals like EUGMP, TGAAustralia, UK MHRAetc. TIL manufactures Tablets, Liquids, Powders in Sachets, and Capsules and with well-known partners for several European companies. We are considered as Pioneers in Amino Acids in India and few known brands include ApetaminT/AstyminT/Astyfer/Neutrosec/Urelog/Peglec/HappenzT. Walk-in Interview Details: Date: Sunday, 28th September ...