273 Ftir Jobs - Page 11

Job Title - CAL- PRD + Level :Senior Manager + S&C- IMU Management Level:6- Senior Manager Location:Mumabi/ B'lore Must have skills: Account management Good to have skills:NA Experience: Minimum 11+ years of experience Educational Qualification: Graduation/ Post Graduation from a premier B School Roles & Responsibilities: Growing business: Contribute to expanding Accentures footprint and share of wallet in client/industry; accountable for portion of business results on the account (at a minimum.) Bring disruptive and innovative ideas to originate new opportunities (while also pursuing business-as-usual opportunities.) Leverage industry networks and partner with experienced CALs to understand...

Ensure that the manufactured products consistently meet established standards, customer specifications, and industry regulations Optimize processes and drive continuous improvement initiatives Product Modification/ Development as per customer need Required Candidate profile B. Sc Chemistry with M. Sc Polymer Science mandatory 12+ years' experience in Quality Assurance & Control in a chemical/ polymer manufacturing company (preferably in polystyrene manufacturing)

Department: Pharma Standard - AD Required Qualification & Experience: M.Sc. in any Life science(s)/Analytical/M-Pharmacy, with 0 - 5 Years of experience in the field of pharmaceutical industry/CRO setup. For Preparative: Experience on instruments like Preparative HPLC and SFC Expertise in Purification of peptides, impurity isolation. For Analytical: Expertise Analytical Method Development of peptides and oligoes. Regular sample analysis for supporting to synthesis team. Handling experience on DAC column packer and media packing will be advantageous. Department: Pharma Standard - Quality Control Required Qualification & Experience: M.Sc. in any Life science(s)/Analytical/M-Pharmacy, with 0 - ...

Department: Pharma Standard - AD Required Qualification & Experience: M.Sc. in any Life science(s)/Analytical/M-Pharmacy, with 0 - 5 Years of experience in the field of pharmaceutical industry/CRO setup. For Preparative: Experience on instruments like Preparative HPLC and SFC Expertise in Purification of peptides, impurity isolation. For Analytical: Expertise Analytical Method Development of peptides and oligoes. Regular sample analysis for supporting to synthesis team. Handling experience on DAC column packer and media packing will be advantageous. ************************************************************************************************** Department: Pharma Standard - Quality Control...

Job Band: Job Band 13 (JB13) Hiring Manager: Akhil Kodiyamtharappel Sadasivan Lead Recruiter: Tino Manimuthu Country: India Our ability to grow, develop new capabilities and serve even more patients around the world depends on associates like you, who are passionate about our mission. Thank you for considering this new opportunity to further unlock your potential. JOB SUMMARY: - Ontime completion of testing, analysis, and documentation with respect to regulatory guidelines. REPORTING: - Reports to Deputy Manager QC ESSENTIAL DUTIES: - Administration/Internal Communications: Responsible for completing testing as part of Chemical, Functional and incoming inspection. Responsible for Document Re...

Preferred candidate profile Looking for a candidate with 2 to 4 years of work experience as QC analyst /AQA reviewer in reputed pharma companies. Should have Knowledge of handling/analytical data review of HPLC, FTIR, UV spectrophotometer, KF Autotitrator, Dissolution apparatus. Have Basic knowledge of CGMP, GDP, Data integrity. Should have Basic knowledge of OOS (Out of specification), OOT (Out of rend), OOC (Out of calibration).

Key Responsibilities Operational Oversight : Manage daily operations, schedule workflows, and oversee process improvements Strategic Planning : Develop and implement short-term and long-term plans; forecast resource and budget needs

Key Responsibilities Perform analytical testing of raw materials, intermediates, and finished APIs using HPLC, GC, UV, and other analytical instruments. Execute analytical method validation, method transfer, and verification as per regulatory guidelines. Ensure compliance with cGMP, GLP, and regulatory standards (ICH, USFDA, EU, WHO) . Maintain accurate documentation, calibration logs, and test reports in compliance with company SOPs. Support investigations, OOS, OOT, and CAPA implementation . Coordinate with QA and Production teams for smooth project execution. Contribute to laboratory upkeep, safety practices, and audit readiness.

The Opportunity Under limited supervision, obtain revenue by verifying transaction information; compute charges and refunds; prepare and mail invoices; identify delinquent accounts and insufficient payments. Collect revenue by reminding delinquent accounts; notify customers of insufficient payments. Pay invoices by verifying transaction information; schedule and prepare disbursements; obtain authorization of payment. Resolves account discrepancies by investigating documentation; issuing stop payments, payments, or adjustments. The Subject Matter Expert role is responsible for identifying and finding end to end solutions in fixing process gaps and ensuring timely payment from customer on outs...

Role & responsibilities Hands on instruments Gas Chromatography, Gel Permeation Chromatography, FTIR, Type B viscosity, color meter and Moisture meter. Measuring ability of Non-volatile content, acid value, amine value, NCO%, Peel adhesion, Shear strength, amine value and appearance. Responsible for inspection of raw material, packing material, In-process & Finished product samples as per standards. Interdepartmental coordination ability. Responsible for inventory management of Chemicals, Glass-wares and consumables. Responsible for equipment management. Reviewing of quality records related to QC activities. Maintain Safety & 5S in Laboratory. Preferred candidate profile Familiar with docume...

Teslas Supplier Industrialization team is responsible for critical raw materials, component production and qualification activities at suppliers. This role will be responsible for selecting, qualifying, scaling battery cell materials (such as NMC, LFP, precursor, graphite, LiOH, cathode electrode, PVDF, LiPF6, etc.) manufacturing processes and quality system at Tesla supplier locations. In this role, you will work closely with many organizations both internal and external to Tesla, taking new battery designs from initial concept through into full production. The battery cell is a critical component in Tesla vehicles and storage systems. This role will have the opportunity to make meaningful ...

Role & responsibilities: Outline the day-to-day responsibilities for this role. Preferred candidate profile: Specify required role expertise, previous job experience, or relevant certifications.

Job Summary: GE Aerospace is seeking a visionary leader to serve as Executive Leader Vice President - Artificial Intelligence (AI). This role will define and execute the AI and data science strategy for commercial engine services, driving innovation and operational excellence. The Executive Leader/VP - AI will lead a high-performing team, foster cross-functional collaboration, and ensure the successful deployment of AI solutions to optimize service operations, reduce downtime, and enhance profitability. Key Responsibilities: Strategic Leadership: Develop and execute a vision for leveraging AI and data science to drive business outcomes, ensuring alignment with organizational goals and long-t...

i. Experienced in independent instrumental analysis of raw material, in process samples, finished product and stability samples of pharmaceutical products. ii. Well versed in analysis of Tablets, capsules, liquids samples, for common test as Assay, Related substances, Dissolution and preservative content analysis as per controlled specification and method of analysis. iii. Should able to operate, calibrate and maintain instruments like HPLC, GC, Dissolution apparatus, UV and FTIR etc. iv. Experience of Empower, Lab solution software shall be recommended. v. Exposure to perform AMV or development shall be preferred. vi. Aware about on line & good documentation practices. vii. Should have know...

At Umendra Life Sciences Pvt. Ltd. , we take quality seriously. Our products are trusted by consumers worldwide, and were looking for a Quality Control (QC) professional to ensure they meet the highest standards. If you're passionate about precision and excellence, this role is for you. Your Role: As part of our QC team , you'll focus on testing raw materials, in-process samples, and finished products to ensure they meet established specifications. Your job is to detect and prevent defects before products reach the market. Key Responsibilities: Conduct physical and chemical testing of raw materials and final products (pH, viscosity, stability, active ingredient analysis). Perform stability s...

Hiring QC – Personal Care & OTC | Umendra Life Sciences | 2–5 Yrs Exp | Bavla, Ahmedabad | HPLC, GC, FTIR, UV

Role & responsibilities Should have Knowledge about IMS system (ISO 9001:2015, ISO 14001:2015 OHSAS 18001:2007, and cGMP, USFDA, FSSC 22000, NABL. Analytical skill for QC instrument, i.e. GLC, HPLC, UV-Visible, FTIR, ICP, K/F, Melting point etc. Regularize the QC activities as per cGMP requirements. RM, PKG, In-process and FG sampling & Analysis. Co-ordination with QC staff, R&D, Commercial and production for quality & dispatch related activities for on time dispatches. Day to day monitoring and execution online all IPQC and FG analysis activities. Resolve the trouble shooting related to QC activities. Knowledge about 21 CFR Part 211, 111 with data integrity (Part-11) Awareness about respons...

Role & responsibilities Ensure All Biopharmaceutical Development Lab Equipment are in state of GLP and Safety Compliance by rectifying equipment breakdowns, maintaining critical spares & consumables and carrying out equipment installations as per approved protocols. Attend breakdown of S1, S2 & S20 Equipment/ Instrument in lab and get it operational with support from instrument vendor and E&M team. Responsible for IQ, OQ, PQ for new instrument installation, calibration and maintain the supporting documents in coordination with DQA and E&M team. Responsible for the equipment requalification and completion of documents coordination with DQA and E&M team. Ensure that the S1, S2 & S20 Equipment/...

Responsibilities: Responsible for Documentation work in QC Department. Candidate must have knowledge of HPLC. Shall maintained all records related to manufacturing Overall looking after the complete filling, packing activities and Procurement of the packing material. To ensure the compliance of safety Requirement Cleanliness Hygiene and Environment in Working Areas. Required Skills: Must be excellent in written and spoken English; net savvy and adept at computer skills Attention for detail Team player Good in communication Required Qualification : - B. Sc./M.Sc. -Chemistry

Responsibilities: Responsible for Documentation work in QC Department Candidate must have Experience of HPLC , GC & Wet Analysis. Shall maintained all records related to manufacturing Overall looking after the complete filling, packing activities and Procurement of the packing material. To ensure the compliance of safety Requirement Cleanliness Hygiene and Environment in Working Areas. Responsible for Domestic / Export/ batch production & their Documents for their smooth Dispatch Activity. Required Skills: Team player Good in communication Required Qualification: - B.Sc/M.Sc - Chemistry

Responsibilities: Responsible for Documentation work in QC Department Candidate must have knowledge of HPLC/GC. Responsible for manufacturing the batch as per MOM or BMR. Shall maintained all records related to manufacturing Overall looking after the complete filling, packing activities and Procurement of the packing material. To ensure the compliance of safety Requirement Cleanliness Hygiene and Environment in Working Areas. Responsible for Domestic / Export/ batch production & their Documents for their smooth Dispatch Activity. Required Skills: Must be excellent in written and spoken English; net savvy and adept at computer skills Attention for detail Team player Good in communication Requ...

Position: Pre-Clinical Designation: Research Associate Job Location: Dholka, Gujarat 1. Study Sample Analysis- Clinical studies 2. Method Development and Method Validation - Preparation of STP And MVP 3. Coordinate with QA & QC department for timely completion of Projects reports 4. Preparation of SOP and method development and method validation documents 5. Maintaining GLP & ensure 100% compliance

Key Job Responsibilities : Operate and troubleshoot instruments such as HPLC, GC, LC, FTIR, AAS and Other microbiology lab instruments. Create and maintain training documentation for individual staff in the Lab. Release and hold product(s) as necessary in the Warehouse Management System Troubleshoot assays and equipment when unexpected results occur. Perform data entry and data analysis, review quality documents, test records and shelf-life program. Work together with the Quality management to improve all Quality functions. Create and maintain quality documentation of equipment and instruments used in the lab; create/revise Standard Operating Procedures