325 Dissolution Jobs - Page 13

Key Responsibilities Quality Strategy & Planning Develop and implement quality control standards, procedures, and policies. Define inspection criteria and quality benchmarks. Team Management Lead and supervise a team of quality inspectors or analysts. Provide training and guidance to QC staff. Manage and supervise QC laboratory activities Use effective negotiation skills to drive alignment and resolve conflict Inspection & Testing Oversee routine inspections and testing of raw materials, in-process, and finished products. Ensure compliance with internal and external specifications and regulations. Documentation & Reporting Maintain detailed records of quality control activities. Analyze QC d...

2 VACACNCIES IN ADL - STABILITY TEAM 1) Stability - Team lead/Manager- Investigational analysis - ADL DEPARTMENT with 10 to 18 yrs of experience in Regulated and Emerging markets. 2) Executive / Scientist - ADL Stability with 6 to 9 yrs of experience in Regulated and Emerging markets. Educational qualification : M.Sc Analytical chemistry Dosage forms : Oral solids, Liquid orals, Opthalmic and injectable products Job description for AD: 1) Will be responsible and accountable for the trouble shooting and investigational analysis of R&D stability samples 2) Sound technical and scientific knowledge for investigation of anomalies. 3) Root cause identification and CAPA for OOT and OOS for developm...

VACANCY FOR TEAM LEADER - ANALYTICAL METHOD DEVELOPMENT (FORMULATIONS) - REGULATED MARKET Experience: 10 to 15 years Designation : Asst. Manager/ManagerEducational qualification : M.Sc Job profile : Need to work independently and should have handled a team of 6 to 8 members for method development and routine testing To guide and mentor analysts with practical training for developing analytical methods. SOP training and Analyst certification for new joinees within the team. Work allocation and planning of daily activities for the team subordinates Monitoring of routine analysis and trouble shooting To support site for critical trouble shooting and investigation Review of raw data , LNB and fi...

Qualification : M. Pharmacy (Analytical)/M.Sc.(Analytical) Experience : 2-3 yrs. (Formulation Experience) Location : Balnagar (Hyderabad) Skills Required: Sound knowledge of Dissolution, Analytical method development for tablets, capsules, oral solutions, ICH stability testing, Water HPLC, UV-Visible Spectrophotometer, KF Auto tiltrotor, Analytical method validations, transfer and verifications as per ICH guidelines and USP/BP guidelines, Analysis of in-process, stability & protocol driven samples. Reports, Protocols and STP, SOPs Preparation. GLP Activities. Chromatographic software like Empower. Prefer Male people & Immediate Joiners.

Experience - 2 Years + In Formulation QC * QC - Finish Product - GC/HPLC/ Dissolution/AAS/UV * QC- In process- HPLC/UV/Dissolution/GC * QC - Validation- HPLC/UV/GC/Dissolution * RM - HPLC * Stability HPLC GC UV Dissolution * RM Reviewer

Job summary We are seeking an individual to perform the Preventive Maintenance and Break Down Maintenance of Analytical Equipment's present in Quality Control . Roles & Responsibilities To perform the preventive and breakdown maintenance of analytical equipment's or Instruments like HPLC, UPLC, GC-HSS, Dissolution Test Appratus, Titrators, FTIR, UV-VIS Spectrophotometer,.... To update the preventive maintenance plan whenever addition of instruments or match the calibration schedule. To prepare the task lists for all analytical equipment's and update them in SAP. To perform the preventive maintenance as per the PM schedule. To make sure of closing the generated PM orders in SAP after performi...

The position is one of a leadership role. Work experience of at least 10 years in the Indian BFSI, real estate and infrastructure domain, of which at least 6 years should be in leading a team of 8 to 10 members wherein the candidate should have worked on and be centrally involved in project management and driving research and consulting engagements with or within banks, HFCs, NBFCs and corporates. Ability to drive business development and acquisition efforts in the above sectors is also critical.

Sales reporting and Analytics We are seeking a detail-oriented and proactive professional to join our Sales Operations team as a Sales Reporting and Analytics Analyst. This role will be responsible for delivering strategic and operational sales insights through regular and ad-hoc reporting, dashboard creation, and data quality management. The ideal candidate will support business units (BU/SBU) with performance tracking, forecasting, and executive-level analytics. Your role Provide timely and accurate sales data for BU/SBU and management reviews. Develop and maintain BAU (Business As Usual) strategic reports on BU sales performance. Conduct on-demand ad-hoc analysis on bookings, pipeline, fo...

Walk-In Drive For Formulation Analytical Research & Development(FAR&D)- Holi Child School, Near Dundigal Police Station, Gandi Maisamma on Friday 22-08-2025. Requirement for Executive - FAR&D - Formulation Analytical Research & Development(FAR&D) Undertake method development, troubleshooting and method validation to GMP and ICH. Investigation of non-conforming samples, CAPAs, data evaluation and reporting. Write cGMP Quality documents including Standard Operating Procedures, laboratory equipment procedures and investigational protocols. Excellent, enthusiastic, clear communication skills, both written and verbal, with a diverse audience are critical to the success of this position. Proven ab...

Walk-In Drive For Formulation Analytical Research & Development(FAR&D)- Qualychrome Research Labs, H.No .5-5-35/128, plot no.177, near Venkateswara Swamy temple, Prashanti Nagar, Kukatpally, Hyderabad, Telangana on Friday 22-08-2025. Requirement for Executive - FAR&D - Formulation Analytical Research & Development(FAR&D) Undertake method development, troubleshooting and method validation to GMP and ICH. Investigation of non-conforming samples, CAPAs, data evaluation and reporting. Write cGMP Quality documents including Standard Operating Procedures, laboratory equipment procedures and investigational protocols. Excellent, enthusiastic, clear communication skills, both written and verbal, wit...

Walk-In Drive For Formulation Analytical Research & Development(FAR&D)- MSN Laboratories, R&D Center, Pashamylaram, Hyderabad on Friday 22-08-2025. Requirement for Executive - FAR&D - Formulation Analytical Research & Development(FAR&D) Undertake method development, troubleshooting and method validation to GMP and ICH. Investigation of non-conforming samples, CAPAs, data evaluation and reporting. Write cGMP Quality documents including Standard Operating Procedures, laboratory equipment procedures and investigational protocols. Excellent, enthusiastic, clear communication skills, both written and verbal, with a diverse audience are critical to the success of this position. Proven ability to i...

Qc Stability and Fg section as analyst. Physical test of tablets, Dissolution Test,Assay(By UV) skills in operating instruments like UV Apparatus, Disintegration Apparatus, Friability Apparat

Roles: Manage Execution: Coordinate onsite IoT implementation and commissioning for DigitalPaani projects. Plan & Track: Develop detailed project plans, monitor progress (e.g., via Jira), and ensure timely delivery. Solve Problems: Support onsite teams to overcome hurdles and keep projects within budget. Requirements: Automation Experience: Skilled in PLCs, sensors, wiring, and electrical panel management. Organized & Practical: Strong at planning, documentation, and onsite execution. Industry Fit: Water industry experience is a plus; large-site execution is ideal but not required.

Roles and Responsibilities Conduct quality control tests on raw materials, in-process samples, finished products, and stability studies using HPLC, GC, UV, Dissolution, LIMS, Microbiology techniques. Ensure compliance with GLP guidelines for laboratory operations and maintain accurate records of test results. Collaborate with cross-functional teams to resolve quality issues and implement corrective actions. Develop and execute protocols for wet analysis testing of pharmaceutical products. Participate in audits conducted by regulatory authorities or internal stakeholders.

Hello, We have urgent opening for the below profile Designation :- Technician / Operator Experience :- 3-5 Years Qualifications :- Diploma in instrumentation Job Responsibilities :- 1) Manage and maintain analytical instruments which includes HPLC, Dissolution, UV Spectrophotometer , GC, Particle size, Milli Q water purification system, Analytical/Precision balance etc. 2) Co-ordination with service engineer for breakdown and preventive maintenance 3) Oversee repair and calibration of instruments/equipments 4) Ensuring adherence to quality standards and best practices to ensure zero downtime 5) Co-ordination with CFT team for PO and spares If you think that you fit the role, please share you...

Principal task: Analytical Method Development by HPLC for all Project. Review the analytical method development data, validation study data and method transfer protocol and reports. Calibration of HPLC system. To maintain GLP/GDP in working environment. Preparation of analytical data and submit for review. Analytical Method Development and Validation. Responsibilities: Calibration of HPLC’s as per SOP and maintenance of HPLC Systems. Maintaining record for all analytical reports by entering all the data in raw data note book and timely release of analytical reports. Preparation & Review of analytical method validation protocol and report as per the current regulatory requirement. As per Prot...

Serves as lead engineer on mid- to large size projects. Provides specialized technical input to studies and design for staff's specific area of expertise. Approves and signs off on work. Provides technical expertise for studies and design efforts. Presents complex technical solutions to clients. Performs quality control reviews of work developed by others. Participates in development of technical proposals. Provides estimates for the engineering budget and schedule to meet requirements on large projects.

Performs specific and limited portions of a broader assignment of an experienced engineer for Electrical /MEP work Gathers and correlates basic engineering data using established and well-defined procedures. Works on detailed or routine engineering assignments involving calculations and relatively simple tests. Proposes approach to solve new problems encountered. Identifies discrepancies in results. Provides guidance to entry level engineers. Performs work in accordance with agreed upon budget and schedule with moderate supervision. Qualifications Bachelors degree in electrical / mechanical engineering or related discipline from a recognized university 5 years of professional experience in r...

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

Job Description: Position: QC Officer Responsibilities: Effectively perform chemical analysis techniques specifically using HPLC, GC, Karl Fischer, Melting Point, IR, and UV-Vis instrumentation. Completes documentation relating to material analysis and enters data into database/software systems. Assist with production activities as required. Laboratory environment requiring the ability to carry out laboratory operating procedures in a safe manner, while maintaining a clean and orderly workspace. Carried out instructions from senior staff. Work effectively with computer software and hardware, including analytical instruments, spreadsheets, and word-processing applications. Maintain and perfor...

Responsibilities: To follow Good Laboratory Practices. Carry out routine analysis & Ensure documents pertaining to day to day analysis. Calibrate instrument used for analysis as per SOP and maintain its record. Method Transfer Activity. Should have experience of handling and calibration of GC, HPLC, KF, UV, Viscometer, Potentiometer, Tintometer, PH Meter etc. Various analyticals methods development and wet analysis along with related documentation. Required Skills Must be excellent in written and spoken English; Net savvy and adept at computer skills. 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

HPLC, Stability test ,