395 Dissolution Jobs - Page 7

Dear Applicants, Greetings from Biophore India !! We have opening for Formulation AR&D Department. Experience : 2 - 6 Years Qualification : B. Pharm /M. Pharm or M Sc Work Location: R&D Centre -Pashamylaram, Isnapur, Sanga Reddy. Job Description 1) Method Development and routine analysis of Assay, Dissolution, Related substances, Content Uniformity, Blend Uniformity. 2) Responsible for Analytical Method Validation activities for solid orals and injectables. 3) Responsible for Routine and Stability analysis activities for solid orals and injectables. 4)Responsible for the Review of documents generated in Method development activity. 5)Responsible for the Preparation and Review of Tentative me...

As a Pharmaceutical Documents Associate at our company, you will play a crucial role in ensuring the quality and compliance of our pharmaceutical products. Your responsibilities will include: - Having experience or sound knowledge in Active Pharmaceutical Ingredients, Finish Product, Packaging Material Standards, Quality Management, and Quality Control. - Demonstrating knowledge or experience in Quality control tests for various formulations and APIs such as Assay, Dissolution, Disintegration, Uniformity of Weight/dosage, Impurity testing, Water content, etc using methods like HPLC, GC, TLC, IR/UV, Disso, etc. - Understanding pharmacopoeia applications and all documentation relevant to QA/QC...

As an Assistant Manager or Team Leader at Synnat Pharma in Visakhapatnam, you will play a crucial role in leading method development, validation, stability studies, and technology transfer activities. Your meticulous nature and extensive experience will be essential in collaborating closely with R&D, QC, and Regulatory teams to support product development and ensure compliance with global pharmaceutical standards. You should possess strong analytical expertise, leadership skills, and a dedication to regulatory compliance and continuous improvement. - Developing, optimizing, and validating analytical methods such as HPLC, GC, UV-Vis, and Dissolution according to ICH and regulatory guidelines....

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...

* Perform pre-formulation studies , R&D trials and support scale-up activities * Conduct R&D trails for oral solid dosage forms *Develop and optimize formulation to meet regulatory and quality reequipments * Document and analyze trial data to improve formulation *Dissolution, Method development , Method Validation

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.

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

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

Job Track Description: Performs tasks based on established procedures. Uses data organizing and coordination skills to perform business support or technical work. Requires vocational training, certifications, licensures, or equivalent experience. General Profile Requires limited prior training or licenses and training certifications. Has basic operational or analytical skills to perform tasks. Works within clearly defined standard operating procedures and adheres to quality guidelines. Work is completed with close supervision and under clearly defined procedures. Functional Knowledge Requires a basic understanding of theories, practices, and procedures. Business Expertise Understanding of ho...

Job Track Description: Performs tasks based on established procedures. Uses data organizing and coordination skills to perform business support or technical work. Requires vocational training, certifications, licensures, or equivalent experience. General Profile Requires limited prior training or licenses and training certifications. Has basic operational or analytical skills to perform tasks. Works within clearly defined standard operating procedures and adheres to quality guidelines. Work is completed with close supervision and under clearly defined procedures. Functional Knowledge Requires a basic understanding of theories, practices, and procedures. Business Expertise Understanding of ho...

Through our dedicated associates, Conduent delivers mission-critical services and solutions on behalf of Fortune 100 companies and over 500 governments - creating exceptional outcomes for our clients and the millions of people who count on them. You have an opportunity to personally thrive, make a difference and be part of a culture where individuality is noticed and valued every day. \n Job Track Description: \n \n Performs tasks based on established procedures. \n Uses data organizing and coordination skills to perform business support or technical work. \n Requires vocational training, certifications, licensures, or equivalent experience. \n \n General Profile \n \n Requires limited prior...

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...

Good knowledge of QC processes and GMP compliance. Skills: MS Office proficiency and strong communication skills. Responsible for quality testing, documentation, and ensuring product compliance with industry standards. Required Candidate profile Experience: 5-6 years in Pharma/API Education: B.Sc / M.Sc in Chemistry Must have hands-on experience with HPLC.

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

Company: Strides Pharma Science Ltd Department: Quality Control (QC) Position: Senior Executive Job Location: Alathur, Chennai Qualification: M.Sc. (Chemistry), B-Pharm, M-Pharm Experience: 4.5 to 8 Years Skills required: Experience on Raw material, In-process, Finished product, Stability and Microbiological testing. Work experience on FDA regulatory plants Flexible to work in shifts Job responsibility: Handling of Sophisticated instruments such as HPLC, GC, UPLC, UV, AAS & Dissolution Tester Analysis in LIMS e-RDS Experience on Microbiological testing Instrument Qualification knowledge on IQ, OQ, PQ. Regards, Srinidhi S HR Talent Acquisition

Role & responsibilities Literature Survey for the assigned project. Analytical method development such as Assay, Dissolution, Related Substances method by HPLC. Analytical method validation of Assay, Dissolution, Related Substances method by HPLC as per ICH guideline by HPLC. 4. Analysis of Initial and stability samples. 5. Carry out basic trouble shooting for instrument related issues, whenever required. Email id- namita.raul@ashishlifescience.com Contact- 8657894640

Job Track Description: Performs tasks based on established procedures. Uses data organizing and coordination skills to perform business support or technical work. Requires vocational training, certifications, licensures, or equivalent experience. General Profile Requires limited prior training or licenses and training certifications. Has basic operational or analytical skills to perform tasks. Works within clearly defined standard operating procedures and adheres to quality guidelines. Work is completed with close supervision and under clearly defined procedures. Functional Knowledge Requires a basic understanding of theories, practices, and procedures. Business Expertise Understanding of ho...

Exciting Career Opportunities at Natco Pharma Limited for the following requirements Work Location: Kothur (Formulation Division) Interview Date: Saturday, 20th September 2025 Time: 9:00 AM to 2:00 PM Venue: Natco House, Road No.-2, Banjara Hills, Hyderabad 500034 (Opp. A.P. Productivity Council) Open Positions: Analyst - Quality Control (OSD & Sterile) Experience: 3 to 5 Years Qualification: B. Pharmacy / M. Pharmacy / M.Sc (Organic/Analytical/General) Chemistry Key Responsibilities: Adherence to GLP, GDP, cGMP, and ALCOA+ standards. Analysis of RM / IP / FP samples, Operation and troubleshooting of instruments such as HPLC, UV, KF, IR, and Dissolution Apparatus. Demonstration of QC testing...

Key Responsibilities: 1. Stability Study Design & Planning Define study protocols, including time points, conditions (temperature, humidity, light exposure), and container types. Collaborate with formulation scientists and regulatory affairs teams to ensure studies align with regulatory guidelines (e.g., ICH, FDA). Plan long-term and accelerated stability testing for new and existing products 2. Compliance & Documentation Document study protocols, deviations, results, and reports. Maintain comprehensive stability study records for internal reference and regulatory submissions. Prepare stability data for inclusion in regulatory filings, ensuring compliance with ICH, FDA, or other relevant gui...

We are seeking a detail-oriented and proactive professional to manage monthly MIS reporting, critical issue tracking, and management approvals across multiple business units. This role requires strong analytical, coordination, and communication skills to ensure timely and accurate reporting for senior leadership. Role & responsibilities Prepare and consolidate Monthly MIS Reports for the multiple departments: Track and report critical issues and ensure timely escalation to management. Coordinate with department heads for data collection, validation, and approvals. Maintain dashboards and ensure accuracy of all reports submitted to senior management. Support in preparing presentations and sum...

Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC etc and automation

Preparing test solutions, compounds, and reagents for conducting tests and advising and coordinating test procedures(qualitative and quantitative chemical and collect/physical analysis of raw materials

Setting strategy for evaluating and implementing new technologies within the Analytical Development department, with a particular emphasis on state-of-the-art separation techniques (HPLC/UPLC/LCMS/GC) and familiar with XRD, DSC

Walk-In Drive For Formulation Analytical Research & Development(FAR&D)- MSN Laboratories, R&D Center, Pashamylaram, Hyderabad on Saturday 20-09-2025. 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...

Conduct chemical synthesis of new and existing agrochemical compounds in the lab. Develop and optimize synthetic routes and reaction conditions to improve yield, purity, and cost-effectiveness.