322 Dissolution Jobs

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...

About the Role 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 findi...

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...

Responsibilities: Ensure timely and Accurately material testing (RAW/ In Process/Finish/ R&D). Accurate and On-time Reporting and documentation at all stages. Proper Calibration. Understanding of analytical chemistry. Hands-on experience in HPLC /GC, wet analysis. Required Skills: Candidate must have good communication skill. Good leadership quality and time management. Ability to work independently and as part of a team. Required Qualification: - B.Sc/M.Sc - Chemistry

Key Responsibilities Responsible for review of stability protocol & report. Responsible for Preparation of Annual Product Quality Review. Responsible for review of Master Packing Card & Master Formula Card. Responsible for preparation and review of Process validation Protocols and reports. Responsible for review of Batch Manufacturing and Batch Packing records Responsible for preparation of batch release certificate and ensuring batch release process performed as per the SOP. Responsible for issuance of Formats, Logbooks, Register, protocol, reports, BMRs and BPRs as per respective procedure. Responsible for review of QC documents such as Specifications and Standard Testing Procedure (RM, bu...

Responsibilities: Experience in Method Validation. Experience in Stability Study. Experience of review Electronic data review and backup systems. Expert in Qualification of analytical instruments like HPLC, GC, AAS, FTIR, UV etc. Expert in Calibration of analytical instruments like HPLC, GC, AAS, FTIR, UV etc. Must have minimum 3+ years of experience as a Reviewer. Must have an experience of reviewing all types of QC software. Must be familiar with cGMP/GLP practices and ICH and FDA Guidelines. Required Skills Must be excellent in written and spoken English; net savvy and adept at computer skills. Logical thinking. Organizing. Good in communication. Required Qualification: - B.Sc/M.Sc - Chem...

Manager - Quality Control (Formulations) 10 to 15 years of experience in Pharmaceutical Industry especially in Formulations Unit. Should have experience in successfully handling Quality Audits. Thorough knowledge in all types of Analytical instruments, analytical methods, HPLC, Method validation and method development etc., Should possess profound knowledge and skills in OSD/Formulations products. Total Quality Management (TQM), preparation and successful implementation of SOP's. Should lead a team in QC department and responsible for TQM. Sound working knowledge in MS Office and computer skills. Responsible for day-to-day and periodical MIS reports. Coordination with Production, QA and othe...

Support lab scientists in planning and executing chemical synthesis experiments. Conduct reactions as per given procedures under supervision. Prepare reagents, solvents, and materials required for synthesis work. Perform product isolation, purifcation, and characterization (e.g., TLC, GC, HPLC, NMR, IR). Maintain accurate experimental records, data sheets, and logbooks. Follow all laboratory safety procedures and ensure compliance with GLP and EHS standards. Assist in scaling up laboratory processes and transferring data to pilot plant teams. Maintain cleanliness and calibration of lab instruments and glassware. Preferred candidate profile M.Sc. in Organic Chemistry. 1 2 years of experience ...

Responsibilities:- Develop and validate analytical methods for raw materials and finished products. Operate instruments like HPLC, GC, UV, IR, and dissolution testers. Prepare method validation protocols and reports as per ICH guidelines. Support stability studies and impurity profiling. Required Skills :- Proficiency in analytical instrumentation and software. Strong documentation and regulatory compliance knowledge. Ability to troubleshoot analytical issues independently. Required Qualification: - B.Pharm/M.Pharm/B.Sc/M.SC - Chemistry

As a Quality Control Analyst, your role involves analyzing Vendor Approval samples, preparing and standardizing solutions, and implementing GLP/GMP requirements. You will be responsible for analyzing Raw Materials, Finished Products, Stability samples, and Packing materials while ensuring compliance with cGMP requirements. Additionally, you will review laboratory chemicals, calibrate instruments like HPLC, UV, IR, Dissolution, KF Potentiometer, and perform Working standard qualification. Maintenance of Stability Incubators and reviewing analytical data, calibration data, and qualification data are also part of your key responsibilities. Qualifications required for this position include a min...

Designation - Executive , Technical Assistant Department - Quality Control, ASL / MVC Qualification - MSC/ BSC / M.Pharm / B.Pharm Experience - 2 Years - 6 Years Job Location - Indrad (Ahmedabad - Mehsana highway) Key Skills - HPLC, Method Validation, Chemical Testing, Instrument Handling, Documentation Interested candidates can apply with their updated cv.

Walk- In - Drive Method Validation/ FML AQA- MSN Laboratories, Formulation Unit - V, RK Puram, Hyderabad on Saturday 15-11-2025. ASRD Responsibilities : 1) Execution of Analytical Method validations for drug products for various markets. 2) Execution of DPDM Method validations for drug products. 3) Analytical method transfers to the Quality control labs. 4) Performing the calibrations of the analytical instruments. 5) Preparation & review of Analytical Method validations protocols and reports. 6) Responsible for cGLP, documentation and implementation of departmental quality systems. AQA Responsibilities : 1. Preparation and Review of AQA SOPs. 2. Review of validation protocols & reports. 3. ...

Dear All, We are seeking a highly motivated and talented Analytical R&D Scientist(Injectables) to join our innovative team. The ideal candidate will have a strong foundation in Analytical development and you will play a crucial role in developing new and improved formulations, ensuring product quality, and meeting regulatory requirements. Location: Hyderabad(Dulapally) Required Experience: 5-7 Years Job Responsibilities: 1. To follow the departmental SOPs 2. To ensure the error free and online documentation. 3. To ensure only calibrated instrument /equipment's are used for analysis. 4. To coordinate with supervisor in developing the methods for dissolution, assay by UV/HPLC and RS by HPLC. 5...

Job Title: Senior QC + QA Trainer (Pharma / Biotech Laboratory) Location: Remote Job type: Part-time Job Summary: We are seeking a highly experienced and knowledgeable QC + QA Trainer to design, develop, and deliver technical training programs for quality control and quality assurance teams. The trainer will be responsible for building competence in analytical testing, documentation practices, GMP compliance, and QA/QC systems within a regulated laboratory environment. Key Responsibilities: Training & Development Develop and deliver structured training programs on QC laboratory techniques, QA systems, and GMP compliance . Conduct practical laboratory training (analytical instruments, wet che...

Role Description This is a full-time role for a Quality Control Analyst, based on-site in Pune. The Quality Control Analyst will be responsible for conducting quality control tests, operating laboratory equipment, and ensuring compliance with quality assurance protocols. Day-to-day tasks include analyzing test results, preparing analytical test reports, and maintaining laboratory records. The role requires strict adherence to standard operating procedures to guarantee the accuracy and integrity of data. Skills required - Proficient in Analytical Skills, Quality Control, and Quality Assurance Hands-on experience with Laboratory Skills and Laboratory Equipment Strong attention to detail and pr...

Key Responsibilities: 1. Routine Analysis & Testing: Perform analysis of raw materials, in-process, finished products, and stability samples as per approved specifications and test procedures. Conduct analysis using instruments such as HPLC, GC, UV-Vis Spectrophotometer, FTIR, Dissolution Tester, pH Meter, and KF Titrator . Ensure analytical results are recorded accurately and reviewed as per GLP and cGMP standards. 2. Documentation & Record Keeping: Prepare and review analytical reports, COAs, and test records. Maintain logbooks, stability registers, and instrument usage records. Ensure compliance with Good Documentation Practices (GDP) and data integrity requirements. 3. Instrument Calibra...

Experience - 3 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

Walk-In Drive For Formulation Analytical Research & Development(FAR&D)- MSN Laboratories, R&D Center, Pashamylaram, Hyderabad on Friday 31-10-2025. 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...

R&D Officer Formulation & Dossier Filing (02 Positions) based in Vapi, Gujarat. The ideal candidate brings 5 to 7 years and a strong record of GMP/cGMP compliance within regulated pharma, chemicals or biotech environments. Key responsibilities include ownership of day-to-day operations, documentation integrity, SOP creation/review, deviation/OOS handling, CAPA and change control management, audit readiness, cross-functional coordination with Production, QC, Engineering and Supply Chain, and proactive risk assessment to protect product quality and patient safety. The role requires hands-on problem solving, stakeholder communication, coaching junior staff, and contribution to continuous improv...

Company: Strides Pharma Science Ltd Department: Quality Control (QC) Position: Trainee Job Location: Alathur Qualification: B-Pharm, M-Pharm Experience: 0 to 1 Year Key responsibilities: Analysis of Material / Product by referring current version of specification STP with relevant material code. Responsible for initial set up of Instrument/Equipment before starting the analysis with relevant online entries in usage Log / LIMS. Perform the Assay and RS by LC/UV/Dissolution, content uniformity by LC analysis with simple and complex products Tests as per SOP/STP. Proper handling of chromatographic column used for analysis. Maintain data integrity and appropriate traceability Regards, Srinidhi S...

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...

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...

Method Validation

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...