395 Dissolution Jobs - Page 2

Core Purpose of the Role: This role involves method development, method validation, method transfer and R&D stability studies by using laboratory instruments like Ultra performance liquid chromatography (UPLC), High Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Ultraviolet (UV) spectrophotometer, Polarimeter, etc. Role Accountabilities: Must have strong hands-on experience in development and validation of Assay & related substances methods for drug substance/drug product. Managing the stability studies for individual projects and stability data analysis, knowledge on stability guidelines and maintaining the sample storage. • Must have experience in handling HPLC, UPLC (E...

As an Assistant Manager or Team Leader at Synnat Pharma in Visakhapatnam, you will be responsible for leading method development, validation, stability studies, and technology transfer activities. Your role will involve collaborating closely with R&D, QC, and Regulatory teams to support product development and ensure compliance with global pharmaceutical standards. Strong analytical expertise, leadership skills, and a dedication to regulatory compliance and continuous improvement are crucial for success in this position. **Key Responsibilities:** - Develop, optimize, and validate analytical methods such as HPLC, GC, UV-Vis, and Dissolution in accordance with ICH and regulatory guidelines. - ...

Dear Applicants, Greeting from Biophore India pharmaceutical Pvt Ltd, We have opening for Formulation AR&D Department . Job Openings: 5 Nos Position : Jr. Research Analyst or Research analyst Job Description: Analytical Method Development. Analytical Method Validation and routine analysis of Assay, Dissolution, Related substances, Content Uniformity, Blend Uniformity for solid orals and injectables. Instruments Handling (Dissolution, HPLC,UV, GC) Responsible for the documentation. Qualification: M.Sc. or M .Pharm. I nterview Date on 5-12-2025 at 9:30 AM-2:30 PM (Friday) Ref to Friends or colleagues. Please Carry below Documents. 1) Update Resume. 2) Education Qualification Certificates (Xero...

Walk In Drive For Quality Control Department In Formulation Division @ Jadcherla Department:- Quality Control Qualification :-BSC | B Pharmacy | MSC | M Pharmacy Experience :- 2 To 8 Years Division :- Formulation Interview Date:- 07-12-2025 Interview Time :- 9.00AM TO 2.00PM Venue Location:- ELITE HOTELS & RESORTSNH44,Bangalore Hyderabad Hwy Jadcherla, Telangana 509301 Contact No:- 040-304338701 | 8954 Note:- Candidate should bring Update Resume , Increment Letter, Pay slips, Bank Statement, Certificates, Aadhar Card & Pan Card We are looking for candidate those who have experience in Quality Control Formulation ( HPLC,GC,UV,Dissalution, LCMS, GCMS). About Company:- MSN Group is the fastest ...

Analytical Method Development for ointments, gels, injectables, BFS & lyophilized products. Hands-on with HPLC/UPLC, LCMS/GCMS, dissolution, stability & impurity profiling. Experience: 510 yrs. Location: Bangalore Food allowance Annual bonus Office cab/shuttle Provident fund Health insurance

Candidate should be competent to handle the assigned activity related to analytical method validation (Test Related substances, Assay, Residual solvents Force degradation), Finished API on HPLC, GC GCMS System as per standard operating procedures. Documentation practices as per GLP and GDP requirements. Candidate should have good learning ability, technical knowledge good analytical skill

Role Overview: You will be responsible for operating HPLC and conducting tests such as Assay and Dissolution, CU & BU, Swab Analysis by HPLC. Your primary focus will be working in the Finished Department, utilizing your practical experience with FP, PV, HT, CTC specifications of all products. Key Responsibilities: - Operating HPLC machine for various tests - Conducting tests including Assay and Dissolution, CU & BU, Swab Analysis by HPLC - Working in the Finished Department - Applying practical experience with FP, PV, HT, CTC specifications of all products Qualifications Required: - 2 to 7 years of experience in a similar role - Position available for Officer / Sr. Officer / Executive level ...

Required Skills & Competencies Strong knowledge of GMP, GLP, OOS/OOT guidelines. Hands-on experience with HPLC/GC/UV instruments.

Role & responsibilities Graduate/Post Graduate in Chemistry with 3 to 5 years of experience in QC, familiar with HPLC/GC/FTIR/UV Preferred candidate profile Graduate/Post Graduate in Chemistry with 3 to 5 years of experience in QC, familiar with HPLC/GC/FTIR/UV Job Location : Sikkim Interested candidates may apply at hr.plant@zuventus.com

Job Title: QC Analyst Business Unit: Global Quality And Compliance Job Grade G12C/G12B Location : Jammu At Sun Pharma, we commit to helping you “Create your own sunshine” — by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community. Are You Ready to Create Your Own Sunshine? As you enter the Sun Pharma world, you will find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.” Key responsibilities: 1) To perform analysis of samples all...

Role & responsibilities Main Role: 1. To perform Stability analysis. 2. Maintenance of operating instruments / equipment. 3. To maintain the assigned Laboratory workplace, instruments and equipment etc. 4. To adhere Good Laboratory Practices (GLP), Good Documentation Practices (GDP), relevant regulatory guidelines and PAL procedure. Preferred candidate profile Detailed description of Main Roles and Responsibilities: 1. Responsible for handling , operating and maintaining HPLC / UV and related instruments to ensure optimal performance. 2. Adherence to Good Laboratory Practices (GLP), Good Documentation Practices (GDP), relevant regulatory guidelines and PAL procedure. 3. Performing stability ...

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...

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...

Title: Officer - Formulation QC Custom Field 2: 2691 Location: Bavla, Gujarat, IN Country/Region: IN State: Guja City: Bavla Company: Dishman Carbogen Amcis Limited Business Unit: General Travel Description: Basic knowledge of Formulation QC related activities like Dissolution, Disintegration, Wet analysis Job Segment: QC, Quality

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 Saturday 06-12-2025. 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, w...

Walk-In Drive For Formulation Analytical Research & Development(FAR&D)- MSN Laboratories, R&D Center, Pashamylaram, Hyderabad on Saturday 06-12-2025. 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...

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...

Role & responsibilities Conduct method development, validation, and stability studies for raw materials, intermediates, and finished formulations. Operate and maintain HPLC, GC, UV, IR, and Dissolution apparatus. Prepare and review analytical protocols, reports, and data sheets in line with cGMP and regulatory guidelines. Support formulation development through analytical evaluation and characterization. Perform impurity profiling, assay, and dissolution studies as per SOPs. Participate in OOS/OOT investigations and implement CAPA. Ensure accurate documentation, instrument calibration, and laboratory safety compliance.

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...

Job Description Responsible for testing of Raw material,IP/ FP and Stability sample as per method of analysis. Should have knowledge for the Method Verification/validation and Method Transfer analysis. Have an exposure on operation, calibration, Qualification and maintenance of laboratory instrument's / equipment's . Should have exposure on sophisticated Instruments i.e. HPLC, Dissolution,FTIR,UV, GC, Autotitrator,Karl fischer,PSD etc. Have an exposure for the preparation of calibration & PM schedule of laboratory instrument's / equipment's. Should have knowledge for the preparation, handling & management of working/reference standards etc. Testing of In-process, Stability and Finished produ...

Responsible for testing of Raw material,IP/ FP and Stability sample as per method of analysis Should have knowledge for the Method Verification/validation and Method Transfer analysis Have an exposure on operation, calibration, Qualification and maintece of laboratory instruments / equipments Should have exposure on sophisticated Instruments ie HPLC, Dissolution,FTIR,UV, GC, Autotitrator,Karl fischer,PSD etc Have an exposure for the preparation of calibration & PM schedule of laboratory instruments / equipments Should have knowledge for the preparation, handling & management of working/reference standards etc Testing of In-process, Stability and Finished product samples,Raw material Should h...

Overall adherence to safe practices and procedures of oneself and the teams aligned. Contributing to development of procedures, practices and systems that ensure safe operations and compliance to company s integrity & quality standards. Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams, and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements always in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team inclu...

Method development like Related compound, Assay, Dissolution and Residual solvents etc. for development projects using instruments like HPLC, IC, GC, Particle size analyzer etc. Prepare method development report along with tentative analytical method. Attain method transfer activity. Method validation like Dissolution, Assay, Related compound and Residual solvents etc. Preparation TT report To keep neat and cleanliness at workplace and follow the Good Laboratory Practices in the Laboratory. Preparation of study protocols with respect to Laboratory. Development batch stability analysis as per stability protocols To attain and complete self-training through QMS. Responsible for COA preparation...