227 Dissolution Jobs - Page 2

Vacancy for Instrument Technician / Officer in Analytical Development Lab Job Location : Kandivali (w), Mumbai Educational qualifications : Diploma in instrumentation Experience: 3- 5 years Job description: 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

You are invited to attend a walk-in interview for the position of Quality Control Analyst at Zydus Lifesciences Limited in Ahmedabad. The interview is scheduled to take place on the 2nd of March, 2025 in Indore. The position is based in our Moriaya unit in Ahmedabad. As a Quality Control Analyst, your responsibilities will include operating various QC equipment such as HPLC, GC, IR, UV, and Dissolution apparatus. Additionally, you will be involved in QC Method Validation and Transfer processes. To be eligible for this position, you should have a minimum educational qualification of B.Sc, M.Sc, B.Pharma, or M.Pharma. Furthermore, candidates with 2 to 8 years of relevant experience in Quality ...

Roles and Responsibility Develop and implement quality control processes to ensure high standards of coding services. Conduct regular audits to identify areas for improvement and provide recommendations for enhancement. Collaborate with cross-functional teams to resolve quality-related issues and improve overall performance. Analyze data to identify trends and patterns, and develop strategies to address them. Develop and maintain quality control documentation, including policies and procedures. Provide training and coaching to team members on quality control best practices. Job Requirements Strong knowledge of quality control principles and practices, particularly in the healthcare industry....

Conduct literature survey, analyze samples (innovator, developmental, stability), Method Development & Validation, Product analysis, documentation, reports, instrument handling & troubleshooting. Required Candidate profile . M.Pharm/ M.Sc./ Skilled in LNB/logbook documentation, test methods, validation/verification, instrument calibration, troubleshooting & data review.

You will be responsible for maintaining quality results, ensuring regulatory compliance, and improving existing systems to prevent non-conformance. This includes operating, calibrating, and maintaining various instruments such as HPLC, Dissolution, Analytical Balance, UV Spectrophotometer, Viscometer, GC, etc. You will also be required to record and maintain online entries in the instrument usage log book and follow good laboratory and documentation practices. Your responsibilities will also include performing analysis as per test request forms, following correct test procedures for analytical validations/verifications, routine analysis, and stability studies. Basic knowledge of method devel...

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

We are hiring for Quality Control for Executive / Senior Executive role Applications are invited for the position of Executive QC and Sr. Executive QC Interested candidates can apply for this position. Required experience: 2 to 10 years Candidates with experience in handling of sophisticated instruments e.g. HPLC, GC, UV, IR, Dissolution apparatuses and other laboratory equipment are preferred. Analysis of RM, In-process, FP Samples. Experience in calibration of all the instruments. Experience in analysis of Process Validation and Cleaning Validation Samples. Well versed with Good Laboratory Practices ,Data integrity concepts, investigations, OOS, OOT and Laboratory Deviations. Exposure of R...

The QC Analyst II position at Piramal Pharma Solutions involves performing analytical chemistry examination testing on raw materials, finished products, or stability samples following approved Standard Operating Procedures (SOPs) and valid methods. This role, which operates during 2nd shift hours, is crucial for ensuring product quality and compliance with regulatory standards. Key responsibilities of the QC Analyst II include conducting chemical or physical testing analysis, documenting and submitting all raw data and results in LIMS, preparing reagents for chemical analysis, and ensuring compliance with compendial (USP/EU) testing requirements as per FDA 21 CFR. Moreover, the incumbent is ...

Hikal Ltd is looking for Officer to join our dynamic team and embark on a rewarding career journey The Senior Officer plays a crucial role in the organization, responsible for overseeing and executing various tasks and projects to ensure the smooth functioning of operations This role requires strong leadership, analytical skills, and the ability to collaborate effectively with team members and stakeholders Key Responsibilities: Leadership:Provide leadership and guidance to team members, fostering a positive work environment Lead by example, demonstrating professionalism, integrity, and dedication to the organization's goals and values Project Management:Manage and coordinate projects from in...

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...

Walk-In Drive For Formulation Analytical Research & Development(FAR&D)- MSN Laboratories, R&D Center, Pashamylaram, Hyderabad on Saturday 06-09-2025. 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...

Job Title: Quality Control Analyst Formulation (OSD & Injectables) Experience: 2 to 8 Years Work Location: MSN Formulation Unit-II, Kothur , Hyderabad Department: Quality Control - Formulations Employment Type: Full-time Job Posting Purpose: We are looking for an experienced and motivated Formulation QC Analyst with 2 to 8 years of hands-on experience in testing Oral Solid Dosage (OSD) and Injectable formulations . This role involves executing and supporting analytical testing, method validation, and regulatory compliance for pharmaceutical products. The ideal candidate will have a strong understanding of GMP/GLP , be proficient with analytical instruments , and have exposure to regulatory a...

1. Execute validation of analytical methods as per ICH guidelines 2. Method Verification 3. Method Transfer 4. Instrument Handling (HPLC,UV-Visible Spectrophotometer) 5. Documentation & Compliance 6. Audit Readiness & Regulatory Support Perks and benefits Bachelor's Accommodation and Travelling facility

Who We Are Together, were on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives Its a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds Working here means working with the worlds leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organizations Essential Medicines List Today, at least 200 million people around the world take one of our medicines every single day An amazing number, but were always looking for new ways to continue making a difference, and new people to make a difference with, The opportu...

About The Role Project Role : VIS & BI Strategy Practitioner Project Role Description : Develop a VIS/BI vision, business case, and modernization strategy; discover and assess VIS/BI opportunities; identify industry- and function-centered VIS/BI use cases; guide clients on industry and function relevant measures and metrics; develop a VIS/BI roadmap and operating model; help drive adoption, decision making and behavior change; measure VIS/BI value. Must have skills : Kinaxis Good to have skills : NAMinimum 5 year(s) of experience is required Educational Qualification : 15 years full time education Summary :As a VIS & BI Strategy Practitioner, you will engage in the development of a comprehen...

Job Description 1. Analysis of stability/Finished product samples and compile the report as per ALCOA procedure, other miscellaneous samples and compile their report. 2. To maintain the instrument usage and maintenance of instrument like Dissolution Test apparatus, UV spectrophotometer, balance, PH meter and Sonicator etc. 3. Ensuring data integrity policy, GDP and its effectiveness up to compliance 4. To maintain the stability chamber and tracker. 5. To maintain the stability chamber and tracker. 6. To ensure charging and withdrawal of stability samples as per approved protocols. Work Experience Education :- B.Pharm/ MSC/ M. Pharm Experience :- 2 to 4 yrs. Education Others Competencies

Excellent Opportunity! Analysts required in the QC department at Unison Pharmaceuticals Pvt Ltd, Moraiya. Apply Now!!! Company: Unison Pharmaceuticals Pvt Ltd Experience: 1-7 Years Qualification: B.Pharma/M.sc/M. Pharma Location: Moriya, Ahmedabad Job Role : Physico Chemical (Analyst)- Friability / DT / Hardness / Thickness / UV Perform physical and chemical analysis for Raw material/ In process / Finished Product based on the test requirements like UV, friability, DT, hardness, thickness, moisture, average weight, and uniformity weight. Prepare documents for each analysis performed and get those checked by the reviewer. HPLC Analyst: Carry out HPLC testing for assay, related substances, dis...

Role Description: Quality control executive Location: Mil Laboratories Pvt. Ltd. 541, GIDC, Manjusar, Ta. Savli, Dist. Vadodara - 391775 Experience: 5 to 6 years Roles Responsibilities:- To perform all the testing related to RM, bulk, FP and stability samples To perform all the testing of packaging materials Handling of QMS documents like SOP, CAPA, repeat analysis, Deviation etc. To manage and lead the team To perform analytical method validation To prepare specifications for different materials New vendor approval Should have working experience of HPLC, GC, UV spectrophotometer, centrifuge etc. What will you need to be successful Preferred experience in sterile pharma plant. Extensive unde...

Scope of Role- The DVA Engineer is responsible for Dimensional Variation Analysis and Tolerance stack up for ongoing and new projects. Knowledge / Experience: 7+ Years Area of Responsibility: DVA Engineer creates and maintains analysis models representing the assembly process, tolerances, and CAD data used for the virtual assembly of a vehicle. He will be responsible for creating reports, communicating results, issues, and recommendations to the customer. Job Requirements: Should have experience in Body Components /Interior Trims/Exterior Trims Domains Should have good working knowledge of GD&T & Tolerance Stack up Analysis Should have good knowledge of GD&T Standard preferred ASME Should ha...

Skill Required 3 to 4 year Pharma background experience for FP , In process and PV samples. Roles and Responsibilites To analyze the samples of in process/FP/Process validation as per work allotted by section in charge/Designee. Preparation of report and submission of reports along with raw data to section in charge/Designee within time. Immediate reporting of any odd observation, incident, OOT and OOS result during analysis to section in charge/Designee. Qualification Required M.sc/B.pharm Relevant skills / Industry experience Should have 2 to 4 year experience. Relevant professional / Educational background M.sc/B.pharm

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

Dear Applicants, Greeting from Biophore India pharmaceutical Pvt Ltd, We have opening for Formulation AR&D Department . Position : Research Analyst or Sr Research Analyst Experience : 3 - 8 Yrs Job Description: Responsible for Analytical Method Development activities solid orals and injectables Responsible for Responsible for Planning and Monitoring of Method development activities and Regular Analysis for solid orals and Injectables. Responsible for Routine and Stability analysis activities for solid orals and injectables. Responsible for the Review of documents generated in Method development activity. Responsible for the Preparation and Review of Tentative method of analysis and Method de...

You will be responsible for analyzing Vendor Approval samples and preparing Standardization of Solutions as needed. You will also need to implement GLP/GMP requirements and analyze Raw Materials, Finished Products, Stability samples, and Packing materials. Ensuring samples and related documentation meet cGMP requirements is crucial. Additionally, you will need to oversee the analysis of Raw Materials, Finished Products, and Stability Samples from outside commercial labs. Reviewing laboratory chemicals, calibrating instruments such as HPLC, UV, IR, Dissolution, KF Potentiometer, and performing Working standard qualification are part of your duties. Maintenance of Stability Incubators, loading...

As the Manager of Analytical Method Development, you will be responsible for the overall development and validation of analytical methods for R&D projects, specifically focusing on oral controlled release dosage forms. Your key responsibilities will include leading the scientific development of new analytical methods, identifying areas for improvement in existing methods, and staying updated on evolving technologies and Regulatory requirements. You will play a crucial role as a member of the new product development team, contributing to the preparation of development proposals, project plans, timelines, and project activity reviews. Your expertise in analytical methods development using tech...

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...