98 Stability Analysis Jobs

Role & responsibilities To perform physical and chemical, instrumental analysis of Raw Material, packaging material, Water samples, In Process, Finished Product Samples and Stability Samples. The candidate should have experience on HPLC, GC UV, IR and Dissolution testing. To perform a Release testing, Dissolution profile study, challenge study ,Hold time study, RLD sample analysis, validation, verification, method transfer activity and API-Verification as when applicable. To perform instrument calibration and working standard qualification. Responsible to adherence of GLP and Health, Safety Environment system in Laboratory. To perform the task assigned by the supervisor/HOD as and when requi...

About The Role Skill required: IX Intelligent Capital Project Operations - Low Carbon Grid Capital Projects Designation: Capital Projects Management Sr Analyst Qualifications: BTech Years of Experience: 5 to 8 years About Accenture Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song all powered by the worlds largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every d...

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...

WORK LOCATION: Baddi, Himachal Pradesh DEPARTMENTS AND EXPERIENCE: Quality Control: Stability/ FP / HPLC/ GC / Microbiology o Qualification & Experience: (02 - 06Years) •B.Sc, B.Pharma & M.Sc with relevant experience o Designations: •Jr. Officer, Officer & Jr.Executive ARD: Stability/ FP /AMV/ HPLC o Qualification & Experience: (02 - 05Years) •B.Sc, B.Pharma , M.Sc & M.Pharma with relevant experience o Designations: •Jr. Research Associate & Research Associate-I INTERVIEW VENUE: o Hotel Le Mariet 9th Km Milestone , Baddi Nalagarh Highway, Krishnapura, Solan, H.P - 174101 NEED TO CARRY: Resume, 3 Month Pay slips, Increment letter, Previous company relieving letters, Education Documents and ID...

We Are Hiring Walk-In Drive for Quality Control (QC) Professionals! Hetero is conducting a walk-in recruitment drive for our Quality Control Department. If you are passionate about pharmaceutical quality systems and ready to build a strong career, we would love to meet you. Interview Date: 02nd November 2025 (Sunday) Time: 9:00 a.m. to 3:00 p.m. Venue: VR ASHOKA GRAND Allwyn X Road, Gachibowli - Miyapur Rd, Towards Kondapur, Hyderabad, Telangana 500049 Work Location: Jadcherla Open Position: Jr. Officer / Officer / Executive / Sr. Executive Department: Quality Control Qualification: B.Sc / B.Pharm / M.Sc / M.Pharm Experience: 19 Years Skill Areas: HPLC, GC, RM, PM, IP/FP, LIMS, Stability, Sa...

Required Analysts for Quality Control Department We are having excellent job opportunities for Quality Control (QC) Department at Amneal Pharmaceuticals, SEZ Matoda Injectable. REQUIREMENT FOR INJECTABLE QUALITY CONTROL DEPARTMENT Designation: Officer/ Sr. Officer /Executive/ Sr. Executive Department: Quality Control Qualification: Diploma/ B.Sc./ M.Sc/ B. Pharm/ M. Pharm Total Experience: 02 to 05 years (Pharma experience only-Injectable is mandatory) Desired Profile: GLP : Operation and Calibration of HPLC (Waters and SHIMADZU), GC, UV, FTIR, K/F, AAS, IC. RM-PM : Analysis of Raw material and Excipients and handling of HPLC (Waters and SHIMADZU), GC(Agilent), UV, FTIR, K/F, AAS, IC. IP-FP ...

We Are Hiring Walk-In Drive for Quality Control (QC) Professionals! Hetero is conducting a walk-in recruitment drive for our Quality Control Department. If you are passionate about pharmaceutical quality systems and ready to build a strong career, we would love to meet you. Interview Date: 02nd November 2025 (Sunday) Time: 9:00 a.m. to 3:00 p.m. Venue: VR ASHOKA GRAND Allwyn X Road, Gachibowli - Miyapur Rd, Towards Kondapur, Hyderabad, Telangana 500049 Work Location: Jadcherla Open Position: Jr. Officer / Officer / Executive / Sr. Executive Department: Quality Control Qualification: B.Sc / B.Pharm / M.Sc / M.Pharm Experience: 1–9 Years Skill Areas: HPLC, GC, RM, PM, IP/FP, LIMS, Stability, S...

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...

WORK LOCATION: Baddi, Himachal Pradesh DEPARTMENTS AND EXPERIENCE: Quality Control: Stability/ FP / HPLC/ GC / Microbiology o Qualification & Experience: (02 - 06Years) •B.Sc, B.Pharma & M.Sc with relevant experience Designations: •Jr. Officer, Officer & Jr.Executive ARD: Stability/ FP /AMV/ HPLC Qualification & Experience: (02 - 05Years) •B.Sc, B.Pharma , M.Sc & M.Pharma with relevant experience Designations: •Jr. Research Associate & Research Associate-I PACKING: Blister& Bottle Packing(ELMACH-3522), Bulk Packing (IMA-PG) Qualification & Experience: (01 - 06Years) •ITI, Diploma & B.Sc with relevant experience Designations: •Jr. Operator, Operators & Sr. Operator INTERVIEW VENUE: oHetero La...

Job Opening Cadila Pharmaceuticals Limited Dholka Position & Department: Executive - Biologicals Analytical Qualifications: M.Sc. Biotechnology Experience: 1-3 Years - Planning and execution of In -process, Bulk and finished product and Stability analysis of all recombinant proteins using different analytical techniques: HPLC, Protein quantification, Gel electrophoresis, Western blot and Dot blot, ELISA - Protein expression and characterization analysis by HPLC for different recombinant vaccines projects. - Analytical method development and Validation for recombinant vaccines as per guidelines. - Data compilation, evaluation and report preparation for the all experiments conducted. - Mainten...

Company Description At TAPI, we're not just a companywe're a community committed to advancing health from the core. As the world's leading supplier of active pharmaceutical ingredients (APIs), we partner with 80% of the top 50 global pharmaceutical companies. With a legacy spanning over 80 years and a portfolio of more than 350 products, as well as custom CDMO services, we're shaping the future of health worldwide. Our strength lies in our peoplea team of over 4,200 professionals across 13 state-of-the-art facilities in Italy, Hungary, the Czech Republic, Croatia, Israel, Mexico, and India. Together, we innovate, solve problems, and deliver excellence. Join us and be part of a mission that t...

We are conducting a WALK-IN DRIVE @ IDPL for multiple openings in our OSD Division (Production, Packing, and Quality Control). Interview Date: 19th October 2025 (Sunday) Timings: 9:30 a.m. to 3:00 p.m. Venue: Talent Acquisition Center, Bhagyaradhi Degree College, 1st Floor, Near IDPL X Road, Hyderabad Work Location: Jadcherla Open Positions: Production (OSD) Operator / Sr. Operator / Officer / Jr. Executive Packing (OSD) — Operator / Sr. Operator / Officer / Jr. Executive Quality Control (OSD) — Officer / Jr. Executive / Executive / Sr. Executive Qualification: I.T.I / Diploma / B.Sc / B.Pharm / M.Sc / M.Pharm Experience: 2–9 years (depending on role) Special Benefit: Join our team and enjoy...

Role & responsibilities Complete Analysis of various raw materials, In-process, Drug substance and finished Products in line with Pharmacopeia method and in-house Specification and test procedures. Change Control, Deviation, Root Cause investigation, CAPA, OOS, OOT, Incidence Calibration of Instruments HPLC , UV-Visible Spectrophotometer, pH Meter,KF Titrator, weight balance. Working standard preparation as per SOP. Ensure the timely analysis of samples GLP, GMP, GDocP (With respect to Regulatory Guidelines) Function in details of various Section of QC/QA(Eg.Raw Material, Finished Product,Stability Study etc. Data Integrity 21 CFR Part 11 Qualification, Calibration, Validation. Maintaining t...

You will be joining WSP as an engineering geologist specializing in Geotechnical Applications, where you will be an essential part of the technical support, Mine Engineering, Stability, and Geology team in Bengaluru/Noida & onsite, dedicated to serving the global mining business. Your role will involve conducting specialized analyses for mining projects while collaborating closely with global leaders in the mining sector. - Assist with geotechnical characterization and assessments for underground, open pit, and mine closure rock mechanics projects. - Plan geotechnical field data collection programs, including health and safety plans and utility locates. - Process and analyze geotechnical dat...

About The Role Skill required: IX Product Engineering Services - Digital Site Designing Designation: Engineering Services Specialist Qualifications: BTech Years of Experience: 7 to 11 years What would you do? The Power System Engineer is responsible for performing detailed analysis of electrical power systems, including transmission, distribution, and generation. The role involves modeling, simulation, and assessment of power systems to ensure their functionality, reliability, and efficiency. The individual will work closely with engineers and stakeholders to identify potential improvements and help design cost-effective solutions. This position requires an in-depth understanding of electric...

About The Role Skill required: IX Product Engineering Services - Digital Site Designing Designation: Engineering Services Specialist Qualifications: BTech Years of Experience: 7 to 11 years What would you do? The Power System Engineer is responsible for performing detailed analysis of electrical power systems, including transmission, distribution, and generation. The role involves modeling, simulation, and assessment of power systems to ensure their functionality, reliability, and efficiency. The individual will work closely with engineers and stakeholders to identify potential improvements and help design cost-effective solutions. This position requires an in-depth understanding of electric...

Role & responsibilities Adequate knowledge of respective guidelines. i.e. ICH, USP,WHO, etc. Stability sample analysis by HPLC/GC/UV/Dissolution apparatus. Preparation of stability testing worksheets. Sample charge and withdrawal as per stability condition. Management of stability samples and stability chambers and maintain the schedule. Preparation of stability trend records and summarize the results Review the stability sample testing data. Review the stability analysis worksheet. Review the stability protocols, samples and stability chambers log records. Review of OOS/OOT and co-ordinate with respective concerns.

Roles and Responsibilities Develop formulations for solid oral dosage forms (tablets) and liquid orals. Conduct formulation research development, stability studies, and analysis to ensure product quality. Prepare trial batches of formulations and document them accurately. Collaborate with cross-functional teams to resolve formulation-related issues. Ensure compliance with regulatory requirements during all stages of formulation development.

About The Role Skill required: IX Product Engineering Services - Digital Site Designing Designation: Engineering Services Senior Analyst Qualifications: BTech Years of Experience: 5 to 8 years What would you do? The Power System Engineer is responsible for performing detailed analysis of electrical power systems, including transmission, distribution, and generation. The role involves modeling, simulation, and assessment of power systems to ensure their functionality, reliability, and efficiency. The individual will work closely with engineers and stakeholders to identify potential improvements and help design cost-effective solutions. This position requires an in-depth understanding of elect...

About The Role Skill required: IX Product Engineering Services - Digital Site Designing Designation: Engineering Services Senior Analyst Qualifications: BTech Years of Experience: 5 to 8 years What would you do? The Power System Engineer is responsible for performing detailed analysis of electrical power systems, including transmission, distribution, and generation. The role involves modeling, simulation, and assessment of power systems to ensure their functionality, reliability, and efficiency. The individual will work closely with engineers and stakeholders to identify potential improvements and help design cost-effective solutions. This position requires an in-depth understanding of elect...

About The Role Skill required: IX Product Engineering Services - Digital Site Designing Designation: Engineering Services Senior Analyst Qualifications: BTech Years of Experience: 5 to 8 years What would you do? The Power System Engineer is responsible for performing detailed analysis of electrical power systems, including transmission, distribution, and generation. The role involves modeling, simulation, and assessment of power systems to ensure their functionality, reliability, and efficiency. The individual will work closely with engineers and stakeholders to identify potential improvements and help design cost-effective solutions. This position requires an in-depth understanding of elect...

B.Sc./M.Sc. with 1–4 years in QC (API). Hands-on with HPLC, GC, UV, and wet analysis. Experienced in raw material, in-process, and finished product testing. Strong in GMP, documentation, and analytical techniques. Required Candidate profile B.Sc./M.Sc. with 1–4 years’ QC experience in API. Proficient in HPLC, GC, wet lab testing, and GMP documentation. Detail-oriented, accurate, and skilled in analytical methods. Perks and benefits GMP GLP plant| Growth| Safety| Compliance| Perks

As an Associate Manager in the Quality Control Department at ZLL-SEZ Oncology Injectable (Alidac), your role is critical and involves the following key responsibilities: - Plan routine activities of the respective section. - Review all analytical raw data and associated documents for accuracy, including calibration/qualification reports, trend data analysis, and quality control testing protocols. - Report and follow up on any discrepancies noticed during the review process, including deviations and incidents. Perform predictive stability analysis on generated data for stability studies. - Log change controls and ensure proper execution following SOPs. Evaluate proposed changes for impact on ...

Main Accountabilities Routine analysis & Stability Analysis (assay, RS, dissolution, water content etc.) of R&D formulation projects (solid & liquid orals, injectables) Daily calibration of pH meters, balances etc. Stability sample management (loading & withdrawal as per stability plan) Preparation of Stability Reports & other protocol based study reports for assigned projects, as applicable Hands-on experience of analytical instrumental techniques (HPLC with chromatographic software etc.) Assisting analytical method development/validation/method transfer activities, as per need Supporting other assigned lab responsibilities for GLP compliance Performance Indicators: Timely execution of assi...

Walk-in Drive @ SEZ-Matoda|| Ahmedabad on 28th Sep '25 (Sunday) for Quality Control Department. We are having excellent job opportunities for Quality Control Department at Amneal Pharmaceuticals, SEZ Matoda Injectable. Interview Venue Details: Date: 28th Sep 25 (Sunday) Time: - 9:00 AM to 3:00 PM Venue : Amneal Pharmaceuticals Plot No 15, 16, 17 Pharmez | Village: Matoda | Sarkhej Bavla Road | Ahmedabad Gujarat - 382220. REQUIREMENT FOR INJECTABLE QUALITY CONTROL DEPARTMENT Designation: Officer/ Sr. Officer /Executive/ Sr. Executive Department: Quality Control Qualification: Diploma/ B.Sc./ M.Sc/ B. Pharm/ M. Pharm Total Experience: 02 to 07 years (Pharma experience only) Desired Profile: GL...