253 Stability Studies Jobs - Page 6

As a Manager R&D Nutraceuticals Products at Mosaic Wellness, you will play a crucial role in leading the development of new formulations, with a specific focus on powders, premixes, and nutri-mixes. Your responsibilities will include formulating innovative nutraceutical products, ensuring regulatory compliance with FSSAI regulations and other quality standards, sourcing and evaluating high-quality raw materials, optimizing manufacturing processes, and collaborating with cross-functional teams for successful product launches. Additionally, you will be required to stay updated with industry trends, new ingredients, and scientific advancements, while maintaining detailed documentation of formul...

Division Department Sub Department 1 Job Purpose Perform sampling, execute and document the analysis of raw materials, packing materials, products assigned for testing and complete all the stability studies in order to ensure its compliance to the laid down quality parameters and predefined specifications / standards and meet SRB targets Key Accountabilities (1/6) Analyse the assigned samples and chromatographic tests for analysis by using the suitable valid procedure and calibrated instruments to ensure the compliance to the set specification / standards Perform analysis for release of RM, PM, FP & water analysis and process/cleaning validation as per commitment dates Perform analysis for s...

Dear All, We are conducting Walk-In Interview on 29th August 2025(Friday) for Quality Assurance and Quality Control( Formulations ) departments. Quality Assurance: Validations - 4-5 Years of experience in Process and Cleaning validations and equipment qualifications Quality Control: IPFP - 4-5 Years of experience in HPLC, GC, UV, Dissolution and RS. Stability - 4-6 Years of experience in Dissolution, GC, UV and Sample management Raw Materials - 2-3 Years of experience in sampling of Raw and Packing materials Analytical Method Validations - 3-5 Years of experience in Method validations, GC and Dissolution instruments GLP - 2-4 Years of experience in management of working and reference standar...

!! Greetings from Natco Pharma Limited..!! We are conducting Walk-in Interview for Formulation Analytical Research & Development Department for our Pharma Division located at Kothur (Near to Shamshabad) Roles: Trainee /Officer / Executive / Sr. Executive / Asst. Manager Qualification: B. Pharmacy / M. Pharmacy (Pharmaceutical Analysis) / M. Sc (Analytical Chemistry) / B.Sc (Chemistry) Experience: 0 to 15 Years (Only freshers who graduated in 2024 or 2025 are eligible to attend) Skills Required: Analytical method development & validation Complex Injectable, Peptide chemistry knowledge preferred Analysis of raw materials, finished products, stability samples, Discriminatory dissolution studies...

As a Research Associate at Naari Pharma, you will play a crucial role in the execution of formulation development activities for solid dosage forms across regulated and semi-regulated markets. Your responsibilities will include conducting literature search and pre-formulation studies, evaluating innovator/RLD products, executing R&D trial batches and scale-up activities, and preparing stability batches. You will also be responsible for documentation tasks such as preparing Master Formula Cards, Product Development Reports, and Stability Protocols, as well as supporting regulatory submissions. You will work closely with cross-functional teams to monitor scale-up and exhibit batches, troublesh...

Responsible for Analysis of RM/IP/FP/PM Samples, analytical reports & documentation, identifying deviations, stability studies, comply with regulatory requirements, Calibration & trouble shooting of Instruments, Audit, cGMP & GLP, Qualifn Protocols.. Required Candidate profile B.Sc/M.Sc.with 4 to 6 yrs exp in API. Sound exp & knowledge of handling GC,HPLC, KF, IR, UV-VISUAL, Spectrophoto, AT, MP/BP etc.Legal compliance, cGMP, GLP, & regulatory guidelines (eg. ICH, USP, EP).

Roles & Responsibilities 1. To support and execute formulation development of mAbs 2. Conducting stability studies as per ICH guidelines. 3. Acquisition, recording, analysis and compilation of data in prescribed formats. 4. Responsible for maintenance and documentation of the developmental work carried out. 5. Supporting procurement/installation of appropriate equipment’s and consumables required for work, whenever applicable. 6. Capturing and compilation of the data generated contemporaneously in eLN (electronic Lab Notebook) and getting the same verified by the manager of the team regularly. 7. Ensuring proper usage and maintenance and calibration of equipment: entering the usage in log bo...

Development of Lyophilized Complex/Peptide Injectable & Biosimilar Product Development (Thaw, filter, fill & Finish). Drug Product R&D Stability, Compatibility & Development Studies. Participate in scale-up, toxicity/clinical exhibit batches of the Drug Products under development. Authoring regulatory filling & TTD Documents i. e. MF, RA, PDR, Stability Study Plan & R&D Stability Studies. Travel Estimate NA Job Requirements Educational Qualification M. Pharm - Pharmaceutics Experience Tenure : 2-6 years

Analyse the assigned samples and chromatographic tests for analysis by using the suitable valid procedure and calibrated instruments to ensure the compliance to the set specification / standards Perform analysis for release of RM, PM, FP & water analysis and process/cleaning validation as per commitment dates Perform analysis for stability samples without any errors as per schedule Check the results of the tests performed, evaluate them against the specifications Review the TDS printed through LIMS for its completion before release Key Accountabilities (2/6) Perform all activities as per current standard procedures by referring to all approved procedures/specifications to ensure compliance t...

Roles and Responsibilities Conduct analytical testing of finished products, including dissolution, UV-Vis, KF, FTIR, and GLP compliance. Develop and validate analytical methods for solid oral OSD products using techniques such as GC, HPLC, and UV spectroscopy. Perform method transfer and validation activities to ensure accuracy and reliability of test results. Collaborate with cross-functional teams to resolve OOS/OOT issues and implement corrective actions. Maintain accurate records of laboratory data, reports, and documentation in accordance with cGMP guidelines.

QA( AQA) To review the Audit Trial Report Review of SOPs pertaining to Quality Control (Chemical & Microbiology) Review of Stability protocols & Report Responsible for investigation and closure of OOL, OOT & OOS. To review the Equipment & usage log books of QC& microbiology. To review the calibration of QC & microbiology equipments Follow up for the closure of deviations/ change controls/CAPAs pertaining to QC area. To log OOS, OOT and OOLs and update the relevant databases and logbooks To Review the analytical method validation/other study Protocols, ROA and Reports Verification of Media Fill vials. Review of EMP, Water trends, specifications and testing Review of STPs & GTP materials/ Prod...

As a valuable member of a dynamic R&D team, you will be contributing to seamless technology transfer, innovative product development, and continuous quality enhancement for successful commercialization of pharmaceutical products across solid, semisolid, and liquid dosage forms. Your responsibilities will include leading and coordinating technology transfer from R&D/CRO to manufacturing sites, monitoring site activities, troubleshooting manufacturing issues, overseeing formulations for quality improvement, and developing new products through pre-formulation, competitor evaluation, formulation development, and stability studies. To excel in this role, you should possess expertise in technology...

The job involves contributing to the technical development and delivery of studies and analysis within the power systems team. This includes delivering consulting work related to various types of power systems studies and analysis such as static studies (e.g., load flow, fault level, reactive compensation), dynamic studies (e.g., stability studies), harmonic analysis, power quality, filter design, transient overvoltage, insulation coordination, control interaction studies, earthing studies, protection coordination, and Arc Flash studies. You will provide technical and project management leadership to support the project team in the successful delivery of consulting work, manage and resource ...

As an R&D Technician, you will play a crucial role in the development of new formulations, materials, and processes while maintaining a strong focus on quality and compliance. Your responsibilities will include conducting laboratory trials, stability studies, and sample evaluations. Additionally, you will collaborate with QA/QC teams to ensure product consistency and reliability. Analyzing data from research experiments and quality assessments will be a key part of your role, providing valuable insights to inform product improvements. It will be essential to maintain accurate documentation for all R&D activities, including technical data sheets, specifications, and trial reports. Ensuring th...

The ideal candidate for this position will join our R&D/F&D team focusing on Oral Solid Dosage (OSD) forms, including pellets and tablets. You will be responsible for conducting pre-formulation and formulation development studies, process validation, stability studies, and technology transfer of new pharmaceutical products while ensuring adherence to ICH guidelines and internal SOPs. Your key responsibilities will include conducting detailed literature reviews to support new product development initiatives. You will evaluate reference products, patents, regulatory status, and formulation strategies. Additionally, you will perform physicochemical characterization of API and excipients, assess...

As the Assistant General Manager for Nasal Spray Formulation Development in the Research & Development department at the R&D Center in Chinchwad, Pune, you will be responsible for leading the development of innovative nasal spray formulations. Your role will involve steering projects from concept to commercial scale-up, focusing on designing, developing, and optimizing nasal spray drug products to ensure regulatory compliance and meet quality standards. You will be leading a team of formulation scientists and collaborating with cross-functional teams to deliver high-quality, cost-effective nasal spray formulations for global markets. Your key responsibilities will include: - Developing and t...

The role involves planning and resource allocation for routine operations within the analytical development function. You will be responsible for ensuring timely analysis of finished products and raw materials for various projects. Your duties will include reviewing analytical data, raw data, daily usage logbooks, and lab notebooks to support operations. You will also be involved in preparing and reviewing critical documents such as Analytical Method validation protocols, reports, method transfer protocols, and Standard Operating Procedures (SOPs). Additionally, you will conduct literature searches and provide guidance on new method development. Another key aspect of the role is to review da...

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

The AGM / DGM Technical Services position requires a candidate with a B.Pharma / M.Pharma qualification and 15 to 20 years of experience in tech transfer activities of solid oral dosage forms for regulated markets. The ideal candidate should have experience in managing a team of 15 to 20 scientists, documentation officers, and technicians. As an AGM / DGM Technical Services in Kandivali, Mumbai, your responsibilities will include planning and executing scale-up and Exhibit batches of solid oral dosage forms for regulated markets such as US, EU, ROW, and Canada. You will be accountable for ensuring the timely initiation of stability studies for exhibit batches and overseeing the technical ser...

As an Executive - Application Lab at Azelis India, your main objective is to develop innovation through formulation, application, sampling, and technical support in the Personal Care and Home Care products industry. You will be responsible for formulating a wide range of products, conducting stability studies, ensuring regulatory compliance, and working on sustainable product concepts aligned with market trends. Your role will also involve providing technical support to customers, conducting product demonstrations, and collaborating with suppliers on new ingredient innovations. In addition, you will manage the HPC application development lab, handle lab operations, support CAPEX planning, an...

You will be part of the Formulation Development team, contributing your expertise in Biologic Formulations and pharmaceutical sciences. Your responsibilities will include conducting literature reviews, formulating biological products, designing and executing experiments, analyzing data using various techniques, calibrating instruments, performing proof-of-concept studies, conducting stability studies, writing scientific reports, and collaborating with cross-functional teams. To excel in this role, you should hold a minimum of a Postgraduate degree (MTech, MPharm) in Pharmaceutical Sciences, Chemistry, or a related field. Proficiency in analytical techniques like HPLC, GC, pH, Osmolality, KF,...

You will be responsible for liaising between various departments such as Planning, Production, Technical Services, Marketing, and Exports. Your roles and responsibilities will include the preparation, review, and implementation of SOPs and STPs. You will be checking all QC related records like analytical reports and logbooks. Additionally, you will be involved in planning and distributing samples for the analysis of Raw Materials, Intermediates, and finished products. You will design and conduct Stability studies as per ICH Guidelines and develop and validate analytical testing methodology used to control raw materials, production intermediates, and final products. Your tasks will also inclu...

The Assistant General Manager - Nasal Spray Formulation Development will play a crucial role in leading the development of innovative nasal spray formulations within the Research & Development (R&D) department of a Pharmaceuticals company. Reporting to the Head of R&D, you will be responsible for driving projects from concept to commercial scale-up, ensuring regulatory compliance and meeting quality standards. Your primary focus will be on designing, developing, and optimizing nasal spray drug products for global markets. Key Responsibilities: - Develop and technology transfer Nasal Sprays, Dry Powder Inhalers, and Soft Mist Inhalers dosage forms for regulated markets like EU and US. - Condu...

Key Accountabilities Accountability Cluster Major Activities / Tasks Develop new analytical methods for analysis of routine as well as stability samples by following proper GLPs to provide results or information regarding products to formulators Perform part method validation, forced degradation studies, excipient compatibility studies, reverse engineering, add-mixture studies, in-use studies, hold-time study and analysis of routine & stability studies Conduct cleaning validation studies Perform analysis of API, excipients and secondary material (packaging material, ink, adhesive etc.) Develop cost effective & time saving analytical method for new or existing product Evaluate the pharmacopei...

YOUR ROLE The Drug Products and Sciences R&D Stability team supports research and development projects for new and existing products. The Research Associate II, Stability Subject Matter Expert, applies sound chemistry and stability planning knowledge to identify and evaluate stability indicating characteristics. The effective integration of chemistry and stability enables establishment of shelf life for new or existing products manufactured for rapidly growing markets and allows for the qualification of product changes on a global scale. The Stability Subject Matter Expert designs strategies and makes recommendations that may be non-routine to address technical, regulatory, and business requ...