69 Assay Jobs

Assay Development & Screening Design, validate, and execute immunology-based assays to screen test molecules. Analyze and interpret experimental data with a focus on accuracy and reproducibility. Reagent & Inventory Management Procure reagents and consumables required for ongoing projects. Monitor procurement timelines to ensure uninterrupted lab operations. Laboratory Operations & Compliance Maintain lab equipment and ensure a clean, safe, and organized workspace. Adhere to SOPs and safety protocols at all times. Technical Expertise: Immuno-oncology assays Bioassays PBMC isolation and banking Flow cytometry and Incucyte analysis Cell culture, including primary cells and engineered cell line...

Role & responsibilities : *Candidate must have good hands on experience in HPLC,Electrophoretic test methods *Candidate must have good hands on experience in cell based test methods. Colorimetric, Spectrophotometer technique's. *Should be able to handle Spectrophotometer, Microplate reader microscope, basic QC instruments and relevant Software's. *Should be systematic in approach and have an idea on GLP & GDP compliance requirements. *Knowledge on QMS elements( OOS, incident Deviation, Change control etc.)

Role & responsibilities Invitro Biology Qualification: PhD/Postdoc (Biotechnology/Biochemistry/) with 0-2 years or M.Sc. with 2 -8 years of experience in various biochemical and cell-based assays to enable screening of NCEs. Hands-on experience on G protein-coupled receptors (GPCRs)/Receptor/Incretin Biology will be preferred Assay development, validation and screening assays for integrated drug discovery program and providing trouble shooting/strategic inputs into the project for achieving the deliverables Meticulously demonstrate consistency of high quality in study plan, reports, and related matter. Critical interpretation and presentation of data to partners. Weekly updates and TCs, e-ma...

Your Responsibilities Provide support at BR India within Discovery Sciences (DSc), focusing on small molecule lead identification and optimization in close collaboration with Novartis colleagues in the US and Switzerland, as well as Indian CROs, to discover and advance innovative therapies addressing areas of high unmet medical need, Make significant contributions to multidisciplinary project teams by developing and implementing in vitro activity assays, including biochemical, cell-based, and biophysical assays, Establish advanced assay protocols at CROs, adapting from internal Novartis SOPs or relevant literature sources, Oversee the transfer and troubleshooting of all assay protocols betwe...

We are looking for a skilled HR professional with strong expertise in Payroll Management, HR Analytics, and Dashboard Reporting, coupled with hands-on experience in Darwinbox HR Core Modules. The ideal candidate will drive operational excellence across payroll processes, ensure compliance, and enable data-driven decision-making through analytics and reporting.

Design and conduct experiments for enzyme discovery, modification, and functional optimization. Purify enzymes using advanced techniques and ensure high activity and purity. Study enzyme kinetics, substrate specificity, and stability under different conditions. Research and implement enzyme applications in industries such as pharmaceuticals, agriculture, bioenergy, and food processing. Collaborate with cross-functional teams, including engineers and scientists, to integrate biocatalysts into broader biochemical processes. Maintain laboratory equipment in good condition and ensure a safe working environment by adhering to safety protocols and procedures. Stay updated with advanced technologie...

Role & responsibilities Candidate should hands on experience on Analytical instrumentation, knowledge of USP chapters, ICH Guidelines . Should have inclination for solving problems encountered during analysis.

Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures 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 at all times 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 i...

Stedman Pharmaceuticals is looking for a dynamic and experienced candidate for the Quality Control (QC) department with hands-on experience in Analytical Method Validation for various dosage forms. Share your Resume to hrd@stedmanpharma.com

As a Pharmaceutical Documents Associate at our company, you will play a crucial role in ensuring the quality and compliance of our pharmaceutical products. Your responsibilities will include: - Having experience or sound knowledge in Active Pharmaceutical Ingredients, Finish Product, Packaging Material Standards, Quality Management, and Quality Control. - Demonstrating knowledge or experience in Quality control tests for various formulations and APIs such as Assay, Dissolution, Disintegration, Uniformity of Weight/dosage, Impurity testing, Water content, etc using methods like HPLC, GC, TLC, IR/UV, Disso, etc. - Understanding pharmacopoeia applications and all documentation relevant to QA/QC...

We are looking for a dynamic and experienced professional to lead our Research & Development efforts within the Bioassay function at Biocon Biologics. This role requires a strong scientific foundation, hands-on expertise in bioassay development, and proven leadership capabilities. The ideal candidate will drive innovation, oversee complex R&D projects, mentor junior scientists, and collaborate cross-functionally to support the organizations strategic goals in biopharmaceutical development. Role & responsibilities: Design, development, optimization and qualification of in vitro cell-based assays (reporter gene assays, proliferation assays, Fc effector assays such as ADC, CDC, ADCP, cellular s...

Experience in various biochemical and cell-based assays to enable screening of NCEs. Hands-on experience on G protein-coupled receptors (GPCRs)/Receptor/Incretin Biology will be preferred Assay development, validation and screening assays for integrated drug discovery program and providing trouble shooting/strategic inputs into the project for achieving the deliverables Meticulously demonstrate consistency of high quality in study plan, reports, and related matter. Strong interpersonal and communication skills. Collaborative mind set

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

Job Opportunity at Natco Pharma Limited (Formulation Unit) Department: Quality Control Position: Chemist / Officer / Executive Qualification: B. Pharmacy / M. Pharmacy / M. Sc Experience: 3 to 5 Years Location: Kothur, Telangana Key Responsibilities: Analysis of finished products, raw materials, and in-process samples Operation and troubleshooting of instruments such as HPLC, UV, KF, IR, and Dissolution Apparatus Testing of Packing Materials Adherence to GLP, GDP, cGMP, and ALCOA+ standards Assay and dissolution testing using HPLC Regulatory exposure in formulation is mandatory Interested candidates may share their CVs at jaganmohan.p@natcopharma.co.in

As a member of the team, you will be responsible for core analytical method development and CMC activities related to Inhalation dosage forms. Your role will involve performing analytical tasks throughout the development process, including scale-up support, method validation, method transfer, release testing, stability testing, drug product characterization, E&L Study, In-vitro study, as well as routine analysis of inhalation dosage forms. You will conduct various tests such as assay, related compound analysis, APSD, DDU, and particulate matter analysis for inhalation dosage forms. The ideal candidate for this position should hold a degree in M. Pharm, M. Sc., or B. Pharm. Amneal is an equal...

This role has been designed as ?Hybridwith an expectation that you will work on average 2 days per week from an HPE office, Who We Are Hewlett Packard Enterprise is the global edge-to-cloud company advancing the way people live and work We help companies connect, protect, analyze, and act on their data and applications wherever they live, from edge to cloud, so they can turn insights into outcomes at the speed required to thrive in todays complex world Our culture thrives on finding new and better ways to accelerate whats next We know varied backgrounds are valued and succeed here We have the flexibility to manage our work and personal needs We make bold moves, together, and are a force for ...

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...

Role & responsibilities: Must Have : Seeking candidates with Hand on expertise with Surface Plasmon Resonance (SPR). Development, performance and troubleshooting of cell-based assays development, qualification and sample analysis for therapeutic protein, monoclonal antibodies. Development, performance and troubleshooting of SPR, ELISA and flow cytometry assays for monoclonal antibodies. Preparation of technical documents. Writing of SOP, Protocol and Reports Preferred candidate profile: Cell based assays development, qualification and sample analysis for therapeutic proteins, monoclonal antibodies. To take charge of the equipment/instruments in the lab and ensure their proper functioning. To...

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...

Responsibilities Collaborate with clients to understand their business requirements and translate them into cloud-based solutions, Design and architect scalable, reliable, and secure cloud solutions on platforms such as Amazon Web Services (AWS), Microsoft Azure, or Google Cloud Platform (GCP), Conduct cloud assessments and provide recommendations on cloud migration strategies, including lift-and-shift, re-platforming, or refactoring, Develop architecture blueprints, diagrams, and documentation that clearly articulate the proposed solutions, Work closely with development teams to ensure cloud architecture best practices are followed throughout the software development lifecycle, Assist in th...

It has been more than 60 years since SYSTRA has garnered expertise that spans the entire spectrum of Mass Rapid Transit System SYSTRA Indias valuable presence in India roots back to 1957, where SYSTRA worked on the electrification of Indian Railways Our technical excellence, holistic approach and the tremendous talent provides a career that puts people who join us at the heart of improving transportation and urban infrastructure efficiency, Understand better who we are by visiting systra in Context BIM Modeller Missions/Main Duties Support the Discipline Lead, BIM Manager and Production Team(s) in day to day BIM implementation activities, Provide progress and performance updates to Disciplin...

QC officer -04 Qc Executive - 01 Perform chromatographic analyses and tests, including HPLC, Gas Chromatography (GC), and Thin-Layer Chromatography (TLC), on raw materials, in-process materials, and finished products. LIMS knowledge preferred. Required Candidate profile We are looking for Male candidate due to work in rotation shift ( First/Second/Night) preferred B.Sc./MSc chemist & required experience of pharma formulation Sterile/Non Sterile product.

Dear Applicants, Greeting from Biophore India pharmaceutical Pvt Ltd, We have opening for Formulation AR&D Department . Job Openings: 4 Nos Position : Research Analyst or Sr Research Analyst Experience : 2 - 7 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 an...

Dear All, We are seeking a highly motivated and talented Analytical R&D Scientist( Oral Solid Dosages ) 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: 2-7 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 b...

You will be responsible for conducting quality control analysis as a QC Analyst, specifically operating HPLC equipment. Your role will involve performing tests such as Assay and Dissolution, CU & BU, and Swab Analysis using HPLC. It is essential that you have experience working in the Finished Department and possess practical knowledge of FP, PV, HT, and CTC specifications for all products. The ideal candidate should have 2 to 7 years of relevant experience for the positions available as Officer, Senior Officer, or Executive. There are a total of 9 vacancies to be filled. Joining our company means being a part of a team that values its employees. We offer a best-in-segment Promotion Policy, ...