59 Assay Jobs

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, ...

We are seeking a highly motivated Research Technician to join the research group of Dr Emre Sayan in School of Cancer Sciences, University of Southampton This exciting role will support research focused on drug discovery and testing to kill metastatic liver, pancreatic and neuroendocrine cancers, The appointed scientist will be using common and cutting-edge techniques The main focus of the project will be on testing the activity of new small molecules in established cancer cell lines and animals Flow cytometry, western blotting, and immuno-fluorescence will be mainly used in addition to a variety of necessary molecular biology, biochemistry and cell biology techniques As part of the team, yo...

Job Title: Invitro BA Scientist Job Location: Bangalore, Hyderabad' About Syngene : Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines • Overall adherence to safe practices and procedures of oneself and the teams ...

Job Title: Invitro ADME Job Location: Bangalore/Hyderabad About Syngene Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures, and SOPs, in letter and spirit. Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned. Con...

Exciting Opportunity Alert - DMPK Roles at Syngene International! Are you passionate about drug discovery and eager to contribute to cutting-edge pharmaceutical research? Join us at Syngene International for the following roles: - ADME Scientist: MSc with 6-9 years or MPharma/Mtech with 3-6 years - Sr AS: MSc with 9-12 years, MPharm/Mtech with 6-9 years - Team Lead: Fresh PhD or MSc with 15-16 years, MPharma with 12-15 years - Sr Team Lead: PhD with 3-5 years of experience - Group Lead: PhD with 5-10 years - Senior Group Lead: PhD with 10+ years Fresh PhD candidates with relevant experience during academics or postdoc are also welcome. Key Skills Required: DMPK In vitro BA and In vitro ADME ...

As a member of our team, your primary responsibilities will include the development and validation of methods for Assay, Dissolution, and related substances. You will also be responsible for the calibration of analytical instruments to ensure accurate and reliable results. Conducting routine and stability samples analysis of OSD formulations will be a key part of your role. To excel in this position, you must possess a good quality mindset and have a thorough understanding of GLP requirements. Your ability to write technical reports and prepare power point presentations will be essential for effectively communicating your findings and recommendations. Join us in this dynamic role where you w...

Planning and executing assay-runs for cell based assays and ELISA as part of Method Development and Method Qualification studies Analysis of the data using parallel line analysis and equivalence testing Writing protocols and reports for Method development and Method qualification studies Maintenance of the cell lines, preparation of cell banks Review of raw data and data recording sheets and to ensure good documentation practices. Planning of day-to-day activities independently. Trouble shooting of the issues (if any) aroused during execution of assay-run. Involving in documents preparation for SOP, STP, MOA.

1) Development of mass spectrometry based methods for analysis of various molecules for pivotal studies such as biosimilarity, comparability etc.. 2)operation and maintenance of mass spectrometry instrument and performing troubleshooting activities 3)developing and carrying out multiple assays aimed at characterization of protein based therapeutics across various stage of the project 4) participate in design, development and implementation of methods for CQA/impurity characterization of molecules. Interpret results,and draw conclusions from multiple stage experiments 5) Author technical documents such as SOP,MoA,study protocol and reports for method and product development

1) Preparationof Analytical method validation Protocols and reports for the relatedsubstances and Assay by HPLC and residual solvents by GC 2) Preparation of Analytical methodvalidation Protocols and reports for the Identification analysis by HPLC,GC andparticle size analyzer and performing the analytical method validations for theIdentification, content and purity analysis by HPLC,GC and Particle sizeanalyzer. 3) Performing the Analytical methodvalidations by HPLC and GC. 4) R esponsible to follow and ensure strict compliance to GLP practices in the laboratory to meet the organizational goal which in line with procedural references. 5) Maintenance of log books and Calibration records as per...

Dear Applicants, Greeting from Biophore India pharmaceutical Pvt Ltd, We have opening for Formulation AR&D Department . Job Openings: 6 Nos Position : Research Analyst or Sr Research Analyst Experience : 2 - 6 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...

We are seeking to hire an innovative and highly motivated Formulation Scientist to join our Biologics RD team . The qualified individual will have at least 3-5 years of relevant industry working experience in developing parenteral formulation, solid and liquid oral dosage forms for use in first-in-human studies. The Formulation Scientist in the Large Molecule Drug Product Development will be a lab-based role, responsible for experimental studies in the pre-formulation, formulation, characterization, and analytical development of therapeutic proteins including monoclonal antibodies, virus-like particles, RNA therapeutics, and subunit-based vaccines. Since most of our clients are based out of ...