Syngene International Limited

Designation Executive Biopharmaceutical Development Job Location Bengaluru India Reporting to ResearchScientist Biopharmaceutical Development Job Grade 9 Operating Unit Biopharmaceuticals Department Biopharmaceutical Development The Company Syngene International Ltd BSE 539268 NSE SYNGENE ISIN INE398R01022 is an integrated research development and manufacturing services company serving the global p

Should be familiar with Analytical instruments and techniques. • Knowledge in Data Interpretation. • Should train the Juniors on SFC techniques and monitor the daily work. • Knowledge in Data Interpretation • Knowledge in handling analytical instruments like Analytical SFC/Chiral HPLC and Preparative SFC • Review daily/monthly laboratory monitoring, verification, and calibration

Primary Responsibility: Ensure material requirements for the new projects with the help of technical teams (MSAT and Manufacturing) and ensure availability as per the project plan. Prepare the production schedule in consultation with the relevant stakeholders and share the same with all the relevant functions on a regular basis. Ensure completion of following activities for the new projects/ p

Primary Responsibilities: Providing consultation to the stakeholders and clients regarding national regulatory aspects, as and when required. Implementing and maintaining process, procedures, and trackers that are essential for national regulatory support function performance in the organization. Identifying the regulatory requirements. Interacting with the regulators and coordinating their i

The ideal candidate will independently execute in-vivo rodent Pharmacokinetic (PK) studies in support of drug discovery in a fast-paced environment. This role requires a good understanding of preclinical ADME, PK parameters, related PK softwares (Kinetica or Phoenix WinNonlin) and pharmacology. The candidate should have ability to manage reportee/s in pharmacokinetics group and will be responsible

Job description: The purpose of MIS role is to produce data-driven reports that help businesses activities. The MIS executive's responsibilities include designing, developing and prepare MIS reports on time and keeping up to date with the latest developments in MIS systems, analyzing reports, operations, and making suggestions for improvement.

Key Responsibilities: Identify and implement state-of-the-art statistical methods for data exploration, visualization, analysis, and integration of cancer genomics/epi-genomics, and other forms of high-dimensional -omics data for patient clinical outcomes Develop and evaluate performance of existing or new assays through statistical inferences Interpret quality control data metrics in NGS meth

Independently prepare, review and finalize the concept sheets Prepare the Clinical Study protocols in compliance to applicable regulatory requirements and associated study documents like ICF, CRF etc. Preparation & finalization of study specific Project Management plans, in consultation with respective Project Manager Write and edit clinical study documents like Concept sheet, Protocols, ICF, CR

Skills Required: * Candidates should have Good Communication & Analytical Skills and should be Good at Medical Terminology (Physiology & Anatomy). Role: Initial file review for identifying merits Subjective review and analysis to identify instances of negligence, factors contributing to it To review surgical procedures, pre and post-surgical care, nursing home negligence To prepare medi

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Syngene International Ltd. (BSE: 539268, NSE: SYNGENE, ISIN: INE398R01022) is integrated contract research, development, and manufacturing organization providing scientific services – from early discovery to commercial supply. Companies' innovative capabilities for novel molecular entities (NMEs) cater to a wide range of industrial sectors, including pharmaceutical, biotechnology, nutrition, animal

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 companys 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 o

Job Title Associate Scientist Job Location Bangalore Job Grade 8I About Syngene Syngene www syngeneintl com is an innovationled 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

Syngene International Ltd is a scientific services company offering services in various industries such as pharmaceuticals, biotechnology, nutrition, animal health, consumer goods and specialty chemicals. It has a team of 5,000 highly qualified employees and state-of-the-art infrastructure and technology to support its culture of scientific innovation.

Designation Executive Biopharmaceutical Development Job Location Bengaluru India Reporting to Associate Manager Biopharmaceutical Development Job Grade 9 Operating Unit Biopharmaceutical Development Department Biopharmaceutical Development The Company Syngene International Ltd BSE 539268 NSE SYNGENE ISIN INE398R01022 is an integrated research development and manufacturing services company serving t

Job Requirements Job Title: Research Associate - Toxicologist (Clinical Team) at Mankind Pharma - Manesar, Gurugram, Haryana Company Name: Mankind Pharma Location: Manesar, Gurugram, Haryana Salary: Not Disclosed (Per year) Qualification: M. Pharm (Pharmacology/Toxicology) / M.Sc. (Toxicology) Job Description: We are seeking a highly skilled and motivated Research Associate - T

Syngene hiring for Safety Assessment as Study Director for GLP in-vivo toxicology studies Qualification: M.Sc/M.Pharma Experience : 3 to 6 years Location: Bangalore Job description Job title: Associate Scientist Job location: Bangalore Job grade: 8-I About Syngene: Syngene (www.syngeneintl.com) is an innovation-led contract research, development and manufacturing organizatio

Designation: Executive Job Location: Bangalore Department: SARC Operations Reporting to: Assistant General Manager Job Grade: 9-I 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 eve

Designation: Executive Job Location: Bangalore Department: Bioanalytical Research Laboratory About Syngene Incorporated in 1993, Syngene International Ltd. is an innovation-focused global discovery, development and manufacturing organization providing integrated scientific services to the pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical indu

Key Responsibilities: • Perform synthetic chemistry reactions, reaction work-ups, purification of the compounds by column chromatography, crystallization, re-crystallization techniques, preparative TLC, and operating lab equipment • Ensure that the samples generated during the course of synthesis are given for analysis and record subsequent results obtained and update the supervisor/group leader

Designation Executive Biopharmaceutical Operations Job Location Bengaluru India Reporting to Deputy Manager Biopharmaceutical Operations Job Grade 9 Operating Unit Biopharmaceutical Department Biopharmaceutical Operations The Company Syngene International Ltd BSE 539268 NSE SYNGENE ISIN INE398R01022 is an integrated research development and manufacturing services company serving the global pharmace

Responsibilities of the Candidate: • Collaborate closely with cross-functional teams, including software engineers, database administrators, and DevOps, to gather requirements and design comprehensive application solutions. • Develop and maintain front-end applications using Node.js, and Angular.js and know other programming languages and relevant frameworks, adhering to best practices for perfor

Key Responsibilities: Routine analysis of in-process and isolated samples Method development and validation Instrument calibrations Documentation Report preparation Miscellaneous lab responsibilities.

Key Responsibilities: Design algorithms under supervision in one or more digital pathology analysis software packages in the quantification of IHC staining expression, including tumor/stroma classification and cellular feature extraction. Document projects, algorithms, and results in detail with the ability to proofread and record results as per regulatory standards. Work collaboratively in pr

Responsibilities: Identifying Key decision makers in the given Database and fix appointments/meetings with them At least reach 100-150 prospective customers per day thru emails Generation/Creation of Database Create, execute and follow-up with the prospects on regular basis, maintain good pipeline in assigned territory/geography/Vertical. Maintaining database (CRM, Excel, etc.) of prospectiv

Requirements: Work as a technical leader and/or partner in cross-functional teams to deliver business needed results. Conduct and manage assigned projects independently including up front knowledge seeking, developing and executing technical plans, collecting and analyzing data, communicating project status and results internally and externally, generating reports and making presentations. Tra

Key Responsibilities • Initiation of QMS elements i.e. Change control, CAPA, deviation, Laboratory Incident, OOS, OOT, Non-Conformity as applicable. • Handling of LMS, LIMS, ELN, TrackWise and EDMS Softwares for routine activities as applicable . • Preparation of Specification, Standard Operating Procedure, Instrument Operating Procedures, General procedures. Observation data sheet, calibration

Key Responsibilities: Shall be responsible for work execution and implementation of Instrumentation & automation initiatives across the organization. Should work with Engineering business partnering teams and OU stakeholders to understand requirements, do the groundwork on data collection, work on the implementation plan, and execute execution. Work for automation in condition monitoring, data a

Role Accountabilities: Record and maintain customer issues on project records, using enterprise solutions for customer relationship and project management Collaborate with cross-functional enabling functions (project management, commercial, etc.) and delivery team to track, monitor and report resolution to issues Track issue history and collaborate with project team to ensure prompt resolution

Roles and Responsibilities Conducting literature search and preparation of Toxicological assessment for Chemicals/ Pharmaceuticals / Medical devices E&L. Preparation and review of Nonclinical overview (NCO) for CTD submission of dossier filing. Preparation and review of Health Based Exposure Limits (PDE/ OEL/ ADI) reports for Pharmaceuticals/ Chemicals. Preparation and review of in silico tox

Role Accountabilities: Timely reporting of deviations and perform appropriate investigations to identify root cause or most probable root cause and proposal & implementation of appropriate CAPA to prevent reoccurrence. Perform appropriate manufacturing investigations for OOS results and Customer Complaints to identify root cause or most probable root cause and proposal & implementation of appro

Core Purpose of the Role: Attend breakdown of Biopharma instruments in R&D lab and get it operational with support from instrument vendor and E&M team. Responsible for IQ,OQ,PQ for new instrument installation, calibration and maintain the supportive documents in coordination with QA and E&M team Get coordination with instrument vendor and E&M team for maintaining spares required to avoid break

Job Purpose: Discovery and Translational Medicine at BBRC/Syngene is seeking an associate scientist to support our novel translational research programs spanning multiple therapeutic areas in oncology, immunology, cardiovascular and fibrosis. As a member of this group, successful candidates are responsible to design, develop and establish robust assays and platform technologies that support b

Key Responsibilities: To perform the role as Clinical Trials - QA auditor to verify compliance with respect to ICH-GCP, applicable regulatory requirements and Study Protocol for Clinical site, Pharmacy, Biometrics, clinical data management and Medical writing activities for patient based (Phase I, II, III and IV) studies. GCP clinical Trial QA auditor with 6-9 years of experience in performing

Key Responsibilities : Protein purification using AKTA Pure & AKTA Avant systems, process development, experience in Affinity, Ion-exchange, HIC chromatography, Column packing and tangential flow filtration. Excellent communication with upstream and analytical team. Diligent documentation skills and experience writing detailed Lab Notebooks. Basic knowledge of bioinformatics is a plus.

Key Responsibilities: Independently perform routine histopathological techniques like grossing, tissue processing, embedding, sectioning and H&E staining Perform robust monoplex IHC automated assays under supervision Perform and support cell culture techniques independently Document & maintain appropriate records Inventory & slides/block Management Perform other lab duties as instructed.

Roles and Responsibilities Perform synthetic chemistry reactions. • Purification of compounds by manual/automated column chromatography or recrystallization techniques. • Submit the samples generated during the course of synthesis for analysis and record results. • Record observations of experiments, results, utilization of resources and other activities related to the reaction in the laborat

Key Responsibilities: Understand and work on exploratory drug discovery programs for the identification of a novel/ validation of existing targets in collaboration with In vitro Pharmacology, Fibrosis, Immunology, Oncology, CV, LDO, and translational research teams Evaluate, develop, and apply cutting-edge methods for the analysis of multi-modal, high-dimensional -omics datasets coming from bot

Key Responsibilities: 1. Working in a team of pathologists, provide Clinical Pathology support to programs/projects at BBRC in close collaboration with the BMS pathology team. 2. Responsible for the development of IHC/ISH assay development, qualification/validation and sample analysis. 3. Works in close collaboration with the scientist/pathologists onsite to support translational pathology

Key Responsibilities: Roles and responsibilities include, but are not limited to the following: Develop, implement, and manage SOPs, work instructions, and compliance policies in support of GLP, GCP, ISO 13485 and CLIA/CAP lab operations. Ensure that record keeping is complete, and records are maintained appropriately by Translational Medicine lab staff. This includes ensuring the requisite

Key Responsibilities: Perform flow cytometer instrument calibration and routine maintenance as per established protocols Perform flow cytometry assay development and method validation Stain and acquire clinical samples on multicolor flow cytometers Perform flow cytometry data analysis and deliver data within timelines Document & maintain appropriate records and electronic lab notebooks Per

Key Responsibilities: Conduct preclinical/laboratory experiments on late stage BMS portfolio compounds to support annual goals and objectives for Translational Medicine (for internal /external, collaborations, compound specific plans etc). Responsible for delivering data in support of translational strategies including biomarkers, patient selection hypotheses, dose and schedule, combination str

Key Responsibilities: Overseeing of standardization and validation of IHC & ISH assays Provide Pathology support to various projects/programs Responsible for reporting of clinical trial samples Work cohesively as a team of pathologists to support pathology and immunohistochemistry workflows Enable and support translational R&D projects in collaboration with network of hospitals Work closely