Qureos Mentor

Syngene International Limited

<div>
 Date: 3 Sept 2025
 
 
 Location:
 
 
 Bangalore, KA, IN, 560099
 
 
 Custom Field 1: Discovery Services
 
 
 
 Job Title: in-vitro Bioanalytical Scientist
 
 
 
 
 Job Location: Bangalore
 
 
 
 
 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
 
 
 
 <ul>
 <li>
 Overall adherence to safe practices and procedures of oneself and the teams aligned
 </li>
 <li>
 Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company&rsquo;s integrity &amp; quality standards
 </li>
 <li>
 Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times.
 </li>
 <li>
 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.
 </li>
 <li>
 Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self
 </li>
 <li>
 Compliance to Syngene&rsquo; s quality standards at all times
 </li>
 <li>
 Hold self and their teams accountable for the achievement of safety goals
 </li>
 <li>
 Govern and Review safety metrics from time to time
 
 
 </li>
 </ul>
 
 Core Purpose Of The Role
 
 
 
 <ul>
 <li>
 To participate in sample processing for PK, ADME assays and handling of LCMS/MS. Ability to adapt to the dynamic team environment
 </li>
 <li>
 Processing of different matrices samples of PK studies
 </li>
 <li>
 Optimization of test compounds manually as well as automated on LCMS/MS
 </li>
 <li>
 Develop methods with the team lead
 </li>
 <li>
 Independently handling of HPLC for UV based samples analysis.
 </li>
 <li>
 Documenting the lab note books online and compound management
 
 
 </li>
 </ul>
 
 Syngene Values
 
 
 
 All employees will consistently demonstrate alignment with our core values
 
 
 <ul>
 <li>
 Excellence
 </li>
 <li>
 Integrity
 </li>
 <li>
 Professionalism
 
 
 </li>
 </ul>
 
 Accountabilities As a Syngene Leader (only For Leadership Hires)
 
 
 
 <ul>
 <li>
 Champion effective Environment, Occupational Health, Safety and Sustainability (EHSS) practices for the company and oversee compliance with those practices within Biologics business. Play an active leadership role in monitoring and verifying safety performance through Gemba walks and other safety-led activities.
 </li>
 <li>
 Foster a corporate culture that promotes an environment, occupational health, safety, and sustainability (EHSS) mindset as well as the highest standards of quality, integrity, and compliance.
 </li>
 <li>
 Put people at the heart of our success by providing clear, active leadership defined by the Syngene leadership framework setting high standards of people management, career planning and talent retention as a priority.
 
 
 </li>
 </ul>
 
 Experience
 
 
 
 <ul>
 <li>
 Minimum 3-5 years of experience in handling ADME assays and HPLC and LCMS/MS
 
 
 </li>
 </ul>
 
 Skills And Capabilities
 
 
 
 <ul>
 <li>
 Expertise in column selection, mobile phase selection, solvent preparations and sample processing techniques such as protein precipitation, liquid-liquid extraction and solid phase extraction is mandatory
 </li>
 <li>
 Sample processing of New chemical entities from various in-vitro and in-vivo studies executed in Preclinical discovery by using appropriate extraction methods
 </li>
 <li>
 Should be able to develop and validate LC-MS based qualitative/quantitative methods and apply them in routine analysis
 </li>
 <li>
 Should be well versed with internet-based literature search and capable of implementing the Learnings as and when required
 </li>
 <li>
 Candidate is expected to have basic understanding in interpretation of Mass/UV Spectra
 </li>
 <li>
 Should ensure preventative maintenance and calibration schedules of HPLC &amp; mass spec by coordinating with vendor and support staff
 </li>
 <li>
 General understanding of Drug metabolism and Pharmacokinetics
 </li>
 <li>
 Should be able to deliver scientific presentation in departmental journal club and write official Project reports
 
 
 </li>
 </ul>
 
 Education
 
 
 
 <ul>
 <li>
 M. Pharm in Pharmaceutical sciences, Pharmaceutical Analysis who has interest and passion for LC/MS related bioanalysis
 
 
 </li>
 </ul>
 
 Equal Opportunity Employer
 
 
 
 It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodation for qualified individuals with disabilities.
</div>

Invitro BA Scientist

<div>
 Date: 8 Sept 2025
 
 
 Location:
 
 
 Bangalore, KA, IN, 560099
 
 
 Custom Field 1: Discovery Services
 
 
 Job Title: in-vitro Bioanalytical Scientist
 
 
 Job Location: Bangalore
 
 
 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
 
 
 
 <ul>
 <li>
 Overall adherence to safe practices and procedures of oneself and the teams aligned
 </li>
 <li>
 Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company&rsquo;s integrity &amp; quality standards
 </li>
 <li>
 Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times.
 </li>
 <li>
 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.
 </li>
 <li>
 Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self
 </li>
 <li>
 Compliance to Syngene&rsquo; s quality standards at all times
 </li>
 <li>
 Hold self and their teams accountable for the achievement of safety goals
 </li>
 <li>
 Govern and Review safety metrics from time to time
 
 
 </li>
 </ul>
 
 Core Purpose Of The Role
 
 
 
 <ul>
 <li>
 To participate in sample processing for PK, ADME assays and handling of LCMS/MS. Ability to adapt to the dynamic team environment
 </li>
 <li>
 Processing of different matrices samples of PK studies
 </li>
 <li>
 Optimization of test compounds manually as well as automated on LCMS/MS
 </li>
 <li>
 Develop methods with the team lead
 </li>
 <li>
 Independently handling of HPLC for UV based samples analysis.
 </li>
 <li>
 Documenting the lab note books online and compound management
 
 
 </li>
 </ul>
 Syngene Values
 
 
 All employees will consistently demonstrate alignment with our core values
 
 
 <ul>
 <li>
 Excellence
 </li>
 <li>
 Integrity
 </li>
 <li>
 Professionalism
 
 
 </li>
 </ul>
 Accountabilities as a Syngene Leader (only for Leadership Hires)
 
 
 <ul>
 <li>
 Champion effective Environment, Occupational Health, Safety and Sustainability (EHSS) practices for the company and oversee compliance with those practices within Biologics business. Play an active leadership role in monitoring and verifying safety performance through Gemba walks and other safety-led activities.
 </li>
 <li>
 Foster a corporate culture that promotes an environment, occupational health, safety, and sustainability (EHSS) mindset as well as the highest standards of quality, integrity, and compliance.
 </li>
 <li>
 Put people at the heart of our success by providing clear, active leadership defined by the Syngene leadership framework setting high standards of people management, career planning and talent retention as a priority.
 
 
 </li>
 </ul>
 
 Experience
 
 
 
 <ul>
 <li>
 Minimum 1-3 years of experience in handling ADME assays and HPLC and LCMS/MS
 
 
 </li>
 </ul>
 
 Skills And Capabilities
 
 
 
 <ul>
 <li>
 Expertise in column selection, mobile phase selection, solvent preparations and sample processing techniques such as protein precipitation, liquid-liquid extraction and solid phase extraction is mandatory
 </li>
 <li>
 Sample processing of New chemical entities from various in-vitro and in-vivo studies executed in Preclinical discovery by using appropriate extraction methods
 </li>
 <li>
 Should be able to develop and validate LC-MS based qualitative/quantitative methods and apply them in routine analysis
 </li>
 <li>
 Should be well versed with internet-based literature search and capable of implementing the Learnings as and when required
 </li>
 <li>
 Candidate is expected to have basic understanding in interpretation of Mass/UV Spectra
 </li>
 <li>
 Should ensure preventative maintenance and calibration schedules of HPLC &amp; mass spec by coordinating with vendor and support staff
 </li>
 <li>
 General understanding of Drug metabolism and Pharmacokinetics
 </li>
 <li>
 Should be able to deliver scientific presentation in departmental journal club and write official Project reports
 
 
 </li>
 </ul>
 Education
 
 
 <ul>
 <li>
 M. Pharm in Pharmaceutical sciences, Pharmaceutical Analysis who has interest and passion for LC/MS related bioanalysis
 
 
 </li>
 </ul>
 
 Equal Opportunity Employer
 
 
 
 It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodation for qualified individuals with disabilities.
</div>

Invitro BA scientist

<div>
 Date: 9 Sept 2025
 
 
 Location:
 
 
 Bangalore, KA, IN, 560099
 
 
 Custom Field 1: Discovery Services
 
 
 Designation: Invitro ADME Scientist
 
 
 Job Location: Bangalore
 
 
 Department: Discovery Biology
 
 
 
 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 industries around the world. Syngene&rsquo;s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&amp;D productivity, speed up time to market and lower the cost of innovation.
 
 
 
 Job Purpose
 
 
 
 <ul>
 <li>
 Highly lab-based role, conducting metabolism, Phys-Chem, Caco-2, LLC-PK1-MDR1, MDCK-II-MDR1, MDCK-II BCRP transporter assays in 24 well/ 96 well plate trans well assays using different matrices with highest quality
 
 
 </li>
 </ul>
 
 Key Responsibilities
 
 
 
 <ul>
 <li>
 Design and execute Caco-2, LLC-PK1-MDR1, MDCK-II-MDR1, MDCK-II BCRP transporter assays in 24 well/ 96 well/384 well plate trans well assays
 </li>
 <li>
 Able to handle Metabolism and Phys-Chem studies
 </li>
 <li>
 Reporting of executed studies without mistakes
 </li>
 <li>
 Raw data compilation, Report preparation, eLN updation on time.
 </li>
 <li>
 Presenting the study results clearly in the cross functional scientific meetings.
 </li>
 <li>
 Follow environment, health, and safety (EHS) requirements at all times in the workplace-ensuring individual and lab/plant safety.
 </li>
 <li>
 Ensure environment, health, and safety (EHS) measures are imparted via training and adhered within the team.
 
 
 </li>
 </ul>
 
 Educational Qualification
 
 
 
 <ul>
 <li>
 M Pharm. in any pharmaceutical science or M Sc. in biological science.
 
 
 </li>
 </ul>
 
 Technical/functional Skills
 
 
 
 <ul>
 <li>
 Comprehensive understanding of in vitro ADME assays and technical expertise in trouble shooting the assays
 </li>
 <li>
 Experience in conducting cell-based assays using wild type and transporter transfected cell lines
 </li>
 <li>
 Good, demonstrated knowledge in software such as Microsoft excel and Graph pad prism
 </li>
 <li>
 Report preparation and review of the reports ready to share with the clients
 </li>
 <li>
 Understanding the functionality, operation and maintenance of the instruments (TEER inst, Microscope, biosafety cabinet, LN2, etc.)
 
 
 </li>
 </ul>
 
 Experience
 
 
 
 <ul>
 <li>
 M Pharm. in pharmaceutical sciences or M SC in biological science with one to four years of Industrial experience in DMPK/ADME research.
 
 
 </li>
 </ul>
 
 Behavioral Skills
 
 
 
 <ul>
 <li>
 Demonstrate ability to be a team player.
 </li>
 <li>
 Commitment to deliver the study reports within the agreed timelines
 </li>
 <li>
 Adaptability to changes in the dynamic lab environment
 </li>
 <li>
 Communicate confidently with colleagues and collaborators in the meetings and presentation of study reports and evidence of publications in the PEER reviewed Journals
 
 
 </li>
 </ul>
 
 Equal Opportunity Employer
 
 
 
 It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities.
</div>

Invitro ADME Scientist

<div>
 Date: 28 Sept 2025
 
 
 Location:
 
 
 Bangalore, KA, IN, 560099
 
 
 Custom Field 1: Discovery Services
 
 
 
 Job Description
 
 
 
 
 Designation:
 
 Computational Chemist (Senior Research Associate) (Level 9)
 
 
 
 Job Location:
 
 Bangalore
 
 
 
 Department:
 
 Computational &amp; Data Sciences
 
 
 
 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 industries worldwide. Syngene&rsquo;s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA, and Herbalife. Its innovative culture is driven by the passion of its 4240-strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&amp;D productivity, speed up time to market, and lower the cost of innovation.
 
 
 
 Job Purpose
 
 
 
 To support drug discovery and material science projects by applying computational modeling, cheminformatics, QSAR/QSPR modeling, and data science techniques.
 
 
 
 Key Responsibilities
 
 
 
 <ul>
 <li>
 Support the design and optimization of small and large molecules using various structure &amp; ligand-based approaches.
 </li>
 <li>
 Implement QSAR/QSPR modeling techniques to predict molecular properties and enhance compound selection.
 </li>
 <li>
 Apply cheminformatics approaches to analyze and interpret chemical and biological data.
 </li>
 <li>
 Utilize data science techniques, including machine learning, to derive insights from computational chemistry datasets.
 </li>
 <li>
 Prepare and submit reports in the relevant format and contribute to design sessions within the team.
 </li>
 <li>
 Provide support to the computational tool/workflow development.
 
 
 </li>
 </ul>
 
 Educational Qualification
 
 
 
 <ul>
 <li>
 Master&rsquo;s degree in Computational Chemistry, Organic Chemistry, Pharmacy, Biotechnology, Life Sciences, or a related field with experience in computational techniques for drug discovery.
 
 
 </li>
 </ul>
 
 Technical/Functional Skills
 
 
 
 <ul>
 <li>
 Strong understanding of computational techniques relevant to drug discovery and material science.
 </li>
 <li>
 Experience with modeling tools such as Schrodinger (Maestro, Bioluminate, Materials Science), MOE, ICM, Cresset, KNIME, and Pipeline Pilot.
 </li>
 <li>
 Expertise in QSAR/QSPR modeling, cheminformatics, and data science approaches in drug discovery.
 </li>
 <li>
 Proficiency in molecular dynamics simulations, quantum chemistry, shape and electrostatic comparison, homology modeling, docking, and pharmacophore modeling.
 </li>
 <li>
 Familiarity with high-performance computing environments, Linux-based clusters, and GPU systems.
 </li>
 <li>
 Knowledge of Python programming is an advantage.
 
 
 </li>
 </ul>
 
 Experience
 
 
 
 <ul>
 <li>
 1-2 years of experience in drug discovery, medicinal chemistry, or computational modeling.
 </li>
 <li>
 Interest in acquiring knowledge and applying innovative techniques to advance medicinal chemistry and material science projects.
 
 
 </li>
 </ul>
 
 Behavioural Skills
 
 
 
 <ul>
 <li>
 Ability to work in a multidisciplinary team with excellent interpersonal skills.
 </li>
 <li>
 Strong analytical and problem-solving skills with a proactive approach to challenges.
 </li>
 <li>
 Effective communication and presentation skills to convey complex scientific information clearly.
 </li>
 <li>
 Ability to adapt to dynamic project requirements and work independently or collaboratively.
 
 
 </li>
 </ul>
 
 Equal Opportunity Employer
 
 
 
 Syngene is committed to providing equal employment opportunities (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. Additionally, Syngene will provide reasonable accommodations for qualified individuals with disabilities.
</div>

Computational Chemist

<div>
 Date: 2 Sept 2025
 
 
 Location:
 
 
 Bangalore, KA, IN, 560100
 
 
 Custom Field 1: Discovery Services
 
 
 
 Job Title
 
 
 :
 
 Study Director - Pharmacokinetics and Immunogenicity Assays
 
 
 
 Job Location:
 
 Bangalore
 
 
 
 Department:
 
 Translational and Clinical Research
 
 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 industries around the world. Syngene&rsquo; s clientele includes world leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA and Herbalife. Its innovative culture is driven by the passion of its 4240- strong team of scientists who work with clients from around the world to solve their scientific problems, improve R&amp; productivity, speed up time to market and lower the cost of innovation.
 
 Job Purpose:
 
 The position holder is responsible for performing bioanalysis which includes performing ligand binding assays related to Pharmacokinetics and Immunogenicity.
 
 Key Responsibilities:
 
 
 
 <ul>
 <li>
 Ensure activities conducted in the bioanalytical lab are in compliance with established SOPs, procedures, systems, regulatory guidance without deviating from established procedures.
 </li>
 <li>
 Regular interaction and participation with Study director, Quality Control (QC) and Quality Assurance (QA) during raw data and reports review, closure of observations and archival.
 </li>
 <li>
 Will be involved in strategic planning for project execution, documentation of data, data analysis, interpretation and presentation of the results
 </li>
 <li>
 Ensure to complete the assigned tasks in timely manner.
 </li>
 <li>
 Actively involved in preparation of SOPs, protocols, method and reports
 </li>
 <li>
 Prepare reagents, buffers and maintain log book for assigned assays
 </li>
 <li>
 Interpret results &ndash; anticipate and understand the issues related to the assay.
 </li>
 <li>
 Participate in, and present data for discussions.
 </li>
 <li>
 Follow environment, health, and safety (EHS) requirements at all times in the workplace ensuring individual and lab/plant safety.
 </li>
 <li>
 Attend training on environment, health, and safety (EHS) measures imparted companyEducational Qualification:
 </li>
 <li>
 Master&rsquo;s degree in Biological Sciences (Preferably Biochemistry background) or a related fieldTechnical/functional Skills:
 </li>
 <li>
 Should have a strong background in immunoassay and bioanalytical Pharmacokinetics and Immunogenicity Assays with a good understanding as per regulatory guidance/ industry practices/internal Standard Operating Protocols.
 </li>
 <li>
 Should have hands-on experience in Ligand Binding Assay (LBA) development, validation and Sample analysis. Knowledge of ELISA and MSD assays are highly desirable.
 </li>
 <li>
 Knowledge and experience with regulatory requirements e.g. Organization for Economic Co-operation and Development (OECD), GXP, 21 CFR Part 11, European Medicines Agency (EMA) and Food and Drug Administration (FDA) guidelines.
 </li>
 <li>
 Manuscript writing ability is preferable
 </li>
 <li>
 Proficiency in software like Laboratory Information Management System (LIMS), GraphPad, Adobe etc.
 
 
 </li>
 </ul>
 
 Experience
 
 
 
 <ul>
 <li>
 6-9 years of experience in immunoassay laboratory. (CRO experience is preferable).Behavioral Skills:
 </li>
 <li>
 Ability to work independently as well as with team members
 </li>
 <li>
 A strong proactive and independent thinker
 </li>
 <li>
 Excellent communication skills - written and oral in English
 </li>
 <li>
 Should have good interpersonal skills
 </li>
 <li>
 Large degree of flexibility and ability to work under strong time pressureEqual Opportunity Employer:
 
 
 </li>
 </ul>
 It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodation for qualified individuals with disabilities.
</div>

ASSOCIATE SCIENTIST