Qureos Mentor

Syngene International Limited

<div>
 Date: 10 Oct 2025
 
 
 Location:
 
 
 Bangalore, KA, IN, 560099
 
 
 Division: Discovery Services
 
 
 
 Job Title: Invivo Pharmacology Scientist
 
 
 
 
 Job Location: Bangalore
 
 
 
 
 JOB PURPOSE (Briefly Describe The Objectives Of The Job)
 
 
 
 Responsible for executing the assigned in vivo efficacy studies in metabolic disorder therapeutic area.
 
 
 
 Key Responsibilities
 
 
 
 <ul>
 <li>
 Responsible to conduct assigned research projects including experiments with utilizing current concepts and recognized standard techniques.
 </li>
 <li>
 Responsible to set up the experimental designs, analysis of data and concluding from the progress.
 </li>
 <li>
 Record laboratory observations information in lab notebooks, database and document the experimental designs.
 </li>
 <li>
 Responsible for data analysis, perform calculations for the result of the experiment.
 </li>
 <li>
 Summarize the research and communicate result of research to the supervisor.
 
 
 </li>
 </ul>
 
 Educational Qualification
 
 
 
 <ul>
 <li>
 M.Pharm Pharmacology
 </li>
 <li>
 M.V.Sc Pharmacology / Pathology
 </li>
 <li>
 M.Sc Neuroscience / Biochemistry / Biotechnology
 
 
 </li>
 </ul>
 
 Work Experience
 
 
 
 0 - 6 years of Industrial experience
 
 
 
 Technical /Functional Skills
 
 
 
 <ul>
 <li>
 Hands-on experience in execution of CNS disease models which includes psychiatric disorders such as anxiety, depression, PTSD etc., and neurological conditions like Alzheimer&rsquo;s disease, Parkinson&rsquo;s disease, cerebral ischemia and epilepsy.
 </li>
 <li>
 Hands-on experience in animal behavioral observation, quantification of animal behavior, experience in stereotaxic surgery, microdialysis, cannulation techniques, immunohistochemistry and ELISA.
 </li>
 <li>
 Will work independently or in association with senior scientists and other associates in the design and execution of in-vivo efficacy experiments in the relevant therapeutic area.
 </li>
 <li>
 Experience in animals handling (rodents and non rodents) such as dosing by various routes, bleeding by various routes, injections by various routes and surgical modalities which includes cannulation etc&hellip;
 </li>
 <li>
 Associate to provide technical, analysis and reporting outcomes of research for projects in relevant therapeutic area.
 </li>
 <li>
 Organizational skills and the ability to work in a highly collaborative environment are required.
 
 
 </li>
 </ul>
 
 Behavioral/Managerial Skills
 
 
 
 <ul>
 <li>
 Good communication skills
 </li>
 <li>
 Excellent interpersonal skills.
 </li>
 <li>
 Good team player
 </li>
 <li>
 Strong documentation Skills.
 
 
 </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>

in vivo pharmacologist

<div>
 Date: 14 Oct 2025
 
 
 Location:
 
 
 Bangalore, KA, IN, 560099
 
 
 Division: Dedicated Centre
 
 
 
 Job Description
 
 
 
 Designation: Research Scientist (7-I)
 
 
 Job Location: Bangalore
 
 
 Department: BBRC PD ARD &ndash; GMP
 
 
 
 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- a 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 (1-2 Lines): Analytical Research and Development working on Analytical GMP testing (AGT), and Syngene BMS Laboratory (SBL) stability programs
 
 
 
 Key Responsibilities
 
 
 
 <ul>
 <li>
 Routine testing of stability samples using chromatographic, dissolution, and wet analytical techniques under a GMP environment following all cGMP practices
 </li>
 <li>
 Performing instrument calibration, method validation, and method transfers
 </li>
 <li>
 Interpretation of stability data and results trending
 </li>
 <li>
 Investigation of OOS/OOT and other laboratory events
 </li>
 <li>
 Preparing the Standard Operating Procedure
 </li>
 <li>
 Preparing stability summary reports and review of final documents
 </li>
 <li>
 Compliance &amp; implementation of quality systems
 </li>
 <li>
 Follow environment, health, and safety (EHS) requirements at all times in the workplace ensuring individual and lab/plant safety
 </li>
 <li>
 Responsible for the activities assigned within the team
 </li>
 <li>
 Deliver analytical results within the established windows and as per applicable guidelines
 </li>
 <li>
 Escalation of issues / non-conformity with applicable procedures/policies
 </li>
 <li>
 Electronic lab notebook documentation
 </li>
 <li>
 Troubleshooting HPLC and dissolution apparatus
 </li>
 <li>
 Miscellaneous lab responsibilities
 
 
 </li>
 </ul>
 Educational Qualifications: M.Sc. Chemistry or M. Pharm
 
 
 
 Technical/Functional Skills
 
 
 
 <ul>
 <li>
 The candidate should have a good educational and theoretical, analytical chemistry background
 </li>
 <li>
 Good knowledge of analytical techniques
 </li>
 <li>
 The candidate should understand instrument calibration, method validation, and routine analysis
 </li>
 <li>
 Good understanding of documentation as per GxP requirements (electronic notebook)
 </li>
 <li>
 The candidate should have good proficiency in MS office tools
 </li>
 <li>
 Experience in stability samples testing and good knowledge of ICH guidelines &amp; cGMP regulatory requirements
 </li>
 <li>
 Must have worked in a cGMP-regulated environment, exposure to regulatory inspections like US FDA, MHRA, etc. is must
 
 
 </li>
 </ul>
 
 Experience:
 
 12-15 years with M.Sc. or 9-11 years with M. Pharm for 7-I
 
 
 
 Behavioral Skills
 
 
 
 <ul>
 <li>
 Strong commitment toward work and a high level of dedication, enthusiasm, and motivation
 </li>
 <li>
 Good speaking-listening-writing skills, attention to detail, proactive self-starter
 </li>
 <li>
 Ability to work successfully in a dynamic environment
 </li>
 <li>
 Should be able to work in a team and flexible for working in shifts.
 </li>
 <li>
 Ability to meet tight deadlines and prioritize workloads.
 
 
 </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>

Research Scientist

<div>
 Date: 14 Oct 2025
 
 
 Location:
 
 
 IN
 
 
 Division: Discovery Services
 
 
 
 Job Title: Junior Analytical Development Scientist - OSD
 
 
 
 
 Job Location: Bengaluru
 
 
 
 
 Department: DPA &ndash; FD
 
 
 
 
 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>
 Analytical development supporting Formulation development
 </li>
 <li>
 Routine analysis of samples
 </li>
 <li>
 Method development
 </li>
 <li>
 Instrument calibrations
 </li>
 <li>
 Documentation
 </li>
 <li>
 Report preparation
 </li>
 <li>
 Miscellaneous lab responsibilities
 
 
 </li>
 </ul>
 
 Role Accountabilities
 
 
 
 <ul>
 <li>
 Candidate should have very good educational and theoretical background.
 </li>
 <li>
 Candidate should have knowledge of calibration, method development and troubleshooting using various instruments like KF auto titrator, dissolution (I, II &amp; IV), spectroscopic instruments e.g. UV spectrometer, IR and Chromatographic instruments e.g. HPLC, GC
 </li>
 <li>
 Knowledge of various regulatory guidelines w.r.t. method development, product development and documentation
 </li>
 <li>
 Knowledge of method development for oral dosage forms w.r.t. tests like assay, degradation products, dissolutions, blend uniformity, content uniformity, cleaning method, etc.
 </li>
 <li>
 Knowledge of specification setting for oral dosage forms, in-process specifications as well as product specifications
 </li>
 <li>
 Knowledge and operating of instruments like LC-MS, GC-MS will be added advantage
 </li>
 <li>
 Good understanding of Documentation as per GxP requirements
 </li>
 <li>
 Online Lab notebook writing
 </li>
 <li>
 Method development report preparation &ndash; Assay, Degradation products, Dissolution, cleaning method, etc.
 </li>
 <li>
 Method of Analysis, Test report, SOP preparation
 </li>
 <li>
 Calibration documentation
 </li>
 <li>
 Review of documents generated by peers or juniors
 </li>
 <li>
 Should be able to search scientific literature on-line
 </li>
 <li>
 Should be a team player and able to coach juniors technically
 
 
 </li>
 </ul>
 
 Syngene Values
 
 
 
 All employees will consistently demonstrate alignment with our core values
 
 
 Excellence
 
 
 Integrity
 
 
 Professionalism
 
 
 
 Experience:
 
 More than 5 years up to 8 years
 
 
 
 Skills And Capabilities
 
 
 
 Candidate should have good proficiency for MS-office tools
 
 
 Should be able to search scientific literature on-line
 
 
 
 Behavioral Skills
 
 
 
 Strong commitment towards work, and a high level of dedication, enthusiasm, motivation, and persuasive ability in a team.
 
 
 Good speaking-listening-writing skills, attention to details, proactive self-starter.
 
 
 Ability to work successfully in a dynamic, ambiguous environment.
 
 
 Ability to meet tight deadlines and prioritize workloads.
 
 
 Ability to develop new ideas and creative solutions.
 
 
 Should be able to work in team and flexible for working in shifts.
 
 
 Should be a focused employee.
 
 
 
 Education:
 
 M.Pharm / M.Sc
 
 
 
 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>

Junior Analytical Development Scientist - OSD

<div>
 Date: 29 Sept 2025
 
 
 Location:
 
 
 Kolthur Shamirpet, Medchal, TG, IN, 500078
 
 
 Division: Discovery Services
 
 
 
 Job Description
 
 
 
 Job title: Associate Scientist
 
 
 Job location: Hyderabad
 
 
 Job grade: 8-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 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 ensure 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>
 Personnel handling this profile will be responsible for conducting reactions and delivering final compounds within a fast turnaround time, meeting the specific requirements of both the project and Syngene. The candidate should be capable of independently designing the synthetic scheme for any target and solve chemistry problems. He or she should ensure that the experimental observations are recorded contemporaneously and in compliance with the Electronic Laboratory Notebook (ELN) policies of the project and Syngene.
 
 
 </li>
 </ul>
 
 Role Accountabilities
 
 
 
 <ul>
 <li>
 Expected to design a synthetic scheme for any given target and to be proactive in identifying rate limiting steps along with the mitigation strategy.
 </li>
 <li>
 The candidate should be well versed in using literature search engines and predictive synthesis tools
 </li>
 <li>
 Perform synthetic chemistry reactions, reaction workups, purification of the compounds by column chromatography, crystallization, re-crystallization techniques, preparative TLC and operating lab equipment&rsquo;s&rsquo;
 </li>
 <li>
 Ensure that the samples generated during synthesis are given for analysis and record subsequent results obtained and update the supervisor / group leader on the progress of synthesis and ensure samples are packed appropriately for shipment
 </li>
 <li>
 Record the observations of experiment/reaction, results, utilization of resources and other activities related to the reaction in the laboratory or e-notebook following guidelines and in timely manner and ensure that the same is handled safely and confidentially.
 </li>
 <li>
 The candidate should be capable of meeting Syngene&rsquo;s productivity expectations (# of compounds/month, # of steps/month and productivity index of around 1.5) without compromising on safety and quality.
 </li>
 <li>
 The candidate should be capable of synthesizing the final compounds at a faster turnaround time.
 </li>
 <li>
 The candidate should have excellent analytical interpretation and purification skills.
 </li>
 <li>
 Ensure that they know the SDS of the chemicals they are handling and aware of emergency response procedures in case of accidental spillage, leakage or fire and ensure proper waste segregation as per EHS norms.
 </li>
 <li>
 Always follow EHS and quality system requirements in the workplace ensuring individual safety and lab safety.
 </li>
 <li>
 Attend all mandatory trainings and update training records as and when trainings are completed.
 </li>
 <li>
 Always ensure confidentiality.
 
 
 </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>
 Specific requirements for this role
 
 
 
 Experience
 
 
 
 <ul>
 <li>
 8-10 years.
 
 
 </li>
 </ul>
 
 Skills And Capabilities
 
 
 
 <ul>
 <li>
 Should have deeper knowledge with concepts of organic synthesis and reaction mechanisms.
 </li>
 <li>
 Should be capable of designing synthetic schemes and troubleshooting synthesis problems independently.
 </li>
 <li>
 Should be excellent in purification and analytical interpretation skills.
 </li>
 <li>
 Familiar with operations of relevant apparatus - instrument / equipment.
 
 
 </li>
 </ul>
 Education
 
 
 <ul>
 <li>
 M.Sc in general or organic chemistry.
 </li>
 </ul>
</div>

Associate Scientist

Join Syngene International Limited and explore 4   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

Syngene International Limited

ABOUT_COMPANY

in vivo pharmacologist

Research Scientist

Junior Analytical Development Scientist - OSD

Associate Scientist