Qureos Mentor

Syngene International Limited

<div>
 Date: 23 Dec 2025
 
 
 Location:
 
 
 Bangalore, KA, IN, 560099
 
 
 Division: Dedicated Centre
 
 
 
 Job Title:
 
 Process Development Scientist-ADC
 
 
 
 Job Location:
 
 Bengaluru
 
 
 
 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>
 </ul>
 
 Core Purpose Of The Role
 
 
 
 Personnel handling this profile will be responsible for performing reactions as per the requirement of the project. They are also responsible for documenting the observations in relevant notebooks. They are to follow instructions from the supervisor and work in a group (or individually) to accomplish the tasks in a timely and efficient manner.
 
 
 
 Key Responsibilities
 
 
 
 <ul>
 <li>
 Perform chemical reactions for the process development of Antibody Drug Conjugates (ADC) that connect an antibody with a potent drug (payload) through a chemical bond in HPAPI facility or in ADC lab. Thereby, suitable prior experience is highly desirable.
 </li>
 <li>
 The selected candidate would handle highly potent active pharmaceutical ingredients (HPAPIs) and cytotoxic compounds.
 </li>
 <li>
 Perform synthetic chemistry reactions, reaction work-ups, purification of the compounds by column chromatography, crystallization, re-crystallization techniques, preparative TLC and operating lab instruments.
 </li>
 <li>
 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 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>
 Ensure that the instrument / equipment are calibrated, undergone preventive maintenance and are kept clean before use and in case of any breakdown, report to maintenance immediately.
 </li>
 <li>
 Ensure that they know the MSDS 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>
 Follow EHS and quality system requirements at all times 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>
 Ensure confidentiality at all times.
 
 
 </li>
 </ul>
 
 Syngene Values:
 
 Follow safety and data integrity guideline.
 
 
 All employees will consistently demonstrate alignment with our core values:
 
 
 <ul>
 <li>
 Excellence
 </li>
 <li>
 Integrity
 </li>
 <li>
 Professionalism
 
 
 </li>
 </ul>
 
 Education:
 
 M.Sc with hands on experience in process chemist in an industry setting
 
 
 
 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>

Process development Scientist-ADC

<div>
 Date: 2 Dec 2025
 
 
 Location:
 
 
 Bangalore, KA, IN, 560099
 
 
 Division: Discovery Services
 
 
 
 Job Title: In Vivo PK scientist
 
 
 
 
 Job Location: Bengaluru
 
 
 
 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:
 
 Conduct of
 
 in vivo
 
 pharmacokinetics study in rodents
 
 
 
 Education:
 
 M. Pharm /PHD (Pharmacology &amp; Toxicology) with an expert in conducting the studies in an industry setting
 
 
 
 Role Accountabilities
 
 
 
 <ul>
 <li>
 Conduct of pharmacokinetic studies in rodents.
 </li>
 <li>
 Documenting the lab notebooks online and compound management.
 </li>
 <li>
 Ability to adapt to the dynamic team environment.
 </li>
 <li>
 Possess the knowledge and exposure to environment, health, and safety (EHS) practices
 </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>
 
 Syngene Values
 
 
 
 All employees will consistently demonstrate alignment with our core values
 
 
 <ul>
 <li>
 Excellence
 </li>
 <li>
 Integrity
 </li>
 <li>
 Professionalism
 
 
 </li>
 </ul>
 
 Skills And Capabilities
 
 
 
 <ul>
 <li>
 Well versed with surgical procedures like cannulation of jugular, femoral, portal vein in rats. Chronic bile duct cannulations in rat and various animal models used for in vivo pharmacokinetics studies.
 </li>
 <li>
 Collection of different vital organs during tissue distribution studies in rodents
 </li>
 <li>
 Pharmacokinetic data analysis using Phoenix WinNonlin and other data analysis tool.
 </li>
 <li>
 Collection of various biological fluids like cerebrospinal fluid, bile, urine, synovial fluid lavage during PK and tissue distribution studies in rodents.
 </li>
 <li>
 Should have preliminary understanding about formulations to be used for pharmacokinetics, efficacy and toxicity studies.
 </li>
 <li>
 Knowledge about regulatory guidelines followed for drug metabolism and pharmacokinetics is desirable.
 
 
 </li>
 </ul>
 
 Behavioral Skills
 
 
 
 <ul>
 <li>
 Ready to take new challenges, committed to work and timelines
 </li>
 <li>
 Should have learning attitude, enthusiastic and hard working
 </li>
 <li>
 Good in communication skills
 </li>
 <li>
 Good work ethics.
 </li>
 <li>
 Good interpersonal skills, and the ability to work effectively in a team environment.
 </li>
 <li>
 Ability to work with co&hyphen;workers professionally.
 </li>
 <li>
 General ability to thrive in a growing infrastructure and culture and also think out of box approach when troubleshooting and problem solving.
 
 
 </li>
 </ul>
 
 Equal Opportunity Employer
 
 
 
 <ul>
 <li>
 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.
 </li>
 </ul>
</div>

Invivo PK Scientist

<div>
 Date: 18 Dec 2025
 
 
 Location:
 
 
 Bangalore, KA, IN, 560099
 
 
 Division: Development Services
 
 
 
 Job Description
 
 
 
 Designation: Formulation Scientist
 
 
 Job Location: Bangalore
 
 
 The Company
 
 
 Syngene International Ltd. (BSE: 539268, NSE: SYNGENE, ISIN: INE398R01022), is an integrated research, development, and manufacturing solutions company serving the global pharmaceutical, biotechnology, nutrition, animal health, consumer goods, and specialty chemical sectors. Syngene&rsquo;s 4500+ scientists offer both the skills and capacity to deliver great science, robust data management and IP security, and quality manufacturing at speed, to improve time-to-market and lower the cost of innovation. With a combination of 1.9 Mn sq ft of specialist discovery, development and manufacturing facilities, as well as dedicated research facilities for Amgen, Baxter, Bristol-Myers Squibb and Herbalife, Syngene works with biotech companies pursuing leading edge science as well as multinationals including GSK and Merck KGaA.
 
 
 Key Result Areas
 
 
 
 Role-specific
 
 
 
 
 Functional Responsibilities:
 
 
 
 <ul>
 <li>
 Design and develop parenteral formulations for complex biologics
 </li>
 <li>
 Execute pre-formulation studies of biologics through rational design principles including structure function assessment, buffer/excipient/stabilizer screening, etc.
 </li>
 <li>
 Plan and execute drug substance/product stability studies, analyze data trend and support assessment of degradation kinetics and assign shelf-life.
 </li>
 <li>
 Author protocols, technical reports and communicate studies outcome to cross-functional groups.
 
 
 </li>
 </ul>
 
 Primary Responsibilities
 
 
 
 <ul>
 <li>
 Should have a strong background in Biologics Parenteral Formulation development including solid and liquid dosage forms
 </li>
 <li>
 Experience in both early and late formulation development of mAbs and fusion proteins
 </li>
 <li>
 Good knowledge on Formulation and Process characterization studies
 </li>
 <li>
 Experienced in handling instruments like Density meter / Osmometer / Viscometer / Turbidity meter / UV Spectrophotometer / HPLC systems
 </li>
 <li>
 Ability to learn quickly, enthusiastic, sincere, positive attitude, hardworking
 </li>
 <li>
 Should have positive temperament, rational/logical thinking and enthusiasm to deliver on time, hardworking and committed.
 </li>
 <li>
 Basic understanding of statistics, DoE and data visualization
 </li>
 <li>
 Should be experienced/demonstrated formulation and process characterization.
 </li>
 <li>
 Authoring Technical documents like PDR, Tech transfer, study reports etc.
 
 
 </li>
 </ul>
 
 Education
 
 
 
 <ul>
 <li>
 M.Pharm or M.Sc. in Life Science/Biotechnology/ Bioprocess Engineering/ Pharmaceuticals/Biopharmaceuticals/ Biopharmaceutical Technology/ Biochemistry or equivalent degree.
 
 
 </li>
 </ul>
 
 Industry Experience
 
 
 
 <ul>
 <li>
 Minimum 6-9 years of relevant practical experience in formulation development for biopharmaceuticals, specifically with mAbs, Proteins and peptides.
 
 
 </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.
 
 
 Pls visit us at https://syngeneintl.com/ to know more about us and what we do.
</div>

Formulation Scientist

<div>
 Date: 23 Dec 2025
 
 
 Location:
 
 
 Bangalore, KA, IN, 560099
 
 
 Division: Dedicated Centre
 
 
 
 Job Description
 
 
 
 Designation: Associate Scientist (8-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>
 Troubleshooting HPLC and dissolution apparatus
 </li>
 <li>
 Interpretation of stability data and results trending
 </li>
 <li>
 Investigation of OOS/OOT and other laboratory events
 </li>
 <li>
 Deliver analytical results within the established windows and as per applicable guidelines
 </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>
 Electronic lab notebook documentation
 </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 preferred
 
 
 </li>
 </ul>
 
 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>

Associate Scientist

<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