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We are Hiring for -Senior Research Associate

1.00 to 3.00 Years   Delhi   12 Jun, 2023
Sygene
Job LocationDelhi
EducationNot Mentioned
SalaryNot Disclosed
IndustryPharma / Biotech
Functional AreaBio Tech / R&D / Scientist
EmploymentTypeFull-time

Job Description

    Designation: Senior Research Associate Job Location: Bangalore Department: Formulation Development Pharmaceutical Development About Syngene Syngene International Ltd. (BSE: 539268, NSE: SYNGENE, ISIN: INE398R01022), is an integrated research, development and manufacturing services company serving the global pharmaceutical, biotechnology, nutrition, animal health, consumer goods and specialty chemical sectors. Syngene s 4500+ scientists offer both skills and the 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 dedicated research facilities for Amgen, Baxter, Bristol-Myers Squibb and Herbalife, as well as 1.9 Mn sq ft of specialist discovery, development and manufacturing facilities, Syngene works with biotech companies pursuing leading edge science as well as multinationals including GSK and Merck KGaA. Key Responsibilities:
    • Responsible for pre-formulation studies, lab-scale trial execution, formulation and process development, execution of scale-up batches, stability studies, and GMP manufacturing activities of drug product based on the scope of the projects. Perform literature search for research purposes.
    • Troubleshooting and problem solving for challenges within projects as required.
    • Interact with cross-functional teams for execution of projects as required.
    • Effectively co-ordinate between teams for cross-functional activities as required.
    • Ensure appropriate GDP for projects as per Syngene policy.
    • Compilation and interpretation of results and report writing
    • Documentation of experiments in laboratory notebook and report writing.
    • Compliance and Adherence to all Syngene quality and safety systems
    Educational Qualification: M. Pharm (pharmaceutics) or MS Pharm (pharmaceutics) Experience: 1 - 3 years Technical Skills: Candidate should have very good educational and theoretical background of solid oral dosage form development (tablet/capsules/pellets)Knowledge of solid state characterization and pre-formulation studiesCandidate should have good proficiency for MS-office toolsShould 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.
    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.,

Keyskills :
continuous improvement facilitationnmrliteraturevalidationsolid state characterizationhplcresearch

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