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Associate Scientist - Pharmaceutical Development

4.00 to 8.00 Years   Kolkata   15 Jun, 2022
Sygene
Job LocationKolkata
EducationNot Mentioned
SalaryNot Disclosed
IndustryPharma / Biotech
Functional AreaGeneral / Other SoftwareBio Tech / R&D / Scientist
EmploymentTypeFull-time

Job Description

    Designation: Associate Scientist Job Location: Bangalore Department: 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. Role Purpose: Responsible for pre-formulation and formulation development, stability studies, scale-up and GMP manufacturing of drug product based on the scope of projects. Expertise expected in terms of complex generic or NCE products which includes but not limited to microspheres/ nanoemulsion/ liposomes. Primary Responsibilities: Project Planning
    • Independently ensuring planning and availability of resources for seamless execution of projects.
    • Manage project related supplies of API, raw materials and packaging components as required.
    • Discussing with clients and aligning to requirements of project proposal.
    Project Execution and management (Expertise expected in terms of complex generic or NCE products which includes but not limited to microspheres/ nanoemulsion/ liposomes)
    • Conduct literature search for research purposes
    • Execute projects related to pre-formulation, formulation, and process development, scale up, Technology transfer and cGMP manufacturing of clinical supplies.
    • Plan and execute stability studies and stability protocol preparation
    • Ensure seamless execution of projects as per committed timelines.
    • Troubleshooting and problem solving for challenges within projects
    • Interact with cross functional teams for execution of projects.
    • Effectively co-ordination between teams for cross functional activities.
    Documentation
    • Ensure appropriate documentation for projects as per Syngene policy.
    • Compilation and interpretation of results and report writing
    • Manage laboratory notebook for all concerned projects. Compile and manage data and write protocols, reports as required.
    • Preparation and review of Master formula records, Batch manufacturing records and Batch packaging records for execution of GMP batches.
    Quality Compliance Compliance and Adherence to all Syngene quality systems EHS Compliance Compliance to Syngene EHS policies and systems Secondary Responsibilities:
    • Support for preparation of SOPs, EOPs, IOPs.
    • Support for client visits and audits.
    Educational Qualification : M Pharma Experience: 4 - 8 years 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 :
data managementanimal healthprotocolsvalidationsopequal employment opportunitydocumentation

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