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Senior Research Associate Pharmaceutical Development

0.00 to 10.00 Years   Bangalore, Karnataka   07 Jun, 2024
Syngene International
Job LocationBangalore, Karnataka
EducationNot Mentioned
SalaryNot mentioned
IndustryNot mentioned
Functional AreaNot Mentioned
EmploymentTypeFull-time

Job Description

JOB DESCRIPTIONDesignation: Senior Research AssociateJob Location: BangaloreDepartment: Pharmaceutical DevelopmentAbout SyngeneSyngene 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. Syngenes 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.Primary Responsibilities:Project Planning

  • Ensure proper planning and availability of resources for seamless execution of projects.
  • Manage project related supplies of API, raw materials and packaging components as required.
  • Discuss with cross functional teams for project related activities
Project Execution and management
  • Conduct literature search for research purposes
  • Execute projects related to pre-formulation, formulation and process development, scale up, Technology transfer and cGMP manufacturing of oral solid products.
  • 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.
  • Execute GMP activities for manual filling of drug in capsule (Dic) and drug in bottle projects.
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 ComplianceCompliance and Adherence to all Syngene quality systemsEHS ComplianceCompliance to Syngene EHS policies and systemsEducational Qualification: M PharmaExperience: 1 - 3 yearsEqual 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. Syngene International

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