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Senior Research Associate-Cdmo

3-6 years
Not Disclosed
10 Jan. 27, 2025
Job Description
Job Type: Full Time Education: B.Sc, M.Sc, B.Pharm, M.Pharm, LifeScience Graduates Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Senior Research Associate - CDMO
Location: Greater Noida, India
Business Unit: R&D
Function: R&D
Level: A4

Company Overview:

Jubilant Ingrevia is a leading global pharmaceutical and life sciences company, actively involved in Pharmaceuticals, Life Science Ingredients, and other sectors such as Drug Discovery Solutions. With a presence in over 100 countries, Jubilant Ingrevia has established itself as a trusted partner to leading pharmaceutical, agrochemical, and life sciences companies.

We are committed to achieving global leadership in our chosen business segments, continuously innovating, and providing cost-effective solutions to our customers. The company is recognized as a "Partner of Choice" for the world's top pharmaceutical and agrochemical companies.


Job Description:

Purpose of the Job:

The Senior Research Associate in CDMO will be responsible for synthesizing Active Pharmaceutical Ingredients (APIs) for new product development. This includes developing synthetic routes while adhering to patent and regulatory guidelines. The role focuses on creating innovative and efficient processes to support the commercialization of pharmaceutical products.

Key Accountabilities:

  • Synthetic Scheme Development: Develop synthetic routes for APIs by exploring non-infringing methods.
  • Literature Research: Conduct literature searches using various search engines and databases to gather relevant information on synthetic methodologies.
  • Chemical Synthesis: Carry out the chemical synthesis of APIs according to the developed routes.
  • Technology Transfer Documentation (TTD): Prepare TTD for successful scale-up and commercialization of developed processes.
  • Scale-Up & Commercialization: Lead the scale-up process and ensure the successful transfer of laboratory-scale processes to production.

Key Interfaces:

  • Internal Interfaces: Work closely with other R&D teams, process chemistry teams, and manufacturing departments to ensure smooth project progression and alignment with organizational goals.
  • External Interfaces: Collaborate with external vendors, contract manufacturing organizations, and clients, as needed, to support development and commercialization efforts.

Education & Experience:

  • Educational Qualification: Ph.D. or M.Sc. in Organic Chemistry.
  • Experience: 3-6 years of relevant experience in organic synthesis and process development, particularly in API development.
  • Desired Certifications: Not specified, but certifications in Process Chemistry, Synthetic Chemistry, or related fields are a plus.

Skills Required:

  • Functional Skills:
    • In-depth knowledge of process chemistry, including synthetic methodologies for API production.
    • Strong background in organic chemistry, with a focus on developing non-infringing synthetic routes for APIs.
    • Experience with developing and handling impurities in chemical synthesis.
    • Ability to scale up processes and develop Technology Transfer Documents (TTD).
  • Behavioral Skills:
    • Strong communication skills, both verbal and written.
    • Excellent problem-solving skills and ability to troubleshoot challenges during synthesis and scale-up.
    • Ability to work effectively in a team-oriented environment and collaborate across functions.
    • Strong attention to detail and a commitment to safety and quality standards.

Desired Experience:

  • 3-6 years of experience in pharmaceutical research and development, with a focus on API synthesis and scale-up processes.

Why Join Us?
At Jubilant Ingrevia, we foster a collaborative and innovative work environment. As part of a global team, you will have the opportunity to work on cutting-edge projects and make a tangible impact on the future of the pharmaceutical and life sciences industries.

If you are passionate about process chemistry and ready to contribute to the development of new pharmaceutical products, we would love to hear from you!

To know more about us, please visit:
www.jubilantingrevia.com


This is a Senior Research Associate - CDMO position based in Greater Noida, offering a dynamic role with opportunities for career growth in a global organization.