Cadila Pharmaceuticals Ltd, a leading name in the pharmaceutical industry, is hiring for the position of Research Associate in Dholka, India. This is an excellent opportunity for professionals in the Research & Development (R&D) sector to join a dynamic team and contribute to innovative pharmaceutical solutions. If you are passionate about formulation development, regulatory compliance, and cutting-edge research, this role is tailored for you.
Job Overview
Job Title: Research Associate
Location: Dholka, India
Category: Research & Development Jobs
Company: Cadila Pharmaceuticals Ltd
Job Code: 18001555
Brand: Research & Development
Key Responsibilities
As a Research Associate at Cadila Pharmaceuticals Ltd, your primary responsibilities will include:
- BOM Preparation: Prepare Bill of Materials (BOM) for new UID activities related to the costing of New Product Developments (NPDs).
- Formulation Development: Ensure timely development and delivery of assigned formulations and projects within agreed timelines and budgets.
- Documentation: Complete document preparation and formulation activities to support pre-clinical, clinical supplies, technology transfer, and exhibit batch manufacturing.
- Regulatory Compliance: Develop non-infringing strategies for novel formulations in compliance with regulatory requirements for US, EU, and ROW markets.
- Lab Activities: Maintain lab notebooks, compile stability data, and track project progress.
- Specification Preparation: Prepare and request specifications for raw materials, packaging materials, in-process controls, and finished products.
- Document Review: Prepare and review documents for exhibit/commercial batches, including master formula cards, product specifications, development reports, and technology transfer dockets.
- Coordination: Collaborate with support functional teams to ensure timely project delivery.
- Equipment Management: Identify product/process-specific equipment and machinery, and maintain records of usage and maintenance.
- Compliance: Ensure adherence to SOPs, Good Laboratory Practices (GLP), and Good Documentation Practices (GDP) in product development.
Qualifications and Skills
- A degree in Pharmacy, Chemistry, or a related field.
- Proven experience in pharmaceutical formulation development and R&D.
- Strong understanding of regulatory requirements for US, EU, and ROW markets.
- Proficiency in documentation and compliance with GLP and GDP.
- Excellent analytical, organizational, and communication skills.
- Ability to work collaboratively in a team-oriented environment.
Why Join Cadila Pharmaceuticals Ltd?
Cadila Pharmaceuticals Ltd is a pioneer in the pharmaceutical industry, known for its commitment to innovation, quality, and patient care. By joining the R&D team, you will be part of a forward-thinking organization that values creativity, professional growth, and cutting-edge research.
