Key Responsibilities:
For QA (Quality Assurance):
- Implement and maintain Quality Management Systems (QMS).
- Conduct internal audits and ensure compliance with GMP, GLP, and regulatory standards.
- Review and approve quality documents, SOPs, and batch records.
- Handle deviations, CAPA, and change control processes.
For QC (Quality Control):
- Perform routine analysis of raw materials, intermediates, and finished products.
- Operate analytical instruments such as HPLC, GC, UV-Vis, FTIR, and others.
- Ensure timely and accurate documentation of test results.
- Conduct stability studies and validate analytical methods.
For RD (Research Development):
- Develop and optimize formulations, processes, or analytical methods for APIs and formulations.
- Perform literature reviews and feasibility studies.
- Support scale-up and technology transfer to manufacturing units.
- Collaborate with cross-functional teams to meet project timelines.
Qualifications:
- Education:MSc in Chemistry (Organic, Inorganic, Integrated, Analytical, Applied, or Pharmaceutical).
- Experience:Freshers are welcome to apply.
Key Skills:
- Strong analytical and problem-solving abilities.
- Knowledge of GMP, GLP, and regulatory requirements for the pharmaceutical industry.
- Proficiency in handling analytical instruments and lab tools.
- Effective communication and documentation skills.
- Ability to work in a fast-paced, collaborative environment.
