Are you a skilled professional looking for a career in the pharmaceutical industry? Cadila Pharmaceuticals Ltd, a leading name in the pharmaceutical sector, is hiring for the position of Quality Control Analyst in Ankleshwar, India. This is an excellent opportunity for individuals passionate about quality assurance, laboratory analysis, and compliance with global standards. Read on to learn more about the job role, responsibilities, and how to apply.
Job Overview
Job Title: Quality Control Analyst
Location: Ankleshwar, India
Company: Cadila Pharmaceuticals Ltd
Key Responsibilities
As a Quality Control Analyst at Cadila Pharmaceuticals Ltd, you will play a crucial role in ensuring the quality and safety of pharmaceutical products. Your primary responsibilities will include:
- Adherence to GLP and Safety Procedures: Maintain compliance with Good Laboratory Practices (GLP) and safety protocols in the laboratory.
- Laboratory Analysis: Perform analysis of raw materials, packing materials, intermediates, APIs, and stability samples as per current specifications and methods.
- CFR 21 Part 11 Compliance: Ensure compliance with CFR 21 Part 11 regulations by following established procedures.
- HPLC Analysis: Conduct HPLC-related analysis for in-process, intermediate, finished products, and returned goods. Perform online documentation and report analysis data in LIMS modules.
- Calibration of Instruments: Perform calibration of laboratory instruments as per schedule and SOPs, ensuring proper documentation and updating of calibration status.
- Quality Incident Management: Report and investigate QI/NQI/OOS/OOT, deviations, and discrepancies in laboratory analysis.
- Data Integrity: Maintain data integrity by ensuring all entries and results align with current specifications and STPs.
- Stability Studies: Prepare stability protocols, perform stability sample analysis, and monitor temperature and humidity conditions in the laboratory.
- Training and Development: Acquire training to stay updated with cGMP systems and technical knowledge.
- Coordination: Collaborate with store departments for urgent raw material analysis and work closely with AR laboratory personnel during analytical method transfers.
Skills and Qualifications
To excel in this role, candidates should possess the following:
- A degree in Pharmacy, Chemistry, or a related field.
- Strong knowledge of GLP, cGMP, and CFR 21 Part 11 compliance.
- Proficiency in HPLC analysis and laboratory instrumentation.
- Attention to detail and strong analytical skills.
- Ability to maintain accurate documentation and ensure data integrity.
- Excellent communication and teamwork skills.
Why Join Cadila Pharmaceuticals Ltd?
Cadila Pharmaceuticals Ltd is a trusted name in the pharmaceutical industry, known for its commitment to quality and innovation. By joining the team, you will:
- Work in a state-of-the-art laboratory environment.
- Gain exposure to global compliance standards and advanced analytical techniques.
- Be part of a dynamic team dedicated to improving healthcare outcomes.
- Enjoy opportunities for professional growth and development.
