Qc Chemist

**Job Overview**:
As a Quality Control Chemist at Macleods Pharmaceuticals Ltd., you will be responsible for performing various analytical tests to assess the quality of raw materials, intermediates, and finished products according to established procedures and regulatory requirements.

**Key Responsibilities**:
1. Analytical Testing: Conduct routine and non-routine analysis of raw materials, in-process samples, and finished products using techniques such as HPLC (High-Performance Liquid Chromatography), GC (Gas Chromatography), UV-Vis Spectroscopy, FTIR (Fourier Transform Infrared Spectroscopy), and wet chemistry methods.

2. Documentation: Maintain accurate and detailed records of all tests performed, including test results, deviations, and any corrective actions taken. Ensure compliance with Good Documentation Practices (GDP) and Good Laboratory Practices (GLP).

3. Instrument Calibration and Maintenance: Perform calibration, troubleshooting, and maintenance of laboratory instruments and equipment to ensure accurate and reliable results.

4. Method Validation and Verification: Assist in method validation and verification studies for new analytical methods or modified existing methods. Ensure that all methods are validated according to regulatory guidelines.

5. Quality Assurance Support: Collaborate with the Quality Assurance (QA) team to investigate and resolve quality-related issues, deviations, and out-of-specification results. Participate in internal audits and inspections as needed.

6. Compliance: Ensure compliance with applicable regulatory requirements, including but not limited to FDA (Food and Drug Administration), ICH (International Council for Harmonisation), and cGMP (current Good Manufacturing Practice) guidelines.

7. Safety: Adhere to all safety protocols and procedures in the laboratory environment. Identify and report any safety hazards or concerns to the appropriate personnel.

8. Continuous Improvement: Participate in continuous improvement initiatives aimed at enhancing laboratory efficiency, productivity, and quality.

**Qualifications and Skills**:

- Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, or a related field.
- Previous experience in a pharmaceutical QC laboratory preferred.
- Proficiency in analytical techniques such as HPLC, GC, UV-Vis spectroscopy, and wet chemistry methods.
- Strong attention to detail and accuracy in record-keeping.
- Good understanding of regulatory requirements and quality systems.
- Excellent communication and teamwork skills.
- Ability to work independently with mínimal supervision.

**Job Types**: Full-time, Permanent

Pay: ₹25,505.29 - ₹40,572.87 per month

**Benefits**:

- Flexible schedule
- Health insurance
- Provident Fund

Schedule:

- Day shift
- Morning shift
- Night shift

**Education**:

- Bachelor's (preferred)

**Experience**:

- total work: 1 year (preferred)

Work Location: In person

Application Deadline: 30/04/2024
Expected Start Date: 01/05/2024