Job Summary:
VIOBILITY Research Private Limited is a qualified and detail-oriented HPLC Analyst to join our Quality Control laboratory. The candidate will be responsible for performing HPLC analysis of pharmaceutical products and water samples, along with assay and dissolution testing to ensure product quality and compliance with regulatory standards. The role involves sample preparation, chromatographic analysis, data interpretation, and maintaining laboratory documentation as per GMP/GLP guidelines.
Key Responsibilities:
- Perform HPLC analysis for raw materials, finished products, and water samples.
- Conduct assay and dissolution testing according to approved analytical methods.
- Prepare samples, standards, reagents, and mobile phases for analysis.
- Analyze chromatographic data and prepare test reports.
- Ensure proper operation, calibration, and maintenance of HPLC instruments.
- Maintain laboratory documentation and records in compliance with GMP/GLP standards.
- Assist in method validation, method transfer, and troubleshooting of analytical methods.
- Follow laboratory safety procedures and quality control protocols.
Qualifications:
- B.Sc / M.Sc in Chemistry, Pharmaceutical Sciences, or related field.
- 1–5 years of experience in HPLC analysis in a pharmaceutical or analytical laboratory.
- Hands-on experience in assay, dissolution testing, and HPLC analysis of waters.
Required Skills:
- Strong knowledge of HPLC operation and chromatographic techniques
- Experience with assay and dissolution testing procedures
- Knowledge of GMP / GLP documentation practices
- Good analytical, problem-solving, and reporting skills
- Attention to detail and ability to work in a laboratory environment
Salary:
Salary will be commensurate with experience and interview performance.
Job Types: Full-time, Permanent
Benefits:
Work Location: In person
