Quality Control / Analytical Chemist

Join Glochem Industries: Quality Control / Analytical Chemist Role Open in Hyderabad

Are you looking for an exciting opportunity in pharmaceutical quality control? Glochem Industries Pvt Ltd is hiring Quality Control / Analytical Chemists to join our team in Bollaram, Hyderabad. If you have experience in HPLC, GC, FTIR, and UV-Vis Spectrophotometry, this role is perfect for you!

Why Join Glochem Industries?

• Leading Pharmaceutical Company with a strong reputation for quality and innovation.
• Global Compliance Standards including USFDA, EUGMP, TGA, PMDA, and KFDA.
• Career Growth with hands-on training in advanced analytical techniques.
• Competitive Salary: ₹2 to ₹4 LPA.

Job Details

• Company: Glochem Industries Pvt Ltd
• Role: Quality Control / Analytical Chemist
• Department: Quality Control / Analytical Department
• Industry: Pharmaceutical
• Location: Bollaram, Hyderabad
• Salary: ₹2 – ₹4 LPA
• Experience: 1-3 years
• Employment Type: Full-time
• Education: B.Sc/M.Sc/B.Pharm/M.Pharm in Chemistry, Pharmacy, or a related field

Key Responsibilities

1. Analytical Testing & Analysis

• Conduct chemical analysis on raw materials, in-process samples, and finished products.
• Use HPLC, GC, FTIR, and UV-Vis Spectrophotometry to ensure product quality.
• Prepare and standardize volumetric solutions and reagents.
• Interpret analytical results and compare them with established specifications.
• Maintain detailed records following GMP/GLP compliance.

2. Instrument Operation & Maintenance

• Operate and maintain HPLC, GC, FTIR, and UV-Vis Spectrophotometers.
• Perform routine instrument calibration and troubleshooting.
• Maintain proper documentation of instrument usage and maintenance logs.

3. Quality Assurance & Compliance

• Ensure all analytical activities comply with USFDA, EUGMP, TGA, PMDA, KFDA.
• Participate in internal and external audits.
• Investigate and document out-of-specification (OOS) results.
• Adhere to GMP/GLP guidelines and data integrity principles.

4. Documentation & Reporting

• Maintain accurate laboratory notebooks.
• Prepare detailed analytical reports and ensure data traceability.
• Manage and archive analytical data as per company policies.
• Contribute to SOP development and validation of new methods.

Candidate Requirements

Education: B.Sc/M.Sc/B.Pharm/M.Pharm in Chemistry, Pharmacy, or related fields

Experience: 1-3 years in pharmaceutical quality control & analysis

Skills: Expertise in HPLC, GC, FTIR, UV-Vis Spectrophotometry

Regulatory Knowledge: Familiarity with GMP/GLP compliance & global pharma regulations

Software Proficiency: Chromeleon (preferred)

Communication: Strong written and verbal communication skills

Company & Vacancy Overview

How to Apply?

📩 Apply Now: Click here to apply

Tagged as: Global Pharma Jobs, Pharmaceutical Careers, Pharmaceutical Jobs