QC Officer HPLC | IP/FP | Documentation | 2 To 4 Years

Quality Control Officer | 2-4 Years | Akola

Are you a Quality Control professional looking for your next career opportunity?

At Leben Life Sciences Pvt. Ltd., an EU-GMP approved pharmaceutical formulation company, we are committed to maintaining the highest standards of quality, compliance, and pharmaceutical excellence.

We are looking for experienced Quality Control Officers to join our QC Department at Akola, Maharashtra.

Key Areas of Expertise

1. HPLC Operations

• Hands-on experience in HPLC analysis of Raw Materials, In-Process, Finished Products, Stability, and Hold Time Study samples.
• Perform analysis as per approved STP, specifications, pharmacopoeial methods, and validated analytical procedures.
• Knowledge of HPLC calibration, system suitability, column handling, and routine troubleshooting.
• Review chromatograms, analytical results, and instrument-related records for accuracy and compliance.
• Hands-on experience with UV-Visible Spectrophotometer will be an added advantage.

2. IP-FP

• Perform analysis of In-Process (IP), Finished Products (FP), Raw Materials, Stability, Hold Time Study, and Process Validation samples.
• Experience in rinse and swab sample analysis as per approved procedures.
• Manage receipt, identification, testing, storage, and disposal of IP/FP and Stability samples.
• Ensure accurate recording, review, and reporting of analytical results with a strong focus on data integrity.
• Candidates with OSD (Oral Solid Dosage) experience will be preferred.

3. QC Documentation

• Prepare, review, and maintain SOPs, Specifications, STPs, and TDSs for RM, PM, IP, FP, Stability, Miscellaneous, and Water.
• Maintain accurate QC analytical records, worksheets, logbooks, calibration records, and laboratory documentation.
• Ensure documentation complies with GLP/GMP, data integrity requirements, and applicable regulatory standards.
• Maintain documentation related to instrument calibration, analytical testing, stability studies, and laboratory activities.
• Handle Progen-related QC activities and maintain associated records.

Educational Qualification

M.Sc. / B.Pharm / M.Pharm

Experience

24 years of relevant experience in Pharmaceutical Quality Control

Job Location

Akola, Maharashtra

Candidates should be willing to work in Akola, Maharashtra.

Preferred Candidate Profile

Candidates with an OSD background and hands-on experience in HPLC, IP/FP analysis, Stability, RM analysis, instrument calibration, GLP/GMP, and QC documentation are encouraged to apply.

Naukri Keywords / Search Tags

Quality Control, QC Officer, QC Executive, Pharmaceutical QC, Pharma QC, HPLC Operations, HPLC Analysis, HPLC Calibration, HPLC, UV, GLP, GMP, IP-FP, In-Process, Finished Product, OSD, Oral Solid Dosage, RM Analysis, Raw Material Analysis, Stability Testing, Hold Time Study, Process Validation, Rinse Sample, Swab Sample, Instrument Calibration, QC Documentation, SOP, STP, Specification, TDS, Water Analysis, Pharmacopoeia, IP, BP, USP, Ph. Eur., Progen, Analytical QC, Pharmaceutical Industry, Pharma Formulation, Akola QC.

Interested?

If you are ready to grow with a dynamic pharmaceutical team and contribute to a quality-driven organization, we would love to hear from you!

Send your updated resume to: [email removed]
For queries: [phone removed]