Quality Control Analyst

Company Description

Iosis Remedies Pvt. Ltd. is a WHO-GMP compliant pharmaceutical manufacturing company located in Baddi, Himachal Pradesh.

We manufacture:

• Solid Oral dosage forms (Tablets, Capsules)
• Liquid Oral dosage forms (Syrups, Suspensions)
• Topical Products (Ointments, Creams)

Our operations focus on quality, compliance, and reliable healthcare delivery.

Role Description

This is a full-time, on-site role for a Quality Control Analyst located in Baddi.

The QC Analyst will be responsible for:

• Testing and analyzing raw materials, in process bulk, finished products, and stability samples
• Operating and maintaining HPLC (preferably Shimadzu/Agilent) and GC (preferably Shimadzu)
• Conducting assay, dissolution, related substances, content uniformity, and other pharmacopoeial tests
• Performing instrument calibration and maintaining logbooks/data integrity
• Documenting results in alignment with GLP, GDP, cGMP, and ALCOA+ principles
• Collaborating with Quality Assurance during deviations, OOS/OOT investigations, and method transfers

• Willingness to work in night shift or rotational shifts is required.

Qualifications

• B.Sc Chemistry / B.Pharm (M.Sc Chemistry is an advantage)
• Minimum 2 years QC laboratory experience in a pharmaceutical formulation plant
• Hands-on experience with HPLC and GC instrumentation
• Strong analytical skills, documentation discipline, and attention to detail
• Understanding of IP/USP/BP/EP methods and regulatory standards

Preferred Skills

• Experience with chromatography software (LabSolutions / Empower / OpenLab / Chromeleon)
• Exposure to

  stability testing, method validation, and audit environments

How to Apply

• Apply Directly via Linkedin or mail your resume on hrd@iosisremedies.com