Job Title

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 standardsPreferred Skills Experience with chromatography software (LabSolutions / Empower / OpenLab / Chromeleon) Exposure tostability testing, method validation, and audit environmentsHow to Apply Apply Directly via Linkedin or mail your resume on hrd@