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 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