QC Chemist / Analyst

Key Duties and Responsibilities: The QC Chemist / Analyst will be responsible for, but not limited to, the following duties:

• Analytical Testing & Laboratory Operations
• Perform routine and non-routine quality control analysis of raw materials, packaging materials, in-process samples, and finished pharmaceutical products in accordance with approved specifications and pharmacopeial methods.
• Conduct HPLC analysis for assay determination, related substances testing, and impurity profiling of APIs and finished dosage forms.
• Perform UV-Visible spectrophotometric, FTIR, and Karl Fischer, melting point analyses as required.
• Carry out dissolution, comparative dissolution, and disintegration testing to support product equivalence and process optimization.
• Ensure accurate analytical weighing and proper use of analytical balances.
• Method Validation & Stability Studies
• Execute analytical method validation and verification in compliance with ICH guidelines and GMP requirements (accuracy, precision, linearity, robustness, specificity).
• Support and manage stability studies including accelerated and long-term studies across relevant climatic zones.
• Monitor and trend stability data and ensure proper operation and monitoring of stability chambers.
• Reagents, Standards & Utilities
• Prepare, standardize, label, and document volumetric solutions and reagents, including stability monitoring.
• Manage primary, secondary, and working reference standards, including qualification, requalification, and inventory control.
• Test pharmaceutical utilities such as purified water for conductivity, pH, and chemical compliance.
• Equipment, Documentation & Compliance
• Perform routine calibration, verification, and qualification of laboratory instruments and equipment.
• Maintain accurate and complete documentation, including SOPs, test records, logbooks, deviation reports, and Certificates of Analysis (COAs).
• Act as custodian of retained and control samples.
• Participate in OOS/OOT investigations, deviation handling, and corrective actions (CAPA).
• Support internal audits, external audits, and regulatory inspections to ensure audit readiness
• Training & Team Support
• Train, mentor, and supervise new laboratory recruits, interns, and trainees.
• Promote adherence to GMP, GLP, data integrity, and laboratory safety practices at all times

Qualifications, Skills and Experience:

• Diploma Science technology chemistry from a recognised institution or a related scientific discipline.
• Minimum of 0–above years’ experience in pharmaceutical quality control and Quality assurance or a GMP-regulated laboratory environment.
• Knowledge on HPLC, UV-Vis, FTIR, dissolution testers, Karl Fischer titrators, and analytical balances.
• Sound knowledge of GMP, GLP, ICH guidelines, and pharmacopeial requirements (USP, BP, EP).
• Proven experience in analytical method validation, impurity profiling, and stability studies.
• Experience in documentation control, SOP writing, and regulatory compliance.
• Key Competencies & Attributes
• High level of integrity, accuracy, and attention to detail
• Strong analytical and problem-solving skills
• Ability to work independently with minimal supervision
• Excellent teamwork, communication, and mentoring skills
• Strong organizational and documentation skills
• Commitment to continuous professional development and quality improvement

How to Apply:

Qualified and interested candidates should submit their CVs to hr@rene.co.ug. Please indicate “QC Chemist / Analyst ” in the subject line of your email.

Deadline: 29th April 2026

NB: Only shortlisted candidates will be contacted.