Rene Industries Limited is seeking a QC Chemist / Analyst for its Quality Control department.

Responsibilities or duties

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

• Analytical Testing & Laboratory Operations
• Method Validation & Stability Studies
• Reagents, Standards & Utilities
• Equipment, Documentation & Compliance
• Training & Team Support

Qualifications or requirements (e.g., education, skills)

Required Qualifications & Experience

• Bachelor’s degree in Chemistry related program from a recognised institution or a related scientific discipline.
• 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

Experience needed

Minimum of 0–above years’ experience in pharmaceutical quality control and Quality assurance or a GMP-regulated laboratory environment.

• Analytical Testing & Laboratory Operations
• Method Validation & Stability Studies
• Reagents, Standards & Utilities
• Equipment, Documentation & Compliance
• Training & Team Support

• HPLC
• UV-Vis
• FTIR
• Dissolution testers
• Karl Fischer titrators
• Analytical balances
• Analytical method validation
• Impurity profiling
• Stability studies
• Documentation control
• SOP writing
• Regulatory compliance
• Integrity
• Accuracy
• Attention to detail
• Analytical skills
• Problem-solving skills
• Teamwork
• Communication skills
• Mentoring skills
• Organizational skills
• Documentation skills
• Continuous professional development
• Quality improvement

• Bachelor’s degree in Chemistry related program 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.