Excutive

• Conduct quality control testing of raw materials inprocess materials and finished products in accordance with established procedures and standards.
• Perform advanced analytical techniques such as HPLC GC UVVIS and titrations for routine and nonroutine analysis.
• Ensure compliance with cGMP (current Good Manufacturing Practice) GLP (Good Laboratory Practice) and other regulatory requirements.
• Review and interpret analytical data perform troubleshooting and assist in investigations of deviations or outofspec results.
• Maintain and calibrate laboratory equipment ensuring they are in proper working condition and compliant with regulatory standards.
• Support the validation and qualification of analytical methods and laboratory instruments.
• Prepare and review stability studies methods specifications and related documents.
• Ensure thorough documentation of all testing analysis and laboratory activities maintaining compliance with GMP guidelines.
• Participate in internal and external audits inspections and quality control reviews.
• Collaborate with crossfunctional teams (Production R&D Regulatory Affairs) to resolve qualityrelated issues and drive continuous improvement.
• Oversee the safe handling and storage of reagents chemicals and controlled substances per safety regulations.

• Bachelor s degree in Pharmaceutical Sciences Chemistry or a related field.
• 47 years of experience in Quality Control within the pharmaceutical or API industry.
• Advanced knowledge of analytical techniques laboratory instrumentation and quality control methodologies.
• Solid understanding of GMP GLP ICH guidelines and other regulatory requirements.
• Strong analytical problemsolving and troubleshooting skills.
• Excellent attention to detail and the ability to work efficiently in a fastpaced compliancedriven environment.
• Effective communication skills and ability to collaborate with crossfunctional teams.
• Ability to work independently with minimal supervision and take initiative in resolving issues.

• Experience in stability studies method validation and handling of highvalue API materials.
• Certification in Quality Management or related fields (e.g. Six Sigma ISO).
• Experience with preparing and handling documentation for regulatory submissions.

project coordination,lab equipment calibration,troubleshooting,documentation compliance,uv-vis,communication,adaptability,problem solving,collaboration,analytical thinking,team collaboration,time management,analytical data interpretation,glp,quality control,quality control testing,gc,titrations,stability studies,method validation,hplc,decision making,cgmp,problem-solving,confidentiality