Job Summary
The role involves executing both qualitative and quantitative analyses of chemical and physical properties of raw materials and end products, ensuring adherence to regulatory standards. This position also encompasses the preparation of technical documentation, conducting in-depth investigations, and delivering training to junior scientists within the quality control lab environment.
Responsibilities
- Conduct qualitative and quantitative assessments of chemical and physical aspects of raw materials and finished products.
- Ensure that all processes meet regulatory compliance requirements.
- Write detailed technical reports based on testing results.
- Carry out investigations on discrepancies and issues that arise in the quality control process.
- Provide mentorship and training to less experienced scientists in the lab.
Qualifications
- High School Diploma with ten years of relevant experience, or a Bachelor’s degree in a science-related discipline with a minimum of five years of experience in GMP pharmaceutical analytical chemistry.
- Expertise in sophisticated analytical techniques and familiarity with documentation standards.
- Proven ability to work independently and in a team-focused environment.
HIKMA provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
