About the Job
Hikma Pharmaceuticals, a global leader in generic and branded medicines for over 45 years, is seeking a dedicated Analyst, QC to join its quality control team in Casablanca, Morocco. This full-time role is critical to ensuring that every product meets rigorous safety and efficacy standards before reaching patients. As a Quality Control Analyst, you will perform chemical and physical analyses, support cGMP compliance, and contribute to continuous improvement initiatives within a fast-paced pharmaceutical environment.
Responsibilities
- Conduct routine and non-routine testing of raw materials, in-process samples, and finished products using analytical techniques such as HPLC, spectroscopy, and wet chemistry.
- Document and review analytical data in accordance with cGMP, ISO 9001, and internal quality standards.
- Investigate out-of-specification (OOS) results and assist in root cause analysis and corrective actions.
- Maintain and calibrate laboratory equipment, ensuring all instruments are in proper working order.
- Support method validation and transfer activities as needed.
- Participate in internal audits and regulatory inspections, providing accurate and timely data.
- Collaborate with cross-functional teams to resolve quality issues and improve processes.
Requirements
- Bachelor’s degree in Chemistry, Pharmacy, Biochemistry, or a related scientific field.
- Minimum 1–2 years of experience in a pharmaceutical QC laboratory (fresh graduates with strong internships may be considered).
- Hands-on experience with analytical instruments (HPLC, GC, UV-Vis, dissolution) is highly preferred.
- Solid understanding of cGMP, ICH guidelines, and pharmacopoeial methods (USP, EP).
- Strong attention to detail, problem-solving skills, and ability to work in a team.
- Proficiency in English and French; Arabic is a plus.
Benefits
- Competitive salary and performance-based bonuses.
- Comprehensive health insurance coverage.
- Opportunities for professional development and career advancement within a global organization.
- Access to ongoing training in analytical techniques and regulatory compliance.
Tips for Success in This Role
- Familiarize yourself with Hikma’s product portfolio and quality policies before your interview to demonstrate genuine interest.
- Highlight any experience with method validation or troubleshooting analytical instruments in your application.
- Emphasize your ability to work under pressure while maintaining accuracy—pharma QC demands precision.
- Show willingness to learn new techniques and adapt to evolving regulatory requirements.