Join to apply for the Quality Control Specialist role at Cpl
Main Responsibilities:
1. Provide analytical expertise for projects, troubleshooting, and investigation of analytical methods and lab technologies.
2. Coordinate analytical testing on projects (validation/transfer), ensuring adherence to schedules.
3. Perform tasks in accordance with cGMP and HSE requirements, following related instructions, procedures, and records.
4. Record all raw data, calculations, and information related to tasks, complying with cGMP and Data integrity standards.
5. Write and review protocols and reports for analytical validation, transfers, and qualification activities.
6. Maintain accurate analytical methods and procedures.
7. Report any quality or HSE events (deviations or OOx) promptly to ensure proper investigation and impact assessment.
8. Participate in investigations to support appropriate analysis and assessment.
9. Conduct trend analysis on method performance to determine the need for revalidation, optimization, or replacement.
10. Ensure lab facilities and instruments are maintained in a quality and safety-compliant state.
11. Support QC team during internal and external audits and inspections.
Qualifications:
1. Higher degree in a scientific or technical discipline (e.g., Chemistry, Biochemistry).
2. At least 3 years of experience in Quality Control, Pharmaceutical Development, Analytical, or Manufacturing in the pharmaceutical industry.
3. Strong knowledge of GMP and regulatory standards.
4. Ability to analyze complex data and laboratory results effectively.
5. High attention to detail for accuracy and compliance.
6. Proactive problem-solving skills.
7. Flexible, adaptable, and open to continuous improvement.
Additional Details:
* Seniority level: Mid-Senior level
* Employment type: Temporary
* Job function: Quality Assurance
* Industry: Staffing and Recruiting
#J-18808-Ljbffr