QC Validation Supervisor
Algorithm s.a.l
Employer Active
Posted 22 hrs ago
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Nationality
Any Nationality
Gender
Not Mentioned
Vacancy
1 Vacancy
Job Description
Roles & Responsibilities
- Supervise and plan validation operations in compliance with GMP/GLP.
- Coordinate with Supply Chain and Quality Assurance to set priorities.
- Ensure deviations/investigations are fully documented and addressed.
- Secure adequate resources with QCL Manager (trained staff, validated methods, and equipment).
- Ensure timely equipment validation and adherence to schedules.
- Apply and monitor good documentation practices per cGMP.
- Prepare and update departmental SOPs as per yearly plan.
- Monitor KPIs and prepare monthly reports.
- Develop team capabilities and encourage teamwork.
- Support other QC tasks in line with competencies as required.
- Abide by company ethics, compliance, and quality standards.
Desired Candidate Profile
Bachelor s degree in chemistry/Biochemistry or related scientific field.
Minimum 3 5 years of experience in Validation or Quality Control within the pharmaceutical industry.
Strong knowledge of GMP/GLP and cGMP requirements.
Experience in method and equipment validation.
Excellent documentation and reporting skills.
Strong leadership, communication, and teamwork abilities.
Detail-oriented, problem-solving mindset.
Company Industry
- Pharma
- Biotech
- Clinical Research
Department / Functional Area
- Quality
- Testing
- QA
- QC
- Inspector
Keywords
- QC Validation Supervisor
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Algorithm s.a.l