Quality Control Supervisor

Genveon İlaç; Gebze; On-site; TRY 500,000 - 800,000; Full time

Job summary

Genveon İlaç is seeking a Quality Control Supervisor for our Gebze production facility. The role supervises QC laboratory activities to ensure compliant release of finished products and maintains GMP, cGMP, and cGLP standards.

You will lead investigations, review results, and coordinate with QA/production to uphold quality and regulatory compliance in a fast-paced environment.

Qualifications

• Bachelor's degree in Chemical Engineering or Chemistry.
• Minimum 6 years of experience in analytical laboratories within the pharmaceutical industry.
• Proven leadership experience and strong managerial skills.
• Solid knowledge of cGMP, cGLP, and SAP systems.
• Ability to thrive in a fast-paced and dynamic environment.
• Team-oriented and customer-focused mindset.
• Strong analytical thinking and decision-making skills.
• Excellent verbal and written communication skills.
• Proficient in MS Office applications.
• Fluent in English (both written and spoken).

Responsibilities

• Ensure full and effective implementation of GMP requirements as defined by the Ministry of Health.
• Manage all aspects of health, safety, quality, and environmental compliance in the responsible area.
• Ensure operations are in line with local legislation, internal guidelines/procedures, and business continuity standards.
• Organize emergency preparedness efforts according to global and local requirements.
• Plan and supervise sampling and laboratory analysis of finished products.
• Review, evaluate, and approve analysis results.
• Perform SAP-based release of finished products.
• Report laboratory data to the Quality Control Manager.
• Lead laboratory investigations and ensure accurate root cause analysis.
• Support team members to complete all analysis and documentation in a timely and accurate manner.
• Safeguard the confidentiality of documents and analytical methods.
• Contribute to cost‑saving and efficiency improvement projects.
• Perform additional responsibilities assigned by management in accordance with methods, procedures, and workflows.

Skills

Leadership

Analytical thinking

Decision making

Communication

Teamwork

Customer focus

English fluency

Adaptability

MS Office

Education

Bachelor's degree in Chemical Engineering or Chemistry

Tools

SAP

Job description

Turkey's young, dynamic, innovative and success-oriented healthcare company that adds innovation to the generic world; GENVEON is looking for a Quality Control Supervisor to be assigned to our production facility in Gebze Plastics Organized Industrial Zone!

QUALIFICATIONS

• Bachelor’s degree in Chemical Engineering or Chemistry,
• Minimum 6 years of experience in analytical laboratories within the pharmaceutical industry,
• Proven leadership experience and strong managerial skills,
• Solid knowledge of cGMP, cGLP, and SAP systems,
• Ability to thrive in a fast-paced and dynamic environment,
• Team-oriented and customer-focused mindset,
• Strong analytical thinking and decision-making skills,
• Excellent verbal and written communication skills,
• Proficient in MS Office applications,
• Fluent in English (both written and spoken).

JOB DESCRIPTION

• Ensure full and effective implementation of GMP requirements as defined by the Ministry of Health,
• Manage all aspects of health, safety, quality, and environmental compliance in the responsible area,
• Ensure operations are in line with local legislation, internal guidelines/procedures, and business continuity standards,
• Organize emergency preparedness efforts according to global and local requirements,
• Plan and supervise sampling and laboratory analysis of finished products,
• Review, evaluate, and approve analysis results,
• Perform SAP-based release of finished products,
• Report laboratory data to the Quality Control Manager,
• Lead laboratory investigations and ensure accurate root cause analysis,
• Support team members to complete all analysis and documentation in a timely and accurate manner,
• Safeguard the confidentiality of documents and analytical methods,
• Contribute to cost‑saving and efficiency improvement projects,
• Perform additional responsibilities assigned by management in accordance with methods, procedures, and workflows.