Quality Control Supervisor

Genveon İlaç; Gebze; In loco; TRY 250.000 - 350.000; Tempo pieno

Descrizione del lavoro

Genveon İlaç in Gebze is seeking a Quality Control Supervisor to oversee GMP compliance, laboratory operations and finished product release. You will lead the QC team, ensure accurate analyses, and maintain safety and environmental standards in a fast-paced pharmaceutical production facility.

The role requires a chemistry or chemical engineering degree, 6+ years in pharmaceutical analytical labs, strong leadership, and fluency in English.

Competenze

• 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).

Mansioni

• 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.

Conoscenze

Leadership experience

Analytical thinking

Communication skills

MS Office

Team-oriented

GMP knowledge

English proficiency

Formazione

Bachelor's degree in Chemical Engineering or Chemistry

Strumenti

SAP systems

Descrizione del lavoro

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.