Pharma Production Specialist: GMP & Process Improvement

Abdi Ibrahim Pharmaceuticals; Esenyurt; On-site; TRY 350,000 - 500,000; Full time

Job summary

Abdi İbrahim seeks a Production Specialist for its Solid Production team at the Esenyurt campus. The role requires a chemical engineering degree and at least 2 years in pharmaceutical production, with strong English and teamwork skills.

Key duties include GMP-compliant process support, SOP creation, protocol preparation, and participation in improvement projects within a collaborative environment.

Qualifications

• Bachelor's degree in chemical engineering.
• At least 2 years of experience in pharmaceutical production.
• Proficiency in English.
• Strong teamwork, communication, and interpersonal skills.
• Excellent problem-solving and decision-making abilities.
• Strong process and time management skills.
• Detail-oriented, analytical, and open to innovation.
• Proficient in Microsoft Office; SAP knowledge preferred.

Responsibilities

• Actively contribute to the implementation, monitoring, documentation, and continuous improvement of production processes in compliance with GMP.
• Ensure that pre-production, production, and post-production activities are carried out accurately, efficiently, and in accordance with procedures and regulations.
• Prepare and revise general and equipment-specific SOPs.
• Prepare manufacturing protocols and revise them per validation reports.
• Actively participate in production-related improvement projects and initiatives.

Skills

Teamwork

Communication

Interpersonal skills

Problem solving

Time management

Detail oriented

Analytical

Innovation

Education

Bachelor's degree in chemical engineering

Tools

SAP

Microsoft Office

Job description

Abdi İbrahim seeks a Production Specialist for its Solid Production team at the Esenyurt campus. The role requires a chemical engineering degree and at least 2 years in pharmaceutical production, with strong English and teamwork skills.

Key duties include GMP-compliant process support, SOP creation, protocol preparation, and participation in improvement projects within a collaborative environment.