Solid Production Responsible at Recordati

Çerkezköy, Marmara Region, Turkey -

Full Time

Start Date

Immediate

Expiry Date

10 Jul, 26

Salary

0.0

Posted On

11 Apr, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Pharmaceutical manufacturing, GMP, Solid dosage production, SAP, OEE, Quality management systems, Process validation, Root cause analysis, CAPA, Equipment qualification, Technical troubleshooting, Team management, Continuous improvement, Kaizen, Analytical thinking, Communication

Industry

Pharmaceutical Manufacturing

Description

Job Purpose Solid Dosage Production Responsible We are looking for a result-oriented and hands-on Solid Dosage Production Responsible to join our pharmaceutical manufacturing team, with strong ownership of shopfloor operations and a solid understanding of production processes.Key Responsibilities JOB DESCRİPTİON: Ensure that production and documentation processes of solid dosage forms (tablets, capsules, etc.) are carried out in full compliance with GMP, Quality Management Systems, OHS, and environmental regulations, Plan, organize, and monitor daily/weekly production activities including granulation, compression, coating, and capsule filling processes, Drive production performance by supporting OEE, quality, and cost improvement initiatives, Manage production orders via SAP, verify material consumption, control stock movements, and ensure accurate production tracking, Support installation, commissioning, and qualification processes (IQ/OQ/PQ) of new equipment and ensure smooth integration into operations, Manage new product introductions, process transfers, and initial production phases to ensure process stabilization, Collaborate with cross-functional teams in technology transfer and validation activities, Manage deviation, OOS, and CAPA processes, including root cause analysis, Monitor team performance and identify training and development needs, Initiate and support continuous improvement projects within the scope of Kaizen initiatives. WHAT WE OFFER: A dynamic and continuously improving working environment Opportunities to take ownership and drive operational excellence Career development and growth opportunities Required Education Required Skills and Experience General Qualifications Bachelor’s degree in Chemical Engineering (preferred), Pharmacy, or Chemistry Minimum 5 years of experience in pharmaceutical manufacturing Preferably experienced in semi-solid and liquid production processes Strong technical understanding of production equipment, maintenance, and troubleshooting Knowledgeable in GMP (Good Manufacturing Practices) with a quality-oriented mindset Strong analytical thinking, problem-solving, and result-driven approach Team player with effective communication skills Good command of English Proficient in MS Office applications For male candidates, military service must be completed Technical Competencies Required Behaviours and Competencies Required Languages Travel required in %

Responsibilities

The role involves managing solid dosage production operations, including granulation, compression, and coating, while ensuring full compliance with GMP and quality standards. Additionally, the position requires driving production performance, managing SAP production orders, and overseeing equipment qualification and process stabilization.