Üretim Asistanı

Recordati Industria Chimica e Farmaceutica S.p.A

Çerkezköy, Turkey
On-site
Gmp compliance
Documentation control
Batch record review
Ensure timely and GMP-compliant control of closed batch manufacturing records and their delivery to the Quality Assurance department

Job Summary

  • Ensure timely and GMP-compliant control of closed batch manufacturing records and their delivery to the Quality Assurance department.
  • Prepare recipes for new or revised products and inform relevant departments, and plan or ensure necessary initial and continuous training for unit personnel.
  • Track and order disinfectants, cleaning cloths, safety equipment, logbooks, forms, and machine cards used in production area disinfection.

Matching Summary

Ensure timely and GMP-compliant control of closed batch manufacturing records and their delivery to the Quality Assurance department.

Skills & Requirements

Must-have

  • GMP compliance
  • documentation control
  • batch record review
  • SOP preparation
  • process validation support

Nice-to-have

  • team player
  • detail-oriented
  • analytical thinking
  • strong communication

Key Requirements

  • Associate's or Bachelor's degree in relevant fields
  • Industry experience
  • Proficiency in MS Office
  • Ability to reside in Çerkezköy, Kapaklı, or Çorlu

Work Rights

Not specified

Tailored Resume

Cover Letter