To ensure that the relevant documentation is made by ensuring the realization of in-process controls, which are the responsibility of the In-Process Control unit at all stages from the beginning of the production and packaging processes.
Contributing to ensuring that the product conforms to the specifications.
To follow the shift plans by managing the organization and work flow of the In-Process Control unit.
To carry out deviation researches about the unit and to ensure that it is closed in a timely manner.
Ensuring compliance with GMP and GLP rules in the In-Process Control unit and in all work areas.
Approving the physical control reports and defect classification forms prepared during packaging processes.
Participating in the meetings held regarding the audit report and audit response report by participating in internal audits when necessary.
General Qualifications:
Bachelor’s degree in Chemistry, Chemical Engineering or Pharmacy departments of universities.
At least 5 years of experience in the pharmaceutical industry.
Preferably experience as a Team Leader / Team Manager.
Knowledge of GMP practices and data security requirements.
Competent in careful, meticulous work and business follow-up.
Open to change, following technological developments, aiming to continuously improve himself and his team; Developed planning and organizational skills.
Proficient in MS Office, QMex and preferably SAP programs.
Completed their military service for male candidates.