Associate Quality Operations


Job description:

Monitoring of manufacturing and maintenance processes. Follow up the solution of compliance issue in production workshop. Batch records review. Deviations / CAPA / Change Control / Complaints handling. Batch records review and batch release

Be responsible for Manufacturing, maintenance and engineering oversight

Review the batch production records and batch release.

Participate in GMP inspection and audit;

Fulfil other routine works assigned by the superior.

 Handling customer complaints.

Investigate deviations and CAPA implementation;

Performing internal Audits

Batch release

Required qualifications:

  • Degree in Chemistry, Biologics, Engineering,Pharmacy or related majors;
  • Former experience, familiar with pharmaceuticals production;
  • Knowledge of GMP;
  • Excellent computer skill;
  • Good communication skills and team work spirit.

Job location

Be'er Tuvia