Job Description

Qualifications and Requirements:

Full knowledge of hematology reagent production processes.
Strong understanding of quality standards and manufacturing requirements for In Vitro Diagnostic (IVD) products.
Proficiency in operating and supervising equipment used in diagnostic reagent manufacturing lines.
Familiarity with Quality Control (QC), Quality Assurance (QA), and production documentation requirements.
Good knowledge of Good Manufacturing Practice (GMP) principles and regulations.
Ability to plan, organize, and manage production activities and personnel.
Strong sense of responsibility, attention to detail, and organizational skills.
Familiarity with medical device and IVD regulatory requirements is considered an advantage.

Employment Type

  • Full Time

Seniority

Details

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