Unit Leader - Live Virus FF at CEVA Animal Health LLC
Magyarország, , Hungary -
Full Time


Start Date

Immediate

Expiry Date

28 Apr, 25

Salary

0.0

Posted On

29 Jan, 25

Experience

3 year(s) or above

Remote Job

No

Telecommute

No

Sponsor Visa

No

Skills

Lyophilization, Pharmaceutical Manufacturing, English, Secondary Education, Regulations

Industry

Pharmaceuticals

Description

WHY CEVA-PHYLAXIA?

  • We dedicate our work to protect animal welfare every day
  • We offer stable employment in a resilient industry
  • We offer comprehensive training opportunities
  • Our business has been growing exponentially
  • You can join a dynamic and enthusiastic team of professionals
  • You can gain unique expertise, exclusively in Hungary
  • Lunchtime is more enjoyable as it is included in working hours

REQUIREMENTS:

  • Relevant higher education degree or, in its absence, a secondary education with at least 4 years of experience in pharmaceutical manufacturing
  • Experience in production, quality control laboratories, or quality assurance
  • Technological knowledge, particularly in vaccine filling, lyophilization, and capping processes
  • Proficiency in English, both spoken and written
  • Knowledge of applying GMP principles and regulations in pharmaceutical manufacturing environments
  • At least 3 years of leadership experience
  • Strong analytical and problem-solving skills
  • Basic IT skills
Responsibilities
  • Ensuring the smooth operation of production processes in compliance with GMP regulations
  • Preparing and reviewing production documentation
  • Coordinating manufacturing processes required for the introduction of new products
  • Validating processes and integrating registration changes into production
  • Ensuring the availability of resources, tools, and equipment, and organizing maintenance work
  • Developing production plans, managing work schedules, and supervising shifts
  • Optimizing and monitoring production inventories and materials
  • Preparing for audits and inspections, presenting the production area during evaluations
  • Managing deviations and changes, and implementing preventive measures
  • Creating reports and performance analyses, and making suggestions for efficiency improvements
  • Supporting the work of subordinates and ensuring necessary training opportunities
  • Monitoring compliance with GMP regulations in the production area
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