Who we are
Fagron is the global market leader in pharmaceutical medicine, and its products are sold to more than 200,000 customers in over 60 countries. The goal of Fagron is: “Together we create the future of the personalized medicine”. Fagron, together with prescribers, pharmacists, and customers, strives to improve medications and help the patient. From our position as market leader, we act locally and think internationally.
About the job

SKILLS/QUALIFICATIONS:

• Must be capable of working in a dynamic, fast-paced, and physically demanding environment with extended periods of standing/walking.
• Must be able to lift 30 pounds and be able to pass, push, and pull to execute aspects of job duty.
• Must be able to repeatedly gown in building dedicated uniform aseptically.
• Computer skills in Microsoft Office products and Outlook.
• Knowledge of/familiarity with pharmaceutical cleanroom environments and operations.
• Exceptional observational skills, ability to think analytically, and possess an attention to detail.
  What’s on offer?
  We offer a dynamic environment where talent and ambition can develop to its fullest. We have an open and informal organization culture, where individuals need to have strong motivation and ability to work independently. Fagron is a widely expanding, international, professional and ambitious pharmaceutical company with multiple growth opportunities. Job opportunity includes competitive salary, comprehensive benefits, performance package, and ability to be part of an international leader in an expanding industry.
  Ready for the challenge?
  Please apply online through careers.fagron.com.
  Job Reference: FA0366

• Responsible for maintaining a safe work environment, working safely and accountable for supporting all health, safety, and environmental Corporate and Site goals.
• Support production operations by means of EM sampling of classified manufacturing, filling, and support areas and operations personnel.
• Support execution of qualification activities and special projects as necessary.
• Successfully interact with and support EM laboratory processes.
• Ensure compliance with current Good Manufacturing Practices (cGMPs) and maintain constant inspection-readiness.
• Ensure integrity of data collected is maintained with accurate and complete documentation.
• Participate in process streamlining and continuous performance improvement.
  Set yourself apart