Validation Administrator

  • Full-time

Company Description

Eurofins Scientific is an international life sciences company which provides a unique range of analytical testing services to clients across multiple industries. The Group believes it is the world leader in food, environment and pharmaceutical products testing and in agroscience CRO services. It is also one of the global independent market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and for supporting clinical studies. In addition, Eurofins is one of the key emerging players in specialty clinical diagnostic testing in Europe and the USA.

 Group's key figures (as of March 2019) are approx. 3.8 billion Euros turnover, over 800 laboratories across 47 countries and about 45,000 staff.

Job Description

  • Help to develop and/or coordinate technical resources to implement test plans and documentation to validate laboratory systems, processes, instruments, and equipment
  • Technical documents must meet regulatory and client requirements and will include, but not be limited to, standard operating procedures and validation plans/protocols
  • Perform all duties accurately and efficiently with the highest level of quality
  • Develop and implement programs to bring laboratory computerized systems, instruments, equipment, and operational systems into compliance with GMP validation requirements
  • Role may also include system administration of pharmaceutical data acquisition systems

Qualifications

The ideal candidate would possess:

  • Knowledge of Windows OS, networking, and instrument PC connectivity and configuration (securities and file structure)
  • Excellent communication (oral and written) and attention to detail
  • Ability to work independently and as part of a team, self-motivation, adaptability, and a positive attitude
  • Ability to learn new techniques, perform multiple tasks simultaneously, keep accurate records, follow instructions, and comply with company policies
  • Understanding of lab instrumentation and/or quality related software tools

Basic Minimum Qualifications:

  • Bachelor's degree in chemistry, microbiology, biology, engineering, computer science, or other related degree concentration, or equivalent directly-related experience (two years of directly related industry experience is equivalent to one full-time year of college in related major)
  • At least one year in the pharmaceutical industry – GxP experience; validation experience required
  • One year of technical writing including investigations, procedures, training, and/or validation documents
  • Authorization to work in the United States indefinitely without restriction or sponsorship

Additional Information

Position is full-time, Monday-Friday, 8 a.m.-5 p.m., with overtime as needed.  

What we Offer:

  • Excellent full time benefits including comprehensive medical coverage, dental, and vision options

  • Life and disability insurance

  • 401(k) with company match

  • Paid vacation and holidays

Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.

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