- Applies GMP/GLP in all areas of responsibility, as appropriate
- Demonstrates and promotes the company vision
- Regular attendance and punctuality
- Applies the highest quality standard in all areas of responsibility
- Demonstrates strong client service skills, teamwork, and collaboration
- Proactively plans and multitasks to maximize productivity
- Meets all quality and productivity metrics and demonstrates strong teamwork and collaboration
- Compliance - Ensure projects are completed in compliance with existing quality systems and are consistent with prior examples. Utilize independent judgement and experience to make quality-based decisions.
- Research - Utilize internal resources and existing procedures to gain knowledge on existing instruments. Assist with research of instrumentation with information obtained from vendors, manuals, and other resources to introduce duplicate/similar instruments and software.
- Technical Writing - Author validation deliverables/documentation in accordance with established validation program. Assist with enhancing instrumentation procedures.
- Training - Provide guidance and coaching within a team environment.
- Validation Support - Accurately update validation program components and maintain LIMS instrument database entries. Perform periodic reviews for chambers and compile and assist with periodic review of computerized systems. Generate monitoring, trending, and departmental reports. Perform routine project close out activities
- Validation Testing - Provide quality project oversight and ensure documentation is complete and reviewed. Summarize results and maintain documentation in an organized GXP compliant manner to demonstrate status
- Conducts all activities in a safe and efficient manner
- Performs other duties as assigned
- Communicates effectively with client staff members
- Bachelors degree in physical science, engineering, or information technology A combination of college and related technical experience will be considered (e.g. Associates with 2 years experience)
- Experience with typing/review of technical reports, protocols, patient/client correspondence, and/or similar professional documents
- Experience authoring instrument validation deliverables (e.g., protocols, test script) within a GXP environment preferred.
This position is full time Monday-Friday 9:00 am-5:00pm with overtime as needed.
Candidates currently living within a commutable distance of Lancaster Pennsylvania are encouraged to apply.
As a Eurofins employee, you will become part of a company that has received national recognition as a great place to work. We offer excellent full-time benefits including comprehensive medical coverage, life and disability insurance, 401(k) with company match, paid holidays and vacation, personal days, and dental and vision options.
Eurofins is a M/F, Disabled, and Veteran Equal Employment Opportunity and Affirmative Action employer.
