Essential Duties and Responsibilities:
- Applies GMP/GLP in all areas of responsibility as appropriate
- 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
- Communicates effectively with client staff members
- Conducts all activities in a safe and efficient manner
- Performs other duties as assigned
- Subject Matter Expert (SME) - Maintain routine instruments in a validated state at all times. Perform assessment trouble-shooting repair. Ensure completion of preventative maintenance routine testing and assigned validation testing.
- Compliance - Ensure all activities are completed on time accurately documented and in compliance with existing quality systems. Ensure that the quality policy program is understood implemented and maintained at all times.
- Productivity - Organize schedule in a manner such that higher priority projects and tasks are completed in a timely manner. Ensure completion of all assigned tasks according to company and department stated TATs.
- Innovation - Active involvement with process improvement initiatives
- Teamwork - Foster teamwork internally and with technical groups to increase overall quality. Take responsibility for group success by assisting and supporting team members.
- Training - Provide guidance and coaching within a team environment
Qualifications :
- Associates degree/Certification in physical science engineering or information technology; combination of college and related technical experience will be considered (e.g. Certificate program with 1 year experience).
- Experience performing and documenting instrument trouble shooting non-routine events and/or validations.
- Strong PC skills and experience.
- Experience with GMP-compliant work practices and systems
- Strong understanding of instrumentation theory
- Authorization to work in the United States indefintely without restriction or sponsorship
Additional Information :
Position is full-time Monday-Friday 2:00 p.m. - 10:00 p.m. OR 10:00 p.m.-6:00 a.m. with overtime as needed. Candidates currently living within a commutable distance of Lancaster PA are encouraged to apply.
We offer excellent full-time benefits including:
- comprehensive medical coverage
- life and disability insurance
- 401(k) with company match
- paid holidays and vacation
- dental and vision options.
To learn more about Eurofins please explore our website
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.
Remote Work :
No
Employment Type :
Full-time
Essential Duties and Responsibilities:Applies GMP/GLP in all areas of responsibility as appropriateApplies the highest quality standard in all areas of responsibilityDemonstrates strong client service skills teamwork and collaborationProactively plans and multitasks to maximize productivityMeets all...
Essential Duties and Responsibilities:
- Applies GMP/GLP in all areas of responsibility as appropriate
- 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
- Communicates effectively with client staff members
- Conducts all activities in a safe and efficient manner
- Performs other duties as assigned
- Subject Matter Expert (SME) - Maintain routine instruments in a validated state at all times. Perform assessment trouble-shooting repair. Ensure completion of preventative maintenance routine testing and assigned validation testing.
- Compliance - Ensure all activities are completed on time accurately documented and in compliance with existing quality systems. Ensure that the quality policy program is understood implemented and maintained at all times.
- Productivity - Organize schedule in a manner such that higher priority projects and tasks are completed in a timely manner. Ensure completion of all assigned tasks according to company and department stated TATs.
- Innovation - Active involvement with process improvement initiatives
- Teamwork - Foster teamwork internally and with technical groups to increase overall quality. Take responsibility for group success by assisting and supporting team members.
- Training - Provide guidance and coaching within a team environment
Qualifications :
- Associates degree/Certification in physical science engineering or information technology; combination of college and related technical experience will be considered (e.g. Certificate program with 1 year experience).
- Experience performing and documenting instrument trouble shooting non-routine events and/or validations.
- Strong PC skills and experience.
- Experience with GMP-compliant work practices and systems
- Strong understanding of instrumentation theory
- Authorization to work in the United States indefintely without restriction or sponsorship
Additional Information :
Position is full-time Monday-Friday 2:00 p.m. - 10:00 p.m. OR 10:00 p.m.-6:00 a.m. with overtime as needed. Candidates currently living within a commutable distance of Lancaster PA are encouraged to apply.
We offer excellent full-time benefits including:
- comprehensive medical coverage
- life and disability insurance
- 401(k) with company match
- paid holidays and vacation
- dental and vision options.
To learn more about Eurofins please explore our website
Eurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.
Remote Work :
No
Employment Type :
Full-time
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