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Eurofins Viracor BioPharma Services · 16 hours ago

Lab Instrument System Admin

Lancaster, PA

Full-time

Onsite

Mid Level

Eurofins Viracor BioPharma Services is an international life sciences company providing analytical testing services. The Lab Instrument System Admin role involves maintaining instrument software, ensuring compliance with quality systems, and providing training to users while conducting research and validation testing.

Biotechnology

No H1B

Responsibilities

Maintain instrument/software in a validated state at all times

Perform assessment, trouble-shooting, repair

Develop and implement CAPA to resolve issues as needed

Ensure completion of preventative maintenance and routine qualification testing

Install, configure software for electronic record compliance

Perform testing to identify gaps and develop remediation as required

Routinely analyze system logs/audit trails, perform software/firmware upgrades, update user account information, and complete periodic system compliance reviews

Determine and/or assist with determining the approach to test and validate instrumentation

Provide technical and risk-based rationale to support approach

Coordinate installation and/or execute testing (as required)

Review testing documentation generated by vendors and/or other team members

Compile and maintain documentation in an organized GXP compliant manner to demonstrate status

Ensure projects are completed in compliance with existing quality systems

Stay current with client, regulatory, validation, IT, and e-record regulations and requirements

Assist with implementing new internal practices and procedures

Research and on-board new instrumentation; Assist with integration of instrumentation into existing data center environments and workflows

Provide technical input for validation deliverables, investigations, and develop/enhance procedures in accordance with established quality programs

Provide training to system users and other admins; Assist with developing training program and procedures

Conducts all activities in a safe and efficient manner

Performs other duties as assigned

Qualification

HPLC TechniquesGMP/GLP ComplianceTechnical WritingMicrosoft WordMicrosoft ExcelCommunication SkillsOrganizational SkillsTeamworkSelf-MotivationAdaptability

Required

Must be eligible to work in the US without immediate OR possible future sponsorship

Strong computer, scientific, and organizational skills

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

Experience in the analysis of therapeutic proteins using various HPLC Techniques including IEX, SEC, HIC and RP and CE including ICE and CE

Excellent oral and written communication skills

The candidate must have effective documentation skills with the ability to author internal technical reports

Experience with Microsoft Word and Excel is required

Bachelor's in physical science (chemistry, engineering, computer science, etc.). Additional years of directly-related experience may be considered in lieu of degree (two years of directly related industry experience is equivalent to one full-time year of college in related major)