Lab Instrument System Admin

• Subject Matter Expert (SME) - 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.
• Validation Testing - 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.
• Applies GMP/GLP in all areas of responsibility as appropriate
• Compliance - 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 - Research and on-board new instrumentation; Assist with integration of instrumentation into existing data center environments and workflows
• Technical Writing - Provide technical input for validation deliverables investigations and develop/enhance procedures in accordance with established quality programs
• Training - 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

Qualifications :

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

The Ideal Candidate would possess:

• 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

Minimum Qualifications:

• Bachelors 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)

Additional Information :

Working schedule will be Full-Time First Shift Monday-Friday 8am-4pm. Candidates currently living within a commutable distance of Lancaster PA are encouraged to apply. 25% travel may be required. This position is NOT remote. 

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 USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.

Remote Work :

No

Employment Type :

Full-time