Job Description
Primary Responsibilities
- Conduct laboratory testing according to established global protocols, timelines and established procedures (SOPs) to generate high-quality, error-free, analytical results.
- Escalate issues potentially impacting patient safety, data quality, service levels.
- Perform and document quality controls per set SOPs and established guidelines.
- Perform and document routine equipment preventative maintenance and repairs.
- Work with instrument vendors to perform day‑to‑day maintenance and instrument troubleshooting.
- Comply with relevant GxP, DoH, CAP and CLIA where locally applicable.
- Perform duties as assigned and other relevant delegated tasks, provide support of all laboratory functions including inventory, stocking, housecleaning, archiving and safety tasks, act as back‑up to colleagues on leave.
- Perform clinical validations; integrate with QC/technical validation.
- Review and release results to clients.
- Run and review required proficiency testing samples.
- Cross‑train appropriate personnel in qualified job tasks.
Level I – Minimum
Level II – Fully meets the qualifications of the Level I plus the following
- Cross‑train appropriate personnel in qualified job tasks.
- Manage issues and resolve escalated issues as appropriate.
Level III – Fully meets the qualifications of the Level I and II plus the following
- Demonstrate leadership and problem‑solving skills through supervision, coaching, mentoring of others as required.
- Assists supervisor in assigned duties such as writing SOPs, implementation of new instruments and software, verification of new study setup and priming.
Qualifications
Position Specifications and Job Requirements
Level I Experience
- Minimum 1 year working in a diagnostic, clinical laboratory working with modern automation.
- Relevant ASCP certification.
- Proficient usage of a commercial grade or customized clinical LIMS.
Level II Experience
- Minimum 4 years working in a diagnostic, clinical laboratory working with modern automation.
- Relevant ASCP certification.
- Proficient usage of a commercial grade or customized clinical LIMS.
Education
- Associate of Applied Science acceptable; Bachelor of Applied Science in Biology, Chemistry, Microbiology or Medical Technology preferred.
- If no Medical Technology degree from an accredited institution, transcripts are required.
Other
- Fluent in English.
- Ability to set and follow priorities, working accurately following set procedures and under deadlines.
- Prolonged usage of analytical and computer systems (>75% time). Ability to lift up to 20 kg (44 lb) from time to time.
- Proficient in good laboratory and documentation practices.
- Ability to multi‑task with different instrumentation.
- Proficient use of Microsoft Office tools.
- Good interpersonal skills.
- Ability to work flexible hours, requested to work weekends on a rotation basis.
- Ability to perform high complexity testing.
- Capable of identifying problems, root causes and solutions, documenting deviations and notifying superiors.
Additional Information
Position is full‑time working Monday‑Friday, 1:00pm‑9:30pm with alternating Saturdays, with overtime as needed. Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply.
Benefits
- 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 Clinical Trial Solutions is a Disabled and Veteran Equal Employment Opportunity employer.