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Dissolution Specialist

External
Eurofins logoEurofins · Lancaster, PA
Full-timeOn-site1w ago
ComplianceSAFe
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Benefits

Excellent full time benefits including comprehensive medical coverage, dental, and vision optionsLife and disability insurance401(k) with company matchPaid vacation and holidaysEurofins USA BioPharma Services is a Disabled and Veteran Equal Employment Opportunity employer.Dental insuranceVision insurance401(k)Paid time offRemote work optionsEquity / stock options

Additional Information

Requires performing a variety of tasks including stocking laboratory supplies, preparing dissolution media solutions, maintaining dissolution/solution storage program, discarding solutions, labelling test tubes/vials, and setting-up/cleaning dissolution baths after use, performing routine maintenance, calibration, and qualification of laboratory equipment (Class II - IV). Working efficiently and independently. 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 and promotes the company vision. 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. Regular attendance and punctuality. Maintains suitable levels of dissolution laboratory supplies. Successfully prepares dissolution media as requested by the technical departments. Maintains the dissolution media carboy cleaning, storage, and discard program. Labels test tubes/vials as requested by the technical departments. Setup and clean dissolution systems after technical use and appropriately discards solutions into the correct waste streams. Assist in maintenance, calibration, and qualification of basic laboratory equipment (Class II - IV). Assist in gathering data for investigations and draft investigation content. Perform ELN Maintenance and calibration logbook entries as required. Understand basic principles of system validation and electronic record compliance from a regulatory standpoint. Maintain dissolution instrumentation in a validated state at all times. Communicates effectively with client staff members. Conducts all activities in a safe and efficient manner. Performs other duties as assigned. Minimum Qualifications; At least one year of related experience in a GMP environment using LIMS, ELN, and Microsoft Office programs. Bachelor of Science (Chemistry focus) Ability to work in the US indefinitely without restriction or sponsorship Working schedule will be Full-Time, M-F 8am-5pm. Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply. No relocation assistance will be given. 25% travel may be required. This position is NOT remote.


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