- Clinical research jobs
- Dissolution Specialist
Dissolution Specialist
Job Description
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.
Qualifications
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
Additional Information
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.
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.
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