Overview
Viral Clearance Services: Background: Bio/pharmaceutical products cannot be marketed or utilized in clinical trials without first establishing that the manufacturing process is capable of removing potential viral contaminants from the finished product. Viral Clearance Services provides assurance to the pharmaceutical industry that the risk is minimal in exposing a customer to a viral contaminated product.
The department deliberately introduces virus into client product intermediates and then measures the ability of the process purification step to remove or inactivate that virus. Multiple steps in a client purification process can be assessed to achieve a cumulative clearance value for a purification process. The testing is designed to satisfy requirements established in the ICH Q5A guidelines. Testing is generally looking for presence/absence of virus plaque forming units (PFU) and comparing the amount of virus that was initially in the sample to the amount of virus in the product containing fraction after the purification has been completed. The Log10 difference between initial titer and the product titer is referred to as a Log Reduction Value.
Responsibilities
* Client purification process - team members assist client in performing their viral clearance study by spiking client sample intermediates with virus for their performance of their purification step.
* Performance of purification processes - team members perform the client purification processes instead of the client being on site to perform them.
* Virus stock preparation - team members perform cell culture manipulation and virus stock propagation to create more virus banks and to improve the titer / purity of virus stocks.
* Instrumentation and testing techniques: AKTA Chromatography systems, Biological Safety Cabinets, Microscopes, and various Laboratory Equipment (including hotplates, balances, pH meters, shakers, electronic pipettors, water baths, centrifuges).
* Continuing investments are made to on-board new technologies for new service offerings and to meet client needs.
* Additional Responsibilities: Completing all training in a timely and complete manner; working with an experienced analyst/mentor performing various tasks and analyses of Bio/pharmaceutical ingredients and products; reviewing or preparing standards and samples for analysis and running any equipment or instrumentation independently and/or with guidance; working efficiently; ensuring that the client receives quality data by reviewing laboratory data for accuracy, clarity, and adherence to GMP and/or GLP regulations.
Qualifications
* Bachelor's degree in biology or related degree concentration and no previous industry laboratory experience required
* Ability to work on the US without immediate or potential future sponsorship
* Good dexterity
* Positive attitude
* Solution driven
* Good work habits (organized, efficient, careful, safety-conscious, accurate)
* Sound scientific logic
* Understanding of instrumentation
* Demonstration of organizational skills
* Ability to work with moderate supervision upon training completion on assigned task
* Ability to handle multitasking
Additional Information
* Working schedule will be Full-Time, First Shift, M-F 8am-4pm.
* Candidates currently living within a commutable distance of Lancaster, PA are encouraged to apply. No relocation assistance will be given. 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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