Entry Level Scientist- Viral Clearance

Viral Clearance Services

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.

Center of Focus

• Virus plaque assays – team members perform cell culture manipulation and virus sample dilutions to yield results of the purification process.
• 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
• Various Laboratory Equipment (including hotplates, balances, pH meters, shakers, electronic pipettors, water baths, centrifuges)

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

• Minimum 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
• Able to work with moderate supervision upon training completion on assigned task
• Able to handle multitasking

The Ideal Candidate would possess the following skills/qualities

• Cell Culture
• Virology
• Plaque Assays
• TCID50
• Virus Production
• AKTA
• Protein Purification
• Viral Filtration
• Virus Inactivation
• AEX (anion exchange)
• CEX (Cation exchange)

Additional Information

• Working schedule will be Full-Time, First Shift, 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

Additional Information

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