Job Description

Document receipt of stability samples and complete inventories. Appropriately handle documentation. Understand stability requirements – protocols, LIMS, storage chamber conditions, labeling of samples and storage positions. Provide support for project managers and laboratory staff. Compose business appropriate communication (i.e. e-mail, document) for client or internal use.

Essential Duties and Responsibilities:

• Applies GMP/GLP in all areas of responsibility, as appropriate
• Demonstrates and promotes the company vision  Regular attendance and punctuality
• Applies quality to all areas of responsibility, understands and promotes quality culture.
• Understand and update LIMS appropriately for protocol and sample activities.
• Manage inventory for incoming project samples; set up stability studies, label samples, and place into chambers.
• Verify sample chamber placement, labeling, container counts, and LIMS entry
• Pull samples from chambers at appropriate intervals; perform periodic chamber inventories
• Maintain contents of stability chambers in an organized manner, monitor and change charts; clean inside of chambers
• Follow all department procedures and SOPs; understand and apply GMP/GLP regulations to daily work; document data according to regulatory requirements
• Attend department meetings
• Independently evaluate and/or provide shipment paperwork, package samples for shipment as needed with additional training.
• Effectively use word, tone, body language to share and receive information.
• Accept and implement process change to support business goals.
• Conducts all activities in a safe and efficient manner
• Performs other duties as assigned

Qualifications

Minimum Qualifications:

• High school diploma + 1 year of relevant experience (minimum) or college degree in related field.
• Ability to work in the US without immediate or potential future sponsorship.
• Computer skills
• Stability experience preferred.
• Good oral and written communication skills
• Attention to detail
• Self-motivated

Additional Information

Working schedule will be Full-Time, First Shift, M-F 9am-5pm. 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.