Laboratory Operations Assistant - Part-Time

Job Description

Job Description

Celerion is committed to swift, exceptional clinical research through translational medicine.  Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.  

We are seeking a detail-oriented and dependable Laboratory Operations Assistant to support daily activities within our bioanalytical department. This role is essential to maintaining the integrity of our laboratory processes and ensuring smooth operations. Responsibilities include handling analytical instruments, managing sample materials, and performing quality control reviews of bioanalytical records and data.

Location: Our Lincoln, NE, location. We are only considering candidates who currently live in the Lincoln area. 

Schedule & Compensation: This is a part-time position working approximately 20 hours per week, Monday–Friday, between 8:00 AM and 5:00 PM, with scheduling flexibility based on your availability. Pay is $17.00/hour. This position does not include benefits. It is an excellent opportunity for students or individuals seeking meaningful part-time experience in a professional laboratory setting. 

Essential Functions:

Laboratory Operations & Compliance

• Prepare, store, inventory, and dispose of laboratory solutions in compliance with EHS standards and applicable SOPs.
• Clean glassware used in solution preparation and maintain general laboratory organization, stocking, and inventory.
• Adhere to all written instructions, SOPs, and working instructions related to job responsibilities.

Sample Management

• Receive, check in, and accurately log biological samples upon arrival.
• Organize and dispose of analytical samples per SOPs and working instructions.
• Store samples for long-term preservation and rack samples for production.
• Ensure proper sample organization and freezer placement; maintain transfer and freezer logs.
• Count and reconcile samples at the conclusion of each study.

Quality Control & Documentation

• Conduct real-time review of production documentation.
• Complete QC reviews of production databases and issue audit findings as appropriate.
• Perform quality control on bioanalytical documents, including BSPs and EDT files.

Requirements:

• High school diploma or GED required; Associate's degree in a related field preferred.
• Post-secondary coursework in science-related disciplines is a plus.
• Basic knowledge of chemistry preferred.
• Strong ability to work independently with minimal supervision.
• Exceptional attention to detail and organizational skills.
• Strong oral and written communication skills.

Special Requirement — Bona Fide Occupational Qualification

This position requires the incumbent to be a non-nicotine/tobacco user. Due to the nature of the work — including the preparation of sensitive solutions and continuous contact with glassware and storage areas — nicotine contamination poses a meaningful risk to study integrity. As a volatile compound, nicotine can compromise results even through trace exposure, including secondhand contact or residual exposure from clothing or nicotine-present environments.

Celerion Values:       Integrity   Trust   Teamwork   Respect

Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.

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We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.