Administrator II, Metrology

Administrator II, Metrology – QPS Holdings, LLC

We are seeking an experienced administrator to perform calibration and maintenance of pipettes and liquid handlers for our Laboratory & Compliance Management (LCM) support unit within the Department of Translational Medicine (TLM). In this role, you will be responsible for performing calibration and maintenance of pipettes and liquid handlers for the TLM team.

$58,000.00/yr - $65,000.00/yr

QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of neuropharmacology, DMPK, toxicology, bioanalysis, translational medicine, early phase clinical and Phase II–IV clinical research services. We strive to employ talented, caring and committed individuals who work collaboratively towards our mission of improving human health and enhancing quality of life.

Team members enjoy challenging and rewarding work and are encouraged to achieve their best. Our culture values diversity, innovation, accountability, teamwork and a friendly atmosphere where performance is recognized and rewarded. We provide unique benefits, training and advancement opportunities and value each team member as both an employee and an individual.

• Perform equipment calibration and documentation per SOP and relevant guidance.
• Provide preventative maintenance on pipettes and liquid handlers.
• Follow GDP documentation for calibration and maintenance activities.
• Visually inspect and/or use testing equipment to determine service issues on pipettes and liquid handlers.
• Troubleshoot problems and identify root causes of repair issues.
• Strictly follow SOPs and safety guidelines.
• Maintain a good working habit, ensuring equipment is calibrated in clean areas and tools are organized and clean.
• Provide input to management on future needs for lab functions.
• Maintain inventory of reagents and consumables.

100% QPS office/facility based in Newark, DE.

• Combination of relevant education and experience that provides sufficient knowledge & skills to ensure incumbent’s success in this role, such as:
• University/College Degree in a relevant scientific discipline, and/or
• Demonstrated experience in CRO, clinical research, or another relevant field.
• Experience in a regulated industry laboratory preferred.

• Good and timely communication skills.
• Strong time management skills, with the ability to work cooperatively and effectively to meet timelines in a fast‑paced setting.
• Ability to learn and work independently, eventually making independent decisions as needed.
• Willingness to adhere to GLPs and other required standards, carefully collecting and organizing data per established criteria.
• Systems and computer proficiency (or ability to learn).

• Great learning opportunities, especially for those new to the field.
• Structured career ladders that provide excellent growth based on personal aspirations.
• Bonuses and merit increases as part of the QPS total rewards approach.
• Solid benefits package, including company‑matched 401(k), group life/AD&D, and short and long‑term disability insurance.
• Park‑like setting in Newark, Delaware.
• Internal committees designed with the needs and enjoyment of QPS employees in mind.

QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote, and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job.

QPS, LLC is a federal contractor and desires priority referrals of protected veterans.

• Entry level

• Full-time

• Information Technology
• Pharmaceutical Manufacturing