Senior Specialist, Lab Steward

QPS, LLCNewark, DE
Onsite

About The Position

Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you!  The Senior Specialist, Lab Steward is part of the Laboratory & Compliance Management (LCM) support unit within the Department of Translational Medicine (TLM) and is responsible for all daily activities that support the smooth operation and regulatory compliance of the main ligand-binding assay laboratory of TLM. Strong attention to detail and the ability to read and understand scientific literature provided by our clients and vendors are critical to being successful in this role. QPS’ Story: Since its inception, 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. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life. Team members enjoy challenging and rewarding work, and are encouraged achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, team work and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals. If this sounds like your ideal work environment, then we would love to speak with you, so apply today! Please visit our website (www.qps.com [http://www.qps.com]) for more information and to see all current openings.

Requirements

  • Combination of relevant education & experience that provides sufficient knowledge & skills to ensure incumbent’s success in this role, such as:
  • University/College Degree in relevant Scientific discipline, and/or
  • Demonstrated experience in CRO, Clinical Research, or other relevant field.

Nice To Haves

  • Experience in a Regulated industry laboratory preferred

Responsibilities

  • Monitor, and address environmental and equipment alarms
  • Help keep the laboratories and all the devices clean, operational and presentable, including regular upkeep of laboratory equipment, such as but not limited to freezers, water baths and balances.
  • Interact with support teams to address maintenance and qualification needs or issues
  • Provide input to management on future needs for lab functions
  • Maintain inventory of reagents and consumables
  • Prepare buffers and solutions for general lab consumption following good laboratory practices
  • Assist in review of lab logbooks to ensure entries are accurate and report any issues to Lab Floor Supervisor for corrections

Benefits

  • Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals.
  • Structured Career Ladders that provide excellent growth based on your personal aspirations.
  • Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance.
  • Solid Benefits package, including Company-matched 401(k), and Company-sponsored 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.
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