Job Openings >> Clinical Operations Specialist I (Must Have Pipetting Exp) - Entry Level
Clinical Operations Specialist I (Must Have Pipetting Exp) - Entry Level
Summary
Title:Clinical Operations Specialist I (Must Have Pipetting Exp) - Entry Level
ID:335917
Department:Development
Description

Position : Clinical Operations Specialist I (Must Have Pipetting Exp)

Location : La Jolla, CA

Duration : 12 Months

Total Hours/week : 40.00

1st shift

Client: Medical Device Company

Job Category: Medical / Clinical Affairs

Level Of Experience: Entry Level

Employment Type: Contract on W2 (Need US Citizens or GC Holders Only)

 

Work hours: 8:00am – 4:30pm

 

3 Must haves on the resume:

Bachelor degree in Chemistry/Biology, pipetting experience, ability to independently manage time/switch between tasks

 

Job Description:

  • The Operations Specialist I is a multi-functional role, responsible for inventory control of materials and finished goods, formulation, packaging, and order fulfillment. The Operation Specialist I also supports Quality Control of finished goods by performing dye labeling reactions and sample preparation.
  • In addition, this position supports laboratory supply receiving and restocking.

 

Duties & Responsibilities:

  • Support security and accuracy of inventory of materials and finished goods through transaction documentation and by conducting physical cycle counts and reconciliation of any discrepancies.
  • Assist in the management of physical inventory within a Glovebox for raw materials, intermediate products, finished goods, analytical samples, and QA Retains.
  • Perform small scale chemical reactions (dye labeling) for Quality Control testing.
  • Fulfill internal requests for samples from inventory and perform sample preparation for quality testing.
  • Perform Aliquoting/Vialing of air and water sensitive finished goods using manual and automated processes and equipment.
  • Perform lyophilization of finished good products.
  • Perform Weight Checks and Packaging of air and water sensitive finished goods within a glovebox.
  • Prepare packaged products for QA inspection and shipments, including all required documentation.
  • Accurately complete required documentation (batch records, data entry, etc.) on time.
  • Receives deliveries of chemicals, materials, and lab supplies. Verifies accuracy of shipment and specifications.
  • Checks materials into inventory management system and restock in proper storage areas.
  • Support document control and data archiving activities as assigned.
  • Promotes a safe work environment. Provide recommendations on maintaining the safety of the work environment.
  • Participates in Environmental Health and Safety programs.
  • Addresses corrective actions whenever a hazard is identified.
  • Notifies supervisor of all observed hazardous conditions or unsafe work practices.
  • Participates in safety audits of safety equipment and laboratory processes.
  • Other responsibilities or projects as assigned by reporting manager.

 

Education & Experience:

  • Typically requires a minimum of a Bachelor’s Degree in Chemistry or Biology with 0-2years relevant experience.

 

Assets:

  • Ability to follow standard operating procedures is essential.
  • Experience with manual (pipette) and automated filling/dispensing is preferred.
  • Prior experience in a chemistry lab is preferred.
  • Experience working in a glovebox is preferred.
  • Proficiency in MS Office Skills (Word, Excel, and PowerPoint) is required.
  • Experience with FileMaker Pro, BMRAM, and DocuNECT is preferred.
  • Must possess strong organizational skills, attention to detail, and the ability to adapt to changing priorities in a fast-paced environment.
  • Be a self-starter, quick learner with the ability to work independently and efficiently.
  • Strong interpersonal communication skills, effective written and oral communications skills.
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