Lab Ops Specialist - Santa Monica, United States - Leadstack Inc

Leadstack Inc

Verified Company

Santa Monica, United States

3 weeks ago

Posted by:

Mark Lane

beBee recruiter

Description

Job Title:
Lab Ops Specialist I

Location:
Santa Monica, CA

Duration: 6 Months Contract

Payrange:
$25/hr - $30/hr on W2 depending on the exp

Hours/Days:
(Tuesday-Sat) Flexible hours.

Everyone at Kite is grounded by one common goal - curing cancer. Every single day, we seek to establish a direct line between that purpose and our day-to-day work.

We are seeking a highly motivated individual to join us as a Lab Ops Specialist I in Quality Control Sample Management in Santa Monica, CA.

Responsibilities:

Perform QC sample receipt, processing and distribution for testing and storage
Perform Apheresis Accession, Inspection, and assist QA with product returns
Maintain, operate equipment and instruments supporting sample processing
Work with internal resources to maintain lab in an optimal state
Perform Cryo sample disposition and shipment
Track inventory of lab supplies and materials
Track inventory of retain samples, stability samples, test materials
Track and distribute samples according to Stability protocols
Troubleshoot standard issues and identify when a deviation from standard process occurs
Gather metric information for use in continuous improvement of areas of responsibility
Data entry and review
Support generation of CoAs for product release
Revise and review SOPs, workinstructions, forms, sampling plans
Monitor the GMP systems currently in place to ensure compliance with documented policies
Assist with audits, walkthroughs, inspections, when necessary
Additional duties as assigned

Basic Qualifications

Bachelor's Degree OR
AA Degree and 1+ years of experience in Quality Control/GMP Environment OR
High School Degree and 3+ years' experience in Quality Control/GMP Environment
Physical requirements: Ability to lift up to 30 lbs

Preferred Qualifications

Degree in biotechnology or related field with Quality Control experience
Working knowledge of GMP, SOPs and quality control processes
Working knowledge of quality systems and regulatory requirements (21 CRF Part 11/210/211)
Ability to communicate and work independently with scientific/technical personnel
Strong written and verbal communication skills
Comfortable in a fastpaced small company environment with direction and able to adjust workload based upon changing priorities
Experience with LIMS
Ability to work with a variable schedule