Job Description

Quality Assurance Expert
Job Number: 20-05044
 
Be a part of a company that supports life-changing healthcare solutions. Eclaro is looking for a Quality Assurance Expert for our client in Carlsbad, CA.
 
Eclaro’s client is a leading manufacturer of lab materials, technology and service supporting the Life Science field. If you’re up to the challenge, then take a chance at this rewarding opportunity!
 
Responsibilities:
  • This key role will be performing activities and reviews in support of the manufacture and disposition of product.
  • As a member of the Client Facing Quality Assurance team, you will be responsible for the critical, quality review of records associated with raw materials and product batch records ensuring compliance with established company procedures and policies as well as cGMP and all related regulatory agencies.
  • Will need to embody the company vision and values.
  • Performing product inspections, line clearances, facility inspections, and general product observation, identifying quality events and assist with associated investigations.
  • May also create, revise, review, and approve controlled documentation, log and monitor data and assist with uploading documentation into shared drive, support the client audits and regulatory inspections.
  • This role will also require  to work independently within prescribed guidelines and effectively collaborate as part of a team.
  • Must also have the ability to work successfully, strategically and tactically in a fast-paced, multi-disciplinary environment with potential for rapidly changing priorities as well as have the ability to obtain direction and commitment to ensure that projects are completed by deadlines and streamlining processes to maximize productivity.
  • Need to be organized and detailed oriented with strong and effective written, verbal, mathematical, and interpersonal communication skills to be successful in this role.
  • Will also perform other Quality Assurance related duties and projects as assigned.
 
Qualifications:
  • Associates degree in a scientific discipline or High School Diploma or GED and 3+ years' experience in cGMP environment
  • 2+ years' experience working in MS Word and Excel for editing documents
 
Preferred Qualifications:
  • Knowledge of governmental regulatory guidelines, directives, and regulations relating to the manufacture of biologics and pharmaceuticals
  • Contract Manufactured Organization (CMO) experience
  • Clean-room experience
 
If hired, you will enjoy the following Eclaro Benefits:
  • 401k Retirement Savings Plan administered by Merrill Lynch
  • Commuter Check Pretax Commuter Benefits
  • Eligibility to purchase Medical, Dental & Vision Insurance through Eclaro
 
If interested, you may contact:
Chris Sta Juana    
christian.sta.juana@eclaro.com
2128047469
Chris Sta Juana | LinkedIn
 

Equal Opportunity Employer: Eclaro values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

Application Instructions

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