Job Description

Life Cycle Specialist - Chemistry Expert
Job Number: 21-16282
 
Be a part of a company that supports life-changing healthcare solutions. Eclaro is looking for a Life Cycle Specialist - Chemistry 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!

Position Overview:
  • Utilized methods for analytical HPLC, titration, UV spectrophotometry, ELISA and HPTLC
  • Analyzed finished products, raw materials, bulk samples, and botanicals utilizing appropriate methods in appropriate turnaround times
  • Performed investigations of out of specification results
  • Contributed to audit readiness and quality audits with ISO
  • Ensured work is in compliance with SOPs and regulatory requirements (ISO 17025)
  • Assisted in selecting and training new chemists
  • Performed test procedures to test integrity of finished products
  • Prepared and maintained documentation for tests conducted throughout the lab
  • Ensured samples were logged accurately and pulled at appropriate time intervals
  • Communicated with other departments to ensure all testing was completed in a timely manner
  • Responsible for supporting client-facing projects as a member of the Life Cycle Management team within Technical Operations. 
  • Will work cross-functionally with the Manufacturing, Process Development, and Quality teams to implement changes to bioprocesses in cGMP production.


Responsibilities:
  • Responsible for activities including:
    • Collaborate cross-functionally with both internal and external stakeholders to implement changes which enable continuous improvement, scale-up, and sustaining of existing cGMP manufacturing processes.
    • Coordinate and drive change orders and related efforts to update manufacturing documentation including batch records, item specifications, forms, SOPs, and bills of material for existing processes.
    • Assist with internal projects to develop and optimize process and product Life Cycle Management and ensure robustness, repeatability, and scalability of cGMP operations.
    • Support the execution of process risk assessments, qualification protocols and reports, and other operational activities that increase safety, reduce operation costs, and maintain cGMP compliance.
    • Interact with multi-disciplinary groups and ensure effective communication.
    • Work both independently and collaboratively as part of a team.
 
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: 
Paul Quibuyen     
Christian.Quibuyen@eclaro.com       
6466952942
Paul Quibuyen | 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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