Job Description

Chemical Engineering
Job Number: 21-15176
Be part of a company that delivers life-changing healthcare solutions. Eclaro is looking for a Chemical Engineering for our client in Saint Louis, MO. 
Eclaro’s client is a leader in the Biopharmaceutical Industry, providing quality, innovative, and affordable medicines that make a difference in the lives of patients all over the world. If you’re up to the challenge, then take a chance at this rewarding opportunity!
  • Open to experience from a new graduate to someone with 2-5 years’ experience.
  • Bachelor’s degree in chemical engineering preferred Advanced Excel user preferred SAP experience
Position Overview:
  • The Product Engineering Specialist is responsible for creating and maintaining production records, specifications and MRP systems for the manufacture of Liquid and Dry Powder Cell Culture Media, Serum, and sterile liquids.
  • The role involves working closely with both internal and external customers and stakeholders to ensure successful product manufacture and ongoing maintenance of the relevant production and quality systems.
  • They will perform the integration of new, modified, transferred, and scaled-up products into site manufacturing processes and systems.
  • Products include all catalog and custom Liquid Media, Dry Powder Media, Serum, ImMEDIAte ADVANTAGE, and sterile solutions.
  • They will build Master Batch Records, Process Instruction Sheets, and other manufacturing documents in the required MRP and electronic document systems.
  • They will create and maintain appropriate routings and other MRP aspects to enable product standard costing and inventory control.
  • They will liaise with internal stakeholders and customers to develop new specifications for custom Cell Culture Media, serum, and sterile liquid products.
  • They will provide information to support customer-driven changes to product specification and product attributes for established custom products.
  • They will process change controls to existing specifications and manufacturing documents using MRP and electronic document systems. They will maintain Standard Operating Procedures for the team to ensure all are relevant, up to date, and globally harmonized with other Cell Culture Media sites.
  • They will serve as a technical resource on the site manufacturing and MRP systems.
  • They will provide support for product investigations / out of specification results, etc.
  • They may support Design Engineers on specific complex projects as needed to achieve success and meet delivery commitments.
  • They will provide data entry / reporting support to the Global Design Team.
  • They will collaborate across sites / regions and with the Cell Culture Media Design Program Management function to ensure processes remain harmonized and improvements are employed globally.
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
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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